PKt8 'QD9D9refs.MYD?,Tang, Q. Shi, S. Q. Huang, H. T. Zhou, L. M.2004Fabrication of highly oriented microstructures and nanostructures of ferroelectric P(VDF-TrFE) copolymer via dip-pen nanolithography21-29!Superlattices and Microstructures361-3Jul-Sep>Microstructures and nanostructures of ferroelectric copolymer poly(vinylidene fluoride-trifluorethylene) [P(VDF-TrFE)] are fabricated on gold via dip-pen nanolithography (DPN). The thickness of the patterns is about I nm after a critical concentration, regardless of the pattern scale. The polymer molecules are well orientated according to an all-trans conformation and have ferroelectric properties on the gold surface through electrostatic interaction, rather than the formation of chemical bonds. Increasing temperature has a positive effect on the growth rate of the P(VDF-TrFE). The electrostatic interaction between the P(VDF-TrFE) and the gold substrate and the intramolecular interaction of polymer molecules play important roles in the growth rate of the P(VDF-TrFE) patterns. (C) 2004 Elsevier Ltd. All rights reserved.://000225425100003ISI:000225425100003 file://S:\SALES\_IMPORTANT_STUFF_HERE\Bibliography_Key_Papers\all publications DPN as of 101006 Copy.Data\PDF\2004 Superlattices & Microstructures Tang Fabricatio-0135437391\2004 Superlattices & Microstructures Tang Fabrication of highly oriented microstructures.pdf?/Su, M. Aslam, M. Fu, L. Wu, N. Q. Dravid, V. P.2004ODip-pen nanopatterning of photosensitive conducting polymer using a monomer ink 4200-4202Applied Physics Letters8421May 24Controlled patterning of conducting polymers at a micro- or nanoscale is the first step towards the fabrication of miniaturized functional devices. Here, we introduce an approach for the nanopatterning of conducting polymers using an improved monomer "ink" in dip-pen nanolithography (DPN). The nominal monomer "ink" is converted, in situ, to its conducting solid-state polymeric form after patterned. Proof-of-concept experiments have been performed with acid-promoted polymerization of pyrrole in a less reactive environment (tetrahydrofuran). The ratios of reactants are optimized to give an appropriate rate to match the operation of DPN. A similar synthesis process for the same polymer in its bulk form shows a high conductance and crystalline structure. The miniaturized conducting polymer sensors with light detection ability are fabricated by DPN using the improved ink formula, and exhibit excellent response, recovery, and sensitivity parameters. (C) 2004 American Institute of Physics.://000221404700021ISI:000221404700021 file://S:\SALES\_IMPORTANT_STUFF_HERE\Bibliography_Key_Papers\all publications DPN as of 101006 Copy.Data\PDF\2004 Applied Physics Letters Su DP nanopatterning of p-1022295630\2004 Applied Physics Letters Su DP nanopatterning of photosensitive conducting polymer.pdf ?Lim, J. H. Mirkin, C. A.2002GElectrostatically driven dip-pen nanolithography of conducting polymers1474-+Advanced Materials1420Oct 16Nanoscale conducting polymer patterns have been fabricated on modified semiconductor substrates using dip-pen nanolithography (DPN). Electrostatic interactions between water-soluble ink materials and charged substrates are the driving force for the generation of stable DPN patterns. The conducting polymers have been characterized by lateral force microscopy (see Figure) and electrochemical methods.://000179034200008ISI:0001790342000081002908001Slides.pptinternal-pdf://2002 AdvMats Lim Electrostatically driven DPN Nanolith-1882359593/2002 AdvMats Lim Electrostatically driven DPN Nanolith.pdfG}?NVega, R. A. Shen, C. K. F. Maspoch, D. Robach, J. G. Lamb tan.ac.kriinternal-pdf://2006_ JPCB_Growth Dynamics of SAM_Ahn-3905701633/2006_ JPCB_Growth Dynamics of SAM_Ahn.pdf s f.ac.ukiinternal-pdf://2006_NL_Fabrication of Biological_Sun-3704538881/2006_NL_Fabrication of Biological_Sun.pdf qic.dtu.dkeinternal-pdf://2005_Fabrication_Biomolecular_Dufva-0913139210/2005_Fabrication_Biomolecular_Dufva.pdf 8Lstrate Interactions59-74 Annals of Biomedical Engineering341internal-pdf://2006_ABE_Sniadecki_Nanotech for cell substrate interactions- 14853 USA.internal-pdf://2005 Biomacromolecules Senaratne Self-assembled monolayers & polymer brushes-4238888971/2005 Biomacromolecules Senaratne Self-assembled monolayers & polymer brushes.pdf hydrogen-passivated silicon with conductive-diamond-coated probes 2053-2056Small312Dec://000251697100012 1613-6810ISI:000251697100012 9ive_Kidambi-3868341765/2008_Tunable resistive_Kidambi.pdf %o,rnal-pdf://2007_Power of the pen_Mirk0F~? Striolo, A.2006GAdsorption of model surfactantlike copolymers on nanopatterned surfacesJournal of Chemical Physics1259SELF-ASSEMBLED MONOLAYERS; TRANSFER RADICAL POLYMERIZATION; DIP-PEN NANOLITHOGRAPHY; POLY(ETHYLENE OXIDE); MOLECULAR-DYNAMICS; GRADUAL VARIATION; NANOMETER-SCALE; BRUSHES; GOLD; PARTICLESArticleSepThe adsorption of polymers, copolymers, surfactants, and biopolymers is often used to engineer surfaces. Towards improving our understanding of polymer adsorption we report simulation results for the adsorption of model copolymers, resembling surfactants, on nanoscale patterned hydrophobic surfaces at infinitely dilute concentrations. The surfactants are composed by a hydrophobic tail and a hydrophilic head. Surfactant adsorption on the hydrophobic surface occurs in the tail-down configuration in which the tail segments are in contact with the surface. We investigate how the presence of a solid hard mask, used to create the nanoscale pattern on the underlying hydrophobic surface, affects the surfactant adsorption. We find that surfactant adsorption on the underlying hydrophobic surface is prevented when the characteristic dimensions of the solid hard mask are less than twice the radius of gyration. We also show that details about mask-surfactant head effective interactions have the potential to alter the characteristics of adsorption. When the mask repels the head segments, the surfactants hardly adsorb on the underlying hydrophobic surface. When the mask strongly attracts the surfactant heads, the surfactants may preferentially adsorb on the mask rather than on the underlying hydrophobic surface. Under these latter circumstances the adsorbed surfactants in some cases assume a head-down configuration in which the head segments are in contact with the mask and the tail segments extend towards the bulk solution. We explain our results in terms of enthalpy and entropy of adsorption and discuss practical implications. (c) 2006 American Institute of Physics.://000240351500045 Times Cited: 0 Cited References: ABBOTT NL, 1992, SCIENCE, V257, P1380 AUGUSTE DT, 2003, BBA-BIOMEMBRANES, V1616, P184 BERGGREN KK, 1995, SCIENCE, V269, P1255 BOYES SG, 2002, MACROMOLECULES, V35, P4960 BRANTLEY EL, 2004, MACROMOLECULES, V37, P1476 CEPAK VM, 1999, CHEM MATER, V11, P1363 CHABINYC ML, 2002, APPL PHYS LETT, V81, P4260 CHAKRABORTY AK, 1991, MACROMOLECULES, V24, P5226 CHAKRABORTY AK, 1996, MRS BULL, V21, P28 CHAKRABORTY AK, 1998, J CHEM PHYS, V108, P1676 CHEN XY, 2004, LANGMUIR, V20, P587 CHUN KY, 2003, J CHEM PHYS, V118, P3252 DAUNTENHAHN J, 1994, MACROMOLECULES, V27, P5399 DENIS FA, 2002, LANGMUIR, V18, P819 DOUGLAS JF, 1989, MACROMOLECULES, V22, P3707 FAN FQ, 2004, LANGMUIR, V20, P3062 GAREL T, 1990, J PHYS A-MATH GEN, V23, L621 GENZER J, 2001, J CHEM PHYS, V115, P4873 GRANVILLE AM, 2004, MACROMOLECULES, V37, P2790 GUTOWSKI WS, 2003, J ADHESION, V79, P445 HANSEN JP, 1986, THEORY SIMPLE LIQUID HARWELL JH, 1993, ADSORPTION MIXED SUR HESTER JF, 2002, J MEMBRANE SCI, V202, P119 HIGGS PG, 1991, J CHEM PHYS, V95, P4506 HUANG YW, 2001, MACROMOLECULES, V34, P3757 HUANG YW, 2002, LANGMUIR, V18, P2280 HUANG YW, 2003, LANGMUIR, V19, P2175 HUANG YW, 2004, J CHEM PHYS, V121, P2264 HUSEMANN M, 1998, ANGEW CHEM INT EDIT, V37, P550 JENNINGS GK, 2003, J AM CHEM SOC, V125, P2950 JORDAN R, 2001, MACROMOLECULES, V34, P1606 KUMAR A, 1992, J AM CHEM SOC, V114, P9188 LAHANN J, 2003, SCIENCE, V299, P371 LEMEINS JF, 2003, COLLOID POLYM SCI, V281, P283 LIN GY, 1994, LANGMUIR, V10, P367 LIU H, 1999, POLYMER, V40, P7285 LIU XG, 2003, ANGEW CHEM INT EDIT, V42, P4785 LU Y, 2005, NANO LETT, V5, P5 MARQUEZ M, IN PRESS LANGMUIR MULLER WT, 1995, SCIENCE, V268, P272 NORDE I, 1995, SURFACE INTERFACIAL PALLANDRE A, 2005, J AM CHEM SOC, V127, P4320 PINER RD, 1999, SCIENCE, V283, P661 QIN SH, 2004, J AM CHEM SOC, V126, P170 SCHMELMER U, 2003, ANGEW CHEM INT EDIT, V42, P559 STRIOLO A, 2001, FLUID PHASE EQUILIBR, V183, P341 STRIOLO A, 2001, J CHEM PHYS, V114, P8565 STRIOLO A, 2004, MOL SIMULAT, V30, P437 STRIOLO A, 2005, J CHEM PHYS, V123 SUN KY, 2004, BIOMATERIALS, V25, P557 SUN TL, 2004, ANGEW CHEM INT EDIT, V43, P357 SUNG WY, 2005, PHYS REV E 1, V71 TARLOV MJ, 1993, J AM CHEM SOC, V115, P5305 TOMLINSON MR, 2003, MACROMOLECULES, V36, P3449 TUMMALA NR, UNPUB WANG JY, 1994, LANGMUIR, V10, P626 WEI X, 2003, J COLLOID INTERF SCI, V264, P296 WILSON DL, 2001, P NATL ACAD SCI USA, V98, P13660 WU T, 2003, MACROMOLECULES, V36, P2448 XIA TK, 1993, SCIENCE, V261, P1310 XIA YN, 1995, J AM CHEM SOC, V117, P3274 XU S, 1999, LANGMUIR, V15, P7244 ZAJAC R, 1997, J CHEM PHYS, V107, P8637 ZHOU F, 2003, ADV FUNCT MATER, V13, P938ISI:000240351500045Univ Oklahoma, Sch Chem Biol & Mat Engn, Sarkeys Energy Ctr T235, Norman, OK 73019 USA. Striolo, A, Univ Oklahoma, Sch Chem Biol & Mat Engn, Sarkeys Energy Ctr T235, Norman, OK 73019 USA. astriolo@ou.edu094709 Artn 094709internal-pdf://2006 JoChemPhys Striolo Adsorption of model surfactantlike-1686979087/2006 JoChemPhys Striolo Adsorption of model surfactantlike.pdf notechnology for Cell-Sub ~?]Slocik, J. M. Beckel, E. R. Jiang, H. Enlow, J. O. Zabinski, J. S. Bunning, T. J. Naik, R. R.2006Site-speciric patterning of biomolecules and quantum dots on functionalized surfaces generated by plasma-enhanced chemical vapor deposition2095-+Advanced Materials1816SELF-ASSEMBLED MONOLAYERS; DIP-PEN NANOLITHOGRAPHY; AQUEOUS-SOLUTION; THIN-FILMS; PROTEIN; NANOPARTICLES; SILICON; DNA; NANOSTRUCTURES; LITHOGRAPHYArticleAugPlasma-enhanced chemical vapor patterned surfaces are used for site-specific attachment of biomolecules and semiconductor quantum dots (QDs; see figure). The fabrication of surfaces with multiple functional building blocks can be used in a single step to create complex multifunctional patterned substrates incorporating self-assembled monolayers (SAMs) and thiol-functionalized quantum dots for a variety of applications.://000240408600002 Times Cited: 0 Cited References: AGARWAL G, 2003, J AM CHEM SOC, V125, P580 AGARWAL G, 2003, J AM CHEM SOC, V125, P7408 AHN SJ, 2005, J AM CERAM SOC, V88, P1171 BERGMAN AA, 1998, LANGMUIR, V14, P6785 BHATNAGAR P, 2006, ADV MATER, V18, P315 CALDERON JG, 1998, J BIOMED MATER RES, V42, P2541 CARUSO F, 2000, LANGMUIR, V16, P9595 DAW R, 1998, BIOMATERIALS, V19, P1717 DYAL A, 2003, J AM CHEM SOC, V34, P1684 FAVIA P, 2003, SURF COAT TECH, V169, P707 FUNG YS, 2001, ANAL CHEM, V73, P5302 GRANT JT, 2005, VACUUM, V80, P12 HAES AJ, 2002, J AM CHEM SOC, V124, P10596 HOLDCROFT S, 2001, ADV MATER, V13, P1753 INEROWICZ HD, 2002, LANGMUIR, V18, P5263 JIANG H, 2004, CHEM MATER, V16, P1292 JUNG D, 2006, SURF COAT TECH, V200, P2886 KAHANA J, 1996, CURRENT PROTOCOLS MO KANE RS, 1999, BIOMATERIALS, V20, P2363 LEE KB, 2003, J AM CHEM SOC, V125, P5588 LEE SH, 2005, SENSOR ACTUAT B-CHEM, V110, P164 LEI CH, 2002, J AM CHEM SOC, V124, P11242 LENIGK R, 2001, LANGMUIR, V17, P2497 LIU MZ, 2002, NANO LETTERS, V2, P863 LOOS K, 2005, LANGMUIR, V21, P5237 MASUDA Y, 2003, CHEM MATER, V15, P2469 NILSSON S, 1995, ANAL CHEM, V67, P3051 SHAPLEY JDL, 2001, THIN SOLID FILMS, V388, P134 SMITH K, 2002, J AM CHEM SOC, V124, P4247 VEISEH M, 2002, LANGMUIR, V18, P6671 VOGT AK, 2003, BIOTECHNOL PROGR, V19, P1562 WADUMESTHRIGE K, 1999, LANGMUIR, V15, P8580 WALBA DM, 2004, LIQ CRYST, V31, P481 WANG C, 2005, ADV MATER, V17, P150 XU H, 2006, J AM CHEM SOC, V128, P3162 ZELIKIN AN, 2006, BIOMACROMOLECULES, V7, P27 ZHANG G, 2005, SMALL, V8, P833 ZHENG HP, 2004, LANGMUIR, V20, P7215ISI:000240408600002USAF, Res Lab, Mat & Mfg Directorate, Dayton, OH 45433 USA. Anteon Corp, Dayton, OH 45431 USA. Naik, RR, USAF, Res Lab, Mat & Mfg Directorate, Dayton, OH 45433 USA. rajesh.naik@wpafb.af.milinternal-pdf://2006 Advanced Materials Slocik Site-specific pat-1418782991/2006 Advanced Materials Slocik Site-specific patterning of biomolecules & quantum dots.pdfCK(?1Sniadecki, N.J. Desai, R.A. Ruiz, S.A. Chen, C.S.2006.Na/8~; HChandekar, A. Sengupta, S. K. Barry, C. M. F. Mead, J. L. Whitten, J. E.2006WTemplate-directed adsorption of block copolymers on alkanethiol-patterned gold surfaces 8071-8077Langmuir2219SELF-ASSEMBLED MONOLAYERS; ATOMIC-FORCE MICROSCOPE; NANOIMPRINT LITHOGRAPHY; POLYMERS; FILMS; WETTABILITY; ADHESION; DENSITY; DOMAINS; MOLDArticleSepFunctionalized alkanethiols have been self-assembled on gold to modify the wetting properties of the surface and promote or hinder the adsorption of block copolymers containing both hydrophobic and hydrophilic blocks. X-ray photoelectron spectroscopy (XPS) studies of spin-coated polyethylene-block-poly(ethylene oxide) (PE-b-PEO) copolymers on 16-mercaptohexadecanoic acid (MHDA)-, octadecanethiol (ODT)-, and 1H,1H,2H,2H-perfluorodecanethiol (PFDT)-covered surfaces have been performed. In the case of an 80 wt% PEO block copolymer, spin-coating on a gold surface precovered with MHDA results in a polymer film thick enough to completely attenuate Au 4f photoelectrons; spin-coating on the more hydrophobic ODT and PFDT monolayers leads to significantly thinner polymer films and incomplete attenuation of the gold photoelectrons. The opposite results are observed when a 20 wt % PEO block copolymer is used. Angle-resolved XPS studies of the 80 wt % PEO block copolymer spin-coated onto an MHDA-covered surface indicate that the PE blocks of the polymer segregate to the near-surface region, oriented away from the hydrophilic carboxylic acid tails of the monolayers; the surface concentration of PE is further enhanced by annealing at 90 degrees C. Microcontact printing and dip-pen nanolithography have been used to pattern gold surfaces with MHDA, and the surfaces have been backfilled with ODT or PFDT, such that the unpatterned regions of the surface are covered with hydrophobic monolayers. In the case of backfilling with PFDT, spin-coating the 80 wt% PEO copolymer onto these patterned surfaces and subsequent annealing results in the block copolymer preferentially adsorbing on the MHDA-covered regions and forming well-defined patterns that mimic the MHDA pattern, as determined by scanning electron microscopy and atomic force microscopy. Significantly worse patterning, characterized by micron-sized polymer droplets, results when the surface is backfilled with ODT instead of PFDT. Using PFDT and MHDA, polymer features having widths as small as 500 nm have been formed. These studies demonstrate a novel method to pattern block copolymers with nanoscale resolution.://000240250600021 Times Cited: 0 Cited References: AGUILAR CA, 2005, BIOMATERIALS, V26, P7642 BAIN CD, 1989, J AM CHEM SOC, V111, P321 BEHL M, 2002, ADV MATER, V14, P588 CHILDS WR, 2002, J AM CHEM SOC, V124, P13583 COLORADO R, 2000, J PHYS ORG CHEM, V13, P796 DECKER EL, 1997, LANGMUIR, V13, P6321 EDWARDS EW, 2004, ADV MATER, V16, P1315 EDWARDS EW, 2005, J POLYM SCI POL PHYS, V43, P3444 FUKUSHIMA H, 2000, J PHYS CHEM B, V104, P7417 GARBASSI F, 1994, POLYM SURFACES, P327 HAWKER CJ, 2005, MRS BULL, V30, P952 HOUSTON JE, 2005, LANGMUIR, V21, P3926 JEGADESAN S, 2006, LANGMUIR, V22, P780 KIM YS, 2005, CHEM MATER, V17, P5867 KISS E, 1996, LANGMUIR, V12, P1651 LAIBINIS PE, 1991, J AM CHEM SOC, V113, P7152 LYUKSYUTOV SF, 2003, APPL PHYS LETT, V83, P4405 MAMIN HJ, 1992, APPL PHYS LETT, V61, P1003 MAURY P, 2005, ADV MATER, V17, P2718 MCCLELLAND GM, 2002, APPL PHYS LETT, V81, P1483 MEYER E, 2000, MACROMOL MATER ENG, V276, P44 MIURA YF, 1998, LANGMUIR, V14, P5821 PARK JS, 2005, LANGMUIR, V21, P2902 SEAH MP, 1979, SURFACE INTERFACE AN, V1, P2 STOYKOVICH MP, 2005, SCIENCE, V308, P1442 SUNDRANI D, 2004, NANO LETT, V4, P273 TOKUHISA H, 2004, LANGMUIR, V20, P1436 VANDEGRAMPEL RD, 2004, LANGMUIR, V20, P145 WAGNER AJ, 2002, LANGMUIR, V18, P1542 WANG H, 2005, LANGMUIR, V21, P2633 WANG MS, 2004, LANGMUIR, V20, P7753 WANG Y, 2005, J PHYS CHEM B, V109, P12376 WATTS JF, 2003, INTRO SURFACE ANAL X, P80 WILBUR JL, 1994, ADV MATER, V6, P600 XIA YN, 1997, ADV MATER, V9, P147 XIANG HQ, 2004, MACROMOLECULES, V37, P5358 YIN YD, 2003, J AM CHEM SOC, V125, P2048ISI:000240250600021Univ Massachusetts, Dept Chem, Lowell, MA 01854 USA. Univ Massachusetts, Ctr High Rate Nanomfg, Lowell, MA 01854 USA. Univ Massachusetts, Dept Plast Engn, Lowell, MA 01854 USA. Whitten, JE, Univ Massachusetts, Dept Chem, 1 Univ Ave, Lowell, MA 01854 USA. James_Whitten@uml.edu2625313603d Block Copolymer.ppt <~? 8Gao, H. Gosvami, N. N. Deng, J. Tan, L. S. Sander, M. S.2006UTemplate-assisted patterning of nanoscale self-assembled monolayer arrays on surfaces 8078-8082Langmuir2219DIP-PEN NANOLITHOGRAPHY; ANODIC ALUMINA FILMS; SOFT LITHOGRAPHY; ALIGNED ARRAYS; FABRICATION; OXIDE; NANOFABRICATION; NANOSTRUCTURES; NANOTUBES; SILVERArticleSepWe report a general, simple, and inexpensive approach to pattern features of self-assembled monolayers (SAMs) on silicon and gold surfaces using porous anodic alumina films as templates. The SAM patterns, with feature sizes down to 30 nm and densities higher than 10(10)/cm(2), can be prepared over large areas (> 5 cm(2)). The feature dimensions can be tuned by controlling the alumina template structure. These SAM patterns have been successfully used as resists for fabricating gold and silicon nanoparticle arrays on substrates by wet-chemical etching. In addition, we show that arrays of gold features can be patterned with 10-nm gaps between the dots.://000240250600022 Times Cited: 0 Cited References: AIZENBERG J, 2003, SCIENCE, V299, P1205 CAI AL, 2002, NANOTECHNOLOGY, V13, P627 CHENG GS, 2002, ADV MATER, V14, P1567 CHU SZ, 2002, ADV MATER, V14, P1752 COJOCARU CS, 2005, NANO LETT, V5, P675 DANIEL MC, 2004, CHEM REV, V104, P293 FELIDJ N, 2002, PHYS REV B, P65 FINNIE KR, 2001, LANGMUIR, V17, P1250 GAO H, 2003, J APPL PHYS, V93, P5602 GATES BD, 2005, CHEM REV, V105, P1171 GEISSLER M, 2004, ADV MATER, V16, P1249 GOLZHAUSER A, 2001, ADV MATER, V13, P806 HE L, 2000, J AM CHEM SOC, V122, P9071 KOVTYUKHOVA NI, 2003, ADV MATER, V15, P780 LEE KB, 2002, SCIENCE, V295, P1702 LEI Y, 2005, J AM CHEM SOC, V127, P1487 LI AP, 1998, J APPL PHYS, V84, P6023 LI FY, 1998, CHEM MATER, V10, P2470 LIU GY, 2000, ACCOUNTS CHEM RES, V33, P457 LOVE JC, 2005, CHEM REV, V105, P1103 LU N, 2002, ADV MATER, V14, P1812 MAOZ R, 2000, ADV MATER, V12, P424 MARTIN CR, 1994, SCIENCE, V266, P1961 MASUDA H, 1995, SCIENCE, V268, P1466 MASUDA H, 2001, ADV MATER, V13, P247 MAURY P, 2005, ADV FUNCT MATER, V15, P451 MCLELLAN JM, 2004, J AM CHEM SOC, V126, P10830 ODOM TW, 2002, LANGMUIR, V18, P5314 PALLANDRE A, 2004, NANO LETT, V4, P365 PINER RD, 1999, SCIENCE, V283, P661 PORTER LA, 2002, NANO LETT, V2, P1369 PRIME KL, 1991, SCIENCE, V252, P1164 RABIN O, 2003, ADV FUNCT MATER, V13, P631 SALAITA K, 2005, SMALL, V1, P940 SANDER MS, 2003, ADV FUNCT MATER, V13, P393 SANDER MS, 2004, ADV MATER, V16, P2052 SANDER MS, 2005, J AM CHEM SOC, V127, P12158 SCHMID H, 2000, MACROMOLECULES, V33, P3042 SMITH RK, 2004, PROG SURF SCI, V75, P1 STAMOU D, 2004, LANGMUIR, V20, P3495 SUN SQ, 2002, NANO LETT, V2, P1223 TARLOV MJ, 1993, J AM CHEM SOC, V115, P5305 TIAN ML, 2005, NANO LETT, V5, P697 WANG H, 2005, J AM CHEM SOC, V127, P14992 WEINBERGER DA, 2000, ADV MATER, V12, P1600 ZHANG H, 2003, NANO LETT, V3, P43ISI:000240250600022Inst Mat Res & Engn, Singapore 117602, Singapore. Gao, H, Inst Mat Res & Engn, Singapore 117602, Singapore. h-gao@imre.a-star.edu.sg{internal-pdf://2006_Langmuir_Template-assisted patterning_Gao-1489457679/2006_Langmuir_Template-assisted patterning_Gao.pdfPc26441259\2006 Langmuir Gao Template -assisted patterning.pdf ~? )Downard, A. J. Tan, E. S. Q. Yu, S. S. C.2006<Controlled assembly of gold nanoparticles on carbon surfaces 1283-1288New Journal of Chemistry309DIP-PEN NANOLITHOGRAPHY; GLASSY-CARBON; ELECTROCHEMICAL OXIDATION; MERCURY-ELECTRODES; PROTEIN ADSORPTION; SILICON SURFACES; FIBER SURFACES; MONOLAYERS; FILMS; IMMOBILIZATIONArticleCitrate-capped gold nanoparticles are electrostatically assembled on amine films attached to carbon surfaces. Primary amines are covalently grafted to carbon surfaces by an electrochemically-assisted method which gives easy control of the number of amine functionalities on the surface, and hence the density of the nanoparticle assembly. Further control of nanoparticle assemblies can be gained by choice of the amine modifier, and by adjusting the nanoparticle concentration, assembly time and pH of the nanoparticle solution. This simple and versatile approach for preparation of tethered nanoparticle assemblies should be compatible with any conducting carbon substrate, giving new materials for applications ranging from catalysis to sensing.://000240109100005 bTimes Cited: 0 Cited References: ADENIER A, 2004, LANGMUIR, V20, P8243 ANTONIADOU S, 1992, J APPL ELECTROCHEM, V22, P1060 BARBIER B, 1990, J ELECTROCHEM SOC, V137, P1757 BECKA AM, 1993, J PHYS CHEM-US, V97, P6233 BROOKSBY PA, 2004, LANGMUIR, V20, P5038 BROOKSBY PA, 2005, LANGMUIR, V21, P11304 BRUST M, 2002, COLLOID SURFACE A, V202, P175 BUTTRY DA, 1999, CARBON, V37, P1929 CHAN EWL, 2002, LANGMUIR, V18, P311 COULON E, 2001, LANGMUIR, V17, P7102 COULON E, 2002, J ORG CHEM, V67, P8513 DANIEL MC, 2004, CHEM REV, V104, P293 DEINHAMMER RS, 1994, LANGMUIR, V10, P1306 DEMERS LM, 2001, ANGEW CHEM INT EDIT, V40, P3071 DEMERS LM, 2002, SCIENCE, V296, P1836 DOWNARD AJ, 1999, ELECTROANAL, V11, P418 DOWNARD AJ, 2000, ELECTROANAL, V12, P1085 DOWNARD AJ, 2005, AUST J CHEM, V58, P275 FRENCH M, 1998, LANGMUIR, V14, P2129 GENESTE F, 2005, NEW J CHEM, V29, P269 GRABAR KC, 1995, ANAL CHEM, V67, P735 GRABAR KC, 1996, J AM CHEM SOC, V118, P1148 HAN XJ, 2003, ANAL CHEM, V75, P6566 HARNISCH JA, 2001, J AM CHEM SOC, V123, P5829 HAYES MA, 1999, ANAL CHEM, V71, P1720 HOEKSTRA KJ, 1996, CHEM MATER, V8, P1865 HUANG XH, 2000, SURF SCI, V459, P183 KOSTECKI R, 2001, THIN SOLID FILMS, V396, P36 LIU JY, 2000, ELECTROCHEM COMMUN, V2, P707 LIU ST, 2002, PHYS CHEM CHEM PHYS, V4, P6059 LIU ST, 2004, NANO LETT, V4, P845 MAYA L, 2002, LANGMUIR, V18, P2392 MENDES PM, 2004, LANGMUIR, V20, P3766 RANGANATHAN S, 2001, ANAL CHEM, V73, P893 SAUNDERS KH, 1985, AROMATIC DIAZO COMPO SEITZ O, 2003, COLLOID SURFACE A, V218, P225 SLOWINSKI K, 1997, J AM CHEM SOC, V119, P11910 SLOWINSKI K, 1999, J PHYS CHEM B, V103, P8544 TANAKA H, 1997, J ELECTROANAL CHEM, V437, P29 TIEN J, 1997, LANGMUIR, V13, P5349 TOGNARELLI DJ, 2005, LANGMUIR, V21, P11119 WANG J, 1998, THIN SOLID FILMS, V327, P591 YAMANOI Y, 2004, LANGMUIR, V20, P1054 ZANELLA R, 2005, J PHYS CHEM B, V109, P16290 ZHANG H, 2002, ADV MATER, V14, P1472 ZHU T, 1999, LANGMUIR, V15, P5197ISI:000240109100005Univ Canterbury, Dept Chem, MacDiarmid Inst Adv Mat & Nanotechnol, Christchurch 1, New Zealand. Downard, AJ, Univ Canterbury, Dept Chem, MacDiarmid Inst Adv Mat & Nanotechnol, Private Bag 4800, Christchurch 1, New Zealand. alison.downard@canterbury.ac.nzinternal-pdf://2006 New Jo of Chem Downard Controlled Assembly of A-1774937615/2006 New Jo of Chem Downard Controlled Assembly of AU nanoparticles on carbon surf.pdf<Ttrolled assembly of au nanoparticles.pdf~? Zhou, D. J. Kang, D. J.2005iCreating functional nanostructured materials at the crossroad of physics, chemistry and materials Science440-468'International Journal of Nanotechnology24Bnanostructure; self-assembled monolayer; layer-by-layer assembly; soft lithography; nanopipet delivery RESONANCE ENERGY-TRANSFER; DIP-PEN NANOLITHOGRAPHY; SELF-ASSEMBLED MONOLAYERS; ATOMIC-FORCE MICROSCOPY; QUANTUM DOTS; HORSERADISH-PEROXIDASE; PROTEIN NANOSTRUCTURES; CONTROLLED DEPOSITION; GOLD NANOPARTICLES; THIN-FILMSReviewControlled assembly and manipulation of three-dimensional (3D) nanostructures with well-defined shapes, profiles and functionalities present a significant challenge to nanotechnology. In this paper we summarise our recent efforts in an attempt to solve this problem by developing a highly selective surface-templated layer-by-layer assembly, where top-down approaches such as soft lithography, focused-ion beam lithography and voltage-controlled nanopipet delivery are combined with bottom-up techniques like self-assembly, molecular recognition and layer-by-layer assembly to controllably deposit and grow 2D to 3D micro/nanostructures with functional materials. This opens up wide applications in highly sensitive biosensors, miniaturised assays, and functional 3D nano-assemblies and devices.://000239797900007 0Times Cited: 0 Cited References: AGARWAL G, 2003, J AM CHEM SOC, V125, P7408 AI H, 2002, BIOMACROMOLECULES, V3, P560 ALBERTI P, 2003, P NATL ACAD SCI USA, V100, P1569 ALIVISATOS AP, 1996, SCIENCE, V271, P933 ALIVISATOS AP, 2004, NAT BIOTECHNOL, V22, P47 BARTLETT PN, 1999, J ELECTROCHEM SOC, V146, P1088 BORNSCHEUER UT, 2003, ANGEW CHEM INT EDIT, V42, P3336 BRUCKBAUER A, 2002, J AM CHEM SOC, V124, P8810 BRUCKBAUER A, 2003, J AM CHEM SOC, V125, P9834 BRUCKBAUER A, 2004, J AM CHEM SOC, V126, P6508 CAMPBELL M, 2000, NATURE, V404, P53 CHAN EWL, 2002, J AM CHEM SOC, V124, P12238 CLAPP AR, 2004, J AM CHEM SOC, V126, P301 CLARK SL, 1997, MACROMOLECULES, V30, P7237 CLARK SL, 1999, ADV MATER, V11, P1031 CRISP MT, 2003, NANO LETT, V3, P173 CUI XQ, 2003, BIOSENS BIOELECTRON, V18, P59 DANIEL MC, 2004, CHEM REV, V104, P293 DAVIS SA, 2003, CURR OPIN SOLID ST M, V7, P273 DECHER G, 1997, SCIENCE, V277, P1232 DELOUISE LA, 2004, ANAL CHEM, V76, P6915 DEMERS LM, 2002, SCIENCE, V296, P1836 DU H, 2003, J AM CHEM SOC, V125, P4012 FAUL CFJ, 2003, ADV MATER, V15, P673 FORSTER T, 1948, ANN PHYSIK, V2, P55 FRANZL T, 2004, NANO LETT, V4, P1599 GEISSLER M, 2004, ADV MATER, V16, P1249 GINGER DS, 2004, ANGEW CHEM INT EDIT, V43, P30 GOLDMAN ER, 2005, J AM CHEM SOC, V127, P6744 GOSLING JP, 1990, CLIN CHEM, V36, P1408 HAMMOND PT, 2004, ADV MATER, V16, P1271 HAN MY, 2001, NAT BIOTECHNOL, V19, P631 HEALEY BG, 1995, SCIENCE, V269, P1078 HENRIKSEN A, 1999, J BIOL CHEM, V274, P35005 HERNE TM, 1997, J AM CHEM SOC, V119, P8916 JAFFAR S, 2004, NANO LETT, V4, P1421 JEON S, 2004, ADV MATER, V16, P1369 JESSEL N, 2003, ADV MATER, V15, P692 JIANG XP, 2001, ADV MATER, V13, P1669 KAWATA S, 2001, NATURE, V412, P697 KIDAMBI S, 2004, J AM CHEM SOC, V126, P4697 KOTOV NA, 1995, J PHYS CHEM-US, V99, P13065 LANG J, 1999, J PHYS CHEM B, V103, P11393 LEE KB, 2003, J AM CHEM SOC, V125, P5588 LI HT, 2004, ANAL CHEM, V76, P4446 LI HW, 2002, NANO LETTERS, V2, P347 LI HW, 2003, LANGMUIR, V19, P1963 LI HW, 2003, NANOTECHNOLOGY, V14, P220 LI JWJ, 2002, NANO LETTERS, V2, P315 LIMOGES B, 2003, J AM CHEM SOC, V125, P9192 LIU DS, 2003, ANGEW CHEM INT EDIT, V42, P5734 LIVNAH O, 1993, P NATL ACAD SCI USA, V90, P5076 MACBEATH G, 2000, SCIENCE, V289, P1760 MAMEDOV AA, 2001, J AM CHEM SOC, V123, P7738 MAMEDOVA NN, 2001, NANO LETTERS, V1, P281 MAO CD, 1999, NATURE, V397, P144 MAO HB, 2002, ANAL CHEM, V74, P379 MATTOUSSI H, 2000, J AM CHEM SOC, V122, P12142 MEDINTZ IL, 2003, NAT MATER, V2, P630 MICHALET X, 2005, SCIENCE, V307, P538 MICHEL B, 2001, IBM J RES DEV, V45, P697 NIEMEYER CM, 2001, ANGEW CHEM INT EDIT, V40, P4128 NIEMEYER CM, 2002, ANGEW CHEM INT EDIT, V41, P3779 OH E, 2005, J AM CHEM SOC, V127, P3270 PEREZLUNA VH, 1999, J AM CHEM SOC, V121, P6469 PEYRATOUT CS, 2004, ANGEW CHEM INT EDIT, V43, P3762 PRIME KL, 1991, SCIENCE, V252, P1164 PUGLIESE L, 1993, J MOL BIOL, V231, P698 RAIMONDI F, 2005, ANGEW CHEM INT EDIT, V44, P2190 RAO SV, 1999, BIOTECHNOL BIOENG, V65, P389 RIEPL M, 2002, LANGMUIR, V18, P7016 ROGACH AL, 2000, CHEM MATER, V12, P1526 ROSI NL, 2005, CHEM REV, V105, P1547 SEEMAN NC, 2003, NATURE, V421, P427 STRYER L, 1967, P NATL ACAD SCI USA, V58, P719 ULMAN A, 1996, CHEM REV, V96, P1533 VIANELLO F, 2000, BIOTECHNOL BIOENG, V68, P488 WAGNER P, 1995, LANGMUIR, V11, P3867 WANG XZ, 2003, CHEM COMMUN, P474 WANG Y, 2003, J AM CHEM SOC, V125, P2830 WEISS S, 1999, SCIENCE, V283, P1676 WHITESIDES GM, 1991, SCIENCE, V254, P1312 WHITESIDES GM, 2001, ANNU REV BIOMED ENG, V3, P335 WHITESIDES GM, 2002, SCIENCE, V295, P2418 WILSON DL, 2001, P NATL ACAD SCI USA, V98, P13660 WILSON DS, 2003, ANGEW CHEM INT EDIT, V42, P494 WU YM, 1998, ENZYME MICROB TECH, V22, P315 WUISTER SF, 2003, NANO LETT, V3, P503 XIA YN, 1999, CHEM REV, V99, P1823 YING LM, 2002, ANAL CHEM, V74, P1380 YING LM, 2003, P NATL ACAD SCI USA, V100, P14629 YING LM, 2005, PHYS CHEM CHEM PHYS, V7, P2859 YURKE B, 2000, NATURE, V406, P605 ZHOU D, 2003, NANO LETT, V3, P1517 ZHOU DJ, 2002, LANGMUIR, V18, P8278 ZHOU DJ, 2003, ANGEW CHEM INT EDIT, V42, P4934 ZHOU DJ, 2003, LANGMUIR, V19, P10557 ZHOU DJ, 2004, LANGMUIR, V20, P9089 ZHOU DJ, 2005, ADV MATER, V17, P1243 ZHOU DJ, 2005, CHEM COMMUN, P4807ISI:000239797900007_Univ Cambridge, Nanosci Ctr, Cambridge CB3 0FF, England. Sungkyunkwan Univ, Dept Phys, Suwon 440746, South Korea. Sungkyunkwan Univ, Sungkyunkwan Adv Inst Nanotechnol, Inst Basic Sci, Ctr Nanotubes & Nanostruct Composites, Suwon 440746, South Korea. Kang, DJ, Univ Cambridge, Nanosci Ctr, 11 JJ Thomson Ave, Cambridge CB3 0FF, England. djkang@skku.edu file://S:\SALES\_IMPORTANT_STUFF_HERE\Bibliography_Key_Papers\all publications DPN as of 101006 Copy.Data\PDF\2005 Intl JoNanotechnology Zhou Creating Functional Nanostructed M-1803519326\2005 Intl JoNanotechnology Zhou Creating Functional Nanostructed Materials.pdf~? Ahmad, F. Shin, K.2006NDendrimers at the air-water interface: surface dynamics and molecular ordering353-371'International Journal of Nanotechnology32-3dendrimers; air-water interface; monolayers; interfacial properties; isotherms DIP-PEN NANOLITHOGRAPHY; DENDRITIC MACROMOLECULES; THIN-FILMS; LANGMUIR-BLODGETT; BLOCK-COPOLYMERS; AMPHIPHILIC DENDRIMERS; TERMINATED DENDRIMERS; ELECTRICAL-PROPERTIES; POLYETHER DENDRIMERS; MONOLAYERSArticleIn recent years considerable effort has been devoted to the fabrication of molecular devices by exploiting ultra thin organic films. Our attention has been focused on dendrimers, one of the most promising candidates for use in preparing highly functionalised devices due to their flexible architecture and unique properties. Thin films of dendrimers provide better control over the inter-distance and the density of the functional groups. In order to generate highly ordered ultra thin films of dendrimers, a prior understanding of their molecular behaviour is required. This review highlights recent investigations and the contribution of Korean researchers to the study of the molecular behaviour and dynamics of dendrimers at interfaces. Here we emphasise the importance of phase isotherms (air-water interface) in understanding the molecular behaviour, molecular interactions, and molecular assembly, together with factors that permit the molecular behaviour to be tuned and controlled.://000239892500012 Times Cited: 0 Cited References: ADRONOV A, 2000, CHEM COMMUN, P1701 AKIMOTO Y, 2000, CHEM PHYS LETT, V326, P383 ALBRECHT TT, 2000, SCIENCE, V290, P2126 BEILINSKA A, 1996, NUCLEIC ACIDS RES, V24, P2176 CALVERT P, 2001, CHEM MATER, V13, P3299 CARDULLO F, 1998, LANGMUIR, V14, P1955 FAIL CA, 2002, LANGMUIR, V18, P264 FELDER D, 2000, ANGEW CHEM INT EDIT, V39, P201 FRECHET JM, 1994, SCIENCE, V263, P1711 FRECHET JMJ, 1999, CHEM MATER, V11, P1267 GRAYSON SK, 2001, CHEM REV, V101, P3819 GRAYSON SK, 2001, CHEM REV, V101, P3819 HAIM AB, 1997, J AM CHEM SOC, V119, P6197 HARKINS WD, 1952, PHYS CHEM SURFACE FI HAWKER CJ, 1990, J AM CHEM SOC, V112, P7638 HIRANO C, 2005, LANGMUIR, V21, P272 HONG BJ, 2003, LANGMUIR, V19, P2357 HUANG E, 1998, NATURE, V395, P755 HYUN J, 2004, J AM CHEM SOC, V126, P7330 JEONG UY, 2002, ADV MATER, V14, P274 JONAS U, 1995, CHEM-EUR J, V1, P243 JUNG SB, 2003, SYNTHETIC MET 1, V135, P75 JUNG SB, 2003, THIN SOLID FILMS, V438, P27 KAMPF JP, 1999, LANGMUIR, V15, P227 KANG JS, 2004, MAT SCI ENG C-BIO S, V24, P281 KANG SZ, 2003, CHEM PHYS LETT, V370, P542 KHOPADE AJ, 2002, NANO LETTERS, V2, P415 KIM H, 2004, BIOMACROMOLECULES, V5, P822 KIM SO, 2003, NATURE, V424, P411 KIRTON GF, 1998, PHYSICA B, V248, P184 KNAPEN JWJ, 1994, NATURE, V372, P659 LANGMUIR I, 1917, J AM CHEM SOC, V39, P1848 LIU YL, 1997, J AM CHEM SOC, V119, P8720 MANSFIELD ML, 1993, MACROMOLECULES, V26, P4262 MANSFIELD ML, 1996, POLYMER, V37, P3835 MATSUI J, 2004, J AM CHEM SOC, V126, P3708 MCKENDRY R, 2002, NANO LETTERS, V2, P713 MOUREY TH, 1992, MACROMOLECULES, V25, P2401 NEWKOME GR, 1985, J ORG CHEM, V50, P2003 NEWKOME GR, 1986, DENDRITIC MOL CONCEP NIERENGARTEN JF, 2001, J AM CHEM SOC, V123, P9743 NIU SJ, 2003, MACROMOLECULES, V36, P2428 NIWA D, 2004, J PHYS CHEM B, V108, P3240 PAO WJ, 2001, PHYS CHEM B, V105, P2170 PARK C, 2001, MACROMOLECULES, V34, P2602 PARK M, 1997, SCIENCE, V276, P1401 PORTER LA, 2002, NANO LETT, V2, P1369 RAYLEIGH L, 1890, P ROY SOC LOND A MAT, V48, P127 REICHMANIS E, 1999, ACCOUNTS CHEM RES, V32, P659 RICHTEREGGER DL, 2001, ANAL CHEM, V73, P5743 ROBERTS G, 1990, LANGMUIR BLODGETT FI SAVILLE PM, 1993, J PHYS CHEM-US, V97, P293 SAVILLE PM, 1995, J PHYS CHEM-US, V99, P8283 SCHENNING APHJ, 1998, J AM CHEM SOC, V120, P8199 SEO YS, 2002, LANGMUIR, V18, P5927 SEO YS, 2004, NANO LETT, V4, P483 SEYREK E, 2004, J PHYS CHEM B, V108, P10168 SHIN K, 2001, LANGMUIR, V17, P4955 SIDORENKO A, 2000, LANGMUIR, V16, P10569 SOHN BH, 2001, J AM CHEM SOC, V123, P12734 SWEET YS, 1997, J CHEM MAT, V7, P1199 TANAKA K, 2003, LANGMUIR, V19, P1196 TOMALIA DA, 1985, POLYM J, V17, P117 TOMALIA DA, 1994, 5728461, US TSUKRUK VV, 1998, ADV MATER, V10, P253 TULLY DC, 2001, CHEM COMMUN, P1229 WALLRAFF GM, 1999, CHEM REV, V99, P1801 WARD M, 2000, ANNU REP PROG CHEM A, V96, P354 WEENER JW, 2000, ADV MATER, V12, P1001 WELLS M, 1996, J AM CHEM SOC, V118, P3988 XU G, 2002, LANGMUIR, V16, P1834 YANG XM, 2000, MACROMOLECULES, V33, P9575 YOON DK, 2003, LANGMUIR, V19, P1154 YOON HC, 2000, ANAL CHEM, V72, P922 ZENG FW, 1997, CHEM REV, V97, P1681 ZHANG L, 2000, LANGMUIR, V16, P3813 ZIMMERMAN SC, 1996, SCIENCE, V271, P1095ISI:000239892500012Gwangju Inst Sci & Technol, Dept Mat Sci & Engn, Kwangju 500712, South Korea. Shin, K, Gwangju Inst Sci & Technol, Dept Mat Sci & Engn, Kwangju 500712, South Korea. kwshin@gist.ac.krinternal-pdf://2006 Intl Journal of Nanotech. Ahmad Dendrimers at the air-w-1003355663/2006 Intl Journal of Nanotech. Ahmad Dendrimers at the air-water interface.pdfXcxournal of Nanotech. Ahmad Dendrimers at the air-water interface.pdf d~?:Jung, J. M. Kwon, K. Y. Ha, T. H. Chung, B. H. Jung, H. T.2006lGold-conjugated protein nanoarrays through block-copolymer lithography: From fabrication to biosensor design 1010-1015Small28-9biosensors; block copolymers; lithography; nanoparticles; proteins SELF-ASSEMBLED MONOLAYERS; SURFACE-PLASMON RESONANCE; DIP-PEN NANOLITHOGRAPHY; CHEMISTRY; ARRAYS; CENTIMETER; SCALEArticleAug://000239717500012 Times Cited: 0 Cited References: ARNOLD M, 2004, CHEMPHYSCHEM, V5, P383 BES L, 2003, MACROMOLECULES, V36, P2493 BOCKSTALLER MR, 2005, ADV MATER, V17, P1331 BRUCKBAUER A, 2004, J AM CHEM SOC, V126, P6508 CHOI DG, 2004, NANOTECHNOLOGY, V15, P970 DANIEL MC, 2004, CHEM REV, V104, P293 DENIS FA, 2002, LANGMUIR, V18, P819 DUVERGER E, 2003, BIOCHIMIE, V85, P167 FALCONNET D, 2004, NANO LETT, V4, P1909 GOODING JJ, 1999, TRAC-TREND ANAL CHEM, V18, P525 GREEN NM, 1990, METHOD ENZYMOL, V184, P51 HAGA T, 2000, G PROTEIN COUPLED RE HOFF JD, 2004, NANO LETT, V4, P853 HOOK F, 2001, LANGMUIR, V17, P8305 JELINEK R, 2004, CHEM REV, V104, P5987 JEOUNG E, 2001, LANGMUIR, V17, P6396 JUNG JM, 2004, ANAL BIOCHEM, V330, P251 KANG MC, 2005, SMALL, V1, P69 KUMER N, 2005, LANGMUIR, V21, P6652 LEE KB, 2002, SCIENCE, V295, P1702 LI HW, 2003, LANGMUIR, V19, P1963 LIENER IE, 1986, LECTINS PROPERTIES F, P33 MICHEL R, 2002, LANGMUIR, V18, P8580 NIEMEYER CM, 2004, NANOBIOTECHNOLOGY, P31 PARK M, 1997, SCIENCE, V276, P1401 PARK TJ, 2004, J AM CHEM SOC, V126, P10512 SALAITA K, 2005, SMALL, V1, P940 SHIBUICHI S, 1996, J PHYS CHEM-US, V100, P19512 VEGA RA, 2005, ANGEW CHEM INT EDIT, V44, P6013 VEGA RA, 2005, ANGEW CHEM, V117, P6167 WHITESIDES GM, 1990, LANGMUIR, V6, P87 ZHANG GJ, 2005, SMALL, V1, P833ISI:000239717500012YKorea Adv Inst Sci & Technol, Dept Chem & Biomol Engn, Lab Organ Optoelect Mat, Taejon 305701, South Korea. Korea Res Inst Biosci & Biotechnol, Res Ctr, Taejon 305600, South Korea. Chung, BH, Korea Adv Inst Sci & Technol, Dept Chem & Biomol Engn, Lab Organ Optoelect Mat, BK-21, Taejon 305701, South Korea. chungbh@kribb.re.kr heetae@kaist.ac.krinternal-pdf://2006 Small Jung Gold-Conjugated Protein Nanoarrays-1959699215/2006 Small Jung Gold-Conjugated Protein Nanoarrays.pdf %' Condensation and Brige Formation.pdf ~?jChristman, K. L. Requa, M. V. Enriquez-Rios, V. D. Ward, S. C. Bradley, K. A. Turner, K. L. Maynard, H. D.20064Submicron streptavidin patterns for protein assembly 7444-7450Langmuir2217DIP-PEN NANOLITHOGRAPHY; LAYER-EXPANSION TECHNIQUE; ANTHRAX TOXIN RECEPTOR; PROTECTIVE ANTIGEN; FOCAL ADHESIONS; OXIDE SURFACES; MOSAIC-VIRUS; LETHAL TOXIN; LITHOGRAPHY; NANOSTRUCTURESArticleAugMicron and submicron-scale features of aldehyde functionality were fabricated in polymer films by photolithography to develop a platform for protein immobilization and assembly at a biologically relevant scale. Films containing the pH-reactive polymer poly(3,3'-diethoxypropyl methacrylate) and a photoacid generator (PAG) were patterned from 500 nm to 40 mu m by exposure to 365 nm (i-line) light. Upon PAG activation and hydrolysis of acetals, aldehyde groups formed. After the films were incubated with a biotinylated aldehyde reactive probe, the X-ray photoelectron spectroscopy results were consistent with biotin being attached to the surface. The background was subsequently passivated by flood exposure and incubation with an aminooxy-terminated poly(ethylene glycol), resulting in a 98% reduction in nonspecific protein adsorption. Protein patterning and assembly was demonstrated using streptavidin, biotinylated anthrax toxin receptor-1, and the protective antigen moiety of anthrax toxin and confirmed by fluorescence microscopy and atomic force microscopy (AFM). AFM demonstrated that 500 nm protein features were achieved. Because of the abundance of biotinylated proteins, this methodology provides a platform for protein immobilization and assembly for various applications in biotechnology.://000239596300057 Times Cited: 0 Cited References: AGARWAL G, 2003, J AM CHEM SOC, V125, P580 AOKI A, 1999, LANGMUIR, V15, P7418 ASTIER Y, 2005, CURR OPIN CHEM BIOL, V9, P576 BHATIA SK, 1992, J AM CHEM SOC, V114, P4432 BRADLEY KA, 2001, NATURE, V414, P225 BRADLEY KA, 2003, BIOCHEM PHARMACOL, V65, P309 BRADLEY KA, 2003, J BIOL CHEM, V278, P49342 BURRIDGE K, 1988, ANNU REV CELL BIOL, V4, P487 BURRIDGE K, 1996, ANNU REV CELL DEV BI, V12, P463 CASE MA, 2003, NANO LETT, V3, P425 CHRISTMAN KL, 2005, LANGMUIR, V21, P8389 CSUCS G, 2003, LANGMUIR, V19, P6104 FALCONNET D, 2004, NANO LETT, V4, P1909 FRIEDLANDER AM, 1986, J BIOL CHEM, V261, P7123 HARRIS JM, 1992, POLYETHYLENE GLYCOL HOFF JD, 2004, NANO LETT, V4, P853 HONG L, 2003, LANGMUIR, V19, P1966 HONG L, 2003, SURF COAT TECH, V169, P211 HYUN J, 2002, NANO LETT, V2, P1203 ICHINOSE N, 1993, CHEM LETT, P1961 KENSETH JR, 2001, LANGMUIR, V17, P4105 KUMAR A, 1993, APPL PHYS LETT, V63, P2002 KWAK SK, 2004, MAT SCI ENG C-BIO S, V24, P151 LEE KB, 2002, SCIENCE, V295, P1702 LEE KB, 2004, NANO LETT, V4, P1869 LEE KJ, 2004, LANGMUIR, V20, P1812 LEMIEUX GA, 1998, TRENDS BIOTECHNOL, V16, P506 LI HW, 2003, LANGMUIR, V19, P1963 LIM JH, 2003, ANGEW CHEM INT EDIT, V42, P2309 LIU J, 1996, COLLOID SURFACE B, V8, P25 MILNE JC, 1993, MOL MICROBIOL, V10, P647 MIYAMOTO S, 1995, J CELL BIOL, V131, P791 NAKAGAWA M, 2002, COLLOID SURFACE A, V204, P1 NAM JM, 2004, ANGEW CHEM INT EDIT, V43, P1246 NOY A, 2002, NANO LETTERS, V2, P109 NURAJE N, 2004, J AM CHEM SOC, V126, P8088 PENA DJ, 2003, LANGMUIR, V19, P9028 PETOSA C, 1997, NATURE, V385, P833 PLATEN J, 2006, SENSORS-BASEL, V6, P361 POGHOSSIAN A, 2005, ELECTROCHIM ACTA, V51, P838 RENAULTT JP, 2003, J PHYS CHEM B, V107, P703 RYAN D, 2004, LANGMUIR, V20, P9080 SCHLICK TL, 2005, J AM CHEM SOC, V127, P3718 SCOBIE HM, 2005, J INFECT DIS, V192, P1047 SHAW LM, 1990, J CELL BIOL, V110, P2167 SMITH JC, 2003, NANO LETT, V3, P883 VOROS J, 2005, MRS BULL, V30, P202 VOSSMEYER T, 1998, J APPL PHYS, V84, P3664 WADUMESTHRIGE K, 1999, LANGMUIR, V15, P8580 WEBER PC, 1989, SCIENCE, V243, P85 WIGELSWORTH DJ, 2004, J BIOL CHEM, V279, P23349 WILSON DL, 2001, P NATL ACAD SCI USA, V98, P13660 XIA YN, 1998, ANGEW CHEM INT EDIT, V37, P551 YIN HB, 2004, NUCLEIC ACIDS RES, V32 ZHOU DJ, 2003, LANGMUIR, V19, P10557ISI:000239596300057Univ Calif Los Angeles, Calif NanoSyst Inst, Dept Microbiol Immunol & Mol Genet, Dept Chem & Biochem, Los Angeles, CA 90095 USA. Univ Calif Santa Barbara, Calif Nanosyst Inst, Dept Mech Engn, Santa Barbara, CA 93106 USA. Maynard, HD, Univ Calif Los Angeles, Calif NanoSyst Inst, Dept Microbiol Immunol & Mol Genet, Dept Chem & Biochem, Los Angeles, CA 90095 USA. maynard@chem.ucla.eduinternal-pdf://2006_Langmuir_Submicron streptavidin patterns for protein assembly-3671179535/2006_Langmuir_Submicron streptavidin patterns for protein assembly.pdf 1Formation-3272973328/2006 JPC Sacha Induced Water;~?SBlattler, T. Huwiler, C. Ochsner, M. Stadler, B. Solak, H. Voros, J. Grandin, H. M.2006&Nanopatterns with biological functions 2237-2264)Journal of Nanoscience and Nanotechnology68Nnanopatterns; biological functions; lithography DIP-PEN NANOLITHOGRAPHY; SELF-ASSEMBLED MONOLAYERS; ELECTRON-BEAM LITHOGRAPHY; SURFACE-PLASMON RESONANCE; POLY(L-LYSINE)-G-POLY(ETHYLENE GLYCOL) LAYERS; EUV INTERFERENCE LITHOGRAPHY; NANOSCALE OPTICAL BIOSENSOR; NANO-STRUCTURED SURFACES; BLOCK-COPOLYMER MICELLES; SILICON-OXIDE SURFACESReviewAugjBoth curiosity and a desire for efficiency have advanced our ability to manipulate materials with great precision on the micrometer and, more recently, on the nanometer scale. Certainly, the semiconductor and integrated circuit industry has put the pressure on scientist and engineers to develop better and faster nanofabrication techniques. Furthermore, our curiosity as to how life works, and how it can be improved from a medical perspective, stands to gain a great deal from advances in nanotechnology. Novel nanofabrication techniques are opening up the possibilities for mimicking the inherently nano-world of the cell, i.e., the nanotopographies of the extracellular matrix (ECM) and the nanochemistry presented on both the cell membrane and the ECM. In addition, biosensing applications that rely on fabrication of high-density, precision arrays, e.g., DNA or gene chips and protein arrays, will gain significantly in efficiency and, thus, in usefulness once it becomes possible to fabricate heterogeneous nanoarrays. Clearly, continued advances in nanotechnology are desired and required for advances in biotechnology. In this review, we describe the leading techniques for generating nanopatterns with biological function including parallel techniques such as extreme ultraviolet interference lithography (EUV-IL), soft-lithographic techniques (e.g., replica molding (RM) and microcontact printing (mu CP)), nanoimprint lithography (NIL), nanosphere lithography (NSL) (e.g., colloid lithography or colloidal block-copolymer micelle lithography) and the nanostencil technique, in addition to direct-writing techniques including e-bearn lithography (EBL), focused ion-beam lithography (FIBL) and dip-pen nanolithography (DPN). Details on how the patterns are generated, how biological function is imparted to the nanopatterns, and examples of how these surfaces can and are being used for biological applications will be presented. This review further illustrates the rapid pace by which advances are being made in the field of nanobiotechnology, owing to an increasing number of research endeavors, for an ever increasing number of applications.://000239780500003 /Times Cited: 0 Cited References: AGARWAL G, 2003, J AM CHEM SOC, V125, P580 AGARWAL G, 2003, J AM CHEM SOC, V125, P7408 AIZAWA M, 2005, J AM CHEM SOC, V127, P8932 AMIJI M, 1992, BIOMATERIALS, V13, P682 AMRO NA, 2000, LANGMUIR, V16, P3006 ANDERSSON AS, 2003, BIOMATERIALS, V24, P3427 ANDRES RP, 1996, SCIENCE, V273, P1690 ARNOLD M, 2004, CHEMPHYSCHEM, V5, P383 BARBUCCI R, 2003, J MATER SCI-MATER M, V14, P721 BEARINGER JP, 1997, LANGMUIR, V13, P5175 BENALI M, 2002, LANGMUIR, V18, P872 BERDONDINI L, 2005, BIOSENS BIOELECTRON, V21, P167 BERNARD A, 1998, LANGMUIR, V14, P2225 BERNARD A, 2000, ADV MATER, V12, P1067 BIETSCH A, 2000, J APPL PHYS, V88, P4310 BOHM I, 1999, APPL SURF SCI, V141, P237 BREHMER M, 2003, J DISPER SCI TECHNOL, V24, P291 BREULMANN M, 2000, 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Paul Scherrer Inst, Lab Micro & Nanotechnol, Villigen, Switzerland. Grandin, HM, ETH, Dept Mat, BioInterface Grp, Lab Surface Sci & Technol, Zurich, Switzerland.K$~?%Ariga, K. Nakanishi, T. Michinobu, T.2006Immobilization of biomaterials to nano-assembled films (self-assembled monolayers, Langmuir-Blodgett films, and layer-by-layer assemblies) and their related functions 2278-2301)Journal of Nanoscience and Nanotechnology68self-assembled monolayer (SAM); Langmuir-Blodgett (LB) film; layer-by-layer (LBL) assembly; protein; DNA; molecular recognition; sensor; reactor AIR-WATER-INTERFACE; QUARTZ-CRYSTAL-MICROBALANCE; FLAVIN ADENINE-DINUCLEOTIDE; ULTRATHIN MULTILAYER FILMS; ORGANIC-INORGANIC HYBRID; DIP-PEN NANOLITHOGRAPHY; POROUS-GLASS PLATE; TRIPEPTIDE-CONTAINING AMPHIPHILES; DIRECTED PROTEIN IMMOBILIZATION; FORCE MICROSCOPIC OBSERVATIONReviewAugFor utilization of highly sophisticated functions of biomaterials in nano-scale functional systems, immobilization of biomaterials on artificial devices such as electrodes via thin film technology is one of the most powerful strategies. In this review, we focus on three major organic ultrathin films, self-assembled monolayers (SAM), Langmuir-Blodgett (LB) films, and layer-by-layer (LBL) assemblies, and from the viewpoints of biomaterial immobilization, typical examples and recent progresses in these film technologies are described. The SAM method allows facile contact between biomaterials and man-made devices, and well used for bio-related sensors. In addition, recent micro-fabrication techniques such as micro-contact printing and dip-pen nanolithography were successfully applied to preparation of biomaterial patterning. A monolayer at the air-water interface, which is a unit structure of LB films, provides a unique environment for recognition of aqueous biomaterials. Recognition and immobilization of various biomaterials including nucleotides, nucleic acid bases, amino acids, sugars, and peptides were widely investigated. The LB film can be also used for immobilization of enzymes in an ultrathin film on an electrode, resulting in sensor application. The LBL assembling method is available for wide range of biomaterials and provides great freedom in designs of layered structures. These advantages are reflected in preparation of thin-film bio-reactors where multiple kinds of enzymes sequentially operate. LBL assemblies were also utilized for sensors and drug delivery systems. 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Supermol Grp, Tsukuba, Ibaraki 3050044, Japan. Ariga, K, Natl Inst Mat Sci, Supermol Grp, 1-1 Namiki, Tsukuba, Ibaraki 3050044, Japan.`~?Naujoks, N. Stemmer, A.2006PCharge patterns as templates for the assembly of layered miomolecular structures 2445-2450)Journal of Nanoscience and Nanotechnology68charge writing; nanofabrication; guided self-assembly; AFM lithography; avidin-biotin reaction DIP-PEN NANOLITHOGRAPHY; PROBE FORCE MICROSCOPY; DRYING DROPS; GAS-PHASE; PARTICLES; SURFACE; LITHOGRAPHY; DEPOSITION; FABRICATION; INTERFACEArticleAugElectric fields are used to guide the assembly of biomolecules in predefined geometric patterns on solid substrates. Local surface charges serve as templates to selectively position proteins on thin-film polymeric electret layers, thereby creating a basis for site-directed layered assembly of biomolecular structures. Charge patterns are created using the lithographic capabilities of an atomic force microscope, namely by applying voltage pulses between a conductive tip and the sample. Samples consist of a poly(methyl methacrylate) layer on a p-doped silicon support. Subsequently, the sample is developed in a water-in-oil emulsion, consisting of a dispersed aqueous phase containing biotin-modified immunoglobulinG molecules, and a continuous nonpolar, insulating oil phase. The electrostatic fields cause a net force of (di)electrophoretic nature on the droplet, thereby guiding the proteins to the predefined locations. Due to the functionalization of the immunoglobulinG molecules with biotin-groups, these patterns can now be used to initiate the localized layer-by-layer assembly of biomolecules based on the avidin-biotin mechanism. By binding 40 nm sized biotin-labelled beads to the predefined locations via a streptavidin linker, we verify the functionality of the previously deposited immunoglobulinG-biotin. All assembly steps following the initial deposition of the immunoglobulinG from emulsion can conveniently be conducted in aqueous solutions. Results show that pattern definition is maintained after immersion into aqueous solution.://000239780500025 Times Cited: 0 Cited References: AGARWAL G, 2003, J AM CHEM SOC, V125, P7408 BERNARD A, 2001, NAT BIOTECHNOL, V19, P866 DEEGAN RD, 2000, PHYS REV E, V61, P475 DICKINSON E, 1999, COLLOID SURFACE B, V15, P161 DOUVAS AM, 2005, ANAL BIOANAL CHEM, V381, P1027 FALCONNET D, 2004, ADV FUNCT MATER, V14, P749 FEDER J, 1976, J APPL PHYS, V47, P1741 FENG J, 2004, COLLOID SURFACE B, V36, P177 FUDOUZI H, 2001, J NANOPART RES, V3, P193 FUDOUZI H, 2002, ADV MATER, V14, P1649 FUDOUZI H, 2002, LANGMUIR, V18, P7648 GARNO JC, 2002, LANGMUIR, V18, P8186 HOFF JD, 2004, NANO LETT, V4, P853 JACOBS HO, 1997, ULTRAMICROSCOPY, V69, P39 JACOBS HO, 2001, SCIENCE, V291, P1763 KAMYSHNY A, 1997, COLLOID SURFACE B, V9, P147 KAMYSHNY A, 1999, J COLLOID INTERF SCI, V212, P74 KIKUKAWA A, 1995, APPL PHYS LETT, V66, P3510 KRINKE TJ, 2001, APPL PHYS LETT, V78, P3708 KRINKE TJ, 2002, PART PART SYST CHAR, V19, P321 LASH JL, 1995, PROTEINS INTERFACES, V2 LEE KB, 2003, J AM CHEM SOC, V125, P5588 MCCLEMENTS DJ, 2004, CURR OPIN COLLOID IN, V9, P305 MESQUIDA P, 2002, MICROELECTRON ENG, V61, P671 MESQUIDA P, 2002, SCANNING, V24, P117 MESQUIDA P, 2002, SURF INTERFACE ANAL, V33, P159 MORT J, 1989, ANATOMY XEROGRAPHY I NAUJOKS N, 2004, COLLOID SURFACE A, V249, P69 NAUJOKS N, 2005, MICROELECTRON ENG, V78, P331 NONNENMACHER M, 1991, APPL PHYS LETT, V58, P2921 SESSLER GM, 1987, ELECTRETS STEMMER A, 2002, CHIMIA, V56, P573 WHITESIDES GM, 2001, ANNU REV BIOMED ENG, V3, P335 WRIGHT WMD, 1998, NANOTECHNOLOGY, V9, P133 YAKHNO T, 2005, NONLINEAR DYNAM, V39, P369 YAP FL, 2005, LANGMUIR, V21, P5233ISI:000239780500025~ETH, Nanotechnol Grp, CH-8092 Zurich, Switzerland. Naujoks, N, ETH, Nanotechnol Grp, Tannenstr 3, CH-8092 Zurich, Switzerland.0 Ζ~?`Schonherr, H. Degenhart, G. H. Dordi, B. Feng, C. L. Rozkiewicz, D. I. Shovsky, A. Vancso, G. J.2006Organic and macromolecular films and assemblies as (bio)reactive platforms: From model studies on structure-reactivity relationships to submicrometer patterning169-208,Ordered Polymeric Nanostructures at Surfaces200BerlinSpringer-Verlag Berlin;biointerfacing; micropatterning; nanopatterning; polymer thin films; surface reactivity ATOMIC-FORCE MICROSCOPY; SURFACE-PLASMON RESONANCE; SUPPORTED LIPID-BILAYERS; QUARTZ-CRYSTAL MICROBALANCE; AQUEOUS 2-PHASE EXTRACTION; NANOMETER-SCALE; GOLD SURFACES; THIN-FILMS; ALKANETHIOLATE MONOLAYERS; PHOSPHOLIPID-BILAYERS#In this contribution we review our recent progress in studies that aim at the understanding of the relationship between structure and surface reactivity of organic thin films on the one hand, and at the micro- and nanofabrication of bioreactive or biocompatible platforms on the other hand. Self-assembled monolayers (SAMs) of n,n'-dithiobis (N-hydroxysuccinimidyl-n-alkano ate) exposing NHS reactive ester groups were studied as model systems for immobilization reactions of DNA, proteins, and receptors. Reaction kinetics and activation energies were determined quantitatively at length scales ranging from millimeters down to nanometers using, for example, surface infrared spectroscopy and in situ inverted chemical force microscopy (iCFM), respectively. The increase in conformational order with increasing alkane segment length was found to result in reduced reactivity due to steric crowding. This drawback of highly organized monolayer architectures and the inherently limited loading can be circumvented by utilizing well-defined macromolecular thin films. Using amine-terminated polyamidoamine (PAMAM) dendrimers immobilized via soft lithography, as well as scanning probe lithography (SPL) approaches (dip-pen nanolithography, DPN) on NHS ester surfaces, robust micrometer and submicrometer patterned (bio)reactive surfaces, which allow one to achieve high molecular loading in coupling reactions for chip-based assays and sensor surfaces, were fabricated. Covalent coupling afforded the required robustness of the patterned assemblies. Finally, we address micro- and nanopatterned bilayer-based systems. SPL was applied in order to fabricate nanoscale biocompatible supramolecular architectures on solid supports. The adsorption of vesicles onto lipid bilayers was spatially controlled and directed in situ with nanometer-scale precision using SPL. This methodology, which provides a platform for research on proteins incorporated in the lipid bilayers comprising the vesicles, does not require that the vesicles are chemically labeled in order to guide their deposition.://000239275000007 Advances in Polymer Science"Times Cited: 0 Cited References: AHMAD J, 1990, LANGMUIR, V6, P1797 ALLARA DL, 1995, BIOSENS BIOELECTRON, V10, P771 AMIRGOULOVA EV, 2004, CHEMPHYSCHEM, V5, P552 AULETTA T, 2004, ANGEW CHEM INT EDIT, V43, P369 BAIN CD, 1989, LANGMUIR, V5, P1370 BASELT DR, 1994, J APPL PHYS, V76, P33 BENNINGHOVEN A, 1994, ANGEW CHEM INT EDIT, V33, P1023 BENTERS R, 2001, CHEMBIOCHEM, V2, P686 BENTERS R, 2002, NUCLEIC ACIDS RES, V30, E1 BERGER CEH, 1995, LANGMUIR, V11, P4188 BERTILSSON L, 1993, LANGMUIR, V9, P141 BEYER D, 1996, ANGEW CHEM INT EDIT, V35, P1682 BOUKOBZA E, 2001, J PHYS CHEM B, V105, P12165 BOXER SG, 2000, CURR OPIN CHEM BIOL, V4, P704 CAMILLONE N, 1993, J CHEM PHYS, V98, P3503 CARPICK RW, 1997, CHEM REV, V97, P1163 CASE MA, 2003, NANO LETT, V3, P425 CASSIE ABD, 1948, DISCUSS FARADAY SOC, V3, P11 CHAPMAN RG, 2001, LANGMUIR, V17, P1225 CHATELIER RC, 1995, LANGMUIR, V11, P4122 CHECHIK V, 1997, LANGMUIR, V13, P6354 CHECHIK V, 1998, LANGMUIR, V14, P99 CHECHIK V, 2000, ADV MATER, V12, P1161 CHEE M, 1996, SCIENCE, V274, P610 CHEN Q, 2004, CHEM MATER, V16, P614 CLARK JH, 1996, CHEM SOC REV, V25, P303 CLINE GW, 1988, J ORG CHEM, V53, P3583 CREAGER SE, 1994, LANGMUIR, V10, P3675 CREMER PS, 1999, J AM CHEM SOC, V121, P8130 CREMER PS, 1999, LANGMUIR, V15, P3893 DAVID C, 1996, MICROELECTRON ENG, V30, P57 DEARO JA, 1997, CHEM PHYS LETT, V277, P532 DEGENHART GH, 2004, LANGMUIR, V20, P6216 DELAMARCHE E, 1994, LANGMUIR, V10, P2869 DORDI B, 2003, LANGMUIR, V19, P5780 DORDI B, 2004, EUR POLYM J, V40, P939 DORDI B, 2004, SURF SCI, V570, P57 DUBOIS LH, 1992, ANNU REV PHYS CHEM, V43, P437 DUFRENE YF, 1997, LANGMUIR, V13, P4779 DUHACHEK SD, 2000, ANAL CHEM, V72, P3709 EVANS SD, 1998, LANGMUIR, V14, P6436 EVERHART DS, 1999, CHEMTECH, V29, P30 FALCONNET D, 2004, ADV FUNCT MATER, V14, P749 FERRETTI S, 2000, TRAC-TREND ANAL CHEM, V19, P530 FINKLEA HO, 1986, LANGMUIR, V2, P239 FODOR SPA, 1991, SCIENCE, V251, P767 FREY BL, 1996, ANAL CHEM, V68, P3187 FRISBIE CD, 1994, SCIENCE, V265, P2071 FRUTOS AG, 2000, LANGMUIR, V16, P2192 FULGHUM JE, 1999, J ELECTRON SPECTROSC, V100, P331 GEHRKE SH, 1998, BIOTECHNOL BIOENG, V58, P416 GINGER DS, 2004, ANGEW CHEM INT EDIT, V43, P30 GODWIN A, 2001, ANGEW CHEM INT EDIT, V40, P594 GONG P, 2004, SURF SCI, V570, P67 GROVES JT, 1997, SCIENCE, V275, P651 GROVES JT, 2002, ACCOUNTS CHEM RES, V35, P149 HAN WQ, 1997, SCIENCE, V277, P1287 HARDER P, 1998, J PHYS CHEM B, V102, P426 HEIBEL C, 1998, ACS SYM SER, V695, P104 HILLBORG H, 1998, POLYMER, V39, P1991 HILLBORG H, 2004, LANGMUIR, V20, P785 HOLMLIN RE, 2001, LANGMUIR, V17, P2841 HOVIS JS, 2000, LANGMUIR, V16, P894 HOVIS JS, 2001, LANGMUIR, V17, P3400 HU K, 1997, LANGMUIR, V13, P5114 HUANG JY, 1994, LANGMUIR, V10, P626 HUANG NP, 2001, LANGMUIR, V17, P489 ISRAELACHVILI JN, 1991, INTERMOLECULAR SURFA JASCHKE M, 1996, J PHYS CHEM-US, V100, P2290 JENKINS ATA, 1999, J AM CHEM SOC, V121, P5274 JENKINS ATA, 2002, LANGMUIR, V18, P3176 JEROME C, 2003, CHEM COMMUN, V2500 JOHNSON KL, 1971, P ROY SOC LOND A MAT, V324, P301 JOYCE SA, 1992, APPL PHYS LETT, V60, P1175 JUNG LS, 2000, J AM CHEM SOC, V122, P4177 KANE RS, 2003, LANGMUIR, V19, P2388 KHADEMHOSSEINI A, 2003, ADV MATER, V15, P1995 KIM JM, 2003, ADV MATER, V15, P1118 KUMAR A, 1994, LANGMUIR, V10, P1498 KUMAR A, 1994, SCIENCE, V263, P60 KUMAR S, 2000, LANGMUIR, V16, P9936 KUNG LA, 2000, LANGMUIR, V16, P6773 LACKOWSKI WM, 1999, LANGMUIR, V15, P7632 LAHANN J, 2002, LANGMUIR, V18, P3632 LAHIRI J, 1999, ANAL CHEM, V71, P777 LAIBINIS PE, 1995, J PHYS CHEM-US, V99, P7663 LARSEN NB, 1997, J AM CHEM SOC, V119, P3017 LEE TR, 1994, LANGMUIR, V10, P741 LI HW, 2002, NANO LETTERS, V2, P347 LI HW, 2003, LANGMUIR, V19, P1963 LIEBAU M, 2001, ADV FUNCT MATER, V11, P147 LIPOWSKY R, 1991, MOL CRYST LIQ CRYST, V202, P17 LIU GY, 2000, ACCOUNTS CHEM RES, V33, P457 LOCKHART DJ, 2000, NATURE, V405, P827 LUSSI JW, 2004, PROG SURF SCI, V76, P55 MALMQVIST M, 1997, CURR OPIN CHEM BIOL, V1, P378 MENDES PM, 2004, CURR OPIN COLLOID IN, V9, P236 MIRKIN CA, 1992, ANNU REV PHYS CHEM, V43, P719 MIZES HA, 1991, APPL PHYS LETT, V59, P2901 MORIGAKI K, 2001, ANGEW CHEM INT EDIT, V40, P172 MORIGAKI K, 2003, LANGMUIR, V19, P6994 MRKSICH M, 2000, CHEM SOC REV, V29, P267 NEOGI P, 1993, J CHEM SOC CHEM COMM, P1134 NIEMEYER CM, 1999, ANGEW CHEM INT EDIT, V38, P2865 NISMAN R, 1994, LANGMUIR, V10, P1667 NOY A, 1997, ANNU REV MATER SCI, V27, P381 NUZZO RG, 1983, J AM CHEM SOC, V105, P4481 OSTUNI E, 1999, COLLOID SURFACE B, V15, P3 OSTUNI E, 2001, LANGMUIR, V17, P5605 OSTUNI E, 2001, LANGMUIR, V17, P6336 OVERNEY RM, 1992, NATURE, V359, P133 PAOLESSE R, 1998, SENSOR ACTUAT B-CHEM, V47, P70 PATHAK S, 2004, LANGMUIR, V20, P6075 PIRRUNG MC, 2002, ANGEW CHEM INT EDIT, V41, P1277 PLANT AL, 1993, LANGMUIR, V9, P2764 POIRIER GE, 1997, CHEM REV, V97, P1117 PORTER MD, 1987, J AM CHEM SOC, V109, P3559 PRIME KL, 1991, SCIENCE, V252, P1164 PRIME KL, 1993, J AM CHEM SOC, V115, P10714 PRUCKER O, 1998, MACROMOLECULES, V31, P592 PRUCKER O, 1998, MACROMOLECULES, V31, P602 PUTKA CS, 2002, BIOTECHNOL BIOENG, V80, P139 RADMACHER M, 1994, BIOPHYS J, V66, P2159 REVIAKINE I, 2000, LANGMUIR, V16, P1806 RICCO AJ, 1998, ACCOUNTS CHEM RES, V31, P289 RINGSDORF H, 1988, ANGEW CHEM INT EDIT, V27, P113 ROWAN B, 2002, LANGMUIR, V18, P9914 RUHE J, 2001, ABSTR PAP AM CHEM 1, V221, U356 SABATANI E, 1987, J ELECTROANAL CH INF, V219, P365 SACKMANN E, 1996, SCIENCE, V271, P43 SAGIV J, 1980, J AM CHEM SOC, V102, P92 SCHENA M, 1995, SCIENCE, V270, P467 SCHENA M, 2003, MICROARRAY ANAL SCHMIDT P, 2000, POLYMER, V41, P4267 SCHONHERR H, 1997, MACROMOLECULES, V30, P6391 SCHONHERR H, 1998, LANGMUIR, V14, P2801 SCHONHERR H, 2000, CHEM MATER, V12, P3689 SCHONHERR H, 2000, J AM CHEM SOC, V122, P3679 SCHONHERR H, 2000, MACROMOLECULES, V33, P4532 SCHONHERR H, 2001, ACS SYM SER, V781, P36 SCHONHERR H, 2003, LANGMUIR, V19, P10843 SCHONHERR H, 2004, LANGMUIR, V20, P11600 SCHONHERR H, 2004, LANGMUIR, V20, P7308 SCHREIBER F, 2004, J PHYS-CONDENS MAT, V16, P881 SCHULZE A, 2001, NAT CELL BIOL, V3, P190 SEIFERT U, 1997, ADV PHYS, V46, P13 SIEGERS C, 2004, CHEM-EUR J, V10, P2831 SIGNAL GB, 1996, ANAL CHEM, V68, P490 SINNIAH SK, 1996, J AM CHEM SOC, V118, P8925 SMITH RK, 2004, PROG SURF SCI, V75, P1 SPINKE J, 1993, J CHEM PHYS, V99, P7012 STAMOU D, 2003, ANGEW CHEM INT EDIT, V42, P5580 STANISH I, 2001, J AM CHEM SOC, V123, P1008 STEVENS F, 1999, LANGMUIR, V15, P207 STOECKLI M, 1999, J AM SOC MASS SPECTR, V10, P67 STORRI S, 1998, BIOSENS BIOELECTRON, V13, P347 SU XD, 2005, LANGMUIR, V21, P348 SULLIVAN TP, 2003, EUR J ORG CHEM JAN, P17 SVEDHEM S, 2003, CHEMBIOCHEM, V4, P339 TANNENBAUM R, 2002, LANGMUIR, V18, P5592 TARLOV MJ, 1993, J AM CHEM SOC, V115, P5305 TOLLNER K, 1997, SCIENCE, V278, P2100 TOOMEY R, 2004, MACROMOLECULES, V37, P882 TURNER NH, 2000, ANAL CHEM, V72, R99 ULMAN A, 1991, INTRO ULTRATHIN ORGA ULMAN A, 1995, CHARACTERIZATION ORG ULMAN A, 1996, CHEM REV, V96, P1533 VANCSO GJ, 1998, ACS SYM SER, V694, P67 VANCSO GJ, 1999, MICROSTRUCTURE MICTR, V741, P317 VANCSO GJ, 2005, ADV POLYM SCI, V182, P55 VANDERWERF KO, 1994, APPL PHYS LETT, V65, P1195 VANOUDENAARDEN A, 1999, SCIENCE, V285, P1046 VANRYSWYK H, 1996, LANGMUIR, V12, P6143 WAGNER P, 1994, FEBS LETT, V356, P267 WAGNER P, 1996, BIOPHYS J, V70, P135 WANG J, 1992, ACS SYM SER, V487, P125 WANG JH, 1997, J AM CHEM SOC, V119, P12796 WATTS TH, 1984, P NATL ACAD SCI USA, V81, P7564 WATTS TH, 1986, NATURE, V320, P179 WESSA T, 1998, FRESEN J ANAL CHEM, V361, P239 WILBUR JL, 1994, ADV MATER, V6, P600 WILBUR JL, 1999, NANOTECHNOLOGY, P339 WIRTH MJ, 1999, CHEM REV, V99, P2843 WOJTYK JTC, 2002, LANGMUIR, V18, P6081 WOUTERS D, 2004, ANGEW CHEM INT EDIT, V43, P2480 XIA YN, 1998, ANNU REV MATER SCI, V28, P153 YAN L, 2004, J MACROMOL SCI-POL C, V44, P175 YANG ZP, 2000, LANGMUIR, V16, P7482 YOSHINAISHII C, 2003, J AM CHEM SOC, V125, P3696 ZHANG ZH, 2003, MACROMOLECULES, V36, P7689 ZHOU XC, 2004, LANGMUIR, V20, P8877 ZHU H, 2002, CURR OPIN CELL BIOL, V14, P173 Review HEIDELBERGER PLATZ 3, D-14197 BERLIN, GERMANYISI:000239275000007:Univ Twente, MESA Inst Nanotechnol, NL-7500 AE Enschede, Netherlands. Univ Twente, Fac Sci & Technol, Dept Mat Sci & Technol Polymers, NL-7500 AE Enschede, Netherlands. Schonherr, H, Univ Twente, MESA Inst Nanotechnol, POB 217, NL-7500 AE Enschede, Netherlands. h.schonherr@tnw.utwente.nl g.j.vancso@tnw.utwente.nlinternal-pdf://2006_Adv Poly Sci_ Organic and macromolec-2883543055/2006_Adv Poly Sci_ Organic and macromolecular films and assemblies as (bio)reactive platforms.pdf MXlbl.govinternal-pdf://2006 JPC Sacha Induced Water Condensation and Brige  ~?BFarkas, N. Ehrman, J. D. Evans, E. A. Ramsier, R. D. Dagata, J. A.20068High-voltage parallel writing on iron nitride thin films 1340-1343(Journal of Vacuum Science & Technology A244LOCAL OXIDATION NANOLITHOGRAPHY; ATOMIC-FORCE MICROSCOPE; DIP-PEN NANOLITHOGRAPHY; MAGNETIC NANOSTRUCTURES; NANO-OXIDATION; METAL-FILMS; LITHOGRAPHY; GROWTH; ZIRCONIUM; SILICONArticleJul-AugWe report large area patterning of sputter-deposited FeN thin films by a high-voltage parallel writing technique that was recently developed to modify ZrN surfaces. Systematically patterned 15-100-nm-thick FeN films consisting of features with well-defined sizes and shapes are obtained by applying high dc voltages between a stamp and the samples. During the process the oxide dissolves, exposing the substrate beneath. This controlled breakdown eliminates the need for any postexposure etching. The single-step imprinting method presented here provides an emerging route to fabricate isolated FeN geometrical structures on silicon substrates for magnetic applications. (c) 2006 American Vacuum Society.://000239048100080 DTimes Cited: 0 Cited References: BAL M, 2002, APPL PHYS LETT, V81, P3479 BASELT DR, 1998, BIOSENS BIOELECTRON, V13, P731 CAVALLINI M, 2003, APPL PHYS LETT, V83, P5286 CHIEN FSS, 2001, J APPL PHYS, V89, P2465 DAGATA JA, UNPUB DREYER M, 2002, J APPL PHYS 3, V91, P8138 FARKAS N, 2003, J VAC SCI TECHNOL A, V21, P1188 FARKAS N, 2004, APPL PHYS LETT, V85, P5691 FARKAS N, 2004, J VAC SCI TECHNOL A, V22, P1879 FARKAS N, 2004, THIN SOLID FILMS, V447, P468 FEHLNER FP, 1970, OXID MET, V2, P59 FU L, 2003, NANO LETT, V3, P757 GALLAGHER WJ, 1997, J APPL PHYS 2A, V81, P3741 GUNDIAH G, 2004, APPL PHYS LETT, V84, P5341 GWO S, 1999, APPL PHYS LETT, V74, P1090 GWO S, 2001, J PHYS CHEM SOLIDS, V62, P1673 HELD R, 1998, PHYSICA E, V2, P748 HINDS KA, 2003, BLOOD, V102, P867 HIROOKA M, 2004, APPL PHYS LETT, V85, P1811 LEIBBRANDT GWR, 1992, PHYS REV LETT, V68, P1947 MELINTE S, 1998, SUPERLATTICE MICROST, V24, P79 NIU C, 2001, J VAC SCI TECHNOL 2, V19, P1947 QIN F, 2003, THIN SOLID FILMS, V444, P179 SHAPIRO EM, 2004, P NATL ACAD SCI USA, V101, P10901 TAKEMURA Y, 2005, ADV ENG MATER, V7, P170 TELLO M, 2003, APPL PHYS LETT, V83, P2339 TERRIS BD, 2000, J APPL PHYS 3, V87, P7004 WEEKES SM, 2005, J APPL PHYS, V97 WOOD DK, 2005, SENSOR ACTUAT A-PHYS, V120, P1 YANG XM, 2003, J VAC SCI TECHNOL B, V21, P3017 YOKOO A, 2003, J VAC SCI TECHNOL B, V21, P2966 YOSHIOKA H, 2000, MAGN RESON IMAGING, V18, P1079 ZHANG ZL, 2004, MAGN RESON MATER PHY, V17, P201ISI:000239048100080Univ Akron, Dept Phys, Akron, OH 44325 USA. Univ Akron, Dept Chem, Akron, OH 44325 USA. Univ Akron, Dept Chem Engn, Akron, OH 44325 USA. Natl Inst Stand & Technol, Div Precis Engn, Gaithersburg, MD 20899 USA. Ramsier, RD, Univ Akron, Dept Phys, Akron, OH 44325 USA. rex@uakron.eduinternal-pdf://2006 Journal of VacScie&TechA Farkas High-voltage parallel-1796539408/2006 Journal of VacScie&TechA Farkas High-voltage parallel.pdf 2v~?'Sacha, G. M. Verdaguer, A. Salmeron, M.2006]Induced water condensation and bridge formation by electric fields in atomic force microscopy 14870-14873Journal of Physical Chemistry B11030JDIP-PEN NANOLITHOGRAPHY; CAPILLARY CONDENSATION; PROBE; OXIDATION; SILICONArticleAugRWe present an analytical model that explains how, in humid environments, the electric field near a sharp tip enhances the formation of water menisci and bridges between the tip and a sample. The predictions of the model are compared with experimental measurements of the critical distance where the field strength causes bridge formation.://000239309500048 Times Cited: 0 Cited References: BATENI A, 2004, LANGMUIR, V20, P7589 BLUHM H, 1998, REV SCI INSTRUM, V69, P1781 CAPELLA B, 1999, SURF SCI REP, V34, P1 DAGATA JA, 2004, J APPL PHYS, V96, P2393 DELAZZER A, 1999, LANGMUIR, V15, P4551 GAO C, 1997, APPL PHYS LETT, V71, P1801 GARCIA R, 1999, J APPL PHYS, V86, P1898 GOMEZMONIVAS S, 2000, APPL PHYS LETT, V76, P2955 GOMEZMONIVAS S, 2001, APPL PHYS LETT, V79, P4048 GOMEZMONIVAS S, 2003, PHYS REV LETT, V91, P56101 ISRAELACHVILI JN, 1991, INTERMOLECULAR SURFA JACKSON JD, 1975, CLASSICAL ELECTRODYN JANG JY, 2004, PHYS REV LETT, V92 KOHONEN MM, 1999, PHYS REV LETT, V82, P4667 LEE KB, 2002, SCIENCE, V295, P1702 MORIMOTO K, 1997, APPL SURF SCI, V117, P652 PARAMONOV PB, 2005, J CHEM PHYS, V123 PINER RD, 1999, SCIENCE, V283, P661 RESTAGNO F, 2000, PHYS REV LETT, V84, P2433 SACHA GM, 2005, APPL PHYS LETT, V86, P23101 SADER JE, 1999, REV SCI INSTRUM, V70, P3967 STIFTER T, 2000, PHYS REV B, V62, P13667 SZOSZKIEWICZ R, 2005, APPL PHYS LETT, V87 THUNDAT T, 1993, SURF SCI LETT, V294, P939 VALENCIA A, 2001, LANGMUIR, V17, P3390 VERDAGUER A, 2005, J CHEM PHYS, V123 VERDAGUER A, 2006, CHEM REV, V106, P1478ISI:000239309500048Univ Calif Berkeley, Div Mat Sci, Lawrence Berkeley Natl Lab, Berkeley, CA 94720 USA. Sacha, GM, Univ Calif Berkeley, Div Mat Sci, Lawrence Berkeley Natl Lab, Berkeley, CA 94720 USA. sgomezmonivas@ ~?LIm, J. Lee, M. Myung, S. Huang, L. Rao, S. G. Lee, D. J. Koh, J. Hong, S. H.2006Directed-assembly of single-walled carbon nanotubes using self-assembled monolayer patterns comprising conjugated molecular wires 3569-3573Nanotechnology1714NDIP-PEN NANOLITHOGRAPHY; DEPOSITION; TEMPLATES; SURFACE; TRANSISTORS; FEATURESArticleJul@Self-assembled monolayer (SAM) patterns on electrodes are often utilized to guide the assembly of single-walled carbon nanotubes (SWCNTs) onto the electrodes to form desired device structures. In this case, the SWCNTs are in contact with the electrodes through the SAM which comprises molecular wires. Presumably, it is desirable to use conjugated molecular wires for a low contact resistance because they have been reported as a better electric conductor than non-conjugated ones. However, until now, the directed-assembly of SWCNTs has been driven mostly via molecular wires with alkane backbones which are known to be relatively poor conductors. Herein, we report large-scale directed-assembly of SWCNTs utilizing SAM patterns comprising conjugated molecular wires. We achieved highly selective adsorption and precision alignment of SWCNTs utilizing polar SAM patterns comprising conjugated molecular wires, while SAM patterns with non-polar terminal groups efficiently prevented adsorption of SWCNTs. Furthermore, we developed a process for assembling a SWCNT across two electrodes coated with conjugated molecular wires, and the electrical conduction through the SWCNT was measured via a conducting atomic force microscope. This result could be an important guideline for large-scale directed-assembly of SWCNT-based devices in the future.://000238969700036 Times Cited: 0 Cited References: BACHTOLD A, 2001, SCIENCE, V294, P1317 BAUGHMAN RH, 1999, SCIENCE, V284, P1340 BEEBE JM, 2002, J AM CHEM SOC, V124, P11268 CHO N, 2006, J CHEM PHYS, V124 DAI HJ, 1996, NATURE, V384, P147 DEHEER WA, 1995, SCIENCE, V270, P1179 FAN SS, 1999, SCIENCE, V283, P512 FRANK S, 1998, SCIENCE, V280, P1744 HONG S, 2000, SUPERLATTICE MICROST, V28, P289 HUANG Y, 2001, SCIENCE, V291, P630 JASCHKE M, 1995, LANGMUIR, V11, P1061 KONG J, 1998, NATURE, V395, P878 KRUPKE R, 2003, SCIENCE, V301, P344 LIU J, 1998, SCIENCE, V280, P1253 LIU J, 1999, CHEM PHYS LETT, V303, P125 MAHAPATRO AK, 2006, APPL PHYS LETT, V88 MANANDHAR P, 2003, PHYS REV LETT, V90 MARTEL R, 1998, APPL PHYS LETT, V73, P2447 MCLEAN RS, 2006, NANO LETT, V6, P55 MYUNG S, 2005, ADV MATER, V17, P2361 NYAMJAV D, 2003, ADV MATER, V15, P1805 PINER RD, 1999, SCIENCE, V283, P661 RAO SG, 2003, NATURE, V425, P36 RUECKES T, 2000, SCIENCE, V289, P94 SAMANTA MP, 1996, PHYS REV B, V53, P7626 SHEEHAN PE, 2002, PHYS REV LETT, V88 WANG YH, 2006, P NATL ACAD SCI USA, V103, P2026 WILBUR JL, 1995, LANGMUIR, V11, P825 XIA YN, 1995, J AM CHEM SOC, V117, P3274ISI:0002389697000363Seoul Natl Univ, Sch Phys, Seoul 151747, South Korea. Seoul Natl Univ, NANO Syst Inst, Seoul 151747, South Korea. Northwestern Univ, Dept Chem, Evanston, IL 60208 USA. Florida State Univ, Dept Phys, Tallahassee, FL 32306 USA. Im, J, Seoul Natl Univ, Sch Phys, Seoul 151747, South Korea. shong@phya.snu.ac.krinternal-pdf://2006 Nanotechnology Im Directed-assembly of single-walled ca-1830201104/2006 Nanotechnology Im Directed-assembly of single-walled carbon nanotubes.pdf their analogs.pdf0-walled carbon nanotubes.pdf8~??Rohde, R. D. Agnew, H. D. Yeo, W. S. Bailey, R. C. Heath, J. R.2006XA non-oxidative approach toward chemically and electrochemically functionalizing Si(111) 9518-9525(Journal of the American Chemical Society12829SELF-ASSEMBLED MONOLAYERS; DIP-PEN NANOLITHOGRAPHY; HYDROGEN-TERMINATED SILICON(111); SELECTIVE FUNCTIONALIZATION; RECOMBINATION VELOCITY; CRYSTALLINE SI(111); ELECTRODE SURFACES; ALKYL MONOLAYERS; CLICK CHEMISTRY; PROTEINArticleJulA general method for the non-oxidative functionalization of single-crystal silicon(111) surfaces is described. The silicon surface is fully acetylenylated using two-step chlorination/alkylation chemistry. A benzoquinone-masked primary amine is attached to this surface via Cu(I)-catalyzed Huisgen 1,3-dipolar cycloaddition ("click" chemistry). The benzoquinone is electrochemically reduced, resulting in quantitative cleavage of the molecule and exposing the amine terminus. Molecules presenting a carboxylic acid have been immobilized to the exposed amine sites. X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FTIR), cyclic voltammetry (CV), and contact angle goniometry were utilized to characterize and quantitate each step in the functionalization process. This work represents a strategy for providing a general platform that can incorporate organic and biological molecules on Si(111) with minimal oxidation of the silicon surface.://000239120700067  Times Cited: 0 Cited References: BABICSAMARDZIJA K, 2005, LANGMUIR, V21, P12187 BANSAL A, 1998, J PHYS CHEM B, V102, P4058 BANSAL A, 2001, J PHYS CHEM B, V105, P10266 BECKMANN N, 2005, P NATL ACAD SCI USA, V102, P14587 BOCK VD, 2006, EUR J ORG CHEM, P51 BOUKHERROUB R, 1999, J AM CHEM SOC, V121, P11513 BUNIMOVICH YL, 2004, LANGMUIR, V20, P10630 BURIAK JM, 1998, J AM CHEM SOC, V120, P1339 CHIDSEY CED, 1990, J AM CHEM SOC, V112, P4301 CICERO RL, 2000, LANGMUIR, V16, P5688 COLLMAN JP, 2004, LANGMUIR, V20, P1051 COLLMAN JP, 2006, LANGMUIR, V22, P2457 CRAIGHEAD HG, 2001, CURR OPIN SOLID ST M, V5, P177 CURRELI M, 2005, J AM CHEM SOC, V127, P6922 DEVARAJ NK, 2005, J AM CHEM SOC, V127, P8600 DEVARAJ NK, 2006, J AM CHEM SOC, V128, P1794 DUMAS P, 1990, PHYS REV LETT, V65, P1124 EFFENBERGER F, 1998, ANGEW CHEM INT EDIT, V37, P2462 FAN R, 2005, NANO LETT, V5, P1633 GIOVANELLI D, 2003, ANAL LETT, V36, P2941 HABER JA, 2002, J PHYS CHEM B, V106, P3639 HODNELAND CD, 2000, J AM CHEM SOC, V122, P4235 HU K, 1997, J PHYS CHEM B, V101, P8298 HURLEY PT, UNPUB ISRAELACHVILI J, 1985, INTERMOLECULAR SURFA JUNG DR, 2001, CRIT REV BIOTECHNOL, V21, P111 JUNG H, 2004, NANO LETT, V4, P2171 KARNIK R, 2005, NANO LETT, V5, P1638 KOLB HC, 2001, ANGEW CHEM INT EDIT, V40, P2004 LEE JK, 2004, LANGMUIR, V20, P3844 LEE KB, 2002, SCIENCE, V295, P1702 LI HM, 2005, J AM CHEM SOC, V127, P14518 LINFORD MR, 1995, J AM CHEM SOC, V117, P3145 LUMMERSTORFER T, 2004, J PHYS CHEM B, V108, P3963 NEMANICK EJ, 2005, THESIS CALTECH NEMANICK EJ, 2006, IN PRESS J PHYS CH B PINER RD, 1999, SCIENCE, V283, P661 RECCIUS CH, 2005, PHYS REV LETT, V95 ROUSSEL C, 2003, CHEMPHYSCHEM, V4, P200 ROYEA WJ, 2000, APPL PHYS LETT, V77, P1988 SIEVAL AB, 1998, LANGMUIR, V14, P1759 SOLARES SD, 2006, J AM CHEM SOC, V128, P3850 STAVIS SM, 2005, J APPL PHYS, V98 STEWART MP, 2001, J AM CHEM SOC, V123, P7821 STRONG L, 1988, LANGMUIR, V4, P546 SUNG MM, 1997, LANGMUIR, V13, P6164 WEBB LJ, 2003, J PHYS CHEM B, V107, P5404 WEBB LJ, 2005, J CHEM PHYS B, V9, P3930 WEBB LJ, 2006, J PHYS CHEM B, V110, P7349 YABLONOVITCH E, 1986, PHYS REV LETT, V57, P249 YEO WS, 2001, CHEM BIOCH, P590 YEO WS, 2003, J AM CHEM SOC, V125, P14994 YEO WS, 2004, ADV MATER, V16, P1352 YOUSAF MN, 1999, J AM CHEM SOC, V121, P4286 YU H, 2006, IN PRESS APPL PHYS L YU HB, 2005, J PHYS CHEM B, V109, P671 YUE M, 2004, J MICROELECTROMECH S, V13, P290 ZHANG Y, 2006, ANAL CHEM, V78, P2001 ZHENG A, 1999, J ORG CHEM, V64, P156 ZHENG GF, 2005, NAT BIOTECHNOL, V23, P1294 ZIRBS R, 2005, LANGMUIR, V21, P8414ISI:000239120700067CALTECH, Div Chem & Chem Engn, Pasadena, CA 91125 USA. Heath, JR, CALTECH, Div Chem & Chem Engn, MC 127-72, Pasadena, CA 91125 USA. heath@caltech.eduinternal-pdf://2006 JACS Rohde Non-Oxidative functionalization of single cyr-3558318608/2006 JACS Rohde Non-Oxidative functionalization of single cyrstal silicon.pdf ITd their analogs-0588899600/2006 CurrentNanoSci Briones Nucleic acids and  ~?8Johannes, M. S. Kuniholm, J. F. Cole, D. G. Clark, R. L.2006NAutomated CAD/CAM-based nanolithography using a custom atomic force microscope236-2397IEEE Transactions on Automation Science and Engineering33atomic force microscopy (AFM); computer-aided design/computer-aided manufacturing (CAD/CAM); lithography; nanotechnology; oxidation DIP-PEN NANOLITHOGRAPHY; SILICON; OXIDATION; AFMArticleJul We report the development of a novel nanolithographic system that combines the design capabilities of computer-aided design/computer-aided manufacturing (CAD/CAM) software with the nanolithographic abilities of the atomic force microscope (AFM). The AFM is a powerful tool for research at the nanoscale and can be used to perform a variety of serial nanolithographic techniques. A custom-built three-axis AFM system, designed to execute nanolithography, has been constructed and interfaced with a CAD/CAM design environment. This technique utilizes the CAD/CAM software to create, in a virtual design environment, the desired nanoscale patterns. Then, using a G-code interpreter and software algorithms to control the three-dimensional motion of the system, the design is replicated automatically by using conventional nanolithographic procedures. In this report, AFM-based anodization lithography on a silicon wafer and subsequent AFM imaging is used to confirm the successful automatic replication of the desired nanoscale patterns.://000239032600006 Times Cited: 0 Cited References: 2004, ACE CONVERTER PROGRA BINNIG G, 1986, ATOMIC FORCE MICROSC, P930 BUSTAMANTE C, 2003, NATURE, V421, P423 DAGATA JA, 1990, APPL PHYS LETT, V56, P2001 DAY HC, 1993, APPL PHYS LETT, V62, P2691 FOTIADIS D, 2002, MICRON, V33, P385 GINGER DS, 2004, ANGEW CHEM INT EDIT, V43, P30 GORDON AE, 1995, J VAC SCI TECHNOL B, V13, P2805 HAFNER JH, 2001, PROG BIOPHYS MOL BIO, V77, P73 JASCHKE M, 1995, LANGMUIR, V11, P1061 PINER RD, 1999, SCIENCE, V283, P661 QUATE CF, 1997, SURF SCI, V386, P259 TELLO M, 2003, APPL PHYS LETT, V83, P2339 WILBUR JL, 1995, ADV MATER, V7, P649 XU S, 1997, LANGMUIR, V13, P127ISI:000239032600006Duke Univ, Dept Mech Engn & Mat Sci, Durham, NC 27708 USA. Johannes, MS, Duke Univ, Dept Mech Engn & Mat Sci, Durham, NC 27708 USA. rclark@duke.eduinternal-pdf://2006 IEEE Johannes Automated CAD-CAM-based Nanolith.-2098809872/2006 IEEE Johannes Automated CAD-CAM-based Nanolith..pdf Ecsic.esinternal-pdf://2006 CurrentNanoSci Briones Nucleic acids an*f)4~?Briones, C. Martin-Gago, J. A.2006JNucleic acids and their analogs as nanomaterials for biosensor development257-273Current Nanoscience23SELF-ASSEMBLED MONOLAYERS; SINGLE-NUCLEOTIDE POLYMORPHISMS; DENSITY OLIGONUCLEOTIDE ARRAYS; DIP-PEN NANOLITHOGRAPHY; ATOMIC-FORCE MICROSCOPY; DNA MICROARRAYS; ELECTROCHEMICAL DETECTION; MASS-SPECTROMETRY; GENE-EXPRESSION; GOLD SURFACESReviewAugNucleic acids are natural biopolymers that store the genetic information of organisms. This makes the detection and characterization of DNA and RNA a relevant task in biotechnology, with applications ranging from medicine to environmental control. During the last decades, a large effort has been focused on the development of biosensors, among them those devoted to the detection of nucleic acids in natural samples and those that include nucleic acids as nanosized capture probes for different biomolecules. DNA microarray technology has been successfully used in biotechnological applications including genotyping and gene expression studies. Nevertheless, the performance of DNA microarrays has a limitation imposed by the need of a previous fluorescent labeling of the target molecule to be analyzed. This encouraged the use of alternative detection methods, such as optical and electrochemical ones, and recently others based on surface characterization techniques. New trends in nanotechnology point towards new tools for manipulating molecules and macromolecules that could be developed as high performance biosensors. This interdisciplinary approach towards the integration of novel biosensors can benefit from the capability of certain polymers to form self-assembled monolayers (SAMs) on different surfaces. Thiol-modified DNA can form SAMs on gold surfaces with reduced efficiency, and the biological activity of the probe is decreased upon adsorption. Therefore, thiolated DNA has a very limited use in biosensor development. These constraints have been successfully by-passed using uncharged, artificial analogs of natural nucleic acids, such as peptide nucleic acids (PNAs), as molecular probes. This contribution reviews the state of the art in the use of nucleic acids and their analogs as biosensor nanomaterials, and summarizes the novel approach towards the development of biosensors based on SAMs of PNAs. 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CSIC, INTA, Ctr Astrobiol, Madrid 28850, Spain. Martin-Gago, JA, CSIC, Inst Ciencia Mat Madrid, Madrid 28049, Spain. gago@icmm.~?Hanumanthu, R. Stebe, K. J.2006YEquilibrium shapes and locations of axisymmetric, liquid drops on conical, solid surfaces227-239?Colloids and Surfaces A-Physicochemical and Engineering Aspects282 dip-pen nanolithography; axisymmetric interface; wettability; wetting gradient; contact angle; surface tension; line tension DIP-PEN NANOLITHOGRAPHY; LINE TENSION; CONTACT ANGLES; INTERFACIAL-TENSION; SIZE DEPENDENCE; SYSTEMS; WETTABILITY; PARTICLES; CYLINDERS; SESSILEArticleJul0Micro- and nano-scale liquid droplets must be precisely placed in proximity to conical solid tips in applications that include AFM tip dip-pen nanolithography. This seemingly simple task is strongly dependent on wetting conditions of the drop on the tip surface. Over a wide range of wetting conditions and drop Volumes, drops can situate far from a conical needle apex at equilibrium, which can hinder the effectiveness of the respective applications. Needle geometry also affects drop location. On a right conical needle, liquid drops that wet the needle surface locate away from the apex. However, by careful consideration of their geometry, needles can be engineered to retain liquid drops near the tip or some other region of interest. In this work, a theoretical model is developed that predicts axisymmetric, equilibrium drop locations and shapes on conical, solid surfaces as a function of drop volume, needle geometry/shape, needle surface wettability (contact angle), liquid surface tension, line tension, and gravity. (c) 2006 Elsevier B.V. All rights reserved.://000238730200025 Times Cited: 0 Cited References: AMIRFAZLI A, 2000, LANGMUIR, V16, P2024 AMIRFAZLI A, 2003, J COLLOID INTERF SCI, V265, P152 AVEYARD R, 1996, J CHEM SOC FARADAY T, V92, P4271 AVEYARD R, 1996, J CHEM SOC FARADAY T, V92, P85 BABU SR, 1987, J COLLOID INTERF SCI, V116, P350 BAUER C, 2000, PHYS REV E B, V62, P2428 CARROLL BJ, 1986, LANGMUIR, V2, P248 DEGENNES PG, 2004, CAPILLARITY WETTING DUNCAN D, 1995, J COLLOID INTERF SCI, V169, P256 GAYDOS J, 1987, J COLLOID INTERF SCI, V120, P76 GETTA T, 1998, PHYS REV E, V57, P655 GINGER DS, 2004, ANGEW CHEM INT EDIT, V43, P31 GU YG, 1996, J COLLOID INTERF SCI, V180, P212 HARTLAND S, 1976, AXI SYMMETRIC FLUID HONG MH, 2000, APPL PHYS LETT, V77, P2604 HOORFAR M, 2005, ADV COLLOID INTERFAC, V114, P103 HUH C, 1983, J COLLOID INTERF SCI, V91, P472 JANG J, 2003, PHYS REV LETT, V90 JANG JK, 2004, J CHEM PHYS, V120, P1157 JANG JY, 2001, J CHEM PHYS, V115, P2721 JANG JY, 2002, J CHEM PHYS, V116, P3875 KREYSZIG E, 1999, ADV ENG MATH LEWIS A, 1999, APPL PHYS LETT, V75, P2689 LUCASSEN J, 1992, LANGMUIR, V8, P3093 MCHALE G, 1997, J COLLOID INTERF SCI, V186, P453 MCHALE G, 2001, OIL GAS SCI TECHNOL, V56, P47 MIRKIN CA, 2001, CHEMPHYSCHEM, V2, P37 MUGELE F, 2005, J PHYS-CONDENS MAT, V17, R705 NAM JM, 2004, ANGEW CHEM INT EDIT, V43, P1246 PINER RD, 1999, SCIENCE, V283, P661 PLATIKANOV D, 1980, J COLLOID INTERF SCI, V75, P612 QU WL, 1998, COLLOID SURFACE A, V144, P275 ROTENBERG Y, 1983, J COLLOID INTERF SCI, V93, P169 SCHELUDKO A, 1976, J CHEM SOC F1, V72, P2815 SIFTER T, 2000, PHYS REV B, V62, P13667 SU M, 2004, APPL PHYS LETT, V84, P4200 TAKATA Y, 2005, LANGMUIR, V21, P8594 TARAZONA P, 1981, J CHEM PHYS, V75, P3114 TOSHEV BV, 1988, LANGMUIR, V4, P489 WIDOM B, 1995, J PHYS CHEM-US, V99, P2803 ZHANG H, 2004, CHEM MATER, V16, P1480ISI:000238730200025Johns Hopkins Univ, Dept Chem & Biomol Engn, Baltimore, MD 21218 USA. Stebe, KJ, Johns Hopkins Univ, Dept Chem & Biomol Engn, 221 Maryland Hall,3400 N Charles St, Baltimore, MD 21218 USA. rhanuma1@jhem.jhu.edu kjs@jhu.eduinternal-pdf://2006 Colloids & Surfaces Hanumanthu Equilibrium Shapes & Locations-2048577040/2006 Colloids & Surfaces Hanumanthu Equilibrium Shapes & Locations.pdfPxids & Surfaces Hanumanthu Equilibrium Shapes & Locations.pdf  ~?(Li, J. Wang, Y. J. Lu, Z. H. Chan, M. S.2006Enhancing deoxyribonucleic acid (DNA) detection sensitivity through microconcentration on patterned fluorocarbon polymer surface34-39Analytica Chimica Acta5711deoxyribonucleic acid (DNA) detection; sensitivity; microconcentration; patterning; hydrophobic surface DIP-PEN NANOLITHOGRAPHY; HYBRIDIZATION KINETICS; OLIGONUCLEOTIDES; LITHOGRAPHY; MICROARRAYS; NANOARRAYS; CAPILLARY; BIOCHIPS; ADHESION; PLASMAArticleJun/A microconcentration concept is proposed to enhance the sensitivity of deoxyribonucleic acid (DNA) hybridization due to evaporation of the hybridization solution on a patterned hydrophobic fluorocarbon polymer (FCP) surface. The combination of microconcentration and hybridization processes provides a tool to manipulate nanoliter solution. To fabricate a patterned DNA microarray with hydrophobic surrounding surface, a plasma polymerization and lift-off protocol was designed so that the process can be carried out in a standard microelectronic fabrication laboratory with minimal adjustments on the equipment. After microconcentration, a 1 mu L hybridization solution can be concentrated to below 10 nL, which improves the hybridization sensitivity by a factor of 100. (c) 2006 Elsevier B.V. All rights reserved.://000238720100006 Times Cited: 0 Cited References: ANDERSSON H, 2001, SENSOR ACTUAT B-CHEM, V75, P136 CHAN V, 1995, BIOPHYS J, V69, P2243 CHEEK BJ, 2001, ANAL CHEM, V73, P5777 CHRISEY LA, 1996, NUCLEIC ACIDS RES, V24, P3040 DEEGAN RD, 1997, NATURE, V389, P827 DEEGAN RD, 2000, PHYS REV E, V61, P475 DEMERS LM, 2002, SCIENCE, V296, P1836 ERICKSON D, 2003, ANAL BIOCHEM, V317, P186 HALPERIN A, 2005, BIOPHYS J, V89, P796 IVANOVA EP, 2002, LANGMUIR, V18, P9539 KANE RS, 1999, BIOMATERIALS, V20, P2363 KOHARA Y, 2002, NUCLEIC ACIDS RES, V30 LEE KB, 2002, SCIENCE, V295, P1702 LEE KB, 2004, NANO LETT, V4, P1869 LEE SH, 2004, SENSOR ACTUAT B-CHEM, V99, P623 LENIGK R, 2001, LANGMUIR, V17, P2497 LIVACHE T, 2003, J PHARMACEUT BIOMED, V32, P687 MAKOHLISO SA, 1998, BIOSENS BIOELECTRON, V13, P1227 MARRIAN CRK, 1996, MICROELECTRON ENG, V32, P173 MATSUMOTO Y, 1998, SENSOR ACTUAT A-PHYS, V66, P308 MULLER U, 2003, J ASS LAB AUTOM, V8, P96 PAPPAERT K, 2003, CHEM ENG SCI, V58, P4921 ROGERS YH, 1999, ANAL BIOCHEM, V266, P23 RUARDIJ TG, 2000, IEEE T BIO-MED ENG, V47, P1593 TOEGL A, 2003, J BIOMOL TECH, V14, P197 WANG Y, 2003, ANAL CHEM, V75, P1130 ZHANG YC, 2003, ANAL CHEM, V75, P3267ISI:000238720100006Hong Kong Univ Sci & Technol, Dept Elect & Elect Engn, Kowloon, Hong Kong, Peoples R China. SE Univ, Minist Educ, Key Lab Mol & Biomol Elect, Nanjing 210096, Peoples R China. Li, J, Hong Kong Univ Sci & Technol, Dept Elect & Elect Engn, Kowloon, Hong Kong, Peoples R China. eelij@ust.hkinternal-pdf://2006 AnaChimActa Li Enhancing DNA detection sensitivity-0035390224/2006 AnaChimActa Li Enhancing DNA detection sensitivity.pdfT00\2006 AnaChimActa Li Enhancing DNA detection sensitivity.pdf ~?(Im, J. Kang, J. Lee, M. Kim, B. Hong, S.2006uSelective adsorption and alignment behaviors of double- and multiwalled carbon nanotubes on bare Au and SiO2 surfaces 12839-12842Journal of Physical Chemistry B11026pDIP-PEN NANOLITHOGRAPHY; THIN-FILM TRANSISTORS; LARGE-SCALE; DEPOSITION; TEMPLATES; FEATURES; GROWTH; PHASE; INKArticleJulWe present the study of selective adsorption and alignment behaviors of double- and multiwalled carbon nanotubes (dwCNTs and mwCNTs) on self-assembled monolayer (SAM) patterns, bare Au, and SiO2 surfaces. dwCNTs and mwCNTs exhibited stronger affinity to polar SAMs, bare Au, and SiO2 surfaces than to nonpolar SAM surfaces. Furthermore, we found the adsorption probability of smaller carbon nanotubes (CNTs) was higher than that of larger CNTs. As proof of concept, we successfully assembled and aligned dwCNTs and mwCNTs on Au and SiO2 substrates without relying on external forces and demonstrated wafer-scale fabrication of back-gate transistors based on dwCNTs with a high yield.://000238645700002 3Times Cited: 0 Cited References: CHO N, 2006, J CHEM PHYS, V124 COFFEY DC, 2005, J AM CHEM SOC, V127, P4564 CUI Y, 2001, SCIENCE, V293, P1289 DEPABLO PJ, 1999, APPL PHYS LETT, V74, P323 DUAN XF, 2003, NATURE, V425, P274 FRANK S, 1998, SCIENCE, V280, P1744 HANNON JB, 2005, LANGMUIR, V21, P8569 HATA K, 2004, SCIENCE, V306, P1362 HONG SH, 2000, SCIENCE, V288, P1808 HUANG Y, 2001, SCIENCE, V291, P630 IIJIMA S, 1991, NATURE, V354, P56 ISRAELACHVILI J, 1992, INTERMOLECULAR SURFA JANSSON PAC, 2004, APPL PHYS LETT, V84, P2256 JASCHKE M, 1995, LANGMUIR, V11, P1061 JAVEY A, 2004, NATURE, V424, P654 KOCABAS C, 2005, SMALL, V1, P1110 LEE NK, 2006, J CHEM PHYS, V124 LIU J, 1999, CHEM PHYS LETT, V303, P125 MANANDHAR P, 2003, PHYS REV LETT, V90 MAYNOR BW, 2001, LANGMUIR, V17, P2575 MYUNG S, 2005, ADV MATER, V17, P2361 NYAMJAV D, 2003, ADV MATER, V15, P1805 OH SJ, 2003, APPL PHYS LETT, V82, P2521 PASHLEY RM, 1981, J COLLOID INTERF SCI, V83, P531 PINER RD, 1999, SCIENCE, V283, P661 RAO SG, 2003, NATURE, V425, P36 SHEEHAN PE, 2002, PHYS REV LETT, V88 WANG YH, 2006, P NATL ACAD SCI USA, V103, P2026 XIA YN, 1995, J AM CHEM SOC, V117, P3274 ZHANG YG, 2001, APPL PHYS LETT, V79, P3155ISI:000238645700002Seoul Natl Univ, Phys & Nanosyst Inst, Seoul 151747, South Korea. Hong, S, Seoul Natl Univ, Phys & Nanosyst Inst, Seoul 151747, South Korea. shong@phya.snu.ac.kr0177367911Slides.pptinternal-pdf://2006 JoPhysChem Im Selective Absorption & Alignment Behaviors-0925139728/2006 JoPhysChem Im Selective Absorption & Alignment Behaviors.pdfPJoPhysChem Im Selective Absorption & Alignment Behaviors.pdf Q~?JWiechmann, M. Enders, O. Leisten, F. Becker, J. M. Haug, R. J. Kolb, H. A.2006Nanoscale lines of supported nanogold particles and lysozyme-nanogold conjugates generated by atomic force microscopy in aqueous solution 1004-1009Surface and Interface Analysis386nanolines; nanogold particles; NHS-lysozyme conjugates; mica; line-scan mode; AFM DIP-PEN NANOLITHOGRAPHY; SCANNING PROBE; NANOWIRE NANOSENSORSArticleJunKThe line-scan mode is applied in aqueous suspensions of NHS-nanogold and NHS - nanogold-lysozyme conjugates to generate tip-induced linelike pattern with a width in the nanometer scale. With increasing ionic strength the spontaneous adsorption of the particles to the mica surface can be reduced. The reduction causes an increase in the processing time, which is necessary to form a continuous line composed of the respective particles. The line width increases with increasing loading force. For NHS-nanogold, a minimal line width of about 40 nm could be achieved. The results were used to connect two opposite macroscopic gold contacts about 5 mu m apart by a line of NHS-nanogold, which appeared to be of continuous structure down to the nanometer scale, according to the corresponding topography. Copyright (C) 2006 John Wiley & Sons, Ltd.://000238329400004 Times Cited: 0 Cited References: BUNIMOVICH YL, 2004, LANGMUIR, V20, P10630 CUI Y, 2001, SCIENCE, V293, P1289 GINGER DS, 2004, ANGEW CHEM INT EDIT, V43, P30 HAHM J, 2004, NANO LETT, V4, P51 HAINFELD JF, 1992, J HISTOCHEM CYTOCHEM, V40, P177 HECHT S, 2003, ANGEW CHEM INT EDIT, V42, P24 HLA SW, 2001, CHEMPHYSCHEM, V2, P361 HONG SH, 1999, SCIENCE, V286, P523 ISRAELACHVILI JN, 1997, INTERMOLECULAR SURFA KRAMER S, 2003, CHEM REV, V103, P4367 LEE KB, 2002, SCIENCE, V295, P1702 LEISTEN F, 2005, IN PRESS J COLLOID I LIM JH, 2002, ADV MATER, V14, P1474 LIU XG, 2002, ADV MATER, V14, P231 MANANDHAR P, 2003, PHYS REV LETT, V90 MCCARTY GS, 1999, CHEM REV, V99, P1983 NYFFENEGGER RM, 1997, CHEM REV, V97, P1195 PINER RD, 1999, SCIENCE, V283, P661 SCALES PJ, 1990, LANGMUIR, V6, P582 WOUTERS D, 2004, ANGEW CHEM INT EDIT, V43, P2480ISI:000238329400004Univ Hannover, Inst Biophys, D-30419 Hannover, Germany. Univ Hannover, Inst Solid State Phys, Dept Nanostruct, D-30167 Hannover, Germany. Kolb, HA, Univ Hannover, Inst Biophys, Herrenhaeuser Str 2, D-30419 Hannover, Germany. kolb@biophysik.uni-hannover.decinternal-pdf://2006_SIA_Nanoscale lines_Wiechmann-1563061008/2006_SIA_Nanoscale lines_Wiechmann.pdf#h Analysis Wiechmann Nanos-2682650205\2006 Surface & Interface Analysis Wiechmann Nanoscale Lines of Supported Nanogold Particles.pdf!~? YLuo, G. Xie, G. Y. Zhang, Y. Y. Zhang, G. M. Zhang, Y. Y. Carlberg, P. Zhu, T. Liu, Z. F.2006?Scanning probe lithography for nanoimprinting mould fabrication 3018-3022Nanotechnology1712DIP-PEN NANOLITHOGRAPHY; SELF-ASSEMBLED MONOLAYERS; HYDROGEN-PASSIVATED SILICON; ATOMIC-FORCE MICROSCOPE; IMPRINT LITHOGRAPHY; NANOMETER-SCALE; TUNNELING MICROSCOPE; LOCAL OXIDATION; NANOSTRUCTURES; NANOFABRICATIONArticleJunWe propose a rational fabrication method for nanoimprinting moulds by scanning probe lithography. By wet chemical etching, different kinds of moulds are realized on Si( 110) and Si( 100) surfaces according to the Si crystalline orientation. The structures have line widths of about 200 nm with a high aspect ratio. By reactive ion etching, moulds with patterns free from the limitation of Si crystalline orientation are also obtained. With closed-loop scan control of a scanning probe microscope, the length of patterned lines is more than 100 mu m by integrating several steps of patterning. The fabrication process is optimized in order to produce a mould pattern with a line width about 10 nm. The structures on the mould are further duplicated into PMMA resists through the nanoimprinting process. The method of combining scanning probe lithography with wet chemical etching or reactive ion etching (RIE) provides a resistless route for the fabrication of nanoimprinting moulds.://000238256300034 Times Cited: 0 Cited References: AHN SW, 2005, MICROELECTRON ENG, V78, P314 AVOURIS P, 1997, APPL PHYS LETT, V71, P285 BEAN KE, 1978, IEEE T ELECTRON DEV, V25, P1185 BECK M, 2002, MICROELECTRON ENG, V61, P441 CHENG X, 2004, MICROELECTRON ENG, V71, P288 CHIEN FSS, 1999, APPL PHYS LETT, V75, P2429 CHIEN FSS, 2002, J APPL PHYS, V91, P10044 CHOU SY, 1995, APPL PHYS LETT, V67, P3114 CHOU SY, 1996, SCIENCE, V272, P85 CHOU SY, 1997, J VAC SCI TECHNOL B, V15, P2897 DAGATA JA, 1990, APPL PHYS LETT, V56, P2001 FONTAINE PA, 1998, J APPL PHYS, V84, P1776 GADEGAARD N, 2003, MACROMOL MATER ENG, V288, P76 GARCIA R, 1998, APPL PHYS LETT, V72, P2295 GARCIA R, 1999, J APPL PHYS, V86, P1898 GINGER DS, 2004, ANGEW CHEM INT EDIT, V43, P30 HOFF JD, 2004, NANO LETT, V4, P853 KOINUMA M, 1996, SURF SCI, V357, P565 KRAMER S, 2003, CHEM REV, V103, P4367 KUO CW, 2003, ADV MATER, V15, P1065 LI HW, 2003, NANOTECHNOLOGY, V14, P220 LIU GY, 2000, ACCOUNTS CHEM RES, V33, P457 MAGNO R, 1997, APPL PHYS LETT, V70, P1855 PINER RD, 1999, SCIENCE, V283, P661 RESNICK DJ, 2003, J VAC SCI TECHNOL B, V21, P2624 RUCHHOEFT P, 1999, J VAC SCI TECHNOL B, V17, P2965 SNOW ES, 1993, APPL PHYS LETT, V63, P749 TUNG YC, 2005, APPL PHYS LETT, V86 WEINBERGER DA, 2000, ADV MATER, V12, P1600 WOUTERS D, 2004, ANGEW CHEM INT EDIT, V43, P2480 XU S, 1997, LANGMUIR, V13, P127 XU S, 1999, LANGMUIR, V15, P7244 YU ZN, 2003, J VAC SCI TECHNOL B, V21, P2089 ZHANG H, 2002, ADV MATER, V14, P1472 ZHANG H, 2003, NANO LETT, V3, P43 ZHANG H, 2004, CHEM MATER, V16, P1480 ZHANG YY, 2005, NANOTECHNOLOGY, V16, P422 ZHENG JW, 2000, LANGMUIR, V16, P4409ISI:000238256300034Peking Univ, Coll Chem & Mol Engn,Beijing Natl Lab Mol Sci, Ctr Nanoscale Sci & Technol, Key Lab Phys & Chem Nanodevices, Beijing 100871, Peoples R China. Lund Univ, Div Solid State Phys, Nanometer Struct Consortium, S-22100 Lund, Sweden. Luo, G, Peking Univ, Coll Chem & Mol Engn,Beijing Natl Lab Mol Sci, Ctr Nanoscale Sci & Technol, Key Lab Phys & Chem Nanodevices, Beijing 100871, Peoples R China. zhutao@pku.edu.cninternal-pdf://2006 Nanotechnology Luo Scanning Probe Lithography for Nanoimprin-2972414224/2006 Nanotechnology Luo Scanning Probe Lithography for Nanoimprinting.pdfT0Dtechnology Luo Scanning Probe Lithography for Nanoimprinting.pdf v~?!DAgheli, H. Malmstrom, J. Larsson, E. M. Textor, M. Sutherland, D. S.2006=Large area protein nanopatterning for biological applications 1165-1171 Nano Letters66QUARTZ-CRYSTAL MICROBALANCE; SELF-ASSEMBLED MONOLAYERS; DIP-PEN NANOLITHOGRAPHY; COLLOIDAL LITHOGRAPHY; SOFT LITHOGRAPHY; NANOSPHERE LITHOGRAPHY; CHEMICAL-PATTERNS; FABRICATION; ADSORPTION; SURFACESArticleJun>Large area nanopatterns of functional proteins are demonstrated. A new approach to analyze atomic force microscopy height histograms is used to quantify protein and antibody binding to nanoscale patches. Arrays of nanopatches, each containing less than 40 laminin molecules, are shown to be highly functional binding close to 1 monoclonal anti-laminin IgG (site by IKVAV sequence) or 3-4 polyclonal anti-laminin IgG's per surface bound laminin. Complementary quartz crystal microbalance measurements indicate higher functionality at nanopatches than on homogeneous surfaces.://000238258300018 Times Cited: 0 Cited References: ARNOLD M, 2004, CHEMPHYSCHEM, V5, P383 BERGKVIST M, 2001, J PHYS CHEM B, V105, P2062 CAI YG, 2005, LANGMUIR, V21, P9274 CHEN CS, 1997, SCIENCE, V276, P1425 CHENG JY, 2002, APPL PHYS LETT, V81, P3657 COX JK, 1999, CURR OPIN COLLOID IN, V4, P52 CURTIS A, 2001, TRENDS BIOTECHNOL, V19, P97 DENIS FA, 2004, LANGMUIR, V20, P9335 DENIS FA, 2005, SMALL, V1, P984 FALCONNET D, 2004, ADV FUNCT MATER, V14, P749 FALCONNET D, 2004, NANO LETT, V4, P1909 GROLL J, 2005, CHEMBIOCHEM, V6, P1782 HANARP P, 2001, J COLLOID INTERF SCI, V1, P26 HANARP P, 2003, COLLOID SURFACE A, V214, P23 HANARP P, 2003, J PHYS CHEM B, V107, P5768 HOOD L, 2004, SCIENCE, V306, P640 HUANG NP, 2001, LANGMUIR, V17, P489 HULTEEN JC, 1995, J VAC SCI TECHNOL A, V13, P1553 KANE RS, 1999, BIOMATERIALS, V20, P2363 KASEMO B, 1998, CURR OPIN SOLID ST M, V3, P451 KENSETH JR, 2001, LANGMUIR, V17, P4105 KRAUSCH G, 2000, ADV MATER, V14, P1579 LEE KB, 2002, SCIENCE, V295, P1702 MACBEATH G, 2000, SCIENCE, V289, P1760 MICHEL R, 2002, LANGMUIR, V18, P8580 PALLANDRE A, 2005, J AM CHEM SOC, V127, P4320 PAVLOVIC E, 2003, NANO LETT, V3, P779 PRIME KL, 1991, SCIENCE, V252, P1164 REIMHULT E, 2004, ANAL CHEM, V76, P7211 RODAHL M, 1995, REV SCI INSTRUM, V66, P3924 SALAITA K, 2005, SMALL, V1, P940 SPATZ JP, 1999, ADV MATER, V11, P149 STEVENS MM, 2005, SCIENCE, V310, P1135 TASHIRO K, 1989, J BIOL CHEM, V264, P16174 WHITESIDES GM, 2001, ANNU REV BIOMED ENG, V3, P335 XIA YN, 1998, ANNU REV MATER SCI, V28, P153 ZHANG GJ, 2005, SMALL, V1, P833ISI:000238258300018Chalmers Univ Technol, Dept Appl Phys, S-41296 Gothenburg, Sweden. Univ Aarhus, iNANO Ctr, DK-8000 Aarhus, Denmark. ETH, Lab Surface Sci & Technol, Dept Mat, CH-8093 Zurich, Switzerland. Sutherland, DS, Chalmers Univ Technol, Dept Appl Phys, S-41296 Gothenburg, Sweden. duncan@inano.dkinternal-pdf://2006 Nano Letters Agheli Large Area Protein Nanopatterning-0725384976/2006 Nano Letters Agheli Large Area Protein Nanopatterning.pdfP#h=406 Nano Letters Agheli Large Area Protein Nanopatterning.pdf ~?"3Fan, X. Tran, D. T. Brennan, D. P. Oliver, S. R. J.20064Microfabrication using elastomeric stamp deformation 11986-11990Journal of Physical Chemistry B11024DIP-PEN NANOLITHOGRAPHY; OPTICAL LITHOGRAPHY; PHOTONIC CRYSTALS; SOFT LITHOGRAPHY; FABRICATION; GOLD; MICROSTRUCTURES; ELECTRONICS; MONOLAYERS; STABILITYArticleJunElastomeric stamp deformation has been utilized for the contact printing (CP) of self-assembled monolayers (SAMs) and, more recently, polymers and proteins. Here, we take advantage of this well-studied phenomenon to fabricate a series of new metal thin-film patterns not present on the original stamp. The rounded patterns are of nanoscale thickness, long-range order, and are created from elastomeric stamps with only straight-edged features. The metal was printed onto the surface of an alpha,omega-alkanedithiol self-assembled monolayer (SAM). The new shapes are controlled by a combination of stamp geometry design and the application of external pressure. Previously published rules on stamp deformation for contact printing of SAMs are invalid because the coating is instead a thin-metal film. This method represents a new pathway to micropatterning metal thin films, leading to shapes with higher complexity than the original lithographic masters.://000238284600055 Times Cited: 0 Cited References: ARSHAK K, 2005, J OPTOELECTRON ADV M, V7, P193 BIETSCH A, 2000, J APPL PHYS, V88, P4310 BRAMBLEY D, 1994, ADV MATER OPT ELECTR, V4, P55 CHOI HW, 2004, J CRYST GROWTH, V268, P527 COLOMBELLI R, 2003, SCIENCE, V302, P1374 DELAMARCHE E, 1997, ADV MATER, V9, P741 DEMERS LM, 2002, SCIENCE, V296, P1836 GATES BD, 2003, J AM CHEM SOC, V125, P14986 GUO QJ, 2004, NANO LETT, V4, P1657 HASAN M, 2002, J AM CHEM SOC, V124, P1132 HUI CY, 2002, LANGMUIR, V18, P1394 JEONG HJ, 1994, SOLID STATE TECHNOL, V37, P39 KUMAR A, 1993, APPL PHYS LETT, V63, P2002 LOO YL, 2002, APPL PHYS LETT, V81, P562 LOO YL, 2002, J AM CHEM SOC, V124, P7654 LOO YL, 2002, J VAC SCI TECHNOL B, V20, P2853 LOO YL, 2003, NANO LETT, V7, P913 OHTERA Y, 2004, OPT ENG, V43, P1022 OKAZAKI S, 1991, J VAC SCI TECHNOL B, V9, P2829 PAINTER O, 1999, SCIENCE, V284, P1819 PEASE RFW, 1992, J VAC SCI TECHNOL B, V10, P278 PINER RD, 1999, SCIENCE, V283, P661 ROGERS JA, 2001, P NATL ACAD SCI USA, V98, P4835 SHARP KG, 2004, LANGMUIR, V20, P6430 SHI WL, 2004, COLLOID SURFACE A, V246, P109 SHINJO T, 2000, SCIENCE, V289, P930 STEINGRUBER R, 2003, MICROELECTRON ENG, V67, P157 TAN L, 2003, J VAC SCI TECHNOL B, V21, P2742 TIEN J, 2002, P NATL ACAD SCI USA, V99, P1758 XIA Y, 1998, ANGEW CHEM INT EDIT, V37, P550 ZAUMSEIL J, 2003, NANO LETT, V9, P1223ISI:000238284600055Univ Calif Santa Cruz, Dept Chem & Biochem, Santa Cruz, CA 95064 USA. Oliver, SRJ, Univ Calif Santa Cruz, Dept Chem & Biochem, 1156 High St, Santa Cruz, CA 95064 USA. soliver@chemistry.ucsc.eduinternal-pdf://2006_JPCB_Microfabrication using elastomeric stamp deformation-0675798800/2006_JPCB_Microfabrication using elastomeric stamp deformation.pdfL0DWFan Microfabrication Elastomeric Stamp Deformation.pdf F~?#KIm, J. Huang, L. Kang, J. Lee, M. Lee, D. J. Rao, S. G. Lee, N. K. Hong, S.2006s"Sliding kinetics" of single-walled carbon nanotubes on self-assembled monolayer patterns: Beyond random adsorptionJournal of Chemical Physics12422tFIELD-EFFECT TRANSISTORS; DIP-PEN NANOLITHOGRAPHY; SURFACE; DEPOSITION; TEMPLATES; FEATURES; PHASE; FILMS; GOLD; INKArticleJun}We present the experimental results and theoretical model describing new adsorption kinetics of single-walled carbon nanotubes (swCNTs) onto self-assembled monolayer (SAM) including their sliding motion. The adsorption behavior of swCNTs on large-size SAM patterns is similar to the Langmuir isotherm, while that on nanoscale patterns shows a significant deviation which can be explained by the sliding motion of adsorbed nanotubes. The '' sliding chamber '' experiment confirms that swCNTs can align along the SAM patterns by sliding motion right above the SAM surfaces. This result provides new scientific insights regarding the adsorption kinetics of one-dimensional nanostructures, and, from a practical point of view, it can be an important guideline to design SAM patterns to assemble carbon nanotubes and nanowires into desired device structures. (c) 2006 American Institute of Physics.://000238279800049 dTimes Cited: 0 Cited References: ANCONA MG, 2003, NANO LETT, V3, P135 ARNOLD MS, 2003, J PHYS CHEM B, V107, P659 CHO N, 2006, J CHEM PHYS, V124 COFFEY DC, 2005, J AM CHEM SOC, V127, P4564 DOI M, 1986, THEORY POLYM DYNAMIC GHOSH S, 2003, SCIENCE, V299, P1042 GIRIFALCO LA, 2000, PHYS REV B, V62, P13104 HANNON JB, 2005, LANGMUIR, V21, P8569 HEO YW, 2004, APPL PHYS LETT, V85, P2274 HONG SH, 1999, SCIENCE, V286, P523 HOUGH LA, 2004, PHYS REV LETT, V93 HUANG Y, 2001, SCIENCE, V291, P630 IIJIMA S, 1991, NATURE, V354, P56 KARPOVICH DS, 1994, LANGMUIR, V10, P3315 KIM P, 1999, SCIENCE, V286, P2148 KRAMERS HA, 1940, PHYSICA, V7, P284 LIU J, 1999, CHEM PHYS LETT, V303, P125 MANANDHAR P, 2003, PHYS REV LETT, V90 MARTEL R, 1998, APPL PHYS LETT, V73, P2447 MICOCCI G, 1997, J VAC SCI TECHNOL A, V15, P34 MYUNG S, 2005, ADV MATER, V17, P2361 NAMJAV D, 2003, ADV MATER, V15, P1805 OH SJ, 2003, APPL PHYS LETT, V82, P2521 PINER RD, 1999, SCIENCE, V283, P661 RAO SG, 2003, NATURE, V425, P36 SHEEHAN PE, 2002, PHYS REV LETT, V88 TANS SJ, 1998, NATURE, V393, P49 WANG YH, 2006, P NATL ACAD SCI USA, V103, P2026 XIA YN, 1995, J AM CHEM SOC, V117, P3274 ZHANG M, 2002, NANOTECHNOLOGY, V13, P212 ZHANG YG, 2001, APPL PHYS LETT, V79, P3155ISI:0002382798000498Seoul Natl Univ, Sch Phys, Seoul 151747, South Korea. Sejong Univ, Dept Phys, Seoul 143743, South Korea. Florida State Univ, Inst Fundamental Phys, Tallahassee, FL 32306 USA. Northwestern Univ, Dept Chem, Evanston, IL 60208 USA. Hong, S, Seoul Natl Univ, Sch Phys, Seoul 151747, South Korea. shong@phya.snu.ac.kr224707 Artn 224707internal-pdf://2006 JoChemPhys Im Sliding kinetics of single-walled carbon-3410526736/2006 JoChemPhys Im Sliding kinetics of single-walled carbon.pdf Kons: Template for directed deposition of biomacromolecules224-230Langmuir241Jan://000251916100034 0743-7463ISI:000251916100034[interD }?$ Mirkin, C. A.2007OThe power of the pen: Development of massively parallel dip-pen nanolithography79-83Acs Nano12Sep://000252012300003 1936-0851ISI:000252012300003iinte nal-pdf://2008_Tunable resist ~?%-Lee, W. K. Caster, K. C. Kim, J. Zauscher, S.2006Nanopatterned polymer brushes by combining AFM anodization lithography with ring-opening metathesis polymerization in the liquid and vapor phase848-853Small272atomic force microscopy; catalysts; electric field microscopy; nanolithography; ring-opening polymerization SCANNING-PROBE LITHOGRAPHY; DIP-PEN NANOLITHOGRAPHY; FREE-RADICAL POLYMERIZATION; SELF-ASSEMBLED MONOLAYERS; SOLVENTLESS POLYMERIZATION; THIN-FILMS; FORCE MICROSCOPY; POLYACETYLENE; SURFACE; SILICONArticleJul://000238159300003 Times Cited: 0 Cited References: AHN SJ, 2002, APPL PHYS LETT, V80, P2592 ARBUCKLE GA, 1994, SYNTHETIC MET, V63, P35 DAGATA JA, 1990, APPL PHYS LETT, V56, P2001 EDWARDS JH, 1980, POLYMER, V21, P595 EDWARDS JH, 1984, POLYMER, V25, P395 FU DG, 2002, ADV MATER, V14, P339 GINGER DS, 2004, ANGEW CHEM INT EDIT, V43, P30 GORMAN CB, 1993, J AM CHEM SOC, V115, P1397 GU HW, 2004, ADV FUNCT MATER, V14, P492 GU HW, 2004, ADV MATER, V16, P1356 HALL JW, 1996, MACROMOLECULES, V29, P546 HARADA Y, 2003, LANGMUIR, V19, P5104 HARRIS RF, 2005, ADV MATER, V17, P39 HYUN J, 2001, MACROMOLECULES, V34, P5644 IVIN KJ, 1997, OLEFIN METATHESIS ME, P472 JEON NL, 1999, APPL PHYS LETT, V75, P4201 JONES DM, 2002, ADV MATER, V14, P1130 JUANG A, 2001, LANGMUIR, V17, P1321 KAHOLEK M, 2004, NANO LETT, V4, P373 KIM NY, 2000, MACROMOLECULES, V33, P2793 KRAMER S, 2003, CHEM REV, V103, P4367 LEE W, 2005, LANGMUIR, V21, P8839 LEI CH, 2003, APPL PHYS LETT, V83, P482 LI QG, 2003, LANGMUIR, V19, P166 LIU GY, 2000, ACCOUNTS CHEM RES, V33, P457 LIU GY, 2002, P NATL ACAD SCI USA, V99, P5165 LIU XG, 2003, ANGEW CHEM INT EDIT, V42, P4785 LYNN DM, 1996, J AM CHEM SOC, V118, P784 MAMIN HJ, 1990, PHYS REV LETT, V65, P2418 PARK LY, 1992, CHEM MATER, V4, P1388 PINER RD, 1999, SCIENCE, V283, P661 SAILOR MJ, 1990, SCIENCE, V249, P1146 SCHERMAN OA, 2001, SYNTHETIC MET, V124, P431 SCHERMAN OA, 2003, J AM CHEM SOC, V125, P8515 STAII C, 2004, NANO LETT, V4, P859 SUGIMURA H, 1995, LANGMUIR, V11, P3623 SUGIMURA H, 1997, NANOTECHNOLOGY, V8, P15 TRNKA TM, 2001, ACCOUNTS CHEM RES, V34, P18 VONWERNE TA, 2003, J AM CHEM SOC, V125, P3831 WECK M, 1999, J AM CHEM SOC, V121, P4088 WIDAWSKI G, 1995, J MATER CHEM, V5, P1847 WOUTERS D, 2003, LANGMUIR, V19, P9033 XU P, 2004, ADV MATER, V16, P628ISI:000238159300003VUSA, Res Off, Res Triangle Pk, NC 27709 USA. Duke Univ, Dept Mech Engn & Mat Sci, Durham, NC 27708 USA. Duke Univ, Ctr Biol Inspired Mat & Mat Syst, Durham, NC 27708 USA. Pohang Univ Sci & Technol, Dept Chem, Pohang 790784, Kyungbook, South Korea. Caster, KC, USA, Res Off, Res Triangle Pk, NC 27709 USA. ken.caster@duke.edu zauscher@duke.eduwinternal-pdf://2006 Small Lee Nanopatterned Polymer Brushes-0575346448/2006 Small Lee Nanopatterned Polymer Brushes.pdfP=4`0306377796\2006 Small Lee Nanopatterned Polymer Brushes.pdf~?&/Plain, J. Pallandre, A. Nysten, B. Jonas, A. M.20062Nanotemplated crystallization of organic molecules892-897Small27crystallization; nanolithography; pattern formation; patterning; physisorption SELF-ASSEMBLED MONOLAYERS; DIP-PEN NANOLITHOGRAPHY; BUILDING-BLOCKS; TEMPLATES; SURFACES; NANOSTRUCTURES; NANOWIRES; CRYSTALS; PATTERNS; DEVICESArticleJul://000238159300012 Times Cited: 0 Cited References: AIZENBERG J, 1999, NATURE, V398, P495 BARALIA GG, 2006, NANOTECHNOLOGY, V17, P1160 BRISENO AL, 2005, J AM CHEM SOC, V127, P12164 CUI Y, 2001, SCIENCE, V291, P851 DAILLANT J, 1999, XRAY NEUTRON REFLECT GU JH, 2004, J AM CHEM SOC, V126, P8098 HOEPPENER S, 2002, ADV MATER, V14, P1036 HOFF JD, 2004, NANO LETT, V4, P853 HUANG Y, 2001, SCIENCE, V291, P630 JONAS U, 2002, P NATL ACAD SCI USA, V99, P5034 KOVTYUKHOVA NI, 2002, CHEM-EUR J, V8, P4355 LEE KB, 2002, SCIENCE, V295, P1702 LEE SW, 2005, ADV MATER, V17, P2749 LEHN JM, 1995, SUPRAMOLECULAR CHEM LIU ST, 2002, NANO LETT, V2, P1055 LIU ST, 2004, NANO LETT, V4, P845 ONCLIN S, 2005, ANGEW CHEM INT EDIT, V44, P6282 ONCLIN S, 2005, ANGEW CHEM, V117, P6438 PALLANDRE A, 2004, NANO LETT, V4, P365 PALLANDRE A, 2005, J AM CHEM SOC, V127, P4320 PALLANDRE A, 2006, ADV MATER, V18, P481 PALLANDRE A, 2006, ELECTROPHORESIS, V27, P584 PARVIZ BA, 2003, IEEE T ADV PACKAGING, V26, P233 PERCEC V, 2002, NATURE, V419, P384 TIAN ZRR, 2003, NANO LETT, V3, P179 TSUKRUK VV, 2004, PHYS REV LETT, V92 WHITESIDES GM, 2002, SCIENCE, V295, P2418 ZHONG ZH, 2003, SCIENCE, V302, P1377ISI:000238159300012LUniv Catholique Louvain, Unite Phys & Chim Hauts Polymeres POLY, B-1348 Louvain, Belgium. Univ Catholique Louvain, Res Ctr Micro & Nanoscop Mat & Elect Devices CeRM, B-1348 Louvain, Belgium. Jonas, AM, Univ Catholique Louvain, Unite Phys & Chim Hauts Polymeres POLY, Pl Croix Sud 1, B-1348 Louvain, Belgium. alain.jonas@uclouvain.beinternal-pdf://2006 Small Plain Nanotemplated crystallization of organic molecules-1900789776/2006 Small Plain Nanotemplated crystallization of organic molecules.pdfPWaLlain Nanotemplated crystallization of organic molecules.pdf `4m, S. K. Lee, H.2006QAnodic oxidation lithography via atomic force microscope on organic resist layers187-195 Polymer-Korea303matomic force microscope; nanolithography; anodic oxidation or anodization; organic resist; self-assembled monolayer; Langmuir-Blodgett film; polymer resist SCANNING TUNNELING MICROSCOPE; SELF-ASSEMBLED MONOLAYERS; DIP-PEN NANOLITHOGRAPHY; ANODIZATION LITHOGRAPHY; NANOMETER-SCALE; PROBE LITHOGRAPHY; SILICON SURFACES; AFM LITHOGRAPHY; PALMITIC ACID; NANOFABRICATIONArticleMayXAtomic force microscope (AFM)-based anodic oxidation lithography has gained great interests in fabricating nanometer scale features on semiconductor or metal substrates beyond the limitation of optical lithography. In this article AFM anodic oxidation lithography and its organic resist layers are introduced based on our previous works. Organic resist layers of self-assembled monolayers, Langmuir-Blodgett films and polymer films are suggested to play a key role in enhancing the aspect ratio of producing features, the lithographic speed, and spatial precision in AFM anodic oxidation lithography.://000238074500001 Times Cited: 0 Cited References: AHN SJ, 2002, APPL PHYS LETT, V80, P2592 AVOURIS P, 1997, APPL PHYS LETT, V71, P285 BABA M, 1990, JPN J APPL PHYS PT 1, V29, P2854 BAE S, 2005, NANOTECHNOLOGY, V16, P2082 BINNIG G, 1982, PHYS REV LETT, V49, P57 BINNIG G, 1986, PHYS REV LETT, V56, P930 BRANDOW SL, 1997, J VAC SCI TECHNOL B, V15, P1818 DAGATA JA, 1990, APPL PHYS LETT, V56, P2001 EIGLER DM, 1990, NATURE, V344, P524 GARFUNKEL E, 1989, SCIENCE, V246, P99 GATES BD, 2005, CHEM REV, V105, P1171 GORDON AE, 1995, J VAC SCI TECHNOL B, V13, P2805 GOULD P, 2003, MAT TODAY, V6, P34 ISRAELACHVILI JN, 1992, INTERMOLECULAR SURFA KIM JC, 1998, JPN J APPL PHYS, V37, P324 KIM SM, 2003, J VAC SCI TECHNOL B, V21, P2398 KOLBE H, 1849, LIEBIGS ANN CHEM, V69, P257 KONSEK SL, 1997, APPL PHYS LETT, V70, P1846 LEE H, 2002, APPL PHYS LETT, V81, P138 LEE HJ, 2003, MATER RES SOC SYMP P, V739, P199 LEE S, 2005, NANOTECHNOLOGY, V16, P3137 LEE SH, 2004, ENCY NANOSCIENCE NAN, P109 LEE W, 2002, LANGMUIR, V18, P8375 LEE W, 2005, LANGMUIR, V21, P8839 LEE WB, 2001, SYNTHETIC MET, V117, P305 LEGRAND B, 1999, APPL PHYS LETT, V74, P4049 LI Q, 2003, LANGMUIR, V19, P66 LIU GY, 2000, ACCOUNTS CHEM RES, V33, P457 LIU JF, 2002, NANO LETT, V2, P937 LYO IW, 1991, SCIENCE, V253, P173 MARSH G, 2003, MAT TODAY, V6, P28 NYFFENEGGER RM, 1997, CHEM REV, V97, P1195 PINER RD, 1999, SCIENCE, V283, P661 RADOJKOVIC P, 1998, APPL PHYS A-MATE S 2, V66, S701 SHEEHAN PE, 2004, APPL PHYS LETT, V85, P1589 SILVER RM, 1987, APPL PHYS LETT, V51, P247 SNOW ES, 1999, APPL PHYS LETT, V75, P1476 SON MS, 2002, J KOREAN PHYS SOC, V41, P949 STIEVENARD D, 1997, APPL PHYS LETT, V70, P3272 SUGIMURA H, 1996, J VAC SCI TECHNOL 1, V14, P1223 TELLO M, 2001, APPL PHYS LETT, V79, P424 ULMAN A, 1991, INTRO ULTRATHIN ORGA VERSEN M, 2000, ULTRAMICROSCOPY, V82, P159 WILDER K, 1998, J VAC SCI TECHNOL B, V16, P6 WOUTERS D, 2004, ANGEW CHEM INT EDIT, V43, P2480 XU S, 1997, LANGMUIR, V13, P127 ZHAO JW, 2002, NANO LETTERS, V2, P137ISI:000238074500001Hanyang Univ, Dept Chem, Seoul 133791, South Korea. Lee, H, Hanyang Univ, Dept Chem, Seoul 133791, South Korea. haiwon@hanyang.ac.kra~?(jLiu, D. G. Gugliotti, L. A. Wu, T. Dolska, M. Tkachenko, A. G. Shipton, M. K. Eaton, B. E. Feldheim, D. L.2006@RNA-mediated synthesis of palladium nanoparticles on Au surfaces 5862-5866Langmuir2213IN-VITRO SELECTION; SELF-ASSEMBLED MONOLAYERS; DIP-PEN NANOLITHOGRAPHY; DNA MONOLAYERS; BOND FORMATION; CATALYTIC RNA; STRANDED-DNA; APTAMERS; GOLD; EVOLUTIONArticleJunRNA catalysts for the shape-controlled synthesis of Pd particles from the precursor complex trisdibenzylideneacetone dipalladium ([Pd-2(DBA)(3)] were recently discovered in our laboratory (J. Am. Chem. Soc. 2005, 127, 17814-17818). In the work described here, RNA codes for hexagonal Pd platelets and Pd cubes were covalently immobilized on gold surfaces and evaluated for their activity toward particle synthesis. When coupled to gold via oligoethylene glycol linkers, both RNA sequences were able to catalyze the formation of Pd particles with the same shape control previously observed in solution. For low surface coverages, the average distance between RNA molecules on the surface was estimated at ca. 300 nm, yet large (e g., dimensions of hundreds of nanometers) Pd hexagons and cubes still formed. This surprising result suggests that a single RNA molecule may be sufficient for nucleating and controlling the shapes of these particles. Finally, the use of surface-bound RNA as a tool for directing the orthogonal synthesis of materials on surfaces was demonstrated. Patterning the RNA code for Pd hexagons next to the code for Pd cubes, followed by incubation in a solution containing [Pd-2(DBA)(3)], resulted in the spontaneous formation of spatially distinct spots of hexagonal and cubic particles.://000238217000056 Times Cited: 0 Cited References: AHMADI TS, 1996, CHEM MATER, V8, P1161 BEAUDRY AA, 1992, SCIENCE, V257, P635 BIETSCH A, 2004, LANGMUIR, V20, P5119 BOCK C, 2004, PROTEOMICS, V4, P609 BURGSTALLER P, 1994, ANGEW CHEM INT EDIT, V33, P1084 BURGSTALLER P, 1996, BIOORG MED CHEM LETT, V6, P1157 BURKE DH, 1996, J MOL BIOL, V264, P650 BURKE DH, 1997, CHEM BIOL, V4, P833 CHAPMAN KB, 1994, CURR OPIN STRUC BIOL, V4, P618 CHUNG SW, 2005, SMALL, V1, P64 COLLETT JR, 2005, METHODS, V37, P4 CONRAD R, 1996, ANAL BIOCHEM, V242, P261 CONRAD RC, 1996, METHOD ENZYMOL, V267, P336 COX JC, 2002, NUCLEIC ACIDS RES, P30 DEMERS LM, 2002, SCIENCE, V296, P1836 ELLINGTON AD, 1990, NATURE, V346, P818 ELLINGTON AD, 1994, CURR BIOL, V4, P427 FAHLMAN RP, 2002, J AM CHEM SOC, V124, P4610 FAMULOK M, 1994, J AM CHEM SOC, V116, P1698 GARDNER TJ, 1995, J AM CHEM SOC, V117, P6927 GATES BD, 2005, CHEM REV, V105, P1171 GUGLIOTTI LA, 2004, SCIENCE, V304, P850 GUGLIOTTI LA, 2005, J AM CHEM SOC, V127, P17814 GUHLKE S, 2003, EUR J NUCL MED MOL I, V30, P1441 KIRKLAND AI, 1993, P ROY SOC LOND A MAT, V440, P589 KLUG SJ, 1999, RNA, V5, P1180 KUMAR PKR, 1995, J CELL BIOCHEM, V34, P6 LAIBINIS PE, 1989, SCIENCE, V245, P845 LAUHON CT, 1995, FASEB J, V9, A1422 LAUHON CT, 1995, J AM CHEM SOC, V117, P1246 LEVICKY R, 1998, J AM CHEM SOC, V120, P9787 LI HY, 2004, J AM CHEM SOC, V126, P418 LORSCH JR, 1994, BIOCHEMISTRY-US, V33, P973 LORSCH JR, 1996, ACCOUNTS CHEM RES, V29, P103 LOVE JC, 2005, CHEM REV, V105, P1103 NAITO K, 2005, CHAOS, V15 NIEUWLANDT D, 2003, CHEMBIOCHEM, V4, P651 OSBORNE SE, 1997, CURR OPIN CHEM BIOL, V1, P5 PANG DW, 2000, ANAL CHEM, V72, P4700 PARK SH, 2005, NANO LETT, V5, P693 PINTO YY, 2005, NANO LETT, V5, P2399 POTYRAILO RA, 1998, ANAL CHEM, V70, P3419 PUNTES VF, 2001, SCIENCE, V291, P2115 PUNTES VF, 2002, TOP CATAL, V19, P145 ROBERTSON DL, 1990, NATURE, V344, P467 SCHILARDI PL, 2005, CHEM-EUR J, V12, P38 SCHNEIDER D, 1992, J MOL BIOL, V228, P862 SEEMAN NC, 2003, CHEM BIOL, V10, P1151 SENGLE G, 2001, CHEM BIOL, V8, P459 TARASOW TM, 1997, NATURE, V389, P54 TUERK C, 1990, SCIENCE, V249, P505 WECKER M, 1996, RNA, V2, P982 WIEGAND TW, 1997, CHEM BIOL, V4, P675 WILSON C, 1995, NATURE, V374, P777 WRIGHT MC, 1996, MOL BIOL CELL S, V7, P1950 XIAO SJ, 2002, J NANOPART RES, V4, P313 YAN AC, 2005, FRONT BIOSCI, V10, P1802 YAN H, 2003, SCIENCE, V301, P1882 YAU HCM, 2002, THIN SOLID FILMS, V413, P218 ZHANG L, 2001, BIOCONJUGATE CHEM, V12, P939 ZHANG RY, 2002, J PHYS CHEM B, V106, P11233ISI:000238217000056N Carolina State Univ, Dept Chem, Raleigh, NC 27695 USA. Univ Colorado, Dept Chem & Biochem, Boulder, CO 80309 USA. Eaton, BE, N Carolina State Univ, Dept Chem, Raleigh, NC 27695 USA. Bruce.Eaton@colorado.edu Dan_Feldheim@ncsu.eduinternal-pdf://2006 Lnagmuir Liu RNA mediated synthesis of palladium nanoparticles-3360473872/2006 Lnagmuir Liu RNA mediated synthesis of palladium nanoparticles.pdf!~?)3Cisneros, D. A. Hung, C. Franz, C. A. Muller, D. J.2006fObserving growth steps of collagen self-assembly by time-lapse high-resolution atomic force microscopy232-245Journal of Structural Biology1543AFM; collagen molecules; growth steps; microfibrils; molecular interactions; self-assembly SCANNING-ELECTRON-MICROSCOPY; DIP-PEN NANOLITHOGRAPHY; I COLLAGEN; EXTRACELLULAR-MATRIX; MECHANICAL-PROPERTIES; BASEMENT-MEMBRANE; MOLECULAR PACKING; PROBE MICROSCOPY; TRABECULAR BONE; OMPF PORINArticleJunInsights into molecular mechanisms of collagen assembly are important for understanding countless biological processes and at the same time a prerequisite for many biotechnological and medical applications. In this work, the self-assembly of collagen type I molecules into fibrils could be directly observed using time-lapse atomic force microscopy (AFM). The smallest isolated fibrillar structures initiating fibril growth showed a thickness of approximate to 1.5 nm corresponding to that of a single collagen molecule. Fibrils assembled in vitro established an axial D-periodicity of 67 nm such as typically observed for in vivo assembled collagen fibrils from tendon. At given collagen concentrations of the buffer solution the fibrils showed constant lateral and longitudinal growth rates. Single fibrils continuously grew and fused with each other until the supporting surface was completely covered by a nanoscopically well-defined collagen matrix. Their thickness of approximate to 3 nm suggests that the fibrils were build from laterally assembled collagen microfibrils. Laterally the fibrils grew in steps of approximate to 4 nm, indicating microfibril formation and incorporation. Thus, we suggest collagen fibrils assembling in a two-step process. In a first step, collagen molecules assemble with each other. In the second step, these molecules then rearrange into microfibrils which form the building blocks of collagen fibrils. High-resolution AFM topographs revealed substructural details of the D-band architecture of the fibrils forming the collagen matrix. These substructures correlated well with those revealed from positively stained collagen fibers imaged by transmission electron microscopy. (c) 2006 Elsevier Inc. All rights reserved.://000238104900002 3Times Cited: 0 Cited References: ABRAMOFF MD, 2004, BIOPHOTONICS INT, V11, P36 AGARWAL G, 2002, BIOCHEMISTRY-US, V41, P11091 AKIYAMA SK, 1990, BIOCHIM BIOPHYS ACTA, V1031, P91 ALLEN DB, 1992, PEDIATRICS, V89, P416 BARRET SD, 2004, IMAGE SXM BASELT DR, 1993, BIOPHYS J, V65, P2644 BELL E, 1979, P NATL ACAD SCI USA, V76, P1274 BERNENGO JC, 1978, BIOCHIM BIOPHYS ACTA, V532, P305 BIGI A, 1997, BIOMATERIALS, V18, P657 BISHOP PN, 2000, PROG RETIN EYE RES, V19, P323 CHAPMAN JA, 1990, ELECTRON MICROSC REV, V3, P143 CHEN CH, 2000, J STRUCT BIOL, V131, P44 CHERNOFF EAG, 1992, J VAC SCI TECHNOL A, V10, P596 CHRISTIANSEN DL, 2000, MATRIX BIOL, V19, P409 COOMBES AGA, 2002, BIOMATERIALS, V23, P2113 DEMERS LM, 2002, SCIENCE, V296, P1836 DRAKE B, 1989, SCIENCE, V243, P1586 ENGEL A, 1997, CURR OPIN STRUC BIOL, V7, P279 ENGEL A, 2000, NAT STRUCT BIOL, V7, P715 ENGEL J, 1998, MATRIX BIOL, V17, P679 FANTNER GE, 2004, BONE, V35, P1013 FREDERIX PLTM, 2003, CURR OPIN CHEM BIOL, V7, P641 GALE M, 1995, BIOPHYS J, V68, P2124 GAYATRI R, 2001, BIOCHEM BIOPH RES CO, V283, P229 GRAHAM HK, 2000, J MOL BIOL, V295, P891 GRINNELL F, 2000, TRENDS CELL BIOL, V10, P362 GRINNELL F, 2003, TRENDS CELL BIOL, V13, P264 GUIDRY C, 1985, J CELL SCI, V79, P67 GUTSMANN T, 2003, BIOPHYS J, V84, P2593 GUTSMANN T, 2005, BIOPHYS J, V89, P536 HABELITZ S, 2002, J STRUCT BIOL, V138, P227 HASSENKAM T, 2004, BONE, V35, P4 HATTORI S, 1999, J BIOCHEM-TOKYO, V125, P676 HO SP, 2005, J STRUCT BIOL, V151, P69 HOFMANN H, 1984, J MOL BIOL, V172, P325 HOHENESTER E, 2002, MATRIX BIOL, V21, P115 HOLMES DF, 1996, J MOL BIOL, V261, P93 HOLMES DF, 2001, P NATL ACAD SCI USA, V98, P7307 HULMES DJ, 1981, NATURE, V293, P239 HULMES DJS, 1981, P NATL ACAD SCI USA, V78, P3567 HULMES DJS, 2002, J STRUCT BIOL, V137, P2 JIANG FZ, 2004, J STRUCT BIOL, V148, P268 JIANG FZ, 2004, MICROSC RES TECHNIQ, V64, P435 JURVELIN JS, 1996, J STRUCT BIOL, V117, P45 KADLER KE, 1987, J BIOL CHEM, V262, P15696 KADLER KE, 1993, INT J EXP PATHOL, V74, P319 KADLER KE, 1996, BIOCHEM J 1, V316, P1 KADLER KE, 2000, MATRIX BIOL, V19, P359 KARRASCH S, 1994, P NATL ACAD SCI USA, V91, P836 KOBAYASHI K, 1985, COLLAGEN REL RES, V5, P253 KUNICKI TJ, 2002, ARTERIOSCL THROM VAS, V22, P14 LEE CH, 2001, INT J PHARM, V221, P1 LEE KB, 2002, SCIENCE, V295, P1702 LIN H, 1999, BIOCHEMISTRY-US, V38, P9956 LLOYD AW, 2002, MED DEVICE TECHNOL, V13, P18 MARSHALL GW, 2001, SURF SCI, V491, P444 MCBRIDE DJ, 1992, MATRIX, V12, P256 MEEK KM, 1979, J BIOL CHEM, V254, P10710 MELLER D, 1997, CELL TISSUE RES, V288, P111 MULLER DJ, 2002, PROG BIOPHYS MOL BIO, V79, P1 MYLLYHARJU J, 2001, ANN MED, V33, P7 MYLLYHARJU J, 2004, TRENDS GENET, V20, P33 ORGEL JPRO, 2001, STRUCTURE, V9, P1061 ORTIZURDA S, 2005, SCIENCE, V307, P1773 OTTANI V, 2002, MICRON, V33, P587 PAIGE MF, 2001, MICRON, V32, P355 PATERLINI MG, 1995, BIOPOLYMERS, V35, P607 PHILIPPSEN A, 2002, BIOPHYS J, V82, P1667 POOLE K, 2005, J MOL BIOL, V349, P380 PROCKOP DJ, 1998, J STRUCT BIOL, V122, P111 PROCKOP DJ, 1998, MATRIX BIOL, V16, P519 PROCKOP DJ, 1999, BIOCHEM SOC T, V27, P15 RASPANTI M, 1989, INT J BIOL MACROMOL, V11, P367 RASPANTI M, 1997, J STRUCT BIOL, V119, P118 RASPANTI M, 2001, MATRIX BIOL, V20, P601 RASPANTI M, 2002, ARCH HISTOL CYTOL, V65, P37 RASPANTI M, 2005, MICROSC RES TECHNIQ, V67, P1 REVENKO I, 1994, BIOL CELL, V80, P67 SATO K, 2000, J BIOL CHEM, V275, P25870 SCHABERT FA, 1995, SCIENCE, V268, P92 SCHWARZ UD, 1994, J MICROSC-OXFORD, V173, P183 SILVER FH, 1979, BIOPOLYMERS, V18, P2523 SILVER FH, 2002, CONNECT TISSUE RES, V43, P569 SILVER FH, 2003, J BIOMECH, V36, P1529 SQUIRE JM, 1980, NATURE, V288, P410 SUN HB, 2000, ANAL BIOCHEM, V283, P153 THALHAMMER S, 2001, J ARCHAEOL SCI, V28, P1061 THOMAS AC, 2003, CARDIOVASC PATHOL, V12, P271 WARD NP, 1986, J MOL BIOL, V190, P107 WESS TJ, 1998, J MOL BIOL, V275, P255 WESS TJ, 2005, ADV PROTEIN CHEM, V70, P341 YANG WC, 2005, J BIOL CHEM, V280, P20680 YUSPA SH, 2005, SCIENCE, V307, P1727ISI:000238104900002Tech Univ Dresden, Ctr Biotechnol, D-01307 Dresden, Germany. Muller, DJ, Tech Univ Dresden, Ctr Biotechnol, D-01307 Dresden, Germany. mueller@biotec.tu-dresden.deinternal-pdf://2006 Jo of StructBio Cisneros Observing growth steps-3495483920/2006 Jo of StructBio Cisneros Observing growth steps.pdf ~?**Kinser, C. R. Schmitz, M. J. Hersam, M. C.2006zKinetics and mechanism of atomic force microscope local oxidation on hydrogen-passivated silicon in inert organic solvents1377-+Advanced Materials1811SCANNED PROBE OXIDATION; DIP-PEN NANOLITHOGRAPHY; FIELD-INDUCED OXIDATION; CHARGE-LIMITED GROWTH; SPACE-CHARGE; NANO-OXIDATION; SURFACES; FABRICATION; NANOFABRICATION; NANOSTRUCTURESArticleJunOConductive atomic force microscope (AFM) nanopatterning on hydrogen-terminated silicon in a hydrophobic organic solvent under ambient conditions produces features consistent with AFM field-induced oxidation. The growth rate of the oxide features (see figure) exhibits modulation consistent with a space-charge-limited growth mechanism.://000238203300006 2Times Cited: 1 Cited References: ALBERTY RA, 1957, J CHEM PHYS, V26, P1231 AVOURIS P, 1997, APPL PHYS LETT, V71, P285 BASU R, 2004, APPL PHYS LETT, V85, P2619 CALLEJA M, 2000, APPL PHYS LETT, V76, P3427 DAGATA JA, 1990, APPL PHYS LETT, V56, P2001 DAGATA JA, 1998, APPL PHYS LETT, V73, P271 DAGATA JA, 1998, J APPL PHYS, V84, P6891 DAGATA JA, 2000, APPL PHYS LETT, V76, P2710 DAGATA JA, 2004, J APPL PHYS, V96, P2386 DEMERS LM, 2002, SCIENCE, V296, P1836 DUBOIS E, 2000, J APPL PHYS, V87, P8148 GORDON AE, 1995, J VAC SCI TECHNOL B, V13, P2805 GREENE ME, 2004, MICROSC RES TECHNIQ, V64, P415 GUISINGER NP, 2004, NANO LETT, V4, P55 HURLEY PT, 2003, J AM CHEM SOC, V125, P11334 JIN H, 2004, LANGMUIR, V20, P6252 KINSER CR, 2005, NANO LETT, V5, P91 LI Y, 2001, J AM CHEM SOC, V123, P2105 LIU ZM, 2003, SCIENCE, V302, P1543 MAOZ R, 1999, ADV MATER, V11, P55 MARTINEZ RV, 2005, NANO LETT, V5, P1161 PAVLOVIC E, 2003, NANO LETT, V3, P779 PINER RD, 1999, SCIENCE, V283, P661 SNOW ES, 2000, APPL PHYS LETT, V76, P1782 STIEVENARD D, 1997, APPL PHYS LETT, V70, P3272 SUEZ I, 2005, NANO LETT, V5, P321 SUGIMURA H, 1997, J AM CHEM SOC, V119, P9226 TELLO M, 2003, APPL PHYS LETT, V83, P2339 TELLO M, 2005, ADV MATER, V17, P1480 TEUSCHLER T, 1995, APPL PHYS LETT, V67, P3144 UHLIG HH, 1956, ACTA METALL, V4, P541 WACASER BA, 2003, APPL PHYS LETT, V82, P808 WOLTERS DR, 1989, J APPL PHYS, V65, P5126 XU S, 1997, LANGMUIR, V13, P127ISI:000238203300006Northwestern Univ, Dept Mat Sci & Engn, Evanston, IL 60208 USA. Hersam, MC, Northwestern Univ, Dept Mat Sci & Engn, 2220 Campus Dr, Evanston, IL 60208 USA. m-hersam@northwestern.eduinternal-pdf://2006 Adv Mat Kinser Kinetics & Mechanism of Atomic Force Microscope-1448765456/2006 Adv Mat Kinser Kinetics & Mechanism of Atomic Force Microscope.pdfTaL(Mat Kinser Kinetics & Mechanism of Atomic Force Microscope.pdf ~?+Chi, Y. S. Choi, I. S.2006Dip-pen nanolithography using the amide-coupling reaction with interchain carboxylic anhydride-terminated self-assembled monolayers 1031-1036Advanced Functional Materials168SCANNING PROBE LITHOGRAPHY; DIELS-ALDER REACTION; FORCE MICROSCOPY; THIN-FILMS; GOLD; INK; SURFACES; NANOSTRUCTURES; FABRICATION; ADSORPTIONArticleMayjHerein we report on a new type of dip-pen nanolithography (DPN), which utilizes an interfacial organic reaction-the amide-coupling reaction - between chemically activated surfaces and amine ink molecules transferred from an atomic force microscopy tip. As a representative of the chemically activated surfaces that could react with amine compounds, we formed a self-assembled monolayer terminating in interchain carboxylic anhydride (ICA) groups on gold, and generated chemically derived nanopatterns using alkylamines as ink molecules. Amine inks showed diffusive behavior similar to thiol inks on gold in conventional DPN, and the pattern sizes were controlled by changing the tip dwell times. In addition, nanopatterns of hydrolyzed ICAs were generated by taking advantage of the participation of the water meniscus in the DPN process and the chemical nature of the ICAs.://000238073100004 Times Cited: 1 Cited References: BENALI M, 2002, LANGMUIR, V18, P872 BLASDEL LK, 2002, LANGMUIR, V18, P5055 CARNO JC, 2003, NANO LETT, V3, P389 CHAPMAN RG, 2000, LANGMUIR, V16, P6927 CHAPMAN RG, 2001, LANGMUIR, V17, P1225 CHI YS, 2005, B KOR CHEM SOC, V26, P361 CHI YS, 2005, LANGMUIR, V21, P11765 DEGENHART GH, 2004, LANGMUIR, V20, P6126 DEMERS LM, 2002, SCIENCE, V296, P1836 FU L, 2003, NANO LETT, V3, P757 GINGER DS, 2004, ANGEW CHEM INT EDIT, V43, P30 HONG SH, 1999, SCIENCE, V286, P523 HONG SH, 2000, SCIENCE, V288, P1808 HUTT DA, 1997, LANGMUIR, V13, P2740 JANG JY, 2001, J CHEM PHYS, V115, P2721 JUNG H, 2003, J AM CHEM SOC, V125, P12096 JUNG H, 2004, NANO LETT, V4, P2171 KRAMER S, 2003, CHEM REV, V103, P4367 KWON Y, 2002, J AM CHEM SOC, V124, P806 LEE JK, 2003, LANGMUIR, V19, P8141 LEE JK, 2004, J PHYS CHEM B, V108, P7665 LEE JK, 2004, LANGMUIR, V20, P3844 LEE JK, 2005, LANGMUIR, V21, P10311 LEE KB, 2003, KOREAN J CHEM ENG, V20, P956 LI Y, 2001, J AM CHEM SOC, V123, P2105 LIAO JH, 2002, CHINESE PHYS LETT, V19, P134 LIM JH, 2002, ADV MATER, V14, P1474 LIU GY, 2000, ACCOUNTS CHEM RES, V33, P457 LOVE JC, 2005, CHEM REV, V105, P1103 MATSUBARA S, 2002, CHEM LETT 0905, P886 MAYNOR BW, 2001, LANGMUIR, V17, P2575 MAYNOR BW, 2002, J AM CHEM SOC, V124, P522 NOY A, 2002, NANO LETTERS, V2, P109 OSTUNI E, 2001, LANGMUIR, V17, P5605 PENN DJ, 2003, LANGMUIR, V19, P9028 PINER RD, 1997, LANGMUIR, V13, P6864 PINER RD, 1999, SCIENCE, V283, P661 PORTER LA, 2002, NANO LETT, V2, P1369 SU M, 2002, J AM CHEM SOC, V124, P1560 SULLIVAN TP, 2003, EUR J ORG CHEM JAN, P17 WEEKS BL, 2002, PHYS REV LETT, V88 WILSON DL, 2001, P NATL ACAD SCI USA, V98, P13660 WOLFENDEN R, 1985, J AM CHEM SOC, V107, P4345 YAN L, 1997, LANGMUIR, V13, P6704 YAN L, 1999, LANGMUIR, V15, P1208 YANG HC, 1996, LANGMUIR, V12, P726ISI:000238073100004Korea Adv Inst Sci & Technol, Dept Chem, Taejon 305701, South Korea. Korea Adv Inst Sci & Technol, Sch Mol Sci BK21, Taejon 305701, South Korea. Choi, IS, Korea Adv Inst Sci & Technol, Dept Chem, Taejon 305701, South Korea. ischoi@kaist.ac.kryinternal-pdf://2006 AdvFuncMats Chi DPN using amide-coupling-3512415760/2006 AdvFuncMats Chi DPN using amide-coupling.pdfP4Ĉ-2927665189\2006_AdvFuncMater_Chi_pdf_AmideCouplingReact.pdf ~?,IAzzaroni, O. Moya, S. E. Brown, A. A. Zheng, Z. Donath, E. Huck, W. T. S.2006|Polyelectrolyte brushes as ink nanoreservoirs for microcontact printing of ionic species with poly(dimethyl siloxane) stamps 1037-1042Advanced Functional Materials168DDIP-PEN NANOLITHOGRAPHY; MOLECULAR PRINTBOARDS; FABRICATION; SURFACEArticleMayIn this work a new variation of microcontact printing is described, which is used to transfer chemical patterns onto different substrates. The approach is based on the use of conventional elastomeric stamps modified with polyelectrolyte brushes. It is demonstrated that, by using stamps modified with brushes acting as preconcentrating/sorbent nanolayers, it is possible to control the uptake of aqueous inks containing ionic species. This controlled uptake can be easily used for site-selective delivery of the loaded species by means of soft lithography. The potential of this approach is demonstrated by creating patterned counterion domains in a flat polyelectrolyte brush and by promoting a site-selective metallization through galvanic displacement reactions with reactive species.://000238073100005 ITimes Cited: 1 Cited References: AULETTA T, 2004, ANGEW CHEM INT EDIT, V43, P369 AZZARONI O, 2005, MACROMOLECULES, V38, P10192 BALMER TE, 2005, LANGMUIR, V21, P622 BIELSALSKI M, 2004, J CHEM PHYS, V120, P8807 BRUCKBAUER A, 2002, J AM CHEM SOC, V124, P8810 BRUININK CM, 2005, CHEM-EUR J, V11, P3988 CAMPBELL CJ, 2005, LANGMUIR, V21, P2637 DELAMARCHE E, 2001, ADV MATER, V13, P1164 DELAMARCHE E, 2003, LANGMUIR, V19, P8749 ELDING LI, 1972, INORG CHIM ACTA, V6, P683 ELS ER, 1997, MINER ENG, V10, P1177 ELS ER, 2000, MINER ENG, V13, P401 KAZAKOVA VI, 1967, ZH NEORG KHIM+, V12, P323 KLAJN R, 2004, NAT MATER, V3, P729 KRAUS T, 2005, LANGMUIR, V21, P7796 LI XM, 2003, NANO LETT, V3, P1449 LOO YL, 2002, J AM CHEM SOC, V124, P7654 MARTIN BD, 1998, LANGMUIR, V14, P3971 MARTIN BD, 2000, LANGMUIR, V16, P9944 MEI Y, 2005, EUR PHYS J E, V6, P341 MOYA SE, 2005, MACROMOL RAPID COMM, V26, P1117 PINER RD, 1999, SCIENCE, V283, P661 SCHELLEKENS J, 2004, MAT RES SOC S P EXS, V2 SUN YG, 2004, J AM CHEM SOC, V126, P3892 WEIBEL DB, 2005, LANGMUIR, V21, P6436 XIA Y, 1998, ANGEW CHEM INT EDIT, V37, P550 YANG KL, 2003, ADV MATER, V15, P1819 YANG ZP, 2000, ADV MATER, V12, P413 ZHAO MQ, 1999, ANGEW CHEM INT EDIT, V38, P364ISI:000238073100005pUniv Cambridge, Dept Chem, Melville Lab Polymer Synth, Cambridge CB2 1EW, England. Univ Cambridge, Nanosci Ctr, Cambridge CB3 0FF, England. CIQA, Saltillo 25100, Coahuila, Mexico. Univ Leipzig, Inst Biophys & Med Phys, D-04107 Leipzig, Germany. Huck, WTS, Univ Cambridge, Dept Chem, Melville Lab Polymer Synth, Lensfield Rd, Cambridge CB2 1EW, England. wtsh2@cam.ac.ukinternal-pdf://2006_Adv Funt Mater_Polyelectrolyte brushes_Azzaroni-3428780560/2006_Adv Funt Mater_Polyelectrolyte brushes_Azzaroni.pdfl(rvoirs-1658351908\2006 Adv Func Mat Azzaroni Polyelectrolyte Brushes Nanorservoirs.pdf~?-'Grodzinski, P. Silver, M. Molnar, L. K.2006>Nanotechnology for cancer diagnostics: promises and challenges307-318&Expert Review of Molecular Diagnostics63Fbiosensor; cancer; image contrast; molecular diagnostics; nanocantilever; nanoparticle; nanotechnology; nanotube; nanowire; quantum dot SEMICONDUCTOR QUANTUM DOTS; NANOMECHANICAL CANTILEVER ARRAY; DIP-PEN NANOLITHOGRAPHY; MRI CONTRAST AGENTS; DNA DETECTION; NANOPARTICLE; NANOCRYSTALS; PROBES; NANOBIOTECHNOLOGY; NANOMATERIALSReviewMay,Despite recent progress in the treatment of cancer, the majority of cases are still diagnosed only after tumors have metastasized, leaving the patient with a grim prognosis. However, there may be an opportunity to drastically reduce the burden of cancer, if the disease can be detected early enough. Nanotechnology is in a unique position to transform cancer diagnostics and to produce a new generation of biosensors and medical imaging techniques with higher sensitivity and precision of recognition. This review examines the in vitro and in vivo diagnostic applications of nanoparticles, and other nanodevices that are likely to have an impact on the field in the future. Future developments that may lead to the realization of multifunctional detection and treatment nonoparticle platforms are also discussed.://000237916000005 Times Cited: 0 Cited References: ALIVISATOS AP, 1996, SCIENCE, V271, P933 ANDERSON SA, 2000, MAGNET RESON MED, V44, P433 ARNTZ Y, 2003, NANOTECHNOLOGY, V14, P86 BRUCHEZ M, 1998, SCIENCE, V281, P2013 BUETOW KH, 2005, SCIENCE, V308, P821 CHAN WCW, 2002, CURR OPIN BIOTECH, V13, P40 CHANG E, 2005, BIOCHEM BIOPH RES CO, V334, P1317 CHEN RJ, 2003, P NATL ACAD SCI USA, V100, P4984 CUI Y, 2001, SCIENCE, V293, P1289 DEJNEKA MJ, 2003, P NATL ACAD SCI USA, V100, P389 DERFUS AM, 2004, NANO LETT, V4, P11 EDWARDS BK, 2005, J NATL CANCER I, V97, P1407 FERRARI M, 2005, BIODRUGS, V19, P203 FERRARI M, 2005, NAT REV CANCER, V5, P161 FODOR SPA, 1991, SCIENCE, V251, P767 FORTINA P, 2005, TRENDS BIOTECHNOL, V23, P168 FRITZ J, 2000, SCIENCE, V288, P316 GABIZON A, 1997, DRUGS S4, V54, P15 GAO XH, 2002, J BIOMED OPT, V7, P532 GAO XH, 2004, NAT BIOTECHNOL, V22, P969 HANAHAN D, 1996, CELL, V86, P353 HANAHAN D, 2000, CELL, V100, P57 HARISINGHANI MG, 2003, NEW ENGL J MED, V348, P2491 HIRSCH LR, 2003, ANAL CHEM, V75, P2377 ILIC B, 2005, NANO LETT, V5, P925 JIN S, 2004, NANO LETT, V4, P915 KIM S, 2004, NAT BIOTECHNOL, V22, P93 KOBAYASHI H, 2004, CURR PHARM BIOTECHNO, V5, P539 KOBAYASHI H, 2004, J NATL CANCER I, V96, P703 KUKOWSKALATALLO JF, 2005, CANCER RES, V65, P5317 LEE KB, 2002, SCIENCE, V295, P1702 LEE KB, 2003, J AM CHEM SOC, V125, P5588 LI J, 2003, NANO LETT, V3, P597 LIM YT, 2003, MOL IMAGING, V2, P50 LIU RH, 2004, ANAL CHEM, V76, P1824 LOUIE AY, 2000, NAT BIOTECHNOL, V18, P321 LOVRIC J, 2005, CHEM BIOL, V12, P1227 MCKENDRY R, 2002, P NATL ACAD SCI USA, V99, P9783 MEDINTZ IL, 2005, NAT MATER, V4, P435 MICHALET X, 2005, SCIENCE, V307, P538 MORAWSKI AM, 2005, CURR OPIN BIOTECH, V16, P89 NAM JM, 2003, SCIENCE, V301, P1884 NAM JM, 2004, J AM CHEM SOC, V126, P5932 NICEWARNERPENA SR, 2001, SCIENCE, V294, P137 NUWAYSIR EF, 2002, GENOME RES, V12, P1749 OBERDORSTER E, 2004, ENVIRON HEALTH PERSP, V112, P1058 PARK SJ, 2002, SCIENCE, V295, P1503 ROSENTHAL A, 1998, SEMIN ONCOL, V25, P315 SALEH OA, 2003, P NATL ACAD SCI USA, V100, P820 SAYES CM, 2004, NANO LETT, V4, P1881 SCHELLENBERGER EA, 2004, CHEMBIOCHEM, V5, P275 SCHMIEDER AH, 2005, MAGNET RESON MED, V53, P621 SITHARAMAN B, 2005, CHEM COMMUN, P3915 TOMALIA DA, 1985, POLYM J, V17, P117 TOMALIA DA, 2005, MAT TODAY, V8, P34 VENDITTO VJ, 2005, MOL PHARM, V2, P302 WALT DR, 2000, SCIENCE, V287, P451 WANG YC, 2005, ANAL CHEM, V77, P4293 WEST JL, 2003, ANNU REV BIOMED ENG, V5, P285 WHITESIDES GM, 2003, NAT BIOTECHNOL, V21, P1161 WICKLINE SA, 2002, J CELL BIOCHEM, V39, P90 WILSON SR, 2002, PERSPECTIVES FULLERE, P155 WINTER PM, 2003, CANCER RES, V63, P5838 WISNER ER, 2003, INVEST RADIOL, V38, P358 WU GH, 2001, NAT BIOTECHNOL, V19, P856 WU XY, 2003, NAT BIOTECHNOL, V21, P41ISI:000237916000005NCI, Sci Applicat Int Res Corp SAIC, Bethesda, MD 20892 USA. Feinstein Kean Healthcare, Cambridge, MA 02142 USA. Grodzinski, P, NCI, Sci Applicat Int Res Corp SAIC, 31 Ctr Dr,MSC 2580,Room 10A52, Bethesda, MD 20892 USA. grodzinp@mail.nih.gov mike.silver@fkhealth.com molnarl@mail.nih.govk ~?.9Crespo-Biel, O. Ravoo, B. J. Huskens, J. Reinhoudt, D. N.2006/Writing with molecules on molecular printboards 2737-2741Dalton Transactions23SELF-ASSEMBLED MONOLAYERS; HOST-GUEST INTERACTIONS; CYCLODEXTRIN MONOLAYERS; FORCE SPECTROSCOPY; BETA-CYCLODEXTRINS; SILICON-OXIDE; GOLD; MULTIVALENT; BINDING; RECOGNITIONArticleNanotechnology aspires to create functional materials with characteristic dimensions of the order 1 - 100 nm. One requirement to make nanotechnology work is to precisely position molecules and nanoparticles on surfaces, so that they may be addressed and manipulated for bottom-up construction of nanoscale devices. Here we review the concept of a "molecular printboard". A molecular printboard is a monolayer of host molecules on a solid substrate on which guest molecules can be attached with control over position, binding strength, and binding dynamics. To this end, cyclodextrins were immobilized in monomolecular layers on gold, on silicon wafers and on glass. Guest molecules ( for example, adamantane and ferrocene derivatives) bind to these host surfaces through supramolecular, hydrophobic inclusion interaction. Multivalent interactions are exploited to tune the binding strength and dynamics of the interaction of guest molecules with the printboard. Molecules can be positioned onto the printboard using supramolecular microcontact printing and supramolecular dip-pen nanolithography due to the specific interaction between the 'ink' and the substrate. In this way, nanoscale patterns can be written and erased on the printboard. Currently, the molecular printboard is exploited for nanofabrication, for example in combination with electroless deposition of metals and by means of supramolecular layer-by-layer deposition.://000238049000002 Times Cited: 0 Cited References: AULETTA T, 2004, ANGEW CHEM INT EDIT, V43, P369 AULETTA T, 2004, J AM CHEM SOC, V126, P1577 BEULEN MWJ, 1998, LANGMUIR, V14, P6424 BEULEN MWJ, 2000, CHEM-EUR J, V6, P1176 BRUININK CM, 2005, CHEM-EUR J, V11, P3988 CRESPOBIEL O, 2005, CHEM-EUR J, V11, P2426 CRESPOBIEL O, 2005, J AM CHEM SOC, V127, P7594 DECHER G, 1997, SCIENCE, V277, P1232 DECHER G, 2003, MULTILAYER THIN FILM DEJONG MR, 2001, CHEM-EUR J, V7, P4164 FRIGGERI A, 1999, CHEM-EUR J, V5, P3595 GATES BD, 2004, ANNU REV MATER RES, V34, P339 GATES BD, 2005, CHEM REV, V105, P1171 HAMMOND PT, 1999, CURR OPIN COLLOID IN, V4, P430 HUISMAN BH, 1995, TETRAHEDRON LETT, V36, P3273 HUISMAN BH, 1996, ADV MATER, V8, P561 HUISMAN BH, 1996, J AM CHEM SOC, V118, P3523 HUSKENS J, 2002, ANGEW CHEM INT EDIT, V41, P4467 JANSEN JFGA, 1994, SCIENCE, V266, P1226 MADOU MJ, 2001, FUNDAMENTALS MICROFA MALLORY GO, 1990, ELECTROLESS PLATING MENOZZI E, 2004, CHEM-EUR J, V10, P2199 MENZ W, 2001, MICROSYSTEM TECHNOLO MULDER A, 2004, J AM CHEM SOC, V126, P6627 MULDER A, 2005, SMALL, V1, P242 NIJHUIS CA, 2004, J AM CHEM SOC, V126, P12266 NIJHUIS CA, 2005, LANGMUIR, V21, P7866 ONCLIN S, 2004, LANGMUIR, V20, P5460 ONCLIN S, 2005, SMALL, V1, P852 SCHIERBAUM KD, 1994, SCIENCE, V265, P1413 SCHONHERR H, 1997, LANGMUIR, V13, P1567 SCHONHERR H, 2000, J AM CHEM SOC, V122, P4963 SCHONHOFF M, 2003, CURR OPIN COLLOID IN, V8, P86 ULMAN A, 1991, INTRO ULTRATHIN ORGA VANVELZEN EUT, 1995, J AM CHEM SOC, V117, P6853 WHITESIDES GM, 2005, SMALL, V1, P172 XIA YN, 1998, ANGEW CHEM INT EDIT, V37, P551ISI:000238049000002Univ Twente, MESA Inst Nanotechnol, Lab Supramol Chem & Technol, NL-7500 AE Enschede, Netherlands. Reinhoudt, DN, Univ Twente, MESA Inst Nanotechnol, Lab Supramol Chem & Technol, POB 217, NL-7500 AE Enschede, Netherlands. d.n.reinhoudt@utwente.nleinternal-pdf://2006_DT_Writing with molecules_Biel-3095023120/2006_DT_Writing with molecules_Biel.pdfhĈlWriting with Molecules-3704513829\2006 Dalton Crespo-Biel Writing with Molecules.pdf~?/Yang, Z. Y. Zhao, Y. P.2006nQM/MM and classical molecular dynamics simulation of histidine-tagged peptide immobilization on nickel surface84-91aMaterials Science and Engineering A-Structural Materials Properties Microstructure and Processing4231-2hybrid QM/MM simulation; IMOMM; CHARMM; histidine; chelate; adhesion DIP-PEN NANOLITHOGRAPHY; GEOMETRY OPTIMIZATION; CRYSTAL-STRUCTURE; QUANTUM; NITRILOTRIACETATE; PROTEINS; PROGRAM; MODELS; IMOMMArticleMayThe hybrid quantum mechanics (QM) and molecular mechanics (MM) method is employed to simulate the His-tagged peptide adsorption to ionized region of nickel surface. Based on the previous experiments, the peptide interaction with one Ni ion is considered. In the QM/MM calculation, the imidazoles on the side chain of the peptide and the metal ion with several neighboring water molecules are treated as QM part calculated by "GAMESS", and the rest atoms are treated as MM part calculated by "TINKER". The integrated molecular orbital/molecular mechanics (IMOMM) method is used to deal with the QM part with the transitional metal. By using the QM/MM method, we optimize the structure of the synthetic peptide chelating with a Ni ion. Different chelate structures are considered. The geometry parameters of the QM subsystem we obtained by QM/MM calculation are consistent with the available experimental results. We also perform a classical molecular dynamics (MD) simulation with the experimental parameters for the synthetic peptide adsorption on a neutral Ni(100) surface. We find that half of the His-tags are almost parallel with the substrate, which enhance the binding strength. Peeling of the peptide from the Ni substrate is simulated in the aqueous solvent and in vacuum, respectively. The critical peeling forces in the two environments are obtained. The results show that the in-tidazole rings are attached to the substrate more tightly than other bases in this peptide. (c) 2006 Elsevier B.V. All rights reserved.://000237817400017 8Times Cited: 0 Cited References: AGARWAL G, 2003, J AM CHEM SOC, V125, P7408 ARICI C, 2002, ANAL SCI, V18, P375 ASSFELD X, 1996, CHEM PHYS LETT, V263, P100 BECKE AD, 1993, J CHEM PHYS, V98, P5648 BROOKS BR, 1983, J COMPUT CHEM, V4, P187 CONTI M, 2000, ANGEW CHEM INT EDIT, V39, P215 CORCHADO JC, 1998, J PHYS CHEM A, V102, P1895 CROWE J, 1994, METHOD MOL BIOL, V31, P371 DEMERS LM, 2002, SCIENCE, V296, P1836 DILABIO GA, 2002, J CHEM PHYS, V116, P9578 FERRE N, 2002, J COMPUT CHEM, V23, P610 FIELD MJ, 1990, J COMPUT CHEM, V11, P700 GAO JL, 1998, J PHYS CHEM A, V102, P4714 HERTWIG RH, 1997, CHEM PHYS LETT, V268, P345 HOCHULI E, 1987, J CHROMATOGR, V411, P177 HONEYCUTT RW, 1970, METHODS COMPUTATIONA, V9, P136 HUMPHREY W, 1996, J MOL GRAPHICS, V14, P33 LUZHKOV V, 1992, J COMPUT CHEM, V13, P199 LYNE PD, 1999, J PHYS CHEM A, V103, P3462 MARSERAS F, 1995, J COMPUT CHEM, V16, P1170 MASERAS F, 1995, J COMPUT CHEM, V16, P1170 MASERAS F, 2000, CHEM COMMUN, P1821 MCCREERY JH, 1976, J AM CHEM SOC, V98, P7191 MERZ KM, 1998, ACS SYM SER, V712, P2 MONTEMAGNO C, 1999, NANOTECHNOLOGY, V10, P225 NOJI H, 1997, NATURE, V386, P299 NUZZO RG, 1983, J AM CHEM SOC, V105, P4481 PETRENKO PA, 2004, RUSS J COORD CHEM+, V30, P813 PONDER JW, TINKER SOFTWARE TOOL SCHAFTENAAR G, 2000, J COMPUT AID MOL DES, V14, P123 SCHMIDT MW, 1993, J COMPUT CHEM, V14, P1347 SCHMITT L, 2000, BIOPHYS J, V78, P3275 SHI XH, 2005, ACTA MECH SINICA, V21, P249 STAUFFER D, 2001, ANN REV COMPUT PHYS, V9, P10 STEPHENS PJ, 1994, J PHYS CHEM-US, V98, P11623 WANG ISY, 1973, J AM CHEM SOC, V95, P8160 YIN J, 2005, MAT SCI ENG A-STRUCT, V409, P160 ZHANG YK, 1999, J CHEM PHYS, V110, P46 Sp. Iss. SIISI:000237817400017Chinese Acad Sci, Inst Mech, State Key Lab Nonlinear Mech, Beijing 100080, Peoples R China. Zhao, YP, Chinese Acad Sci, Inst Mech, State Key Lab Nonlinear Mech, Beijing 100080, Peoples R China. yzhao@lnm.imech.ac.cncinternal-pdf://2006_QM-MM and classical molecular-1533369871/2006_QM-MM and classical molecular.pdf~?02Yang, M. Sheehan, P. E. King, W. P. Whitman, L. J.2006jDirect writing of a conducting polymer with molecular-level control of physical dimensions and orientation 6774-6775(Journal of the American Chemical Society12821tDIP-PEN NANOLITHOGRAPHY; FIELD-EFFECT TRANSISTORS; CONJUGATED POLYMERS; NANOSTRUCTURES; DEPOSITION; NANOWIRES; FILMSArticleMay://000237816300006 Times Cited: 0 Cited References: AASMUNDTVEIT KE, 2000, MACROMOLECULES, V33, P3120 FORREST SR, 1997, CHEM REV, V97, P1793 GINGER DS, 2004, ANGEW CHEM INT EDIT, V43, P30 HOOFMAN RJOM, 1998, NATURE, V392, P54 HOROWITZ G, 1998, ADV MATER, V10, P365 JANG SY, 2004, J AM CHEM SOC, V126, P9476 LIM JH, 2002, ADV MATER, V14, P1474 MAYNOR BW, 2002, J AM CHEM SOC, V124, P522 MCCULLOUGH RD, 1998, ADV MATER, V10, P93 NELSON BA, 2006, APPL PHYS LETT, P88 NOY A, 2002, NANO LETTERS, V2, P109 NYAMJAV D, 2003, ADV MATER, V15, P1805 PARK KC, 1997, MACROMOLECULES, V30, P3175 PINER RD, 1999, SCIENCE, V283, P661 PROSA TJ, 1992, MACROMOLECULES, V25, P4364 SANDBERG HGO, 2002, LANGMUIR, V18, P10176 SHEEHAN PE, 2004, APPL PHYS LETT, V85, P1589 SIRRINGHAUS H, 1998, SCIENCE, V280, P1741 SIRRINGHAUS H, 1999, NATURE, V401, P685ISI:000237816300006USN, Res Lab, Washington, DC 20375 USA. Georgia Inst Technol, Woodruff Sch Mech Engn, Atlanta, GA 30332 USA. Whitman, LJ, USN, Res Lab, Washington, DC 20375 USA. whitman@nrl.navy.milinternal-pdf://2006 JACS Yang Direct Writing of a Conducting Polymer-2977662224/2006 JACS Yang Direct Writing of a Conducting Polymer.pdf~?10Leisten, F. Wiechmann, M. Enders, O. Kolb, H. A.2006pGeneration of nanostructures of mica supported lysozyme molecules in aqueous solution by atomic force microscopy508-514(Journal of Colloid and Interface Science2982nanostructures; lysozyme; mica; AFM DIP-PEN NANOLITHOGRAPHY; DER-WAALS CONTRIBUTIONS; EGG-WHITE LYSOZYME; PROTEIN ADSORPTION; MUSCOVITE MICA; SOLID-SURFACES; LAYERS; CRYSTALLIZATION; ELASTICITY; RESOLUTIONArticleJunNanostructures of lysozyme molecules adsorbed to mica were generated by the tip of an atomic force microscope in contact, tapping, and force-distance mode in aqueous solution. In contact mode at high ionic strength and adjusted lysozyme concentration a monolayer of defined pattern and orientation could be formed by the scan process of the tip. A lysozyme monolayer with minimal pattern size of about 60 unit was achieved by line scan. At larger loading forces besides a monolayer also 3D-aggregates of lysozyme molecules could be generated. In force-distance mode the volume of 3D-aggregates grows with increasing generation time, lysozyme concentration in the bulk phase, loading force, and frequency of up- and down-movement of the substrate toward the fixed cantilever. In tapping mode 3D-aggregates could be generated as well. It is postulated that reduction of electrostatic interaction between the oppositely charged lysozyme molecules and mica surface by sufficient high ionic strength is essential for monolayer formation. It is discussed that for the underlying mechanism of monolayer generation in contact mode lysozyme molecules of the bulk phase adsorb to the tip, become pulled off and attach to the mica surface by the scan process of the tip. (c) 2006 Elsevier Inc. All rights reserved.://000237909100002 JTimes Cited: 0 Cited References: BERGSTROM L, 1997, ADV COLLOID INTERFAC, V70, P125 BLAKE CCF, 1965, NATURE, V206, P757 BLOMBERG E, 1994, LANGMUIR, V10, P2325 BLOMBERG E, 1998, BIOMATERIALS, V19, P371 CACIOPPO E, 1991, J CRYST GROWTH, V114, P286 CARLSSON F, 2004, J PHYS CHEM B, V108, P9871 CZAJKOWSKY DM, 2003, J MICROSC-OXFORD 1, V211, P1 DEMERS LM, 2002, SCIENCE, V296, P1836 ENDERS O, 2004, BIOPHYS J, V87, P2522 FERMANI S, 2001, J CRYST GROWTH, V224, P327 FRITZ M, 1995, LANGMUIR, V11, P3529 GINGER DS, 2004, ANGEW CHEM INT EDIT, V43, P30 GRAY JJ, 2004, CURR OPIN STRUC BIOL, V14, P110 HAGGERTY L, 1993, BIOPHYS J, V64, P886 HLADY V, 1996, CURR OPIN BIOTECH, V7, P72 HONG SH, 1999, SCIENCE, V286, P523 ISRAELACHVILI JN, 1997, INTERMOLECULAR SURFA KIM DT, 2002, LANGMUIR, V18, P5841 KRAMER S, 2003, CHEM REV, V103, P4367 LEE KB, 2002, SCIENCE, V295, P1702 LI HY, 1999, ACTA CRYSTALLOGR D 5, V55, P1023 LIM JH, 2002, ADV MATER, V14, P1474 LIU XG, 2002, ADV MATER, V14, P231 MALMSTEN M, 1998, J COLLOID INTERF SCI, V207, P186 MCPHERSON A, 2004, METHODS, V34, P254 MONDON M, 2003, ANAL BIOANAL CHEM, V375, P849 MULLER DJ, 1997, BIOPHYS J, V73, P1633 MULLER DJ, 1997, J STRUCT BIOL, V119, P172 NAKANISHI K, 2001, J BIOSCI BIOENG, V91, P233 PINER RD, 1999, SCIENCE, V283, P661 RADMACHER M, 1994, BIOPHYS J, V66, P2159 RADMACHER M, 1994, LANGMUIR, V10, P3809 RADMACHER M, 1994, SCIENCE, V265, P1577 RAVICHANDRAN S, 2000, BIOPHYS J 1, V78, P110 ROTH CM, 1993, LANGMUIR, V9, P962 ROTH CM, 1995, LANGMUIR, V11, P3500 SCALES PJ, 1988, J COLLOID INTERF SCI, V124, P391 SCALES PJ, 1990, LANGMUIR, V6, P582 SCHAPER A, 1997, J CHEM PHYS, V106, P8587 SPEZIALE S, 2003, BIOPHYS J, V85, P3202 TANFORD C, 1972, BIOCHEMISTRY-US, V11, P2192 TILTON RD, 1993, LANGMUIR, V9, P2102 WIECHMANN M, 2001, ULTRAMICROSCOPY, V86, P159 WIECHMANN M, 2006, IN PRESS SURF INTERF WOUTERS D, 2004, ANGEW CHEM INT EDIT, V43, P2480ISI:000237909100002Univ Hannover, Inst Biophys, D-30419 Hannover, Germany. Kolb, HA, Univ Hannover, Inst Biophys, Herrenhaeuserstr 2, D-30419 Hannover, Germany. kolb@biophysik.uni-hannover.deinternal-pdf://2006 JoColloid&interfSci Leisten Generation of nanos-0628897296/2006 JoColloid&interfSci Leisten Generation of nanos.pdf ~?2$Djenizian, T. Balaur, E. Schmuki, P.2006<Direct immobilization of DNA on diamond-like carbon nanodots 2004-2007Nanotechnology178vSELF-ASSEMBLED MONOLAYERS; DIP-PEN NANOLITHOGRAPHY; COVALENT ATTACHMENT; GENE-EXPRESSION; SURFACES; MICROSCOPY; ARRAYSArticleApr We report an alternative technique for the immobilization of biological species in the sub-100 nm range. The feasibility of attaching DNA to electron-beam-deposited diamond-like carbon nanodots has been demonstrated. The key point of this approach is that direct patterning of a glass substrate is combined with a resist-free technique. Compared with conventional writing approaches, the high-resolution method presented here is simple, flexible, and compatible with the manipulation of a wide range of biological species.://000237813000036 Times Cited: 0 Cited References: ALLONGUE P, 2000, ELECTROCHIM ACTA, V45, P4591 ARENKOV P, 2000, ANAL BIOCHEM, V278, P123 BRAUN E, 1998, NATURE, V391, P775 BROERS AN, 1964, P 1 INT C EL ION BEA, P181 CULLEN P, 2002, EXPERT OPIN THER PAT, V12, P1783 DELAMARCHE E, 1997, SCIENCE, V276, P779 DEMERS LM, 2002, SCIENCE, V296, P1836 DONTHA N, 1997, ANAL CHEM, V69, P2619 EFFENBERGER F, 1998, ANGEW CHEM INT EDIT, V37, P2462 FODOR SPA, 1991, SCIENCE, V251, P767 FREY BL, 1996, ANAL CHEM, V68, P3187 GEYER W, 2001, J VAC SCI TECHNOL B, V19, P2732 HARNETT CK, 2000, APPL PHYS LETT, V76, P2466 HUGHES TR, 2001, NAT BIOTECHNOL, V19, P342 JOHNSSON B, 1991, ANAL BIOCHEM, V198, P268 KOOPS HWP, 1995, NUCL INSTRUM METH A, V363, P1 KRICKA LJ, 1995, MICROFABRICATED IMMU LEE KB, 2002, SCIENCE, V295, P1702 LOCKHART DJ, 2000, NATURE, V405, P827 LOSCHER F, 1998, LANGMUIR, V14, P2786 MACKEY BL, 2001, J PHYS CHEM B, V105, P3803 MIURA N, 1997, APPL SURF SCI, V114, P269 MRKSICH M, 1995, TRENDS BIOTECHNOL, V13, P228 NIEMEYER CM, 2003, NUCLEIC ACIDS RES, V31 PINER RD, 1999, SCIENCE, V283, P661 SCHENA M, 1995, SCIENCE, V270, P467 SCHOSSLER C, 1997, J VAC SCI TECHNOL B, V15, P1535 SEHGAL D, 1994, ANAL BIOCHEM, V218, P87 SIEBER I, 2003, ELECTROCHEM SOLID ST, V6, C1 STROTHER T, 2000, NUCLEIC ACIDS RES, V28, P3535 SWAN AK, 2003, IEEE J SEL TOP QUANT, V9, P294ISI:000237813000036&Univ Aix Marseille 1, Ctr St Jerome, CNRS, MADIREL,UMR 6121, F-13397 Marseille 20, France. Univ Erlangen Nuremberg, Dept Mat Sci, D-91058 Erlangen, Germany. Djenizian, T, Univ Aix Marseille 1, Ctr St Jerome, CNRS, MADIREL,UMR 6121, F-13397 Marseille 20, France. thierry.djenizian@up.univ-mrs.frinternal-pdf://2006_NanoTech_Direct immobilization of DNA_Djenizian-1602304016/2006_NanoTech_Direct immobilization of DNA_Djenizian.pdf\%\787092266\2006 Nanotechnology Djenizian Direct Immobilization of DNA.pdf ~?3DMyung, S. Im, J. Huang, L. Rao, S. G. Kim, T. Lee, D. J. Hong, S. H.2006N"Lens" effect in directed assembly of nanowires on gradient molecular patterns 10217-10219Journal of Physical Chemistry B11021yWALLED CARBON NANOTUBES; DIP-PEN NANOLITHOGRAPHY; TRANSISTORS; MONOLAYERS; SEPARATION; TEMPLATES; FEATURES; SURFACE; GOLDArticleJunWe report a new phenomenon, named here as the "lens" effect, in the directed-assembly process of nanowires (NWs) on self-assembled monolayer (SAM) patterns. In this process, the adsorption of NWs is focused in the nanoscale regions at the center of microscale SAM patterns with gradient surface molecular density just like an optical lens focuses light. As a proof of concepts, we successfully demonstrated the massive assembly of V2O5 NWs and single-walled carbon nanotubes (swCNTs) with a nanoscale resolution using only microscale molecular patterning methods. This work provides us with important insights about the directed-assembly process, and from a practical point of view, it allows us to generate nanoscale patterns of NWs over a large area for mass fabrication of NW-based devices.://000237844900003 )Times Cited: 1 Cited References: BACHTOLD A, 2001, SCIENCE, V294, P1317 BAIN CD, 1989, LANGMUIR, V5, P1370 BAUGHMAN RH, 1999, SCIENCE, V284, P1340 COFFEY DC, 2005, J AM CHEM SOC, V127, P4564 DAI HJ, 1996, NATURE, V384, P147 DEHEER WA, 1995, SCIENCE, V270, P1179 FRANK S, 1998, SCIENCE, V280, P1744 GUO J, 2002, APPL PHYS LETT, V81, P1486 HANNON JB, 2005, LANGMUIR, V21, P8569 HUANG Y, 2001, SCIENCE, V291, P630 KONG J, 1998, NATURE, V395, P878 KRUPKE R, 2003, SCIENCE, V301, P344 LIU J, 1999, CHEM PHYS LETT, V303, P125 MARTEL R, 1998, APPL PHYS LETT, V73, P2447 MYUNG S, 2005, ADV MATER, V17, P2361 NAMJAV D, 2003, ADV MATER, V15, P1805 OH SJ, 2003, APPL PHYS LETT, V82, P2521 PINER RD, 1999, SCIENCE, V283, P661 RAO SG, 2003, NATURE, V425, P36 RUECKES T, 2000, SCIENCE, V289, P94 SHEEHAN PE, 2002, PHYS REV LETT, V88 WANG YH, 2006, P NATL ACAD SCI USA, V103, P2026 WILBUR JL, 1995, LANGMUIR, V11, P825 XIA YN, 1995, J AM CHEM SOC, V117, P3274ISI:0002378449000036Seoul Natl Univ, Sch Phys, Seoul 151747, South Korea. Seoul Natl Univ, NANO Syst Inst, Seoul 151747, South Korea. Northwestern Univ, Dept Chem, Evanston, IL 60208 USA. Florida State Univ, Dept Phys, Tallahassee, FL 32306 USA. Hong, SH, Seoul Natl Univ, Sch Phys, Seoul 151747, South Korea. shong@phya.snu.ac.krUinternal-pdf://2006_JPCB_Lens effect_Myung-3503767060/2006_JPCB_Lens effect_Myung.pdfPl-Chem Myung Lens effect in directed assembly of nanowires.pdf ~?4Weeks, B. L. DeYoreo, J. J.2006PDynamic meniscus growth at a scanning probe tip in contact with a gold substrate 10231-10233Journal of Physical Chemistry B11021vDIP-PEN NANOLITHOGRAPHY; ATOMIC-FORCE MICROSCOPY; ELECTRON-MICROSCOPY; CONDENSATION; NUCLEATION; DEPOSITION; TRANSPORTArticleJunEnvironmental scanning electron microscopy was used to investigate the dynamic meniscus growth at a cantilever in contact with a substrate. The meniscus was observed to take many minutes to reach an equilibrium state. The observed growth rate is similar to initial patterning rates observed from dip-pen nanolithography and suggest that the meniscus growth may be the rate-limiting step in initial pattering rates.://000237844900007 UTimes Cited: 0 Cited References: ADAMSON AW, 1997, PHYS CHEM SURFACES CARSLAW HS, 1959, CONDUCTION HEAT SOLI GINGER DS, 2004, ANGEW CHEM INT EDIT, V43, P30 GOKHALE SJ, 2003, J COLLOID INTERF SCI, V259, P354 HAMPTON JR, 2005, J PHYS CHEM B, V109, P23118 HAMPTON JR, 2006, J AM CHEM SOC, V128, P1648 HE MY, 2001, J CHEM PHYS, V114, P1355 JANG J, 2003, PHYS REV LETT, V90 JASCHKE M, 1995, LANGMUIR, V11, P1061 PETERSON EJ, 2004, J PHYS CHEM B, V108, P15206 PINER RD, 1999, SCIENCE, V283, P661 RESTAGNO F, 2000, PHYS REV LETT, V84, P2433 SCHENK M, 1998, J APPL PHYS, V84, P4880 SEDIN DL, 2000, ANAL CHEM, V72, P2183 SHARMA A, 1998, LANGMUIR, V14, P4915 SHEEHAN PE, 2002, PHYS REV LETT, V88, P15 WEEKS BL, 2002, PHYS REV LETT, V88 WEEKS BL, 2005, LANGMUIR, V21, P8096ISI:000237844900007Texas Tech Univ, Dept Chem Engn, Lubbock, TX 79409 USA. Lawrence Livermore Natl Lab, Livermore, CA 94551 USA. Weeks, BL, Texas Tech Univ, Dept Chem Engn, Lubbock, TX 79409 USA. Brandon.weeks@ttu.edu4060582753Slides.pptminternal-pdf://2006_JPCB_Dynamic meniscus growth_Weeks-2061232148/2006_JPCB_Dynamic meniscus growth_Weeks.pdf,%\9@ic Meniscus Growth.pdf |~?5!Sheu, J. T. Wu, C. H. Chao, T. S.2006fSelective deposition of gold particles on dip-pen nanolithography patterns on silicon dioxide surfaces 3693-3697^Japanese Journal of Applied Physics Part 1-Regular Papers Brief Communications & Review Papers454Bdip-pen nanolithography; AFM tip; N-(2-aminoethyl)-3-aminopropyltrimethoxysilane; gold nanoparticles; X-ray photoelectron spectroscopy; lateral force microscopy NANOPARTICLE PROBES; LITHOGRAPHY; NANOSTRUCTURES; DNAArticleApr We report a novel platform to perform selective deposition of gold nanoparticles on dip-pen nanolithographic patterns on SiO2 surfaces. An "inked" atomic force microscope (AFM) tip was adopted to deposit 2.2mM organic N-(2-aminoethyl)-3aminopropyltriniethoxysilane (AEAPTMS) Molecules in nanopatterns through a water meniscus onto a SiO2, substrate under ambient conditions; the molecules act as linkers for the selective deposition of gold nanoparticles on the SiO2 surface. Conditions for dip-pen nanolithography of organic nanopatterns of AEAPTMS were investigated. In addition, gold nanoparticles with negatively-charged citrate Surfaces were deposited selectively on top of the organic patterns. X-ray photoelectron spectroscopy was then used to evaluate the presence of gold nanoparticles on the SiO2 surface. Lateral force microscopy was utilized to differentiate the surface between oxidized semiconductors and patterned areas with monolayer of AEAPTMS. Linewidths down to 60 nm have been successfully achieved by this method.://000237570600170 Times Cited: 0 Cited References: ALBRECHT M, 2002, APPL PHYS LETT, V81, P2875 BOGUNIAKUBIK K, 2002, BIOSYSTEMS, V65, P123 CUI Y, 2004, NANO LETT, V4, P1093 ELGHANIAN R, 1997, SCIENCE, V277, P1078 FRENS G, 1973, NATURE-PHYS SCI, V241, P20 IVANISEVIC A, 2001, J AM CHEM SOC, V123, P7887 JIN RC, 2001, SCIENCE, V294, P1901 JUNG H, 2003, J AM CHEM SOC, V125, P12096 LEE KB, 2003, J AM CHEM SOC, V125, P5588 LEE W, 2004, LANGMUIR, V20, P5262 LI MT, 2001, APPL PHYS LETT, V78, P3322 LU Y, 2002, NANO LETTERS, V2, P785 PARK SJ, 2002, SCIENCE, V295, P1503 SHEU JT, 2002, J VAC SCI TECHNOL B, V20, P2824 TATON TA, 2000, SCIENCE, V289, P1757 THOMAS PJ, 2004, J MATER CHEM, V14, P625 XIA YN, 1999, CHEM REV, V99, P1823 XIAO Y, 2003, SCIENCE, V299, P1877 ZHANG H, 2003, NANOTECHNOLOGY, V14, P1113 ZHENG JW, 2000, LANGMUIR, V16, P4409ISI:000237570600170+Natl Chiao Tung Univ, Inst Nanotechnol, Hsinchu 30050, Taiwan. Natl Chiao Tung Univ, Inst Electrophys, Hsinchu 30050, Taiwan. Natl Synchrotron Radiat Res Ctr, Hsinchu 30076, Taiwan. Sheu, JT, Natl Chiao Tung Univ, Inst Nanotechnol, 1001 Ta Hsueh Rd, Hsinchu 30050, Taiwan. jtsheu@faculty.nctu.cdu.twkinternal-pdf://2006_JJAP_Selective deposition of_Sheu-0702635796/2006_JJAP_Selective deposition of_Sheu.pdfX-Geposition-3459323940\2006 JapJoAppPhys Sheu Selective deposition.pdf ~?6!Willner, I. Baron, R. Willner, B.2006&Growing metal nanoparticles by enzymes 1109-1120Advanced Materials189FUNCTIONALIZED AU NANOPARTICLES; SURFACE-PLASMON RESONANCE; DIP-PEN NANOLITHOGRAPHY; ELECTROCHEMICAL DETECTION; AMPEROMETRIC BIOSENSORS; ELECTRICAL DETECTION; BIOCATALYTIC GROWTH; DNA-HYBRIDIZATION; GOLD NANOPARTICLE; OPTICAL-DETECTIONArticleMayAEnzymes act as catalysts for the growth of metallic nanoparticles (NPs). The enzyme-mediated growth of metallic NPs provides a general means to follow biocatalysed transformations, and to develop optical sensors for different substrates such as glucose, L-DOPA, alcohols, lactate or nerve gas analogs. Enzymes modified with Au NPs act as biocatalysts for the fabrication of metallic nanowires. The dip-pen nanolithography of NP-functionalized enzymes on Si surfaces yields biocatalytic templates that enable the orthogonal evolution of nanowires consisting of different metals.://000237640200001 Times Cited: 0 Cited References: AHMAD A, 2005, J BIOMED NANOTECH, V1, P47 ANGELETTI C, 2004, DIAGN CYTOPATHOL, V31, P33 AUTHIER L, 2001, ANAL CHEM, V73, P4450 BARON R, 2005, ANAL CHEM, V77, P1566 BASNAR B, 2006, ADV MATER, V18, P713 BRAUN E, 1998, NATURE, V391, P775 CAO YWC, 2002, SCIENCE, V297, P1536 DEMERS LM, 2000, ANAL CHEM, V72, P5535 DUBERTRET B, 2001, NAT BIOTECHNOL, V19, P365 GILL R, 2005, ANGEW CHEM INT EDIT, V44, P4554 GINGER DS, 2004, ANGEW CHEM INT EDIT, V43, P30 GREGG BA, 1991, J PHYS CHEM-US, V95, P5976 HABERMULLER L, 2000, FRESEN J ANAL CHEM, V366, P560 HE L, 2000, J AM CHEM SOC, V122, P9071 HELLER A, 1990, ACCOUNTS CHEM RES, V23, P128 HELLER A, 1992, J PHYS CHEM-US, V96, P3579 KATAKIS I, 1997, MIKROCHIM ACTA, V126, P11 KATZ E, 2004, ANGEW CHEM INT EDIT, V43, P6042 KATZ E, 2004, ELECTROANAL, V16, P19 KLAUS T, 1999, P NATL ACAD SCI USA, V96, P13611 LYON LA, 1998, ANAL CHEM, V70, P5177 MEDINTZ IL, 2005, NAT MATER, V4, P435 MIRKIN CA, 1996, NATURE, V382, P607 MOLLER R, 2005, NANO LETT, V5, P1475 NIEMEYER CM, 2001, ANGEW CHEM INT EDIT, V40, P4128 PARK SJ, 2002, SCIENCE, V295, P1503 PATOLSKY F, 2003, J AM CHEM SOC, V125, P13918 PATOLSKY F, 2004, NAT MATER, V3, P692 PAULUHN J, 1987, TOXICOLOGY, V46, P177 PAVLOV V, 2004, J AM CHEM SOC, V126, P11768 PAVLOV V, 2005, NANO LETT, V5, P649 PRIYABRATA P, 2001, ANGEW CHEM INT EDIT, V40, P3585 SHANKAR SS, 2004, NAT MATER, V3, P482 SHLYAHOVSKY B, 2005, SMALL, V1, P213 URBAN M, 2003, REV SCI INSTRUM, V74, P1077 VELEV OD, 1999, LANGMUIR, V15, P3693 VILLATTE F, 1998, BIOSENS BIOELECTRON, V13, P157 WANG J, 2001, ANAL CHEM, V73, P5576 WEIZMANN Y, 2004, NANO LETT, V4, P787 WILLNER I, 2000, ANGEW CHEM INT EDIT, V39, P1180 WILLNER I, 2002, TALANTA, V56, P847 WOUTERS D, 2004, ANGEW CHEM INT EDIT, V43, P2480 XIAO Y, 2003, SCIENCE, V299, P1877 XIAO Y, 2004, ANGEW CHEM INT EDIT, V43, P4519 XIAO Y, 2005, CHEM-EUR J, V11, P2698 XIAO Y, 2005, LANGMUIR, V21, P5659 ZAYATS M, 2005, J AM CHEM SOC, V127, P12400 ZAYATS M, 2005, NANO LETT, V5, P21ISI:000237640200001Hebrew Univ Jerusalem, Inst Chem, IL-91904 Jerusalem, Israel. Willner, I, Hebrew Univ Jerusalem, Inst Chem, IL-91904 Jerusalem, Israel. willnea@vms.huji.ac.ilkinternal-pdf://2006_JJAP_Selective deposition of_Sheu-1793334036/2006_JJAP_Selective deposition of_Sheu.pdf|9@Xtal Nanoparticles by Enzymes-1034441826\2006 Adv Mat Willner Growing Metal Nanoparticles by Enzymes.pdf ~?7KLee, S. W. Oh, B. K. Sanedrin, R. G. Salaita, K. Fujigaya, T. Mirkin, C. A.2006WBiologically active protein nanoarrays generated using parallel dip-pen nanolithography1133-+Advanced Materials189SELF-ASSEMBLED MONOLAYERS; SCANNING PROBE LITHOGRAPHY; IMMOBILIZED PROTEINS; COVALENT ATTACHMENT; OXIDE SURFACES; TAPPING-MODE; NANOFABRICATION; ARRAYS; MICROARRAYS; PATTERNSArticleMayAmine-active N-hydroxysuccinimide-terminated alkyl thiol templates are generated using parallel dip-pen nanolithography (DPN) and are used to covalently couple protein A/G. The protein arrays generated (see figure) are used to capture antibodies through affinity binding, while preserving their biological recognition properties. The versatility of the parallel DPN method for making many similar structures in a relatively high-throughput manner (14 000 dots in 10 min) is described.://000237640200003 Times Cited: 0 Cited References: AGARWAL G, 2003, J AM CHEM SOC, V125, P580 AYBAY C, 2003, IMMUNOL LETT, V85, P231 BERNARD A, 1998, LANGMUIR, V14, P2225 BIEBRICHER A, 2004, J BIOTECHNOL, V112, P97 BLAWAS AS, 1998, BIOMATERIALS, V19, P595 BOYLE MDP, 1987, BIO-TECHNOL, V5, P697 BROOKS SA, 1999, J AM CHEM SOC, V121, P8044 BROWNINGKELLEY ME, 1997, LANGMUIR, V13, P343 BULLEN D, 2004, APPL PHYS LETT, V84, P789 CABRITA JF, 2005, ELECTROCHIM ACTA, V50, P2117 CLEVELAND JP, 1998, APPL PHYS LETT, V72, P2613 DEGENHART GH, 2004, LANGMUIR, V20, P6216 DEMERS LM, 2002, SCIENCE, V296, P1836 DULCEY CS, 1991, SCIENCE, V252, P551 FALCONNET D, 2004, ADV FUNCT MATER, V14, P749 GINGER DS, 2004, ANGEW CHEM INT EDIT, V43, P30 HERGENROTHER PJ, 2000, J AM CHEM SOC, V122, P7849 HONG SH, 1999, SCIENCE, V286, P523 HONG SH, 2000, SCIENCE, V288, P1808 JOHNSON CP, 2003, BIOCONJUGATE CHEM, V14, P974 JUN Y, 2004, BIOMATERIALS, V25, P3503 KANE RS, 1999, BIOMATERIALS, V20, P2363 KENSETH JR, 2001, LANGMUIR, V17, P4105 LEE KB, 2003, J AM CHEM SOC, V125, P5588 LEE KB, 2004, NANO LETT, V4, P1869 LEE SW, 2005, ADV MATER, V17, P2749 LI XM, 2004, J MATER CHEM, V14, P2954 LIM JH, 2003, ANGEW CHEM INT EDIT, V42, P2309 LIU GY, 2000, ACCOUNTS CHEM RES, V33, P457 LIU XG, 2005, SCIENCE, V307, P1763 LYNCH M, 2003, PROTEOMICS, V4, P1695 MACBEATH G, 2000, SCIENCE, V289, P1760 NAM JM, 2004, ANGEW CHEM INT EDIT, V43, P1246 NG HT, 2002, LANGMUIR, V18, P6324 OWAKU K, 1995, ANAL CHEM, V67, P1613 PALEGROSDEMANGE C, 1991, J AM CHEM SOC, V113, P12 PETER M, 2004, J AM CHEM SOC, V126, P11684 PINER RD, 1999, SCIENCE, V283, P661 PRIME KL, 1993, J AM CHEM SOC, V115, P10714 SALAITA K, 2005, SMALL, V1, P940 SERVICE RF, 2002, SCIENCE, V298, P2322 SMITH JC, 2003, NANO LETT, V3, P883 STJOHN PM, 1998, ANAL CHEM, V70, P1108 TAN JL, 2002, LANGMUIR, V18, P519 VEGA RA, 2005, ANGEW CHEM INT EDIT, V44, P6013 VIJAYENDRAN RA, 2001, ANAL CHEM, V73, P471 VIJAYKUMAR S, 1987, J MOL BIOL, V194, P531 WADUMESTHRIGE K, 1999, LANGMUIR, V15, P8580 WAGNER P, 1996, J VAC SCI TECHNOL B, V14, P1466 WAUDMESTHRIGE K, 2001, BIOPHYS J, V80, P1891 WILCOP T, 2004, LANGMUIR, V20, P1114 WILSON DL, 2001, P NATL ACAD SCI USA, V98, P13660 XU P, 2004, ADV MATER, V16, P628 XU P, 2005, J AM CHEM SOC, V127, P11745 YAM CM, 2005, J COLLOID INTERF SCI, V285, P711 YIN HB, 2004, NUCLEIC ACIDS RES, V32 ZHANG M, 2002, NANOTECHNOLOGY, V13, P212 ZHENG T, 2005, J AM CHEM SOC, V127, P9982 ZHU H, 2001, SCIENCE, V293, P2101ISI:000237640200003Northwestern Univ, Dept Chem, Evanston, IL 60208 USA. Northwestern Univ, Inst Nanotechnol, Evanston, IL 60208 USA. Mirkin, CA, Northwestern Univ, Dept Chem, 2145 Sheridan Rd, Evanston, IL 60208 USA. chadnano@northwestern.edu0116415078Inserts.pptinternal-pdf://2006 AdvMat Lee Biologically active protein nanoarrays-3118885396/2006 AdvMat Lee Biologically active protein nanoarrays.pdfTGad028\2006 AdvMat Lee Biologically active protein nanoarrays.pdf~?81Faure, C. Guillot, S. Weisbecker, P. Saadaoui, H.2006FMultilamellar-vesicle-assisted electrodeposition of inorganic nanodots1141-+Advanced Materials189DIP-PEN NANOLITHOGRAPHY; PLANAR MODEL CATALYSTS; COLLOIDAL LITHOGRAPHY; NANOFABRICATION; PT/ALUMINA; DEPOSITION; PT/CERIA; CLUSTERS; SURFACES; PHASEArticleMayNanodots are produced over large areas with controlled size and density in a new single-step, low-cost process. This process is based on surfactant-made multilamellar vesicles that serve as nanovectors. Copper ions are incorporated inside vesicles by chemical complexation. Vesicles are attracted under a DC electric field towards an electrode, where they are reduced to produce the metal nanodots shown in the figure.://000237640200005 RTimes Cited: 0 Cited References: AWSCHALOM DD, 1999, NANOTECHNOLOGY, V1, C412 CHEN SC, 1997, SCIENCE, V276, P1425 DAVIES ST, 1996, VACUUM, V47, P455 DENIS FA, 2002, LANGMUIR, V18, P819 DIAT O, 1993, J PHYS II, V3, P1427 DIAT O, 1993, J PHYS II, V3, P9 DOGTEROM M, 1996, J CELL BIOL, V133, P125 FAURE C, 1998, EUR PHYS J B, V5, P87 FAURE C, 2000, J ELECTROCHEM SOC, V147, P575 FAURE C, 2003, J PHYS CHEM B, V107, P4738 GUSMAN H, 2001, BBA-PROTEIN STRUCT M, V1545, P86 HEIZ U, 2000, J PHYS D, V33, P85 KASEMO B, 1998, CURR OPIN SOLID ST M, V3, P451 KOLB DM, 1997, SCIENCE, V275, P1097 LEE KB, 2002, SCIENCE, V295, P1702 LIU K, 2002, APPL PHYS LETT, V81, P4434 MASUDA H, 1998, JPN J APPL PHYS 2, V37, L1090 MCCORD M, 1997, HDB MICROLITHOGRAPHY, V1, CH2 OSTERLUND L, 2003, J CATAL, V215, P94 PINER RD, 1999, SCIENCE, V283, P661 SARKAR DK, 2003, J PHYS CHEM B, V107, P2879 WALES DJ, 1996, SCIENCE, V271, P925 WEI YY, 1988, ACTA CRYSTALLOGR C, V44, P73 WERDINIUS C, 2003, LANGMUIR, V19, P458ISI:000237640200005CNRS, Ctr Rech Paul Pascal, F-33600 Pessac, France. Lab Composites Thermostruct, F-33600 Pessac, France. Faure, C, CNRS, Ctr Rech Paul Pascal, 115 Ave Dr Albert Schweitzer, F-33600 Pessac, France. faure@crpp-bordeaux.cnrs.frointernal-pdf://2006_Adv Mat_Multilamellar-vesicle_Faure-2884350996/2006_Adv Mat_Multilamellar-vesicle_Faure.pdfXnle-assisted electrodeposition-0433504298\2006 AdvMat Faure Multilamellar-vesicle-assisted electrodeposition.pdf ~?95Tzeng, S. D. Lin, K. J. Hu, J. C. Chen, L. J. Gwo, S.2006yTemplated self-assembly of colloidal nanoparticles controlled by electrostatic nanopatterning on a Si3N4/SiO2/Si electret1147-+Advanced Materials189DIP-PEN NANOLITHOGRAPHY; GOLD NANOPARTICLES; NANOMETER-SCALE; CHARGE STORAGE; MICROSCOPY; DEPOSITION; MONOLAYERS; NANOXEROGRAPHY; MANIPULATION; RESOLUTIONArticleMayControlled self-assembly of colloidal nanoparticles onto an electrically nanopatterned electret film is presented (see figure; EFM: electrostatic force microscopy). An unprecedented reolution of 30 nm is achieved for both charge patterning and nanoparticle assembly. Furthermore, only a close-packed monolayer of nanoparticles is assembled, allowing better structural control and the possibility of forming hierarchical nanoparticle structures.://000237640200006 Times Cited: 1 Cited References: AIZENBERG J, 2000, PHYS REV LETT, V84, P2997 ANDRES RP, 1996, SCIENCE, V273, P1690 BARRETT RC, 1991, J APPL PHYS, V70, P2725 BARRY CR, 2003, APPL PHYS LETT, V83, P5527 BARRY CR, 2005, NANO LETT, V5, P2078 BIEBUYCK HA, 1994, LANGMUIR, V10, P1825 BRUST M, 1994, J CHEM SOC CHEM COMM, P801 BULLEN D, 2005, APPL PHYS LETT, V84, P789 CHENG WL, 2004, J PHYS CHEM B, V108, P24 CHIEN FSS, 2000, APPL PHYS LETT, V76, P360 FUDOUZI H, 2001, J NANOPART RES, V3, P193 FUDOUZI H, 2002, ADV MATER, V14, P1649 FUJIWARA I, 1996, JPN J APPL PHYS 1, V35, P2764 GIERSIG M, 1993, LANGMUIR, V9, P3408 GINGER DS, 2004, ANGEW CHEM INT EDIT, V43, P30 HAN YL, 2003, PHYS REV LETT, V91 JACOBS HO, 1999, SURF INTERFACE ANAL, V27, P361 JACOBS HO, 2001, SCIENCE, V291, P1763 JACOBS HO, 2002, ADV MATER, V14, P1553 LIU ST, 2004, NANO LETT, V4, P845 MAMIN HJ, 1995, IBM J RES DEV, V39, P681 MAOZ R, 2000, ADV MATER, V12, P725 MESQUIDA P, 2001, ADV MATER, V13, P1395 MINNE SC, 1998, APPL PHYS LETT, V72, P2340 MURRAY CB, 2000, ANNU REV MATER SCI, V30, P545 PAI DM, 1993, REV MOD PHYS, V65, P163 PINER RD, 1999, SCIENCE, V283, P661 PUNTES VF, 2001, SCIENCE, V291, P2115 SESSLER GM, 1998, ELECTRETS, V1, CH7 SHIPWAY AN, 2000, CHEMPHYSCHEM, V1, P18 SUGIMURA H, 1995, LANGMUIR, V11, P3623 SUGIMURA H, 1997, J AM CHEM SOC, V119, P9226 SUN YG, 2002, SCIENCE, V298, P2176 TIEN J, 1997, LANGMUIR, V13, P5349 TZENG SD, UNPUB TZENG SD, 2002, APPL PHYS LETT, V81, P5042 VETTIGER P, 2002, IEEE T NANOTECHNOL, V1, P39 WRIGHT WMD, 1998, NANOTECHNOLOGY, V9, P133ISI:000237640200006|Natl Tsing Hua Univ, Dept Phys, Hsinchu 300, Taiwan. Natl Tsing Hua Univ, Ctr Mat Sci, Hsinchu 300, Taiwan. Natl Chung Hsing Univ, Dept Chem, Taichung 402, Taiwan. Natl Chung Hsing Univ, Ctr Nanosci & Nanotechnol, Taichung 402, Taiwan. Natl Tsing Hua Univ, Dept Mat Sci & Engn, Hsinchu 300, Taiwan. Gwo, S, Natl Tsing Hua Univ, Dept Phys, Hsinchu 300, Taiwan. gwo@phys.nthu.edu.twinternal-pdf://2006 Adv Mat Tzeng Templated self-assembly of colloidal nanoparti-1240355348/2006 Adv Mat Tzeng Templated self-assembly of colloidal nanoparticles.pdfTadat Tzeng Templated self-assembly of colloidal nanoparticles.pdf ~?:Aizawa, M. Buriak, J. M.2006_Nanoscale patterning of two metals on silicon surfaces using an ABC triblock copolymer template 5877-5886(Journal of the American Chemical Society12817DIP-PEN NANOLITHOGRAPHY; AMPHIPHILIC BLOCK-COPOLYMERS; ELECTRON-BEAM LITHOGRAPHY; SHELL-CORONA MICELLES; THIN-FILMS; GOLD NANORODS; NANOPARTICLE MONOLAYERS; GALVANIC DISPLACEMENT; SILVER NANOPARTICLES; POLYMER ELECTROLYTEReviewMayPatterning technologically important semiconductor interfaces with nanoscale metal films is important for applications such as metallic interconnects and sensing applications. Self-assembling block copolymer templates are utilized to pattern an aqueous metal reduction reaction, galvanic displacement, on silicon surfaces. Utilization of a triblock copolymer monolayer film, polystyrene-block-poly(2-vinylpyridine)block-poly(ethyleneoxide) (PS-b-PVP-b-PEO), with two blocks capable of selective transport of different metal complexes to the surface (PEO and P2VP), allows for chemical discrimination and nanoscale patterning. Different regions of the self-assembled structure discriminate between metal complexes at the silicon surface, at which time they undergo the spontaneous reaction at the interface. Gold deposition from gold(Ill) compounds such as HAuCl4(aq) in the presence of hydrofluoric acid mirrors the parent block copolymer core structure, whereas silver deposition from Ag(I) salts such as AgNO3(aq) does the opposite, localizing exclusively under the Corona. By carrying out gold deposition first and silver second, sub-100-nm gold features surrounded by silver films can be produced. The chemical selectivity was extended to other metals, including copper, palladium, and platinum. The interfaces were characterized by a variety of methods, including scanning electron microscopy, scanning Auger microscopy, X-ray photoelectron spectroscopy, and atomic force microscopy.://000237389900059 KTimes Cited: 1 Cited References: AIZAWA M, 2005, J AM CHEM SOC, V127, P8932 AIZAWA M, 2005, NANO LETT, V5, P815 ALLRED DB, 2005, NANO LETT, V5, P609 ANTONIETTI M, 1995, ADV MATER, V7, P1000 ANTONIETTI M, 1996, MACROMOLECULES, V29, P3800 BALSARA NP, 2002, CHEM NANOSTRUCT MAT, P317 BLACK CT, 2004, IEEE T NANOTECHNOL, V3, P412 BOEKER A, 2001, MACROMOLECULES, V34, P7477 BRONSTEIN L, 1999, CHEM MATER, V11, P1402 BRONSTEIN LH, 1999, LANGMUIR, V15, P6256 BRONSTEIN LM, 1998, INORG CHIM ACTA, V280, P348 BRONSTEIN LM, 2005, J PHYS CHEM B, V109, P18786 CHEMLA M, 2003, J ELECTROANAL CHEM, V559, P111 CHEN Z, 2004, J ELECTROCHEM SOC, V151, R360 CHENG JY, 2004, PHYS REV B, V70 COTTON FA, 1999, ADV INORG CHEM, P1101 COTTON FA, 1999, ADV INORG CHEM, P868 COX JK, 1999, CURR OPIN COLLOID IN, V4, P52 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P2126 VAMVAKAKI M, 2004, FARADAY DISCUSS, V128, P129 WAGNER CD, 2003, NIST XRAY PHOTOELECT WAN JL, 2005, CHEM MATER, V17, P5613 WANG LY, 2005, COLLOID SURFACE A, V257, P231 WEBBER SE, 1998, J PHYS CHEM B, V102, P2618 WEI ZQ, 2004, LANGMUIR, V20, P11301 WEI ZQ, 2004, LANGMUIR, V20, P4322 WONG EW, 2005, CHEM MATER, V17, P237 YAMAMOTO M, 2004, CHEM LETT, V33, P1340 ZAMBELLI T, 2001, J ELECTROCHEM SOC, V148, C614 ZAMBORINI FP, 2003, ANAL CHIM ACTA, V496, P3 ZEHNER RW, 1999, LANGMUIR, V15, P6139 ZHANG DB, 2001, CHEM MATER, V13, P2753ISI:000237389900059Univ Alberta, Natl Inst Nanotechnol, Edmonton, AB T6G 2G2, Canada. Univ Alberta, Dept Chem, Edmonton, AB T6G 2G2, Canada. Aizawa, M, Univ Alberta, Natl Inst Nanotechnol, Edmonton, AB T6G 2G2, Canada. maizawa@ualberta.ca jburiak@ualberta.cainternal-pdf://2006 JACS Aizawa Buriak Nanoscale Patterning Silicon Surfaces-2582579220/2006 JACS Aizawa Buriak Nanoscale Patterning Silicon Surfaces.pdfPnHJACS Aizawa Buriak Nanoscale Patterning Silicon Surfaces.pdfX~?;*Unal, K. Frommer, J. Wickramasinghe, H. K.2006BUltrafast molecule sorting and delivery by atomic force microscopy183105Applied Physics Letters88184DIP-PEN NANOLITHOGRAPHY; ELECTROPHORESIS; WATER; DNAArticleMayAn atomic force microscope (AFM) is tailored to perform ultrafast electrophoretic differentiation of molecules on populations of < 0.1 zeptomoles (10(-22) moles) on the surface of a probe tip. The driving force for differentiation is a large electric field applied over the length of an AFM tip that results in enhanced differential mobilities stemming from the confinement of the water layer on the tip surface. In a demonstration on DNA oligonucleotides, a 5-mer and a 16-mer exhibit migration times of 15 and 5 ms, respectively, approximately five orders of magnitude faster than in conventional capillary electrophoresis. (c) 2006 American Institute of Physics.://000237321600075 FTimes Cited: 0 Cited References: DONG Q, 2003, ELECTROPHORESIS, V24, P3323 EIGLER DM, 1990, NATURE, V344, P524 FABRIZIO EF, 2003, ANAL CHEM, V75, P5012 HO C, 2005, P NATL ACAD SCI USA, V102, P10445 KARNIK R, 2005, NANO LETT, V5, P943 LYUBCHENKO Y, 1993, P NATL ACAD SCI USA, V90, P2137 OPITZ A, 2002, SURF SCI, V504, P199 PAPRA A, 2001, LANGMUIR, V17, P1457 PINER RD, 1999, SCIENCE, V283, P661 SHEEHAN PE, 2004, APPL PHYS LETT, V85, P1589 STEIN D, 2004, PHYS REV LETT, V93 STELLWAGEN E, 2003, BIOCHEMISTRY-US, V42, P11745ISI:000237321600075IBM Corp, IBM Res Div, Almaden Res Ctr, San Jose, CA 95120 USA. Unal, K, IBM Corp, IBM Res Div, Almaden Res Ctr, 650 Harry Rd, San Jose, CA 95120 USA. hkwick@us.ibm.com183105 Artn 183105internal-pdf://2006 AppPhysLtrs Unal Ultrafast molecular sorting-0569370388/2006 AppPhysLtrs Unal Ultrafast molecular sorting.pdf<8trs Unal Ultrafast molecular sorting.pdf~?<5Basabe-Desmonts, L. Reinhoudt, D. N. Crego-Calama, M.2006XCombinatorial fabrication of fluorescent patterns with metal ions using soft lithography1028-+Advanced Materials188SELF-ASSEMBLED MONOLAYERS; DIP-PEN NANOLITHOGRAPHY; MOLECULAR PRINTBOARDS; POLY(DIMETHYLSILOXANE); PRINCIPLES; PROTEINS; SENSORSArticleApr A new combinatorial methodology for the fabrication and direct visualization of fluorescent and metal-ion micrometer patterns is presented. Microcontact printing is used to transfer different metal salts onto a variety of fluorescent monolayers on glass (see figure).://000237371800010 ZTimes Cited: 0 Cited References: AULETTA T, 2004, ANGEW CHEM INT EDIT, V43, P369 BASABEDESMONTS L, 2004, J AM CHEM SOC, V126, P7293 BERNARD A, 2000, ADV MATER, V12, P1067 BOHR MT, 2002, IEEE T NANOTECHNOL, V1, P56 CREGOCALAMA M, 2001, ADV MATER, V13, P1171 DELAMARCHE E, 2003, LANGMUIR, V19, P8749 GEISSLER M, 2004, ADV MATER, V16, P1249 GINGER DS, 2004, ANGEW CHEM INT EDIT, V43, P30 GREENE ME, 2004, MICROSC RES TECHNIQ, V64, P415 MA DI, 2002, CHEM MATER, V14, P4586 MAHALINGAM V, 2004, LANGMUIR, V20, P11756 OLAH A, 2005, APPL SURF SCI, V239, P410 PORTER LA, 2002, NANO LETT, V2, P1369 RENAULT JP, 2002, ANGEW CHEM INT EDIT, V41, P2320 SHTEIN M, 2004, J APPL PHYS, V96, P4500 STOLL G, 2002, J PERIPHER NERV SYST, V7, P13 VALEUR B, 2000, COORDIN CHEM REV, V205, P3 VOSSMEYER T, 1998, J APPL PHYS, V84, P3664 WU T, 2003, J MATER SCI, V38, P4471 XIA YN, 1999, CHEM REV, V99, P1823 YANG KL, 2003, ADV MATER, V15, P1819 ZHENG HP, 2002, LANGMUIR, V18, P4505 ZIMMERMAN R, 2005, J MATER CHEM, V15, P2772ISI:000237371800010Univ Twente, Dept Supremol Chem & Technol, MESA, Inst Nanotechnol, NL-7500 AE Enschede, Netherlands. Crego-Calama, M, Univ Twente, Dept Supremol Chem & Technol, MESA, Inst Nanotechnol, POB 217, NL-7500 AE Enschede, Netherlands. m.cregocalama@utwente.nlinternal-pdf://2006 Adv Mat Basabe-Desmonts Combin Fab of Flourescent Patterns-3790750996/2006 Adv Mat Basabe-Desmonts Combin Fab of Flourescent Patterns.pdfPH Mat Basabe-Desmonts Combin Fab of Flourescent Patterns.pdf8 ary, S. P. Liu, C. Y. Apuzzo, M. L. J.2006pToward the emergence of nanoneurosurgery: Part II - Nanomedicine: Diagnostics and imaging at the nanoscale level805-822 Neurosurgery585nanoarrays; nanofluidics; nanoimaging; nanomedicine; nanoneurosurgery; nanoparticles; nanoscience; nanoshells; nanosurgery; nanotechnology; quantum dots DIP-PEN NANOLITHOGRAPHY; LYMPH-NODE METASTASES; ULTRASMALL SUPERPARAMAGNETIC PARTICLES; NANOMECHANICAL CANTILEVER ARRAY; NANOPARTICLE-BASED DETECTION; IRON-OXIDE NANOPARTICLES; QUANTUM DOTS; IN-VIVO; MOLECULAR-INTERACTIONS; NANOWIRE NANOSENSORSReviewMayTHE NOTION OF nanotechnology has evolved since its inception as a fantastic conceptual idea to its current position as a mainstream research initiative with broad applications among all divisions of science. In the first part of this series, we reviewed the structures and principles that comprise the main body of knowledge of nanoscience and nanotechnology (58). This article reviews and discusses the applications of nanotechnology to biological systems that will undoubtedly transform the foundations of disease diagnosis, treatment, and prevention in the future. Specific attention is given to developments in diagnostics and imaging at the nanoscale level. The use of nanoparticles and nanomaterials as biodetection agents for deoxyribonucleic acid and proteins is presented. In addition, nanodevices, such as nanowires, nanotubes, and nanocantilevers, can be combined with nanoarrays and nanofluidics to create integrated and automated nanodetection platforms. Molecular imaging modalities based on quantum dots and magnetic nanoparticles are also discussed. This technology has been extended to the imaging of intracranial neoplasms. Further innovation within these disciplines will form the basis for the development of mature nanomedicine. 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CALTECH, Div Chem & Chem Engn, Pasadena, CA 91125 USA. Apuzzo, MLJ, 1420 San Pablo St,PMB A-106, Los Angeles, CA 90033 USA. neurosurgery-journal@hsc.usc.edufile://S:\SALES\_IMPORTANT_STUFF_HERE\Bibliography_Key_Papers\all publications DPN as of 101006 Copy.Data\PDF\2006 Neurosurgery Leary Emergence of Nanoneurosurgery Part II-2020454723\2006 Neurosurgery Leary Emergence of Nanoneurosurgery Part II.pdf-~?>2Hurst, S. J. Payne, E. K. Qin, L. D. Mirkin, C. 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PHYS LETT, V363, P123ISI:000237155200003Northwestern Univ, Dept Chem, Evanston, IL 60208 USA. Northwestern Univ, Int Inst Nanotechnol, Evanston, IL 60208 USA. Mirkin, CA, Northwestern Univ, Dept Chem, 2145 Sheridan Rd, Evanston, IL 60208 USA. chadnano@northwestern.eduinternal-pdf://2006 AngeChemie Hurst Multisegmented One- dimensional Nanorods-1224467476/2006 AngeChemie Hurst Multisegmented One- dimensional Nanorods.pdfPtgeChemie Hurst Multisegmented One- dimensional Nanorods.pdf ~??8Nie, Y. R. Li, W. An, L. J. Zhu, D. F. Wang, Z. Yang, B.2006}Fabricating ordered 2D arrays of magnetic rings on patterned self-assembly monolayers via dewetting and thermal decomposition229-234?Colloids and Surfaces a-Physicochemical and Engineering Aspects2781-3pattern; SAMs; magnetic rings; dewetting; thermal decomposition DIP-PEN NANOLITHOGRAPHY; NANOPARTICLE RINGS; FLUX CLOSURE; NANOSTRUCTURES; SURFACESArticleAprOThrough the combination of microcontact printing (mu CP), dewetting and thermal decomposition, ordered 2D arrays of magnetic rings were fabricated. Firstly, patterned hydrophilic and hydrophobic self-assembly monolayers (SAMs) with the dispersed round regions hydrophilic and the continuous regions hydrophobic were obtained by mu CP. Then by dewetting, ordered 2D arrays of iron (III) acetylacetonate (Fe(acac)(3)) rings were fabricated onto the patterned SAMs. Subsequently the Fe(acac)(3) rings were transformed into magnetite (Fe3O4) rings using thermal decomposition at an elevated temperature (300 degrees C). The patterned structures were characterized by optical microscopy, field emission scanning electron microscopy (FESEM), atomic force microscopy (AFM), and magnetic force microscopy (MFM). (c) 2006 Elsevier B.V. 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Tianjin Univ Sci & Technol, Coll Sci, Tianjin 300222, Peoples R China. Yang, B, Jilin Univ, Coll Chem, Key Lab Supramol Struct & Mat, Changchun 130012, Peoples R China. byangchem@jlu.edu.cninternal-pdf://2006 Colloids & Surfaces Nie Fabricating ordered 2D arrays-4043137300/2006 Colloids & Surfaces Nie Fabricating ordered 2D arrays.pdfP /406 Colloids & Surfaces Nie Fabricating ordered 2D arrays.pdf6^~?@1Verdaguer, A. Sacha, G. M. Bluhm, H. 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Lawrence Berkeley Lab, Div Mat Sci, Berkeley, CA 94720 USA. Univ Calif Berkeley, Lawrence Berkeley Lab, Div Chem Sci, Berkeley, CA 94720 USA. Salmeron, M, Univ Calif Berkeley, Lawrence Berkeley Lab, Div Mat Sci, Berkeley, CA 94720 USA. salmeron@stm.lbl.govinternal-pdf://2006 Chem Reviews Verdaguer Molecular Structure of Water at Inte-4093508116/2006 Chem Reviews Verdaguer Molecular Structure of Water at Interfaces.pdfXtlem Reviews Verdaguer Molecular Structure of Water at Interfaces.pdf0~?A/Leary, S. P. Liu, C. Y. Yu, C. Apuzzo, M. L. J.2005Toward the emergence of nanoneurosurgery: Part I - Progress in nanoscience, nanotechnology, and the comprehension of events in the mesoscale realm606-633 Neurosurgery574nanoscience; nanotechnology; mesoscale; nanofabrication; nanoelectrornechanical systems; molecular manufacturing; nanocomputation; nanomedicine; nanoneurosurgery ATOMIC-FORCE MICROSCOPY; SCANNING TUNNELING MICROSCOPY; DIP-PEN NANOLITHOGRAPHY; SILICON (111)-(7X7) SURFACE; WALL CARBON NANOTUBES; NANOELECTROMECHANICAL SYSTEMS; MOLECULAR ELECTRONICS; HIGH-RESOLUTION; SUPRAMOLECULAR CHEMISTRY; CRYSTALLINE NANOWIRESReviewOctSince its original conception in 1959, the notion of nanotechnology and its potential ramifications have not only created fascination, but also intense scientific effort and scrutiny. Currently, research activities are being principally conducted in mesoscale, the realm between nanoscale and macroscale, with the rudiments of nanoscience being defined in realities and principles that will determine activities and discoveries in the future. This paper reviews and discusses the evolution of nanoscience, its contemporary status, and the discoveries that currently constitute the main components of the body of knowledge from a neurosurgical perspective. Specific attention is given to the developments in imaging, fabrication, nanostructures, nanoelectromechanical systems, molecular manufacturing, nanocomputation, and emerging physical and chemical concepts in mesoscale, as they will establish foundations for the realization of nanomedicine and nanoneurosurgery.://000236681500012 'Times Cited: 4 Cited References: *INT WORK GROUP NA, 1999, OSTP COMM TECHN MARC AJAYAN PM, 2001, TOP APPL PHYS, V80, P391 ALBERTI P, 2003, P NATL ACAD SCI USA, V100, P1569 ALBERTI P, 2004, CELL MOL BIOL, V50, P241 ALI MY, 2004, BIOPHYS J, V86, P3804 APUZZO MLJ, 2001, NEUROSURGERY, V49, P765 APUZZO MLJ, 2002, CLIN NEUROSURG, V49, P159 ASHKIN A, 1986, OPT LETT, V11, P288 AVIRAM A, 1974, CHEM PHYS LETT, V29, P277 BACHTOLD A, 2001, SCIENCE, V294, P1317 BADJIC JD, 2004, SCIENCE, V303, P1845 BALZANI V, 2002, P NATL ACAD SCI USA, V99, P4814 BARGATIN I, 2003, PHYS REV LETT, V91 BARO AM, 1985, NATURE, V315, P253 BAUGHMAN RH, 1999, SCIENCE, V284, P1340 BAUGHMAN RH, 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CALTECH, Div Chem & Chem Engn, Pasadena, CA 91125 USA. Univ So Calif, Dept Radiat Oncol, Keck Sch Med, Los Angeles, CA USA. Apuzzo, MLJ, 1420 San Pablo St PMB A-106, Los Angeles, CA 90033 USA. neurosurgery-journal@hsc.usc.edufile://S:\SALES\_IMPORTANT_STUFF_HERE\Bibliography_Key_Papers\all publications DPN as of 101006 Copy.Data\PDF\2005 Neurosurgery Leary Emergence of Nanoneurosurgery Part 1-2607959107\2005 Neurosurgery Leary Emergence of Nanoneurosurgery Part 1.pdf 5~?BCJang, S. G. Choi, D. G. Kim, S. Jeong, J. H. Lee, E. S. Yang, S. M.2006>Nanoscopic Pd line arrays using nanocontact printed dendrimers 3326-3331Langmuir227SELF-ASSEMBLED MONOLAYERS; DIP-PEN NANOLITHOGRAPHY; STAMP DEFORMATION; SOFT LITHOGRAPHY; PATTERN TRANSFER; ETCH RESISTS; FABRICATION; MICROSTRUCTURES; PALLADIUM; MULTILAYERSArticleMarHigh-density Pd line arrays with 55 nm line-width were obtained using nanocontact-printed dendrimer monolayers. Elastomeric PDMS stamps for nanocontact printing were replicated from silicon master molds which were fabricated by UV nanoimprinting in combination with reactive ion etching. The fabrication method effectively controlled the aspect ratios of high-density lines for resolving the problems encountered in both replicating silicon masters to PDMS stamps and printing with the replicated PDMS stamps. Using the PDMS nanostamp with an optimized aspect ratio, a self-assembled monolayer of dendrimer was patterned on a Pd film via nanocontact printing, which was facilitated by the strong interaction between Pd and amine groups of the dendrimer. The patterned self-assembled monolayer was used as an etch-resist mask against the wet etchant of Pd, leaving behind a high-density Pd line array over large areas. The resulting functional Pd nanopattem is of practical significance in microelectronics and bio- or gas-sensing devices.://000236843300065 Times Cited: 0 Cited References: ARRINGTON D, 2002, LANGMUIR, V18, P7788 BANGAR MA, 2004, CHEM MATER, V16, P4955 COLBURN M, 1999, P SOC PHOTO-OPT 1&2, V3676, P379 DELAMARCHE E, 1997, ADV MATER, V9, P741 GORMAN CB, 1995, CHEM MATER, V7, P526 HUCK WTS, 1999, LANGMUIR, V15, P6862 HUI CY, 2002, LANGMUIR, V18, P1394 JEONG JH, 2004, MICROELECTRON ENG, V75, P165 KIM E, 1996, ADV MATER, V8, P139 KUMAR A, 1993, APPL PHYS LETT, V63, P200 LANDIS S, 2000, PHYS REV B, V62, P12271 LI HW, 2002, NANO LETTERS, V2, P347 LOVE JC, 2002, J AM CHEM SOC, V124, P1576 MCKENDRY R, 2002, NANO LETTERS, V2, P713 MONIZ BJ, 1994, METALLURGY ODOM TW, 2002, LANGMUIR, V18, P5314 PINER RD, 1999, SCIENCE, V283, P661 RETTNER CT, 2002, IEEE T MAGN 1, V38, P1725 ROGERS JA, 1997, ADV MATER, V9, P475 ROGERS JA, 1998, J VAC SCI TECHNOL B, V16, P88 SHARP KG, 2004, LANGMUIR, V20, P6430 TOKUHISA H, 1998, J AM CHEM SOC, V120, P4492 WOLFE DB, 2002, APPL PHYS LETT, V80, P2222 XIA YN, 1995, CHEM MATER, V7, P2332 XIA YN, 1996, MICROELECTRON ENG, V32, P255 ZHANG HL, 2004, NANO LETT, V4, P1513 ZHOU F, 2003, ADV MATER, V15, P1367ISI:000236843300065&Korea Adv Inst Sci & Technol, Dept Chem & Biomol Engn, Taejon 305701, South Korea. Korea Inst Machinery & Mat, Nano Mech Syst Res Ctr, Taejon 305343, South Korea. Yang, SM, Korea Adv Inst Sci & Technol, Dept Chem & Biomol Engn, 373-1 Guseong Dong, Taejon 305701, South Korea. smyang@kaist.ac.krwinternal-pdf://2006 Langmuir Jang Nanoscopic Pd line arrays-0016711700/2006 Langmuir Jang Nanoscopic Pd line arrays.pdfP/4w-1410247999\2006 Langmuir Jang Nanoscopic Pd line arrays.pdf ~?C4Majumdar, G. Gogoi, S. K. Paul, A. Chattopadhyay, A.2006=Lithography for imprinting colored patterns with quantum dots 3439-3444Langmuir227DDIP-PEN NANOLITHOGRAPHY; NANOPARTICLES; NANOSTRUCTURES; LUMINESCENCEArticleMarOIn this article, we report a new form of lithography that involves a reaction between a gas and an ion embedded in a polymer film. The principle is based on a combination of top-down and bottom-up approaches in which a transmission electron microscope grid is placed on a poly(vinylpyrrolidone) film containing Cd2+ ions, which is then exposed to H2S gas. This leads to the generation of a fluorescent yellow pattern due to the formation of US nanoparticles on exposed parts of the film. Also, we have used the same method to generate patterns in two colors by starting with a green fluorescent dye incorporated into the film and following the same procedure in which patterned yellow-orange US nanoaparticles are distributed over the background fluorescence of the dye. We have used fluorescence microscopy, UV-vis and fluorescence spectroscopy, transmission electron microscopy, atomic force microscopy. and X-ray diffraction methods for the characterization of the products and patterns. This method could possibly be a fairly general method of generating patterned materials on 2D and 3D substrates.://000236843300082 Times Cited: 0 Cited References: CHOU SY, 2002, NATURE, V417, P835 CHOWDHURY D, 2001, NANO LETTERS, V1, P409 CROOK R, 2003, NATURE, V424, P752 GINGER DS, 2004, ANGEW CHEM INT EDIT, V43, P30 GROSSO D, 2004, NAT MATER, V3, P787 HAYNES CL, 2003, NANO LETT, V3, P939 HUA F, 2004, THIN SOLID FILMS, V449, P222 ITO T, 2000, NATURE, V406, P1027 JIANG P, 2005, ADV MATER, V17, P179 JUNG YJ, 2002, NANO LETT, V3, P561 LAKOWICZ JR, 1999, J PHYS CHEM B, V103, P7613 LAKOWICZ JR, 2000, ANAL BIOCHEM, V280, P128 LIN XM, 2001, APPL PHYS LETT, V78, P1915 MAHTAB R, 1995, J AM CHEM SOC, V117, P9099 NAIR PS, 2002, CHEM COMMUN, P564 OLSON CE, 2002, NAT MATER, V1, P225 RATNER M, 2003, NANOTECHNOLOGY GENTL, P1 SONE ED, 2002, ANGEW CHEM INT EDIT, V41, P1706 SU M, 2002, APPL PHYS LETT, V80, P4434 WEI BQ, 2002, NATURE, V416, P495 WOUTERS D, 2004, ANGEW CHEM INT EDIT, V43, P2480 XIA Y, 1998, ANGEW CHEM INT EDIT, V37, P550ISI:000236843300082Indian Inst Technol, Dept Chem, Gauhati 781039, India. Indian Inst Technol, Ctr Nanotechnol, Gauhati 781039, India. Paul, A, Indian Inst Technol, Dept Chem, Gauhati 781039, India. arun@iitg.ernet.ininternal-pdf://2006 Langmuir Majumdar Lithography for Imprinting Colored Patterns-4294945556/2006 Langmuir Majumdar Lithography for Imprinting Colored Patterns.pdfPluir Majumdar Lithography for Imprinting Colored Patterns.pdf ~?DBValiokas, R. Vaitekonis, A. Klenkar, G. Trinkunas, G. Liedberg, B.2006mSelective recruitment of membrane protein complexes onto gold substrates patterned by dip-pen nanolithography 3456-3460Langmuir228SELF-ASSEMBLED MONOLAYERS; PHOTOSYNTHETIC REACTION CENTERS; ATOMIC-FORCE MICROSCOPY; RHODOBACTER-SPHAEROIDES; IMMOBILIZATION; FABRICATION; ADSORPTION; NANOSTRUCTURES; ARCHITECTURE; NANOARRAYSArticleAprkDip-pen nanolithography (DPN) is employed to develop a generic array platform for the selective recruitment of membrane protein complexes. An atomic force microscope tip inked with HS(CH2)(16)NH2 is used to generate amino-terminated domains on gold. These domains can be arranged into microscopic and submicroscopic patterns, and the untreated gold substrate is subsequently blocked with HS(CH2)(2)CONH(CH2CH2O)(15)CH3, a compound known to resist the unspecific binding of proteins and cells. The patterned gold substrate is exposed to an enriched membrane fraction from mutant Rhodobacter sphaeroides, which contains photosynthetic core complexes consisting of the reaction center and the light-harvesting complex LH1. The selective recruitment to the patterned domains, governed primarily by electrostatic interactions, is confirmed by contact mode atomic force microscopy.://000236745700004 Times Cited: 0 Cited References: BAHATYROVA S, 2004, NATURE, V430, P1058 BENESCH J, 2001, J BIOMAT SCI-POLYM E, V12, P581 CHEN SF, 2003, LANGMUIR, V19, P2859 CHEUNG CL, 2003, J AM CHEM SOC, V125, P6848 CHOI HG, 2002, COLLOID SURFACE B, V23, P327 CIOBANU M, 2005, LANGMUIR, V21, P692 DAS R, 2004, NANO LETT, V4, P1079 DEMERS LM, 2002, SCIENCE, V296, P1836 FANG Y, 2002, J AM CHEM SOC, V124, P2394 FREIBERG A, 1996, PHOTOSYNTH RES, V48, P309 GINGER DS, 2004, ANGEW CHEM INT EDIT, V43, P30 HARDER P, 1998, J PHYS CHEM B, V102, P426 HE JA, 1998, LANGMUIR, V14, P1674 KRAMER S, 2003, CHEM REV, V103, P4367 LEE I, 2000, J PHYS CHEM B, V104, P2439 LEE KB, 2002, SCIENCE, V295, P1702 MALYSHEVA L, 2003, CHEM PHYS LETT, V370, P451 PETERSON EJ, 2004, J PHYS CHEM B, V108, P15206 PINER RD, 1999, SCIENCE, V283, P661 ROZHOK S, 2003, J PHYS CHEM B, V107, P751 RUNDQVIST J, 2005, LANGMUIR, V21, P2981 SCHEURING S, 2003, P NATL ACAD SCI USA, V100, P1690 SCHONHERR H, 2004, LANGMUIR, V20, P7308 SCHWARTZ PV, 2002, LANGMUIR, V18, P4041 SHEEHAN PE, 2002, PHYS REV LETT, V88 SIEBERT CA, 2004, EMBO J, V23, P690 SMITH JC, 2003, NANO LETT, V3, P883 TINAZLI A, 2005, CHEM-EUR J, V11, P5249 TRAMMELL SA, 2004, BIOSENS BIOELECTRON, V19, P1649 WADUMESTHRIGE K, 1999, LANGMUIR, V15, P8580 WADUMESTHRIGE K, 2001, BIOPHYS J, V80, P1891 WALZ T, 1998, J MOL BIOL, V282, P833 WEEKS BL, 2002, J PHYS REV LETT, V88 XU S, 1997, LANGMUIR, V13, P127 ZHANG H, 2003, NANOTECHNOLOGY, V14, P1113 ZHOU DJ, 2003, LANGMUIR, V19, P10557ISI:000236745700004Inst Phys, Mol Cpds Phys Lab, LT-02300 Vilnius, Lithuania. Linkoping Univ, Div Mol Phys, Dept Phys Chem & Biol, S-58183 Linkoping, Sweden. Valiokas, R, Inst Phys, Mol Cpds Phys Lab, Savanoriu 231, LT-02300 Vilnius, Lithuania. valiokas@ar.fi.ltinternal-pdf://2006 Langmuir Valiokas Selective Recruitment of Membrane Pro-3741334805/2006 Langmuir Valiokas Selective Recruitment of Membrane Protein Complexes.pdfTwValiokas Selective Recruitment of Membrane Protein Complexes.pdf R~?EIJegadesan, S. Taranekar, P. Sindhu, S. Advincula, R. C. Valiyaveettil, S.2006|Electrochemically nanopatterned conducting coronas of a conjugated polymer precursor: SPM parameters and polymer composition 3807-3811Langmuir228SCANNING TUNNELING MICROSCOPE; ATOMIC-FORCE MICROSCOPY; DIP-PEN NANOLITHOGRAPHY; ANODIZATION LITHOGRAPHY; CONSTRUCTIVE NANOLITHOGRAPHY; PALMITIC ACID; NETWORK FILMS; SILICON; TIP; NANOFABRICATIONArticleAprHere we describe the formation of precisely controlled corona-type nanopatterns on electroactive polymer precursor films using scanning probe microscopy (SPM) methods. The binary composition of electroactive groups in the polymer triggers the formation of corona-type nanopatterns at particular voltages and tip writing speeds through the electrooxidation of the polymer precursor film. Various parameters Such as tip speed and applied bias were explored in the nanopatterning process. and the formation of a conductive nanopattern was investigated using conducting atomic force microscopy (C-AFM). The formation of the nanopattern was attributed to the flow of electrons from the AFM tip to the polymer film in a controlled electric field distribution. We also report a new method to distinguish the polymer composition and distribution of a polymer blend film by characterizing biasing differences in the patterning of a polymer film.://000236745700054 Times Cited: 0 Cited References: AHN SJ, 2002, APPL PHYS LETT, V80, P2592 AHN SJ, 2002, ULTRAMICROSCOPY, V91, P171 BAE S, 2005, NANOTECHNOLOGY, V16, P2082 BARD AJ, 1990, ACCOUNTS CHEM RES, V23, P357 CAI YG, 2005, J AM CHEM SOC, V127, P16287 DENG SX, 2002, CHEM MATER, V14, P4073 HOLDCROFT S, 2001, ADV MATER, V13, P1753 INAOKA S, 2002, MACROMOLECULES, V35, P2426 JANG SY, 2004, J AM CHEM SOC, V126, P9476 JEGADESAN S, 2005, ADV MATER, V17, P1282 JEGADESAN S, 2006, LANGMUIR, V22, P780 KIRCHNER V, 2001, ACCOUNTS CHEM RES, V34, P371 KOLB DM, 1997, SCIENCE, V275, P1097 LAAN M, 2005, J PHYS D, V36, P2667 LEE K, 1982, J PHYS CHEM-US, V86, P1985 LEE W, 2005, LANGMUIR, V21, P8839 LEMESHKO S, 2001, NANOTECHNOLOGY, V12, P273 LI W, 1996, J PHYS CHEM-US, V100, P20103 LI Y, 2001, J AM CHEM SOC, V123, P2105 LYUKSYUTOV SF, 2003, NANOTECHNOLOGY, V14, P716 LYUKSYUTOV SF, 2003, NAT MATER, V2, P468 MAOZ R, 2000, ADV MATER, V12, P424 PARK MK, 2001, LANGMUIR, V17, P7670 PINER RD, 1999, SCIENCE, V283, P661 SIRRINGHAUS H, 1998, SCIENCE, V280, P1741 SUGIMURA H, 1994, J PHYS CHEM-US, V98, P4352 TARANEKAR P, 2002, LANGMUIR, V18, P7943 TARANEKAR P, 2005, MACROMOLECULES, V38, P3679 TELLO M, 2005, ADV MATER, V17, P1480 WOUTERS D, 2003, LANGMUIR, V19, P9033 XIA C, 2001, LANGMUIR, V17, P7893 ZHAO L, 2005, J ELECTROSTAT, V63, P337ISI:0002367457000548Natl Univ Singapore, Dept Chem, Singapore 117543, Singapore. Natl Univ Singapore, Nanosci & Nanotechnol Initiat, Singapore 117543, Singapore. Univ Houston, Dept Chem, Houston, TX 77204 USA. Advincula, RC, Natl Univ Singapore, Dept Chem, 3 Sci Dr 3, Singapore 117543, Singapore. radvincula@uh.edu chmsv@nus.edu.sginternal-pdf://2006 Langmuir Jegadesan Direct Electrichemical Nanpatterning-2701177365/2006 Langmuir Jegadesan Direct Electrichemical Nanpatterning.pdfd1\2006 Langmuir Jegadesan Electrochemically Nanopatterned conducting coronas.pdfFΖ~?FXu, P. Singh, A. Kaplan, D. L.2006TEnzymatic catalysis in the synthesis of polyanilines and derivatives of polyanilines69-94&Enzyme-Catalyzed Synthesis of Polymers194BerlinSpringer-Verlag BerlinSOLUBLE CONDUCTING POLYANILINE; LIGHT-EMITTING-DIODES; HORSERADISH-PEROXIDASE; PHENOL DERIVATIVES; POLY(VINYLPHOSPHONIC ACID); ANILINE DERIVATIVES; MOLECULAR-COMPLEX; 2-STEP MECHANISM; KINETIC EVIDENCE; LANGMUIR TROUGHEnzyme catalysis in the synthesis of polyaniline is reviewed. Oxidoreductase enzymes and biomimetic catalysts have been used for the polymerization in aqueous, aqueous organic, and interfacial or templating environments to optimize polymer features. The results showed significant structural control in the presence of templates to produce water soluble and processable polymeric materials. Dip-pen nanolithography technology has also been used to process these materials into conducting nano-wires and thus provides new opportunities for the formation of electrical contacts among biological components for various applications such as synthetic biological interfaces.://000236575900003 Advances in Polymer ScienceTimes Cited: 0 Cited References: AGBOR NE, 1997, SENSOR ACTUAT B-CHEM, V41, P137 AIZAWA M, 1990, J BIOTECHNOL, V14, P301 AKKARA JA, 1992, INDIAN J CHEM B, V31, P855 AKKARA JA, 2000, MACROMOLECULES, V33, P2377 ALVA KS, 1998, CHEM MATER, V10, P1270 ALVAREZ S, 2003, J APPL POLYM SCI, V88, P369 BARTLETT PN, 1998, ANAL CHEM, V70, P3685 BRUNO FF, 1995, IND ENG CHEM RES, V34, P4009 BRUNO FF, 1995, LANGMUIR, V11, P889 BRUNO FF, 2003, J MACROMOL SCI PUR A, V40, P1327 CHAN HSO, 1995, J AM CHEM SOC, V117, P8517 CHATTOPADHYAY K, 2000, BIOCHEMISTRY-US, V39, P263 CHEN SA, 1994, J AM CHEM SOC, V116, P7939 CHEN SA, 1995, J AM CHEM SOC, V117, P10055 CHEN SA, 1996, MACROMOLECULES, V29, P3950 DEGRAND C, 2001, ANALYST, V126, P887 DIAZ AN, 1995, J PHOTOCH PHOTOBIO A, V87, P99 DIAZ AN, 1998, J PHOTOCH PHOTOBIO A, V113, P27 FERREIRA ML, 2003, MACROMOL BIOSCI, V3, P179 GENIES EM, 1988, J APPL ELECTROCHEM, V18, P285 GILABERT MA, 2004, BBA-PROTEINS PROTEOM, V1699, P235 GOSPODINOVA N, 1993, POLYMER, V34, P1330 GOSPODINOVA N, 1993, POLYMER, V34, P2434 GOSPODINOVA N, 1994, POLYMER, V35, P3102 GUSTAFSSON G, 1992, NATURE, V357, P477 HODGSON M, 1989, J BIOLUM CHEMILUM, V3, P21 JAKOWSKI JD, 2001, 0149733, WO, APPL JELLE BP, 1993, J ELECTROCHEM SOC, V140, P3560 JIN Z, 2001, SYNTHETIC MET, V122, P237 JOO J, 1994, APPL PHYS LETT, V65, P2278 KARAMYSHEV AV, 2003, ENZYME MICROB TECH, V33, P556 KOBAYASHI S, 2001, CHEM REV, V101, P3793 KU BC, 2003, J MACROMOL SCI PUR A, V40, P1335 LIU G, 1997, MACROMOLECULES, V30, P5660 LIU W, 1999, J AM CHEM SOC, V121, P11345 LIU W, 1999, J AM CHEM SOC, V121, P71 LIU W, 1999, SYNTHETIC MET, V101, P738 LIU W, 2002, LANGMUIR, V18, P9696 MACDIARMID AG, 1987, SYNTHETIC MET, V18, P285 MACDIARMID AG, 1997, SYNTHETIC MET, V84, P27 NAGARAJAN R, 2000, MACROMOLECULES, V33, P9542 NAGARAJAN R, 2001, J MACROMOL SCI PURE, V38, P1519 NAGARAJAN R, 2001, MACROMOLECULES, V34, P3921 NAOI K, 1988, ELECTROCHEM J SOC, V135, C119 NGUYEN MT, 1994, MACROMOLECULES, V27, P3625 PILETSKY S, 2003, BIOTECHNOL BIOENG, V82, P86 PINA DG, 2001, EUR J BIOCHEM, V268, P120 REGELSBERGER G, 1999, BIOCHEMISTRY-US, V38, P10480 RODRIGUEZLOPEZ JN, 2000, BIOCHEMISTRY-US, V39, P13201 ROY S, 2002, BIOMACROMOLECULES, V3, P937 RYABOV AD, 1999, CHEM MATER, V11, P600 RYU KG, 1993, BIOTECHNOL BIOENG, V42, P807 SAHOO SK, 2001, J MACROMOL SCI PURE, V38, P1315 SAHOO SK, 2002, J MACROMOL SCI PUR A, V39, P1223 SAHOO SK, 2002, POLYM MAT SCI ENG, V87, P394 SAHOO SK, 2004, MACROMOLECULES, V37, P4130 SAKHAROV IY, 2002, BIOCHIM BIOPHYS ACTA, V1598, P115 SAKHAROV IY, 2004, SYNTHETIC MET, V142, P127 SAKURAGAWA A, 1998, ANAL CHIM ACTA, V374, P191 SAMUELSON L, 2001, SYNTHETIC MET, V119, P271 SAMUELSON LA, 1998, MACROMOLECULES, V31, P4376 SANCHEZ FG, 1995, J LUMIN, V65, P33 SHAN JY, 2000, POLYM ADVAN TECHNOL, V11, P288 SHAN JY, 2003, POLYM ADVAN TECHNOL, V14, P330 SHRIDHARA K, 1997, MACROMOLECULES, V30, P4024 SKOTHEIM TA, 1998, HDB CONDUCTING POLYM SOLOMON EI, 1993, SCIENCE, V259, P1575 SOLOMON EI, 1996, CHEM REV, V96, P2563 TAKAMUKU S, 2003, SYNTHETIC MET 1, V135, P331 THIYAGARAJAN M, 2003, J AM CHEM SOC, V125, P11502 THIYAGARAJAN M, 2003, J MACROMOL SCI PUR A, V40, P1347 TRIPATHY SK, 1999, SYNTHETIC MET, V102, P893 VERGHESE MM, 1996, CHEM MATER, V8, P822 WANG X, 1999, SYNTHETIC MET, V107, P117 WEI XL, 1995, SYNTHETIC MET, V74, P123 WESTERWEELE E, 1995, ADV MATER, V7, P788 WOOD AS, 1991, MOL PLAST, V68, P47 XU F, 1996, BIOCHEMISTRY-US, V35, P7608 XU P, 2003, POLYM PREP-ACS, V44, P948 XU P, 2004, ADV MATER, V16, P628 YAROPOLOV AI, 1994, APPL BIOCHEM BIOTECH, V49, P257 Review HEIDELBERGER PLATZ 3, D-14197 BERLIN, GERMANYISI:000236575900003kTufts Univ, Dept Biomed Engn, Medford, MA 02155 USA. Tufts Univ, Dept Chem & Biol Engn Bioengn, Medford, MA 02155 USA. Tufts Univ, Ctr Biotechnol, Medford, MA 02155 USA. Harvard Univ, Sch Med, Dept Radiol, Boston, MA 02155 USA. Kaplan, DL, Tufts Univ, Dept Biomed Engn, Medford, MA 02155 USA. peng.Xu@tufts.edu amarjit_singh@hms.harvard.edu david.kaplan@tufts.eduginternal-pdf://2006_AdvPoly Sci_Enzymatic catalysis-1896400405/2006_AdvPoly Sci_Enzymatic catalysis.pdf vt@tue.nlkinternal-pdf://2006_CN_Guided self-assembly_Hoeppener-2769022741/2006_CN_Guided self-assembly_Hoeppener.pdf=D~?GEHoeppener, S. Susha, A. S. Rogach, A. L. Feldmann, J. Schubert, U. S.2006Guided self-assembly of Fe3O4 nanoparticles on chemically active surface templates generated by electro-oxidative nanolithography135-141Current Nanoscience22=electro-oxidative nanolithography; surface patterning; scanning force microscopy; Fe3O4 nanoparticles; self-assembly; nanofabrication DIP-PEN NANOLITHOGRAPHY; MAGNETIC NANOPARTICLES; CONSTRUCTIVE NANOLITHOGRAPHY; NANOCRYSTAL SUPERLATTICES; FORCE MICROSCOPY; NANOSTRUCTURES; MONOLAYERS; COBALT; GOLD; FUNCTIONALIZATIONArticleMayAn approach for the site-selective binding of magnetic Fe3O4 particles onto predefined surface templates is reported. Chemically active surface patterns are prepared by electro-oxidative nanolithography performed with the conductive tip of a scanning probe microscope on n-octadecyltrichlorosilane (OTS) monolayers self-assembled on silicon. The chemical functionalization allows prefabricated nanoparticles with an organic ligand shell to attach selectively on these surface sites, just by immersing the sample into the particle solution. Besides the use of the active surface patterns to guide the assembly of Fe3O4 nanoparticles with nanometer precision, several aspects of the patterning process are briefly discussed in terms of optimization of the obtainable line width.://000236841400007 Times Cited: 0 Cited References: ALIEV FG, 1999, ADV MATER, V11, P1006 BERRY CC, 2003, J PHYS D APPL PHYS, V36, R198 DEMERS LM, 2002, SCIENCE, V296, P1836 ENGELMANN S, 2005, J MAGN MAGN MATER, V293, P685 GINGER DS, 2004, ANGEW CHEM INT EDIT, V43, P30 GRAF H, 2002, APPL PHYS LETT, V80, P1264 GUO J, 2005, SMALL, V1, P737 HOEPPENER S, 2002, ADV MATER, V14, P1036 HOEPPENER S, 2005, IN PRESS ADV FUNCT M HOEPPENER S, 2005, SMALL, V1, P628 HONG SH, 1999, SCIENCE, V286, P523 KIM BS, 2005, NANO LETT, V5, P1987 KIM DK, 2005, J APPL PHYS, V97 LAGAE L, 2002, J APPL PHYS 2, V91, P7445 LI Z, 2004, CHEM MATER, V16, P1391 LIBIOULLE L, 1999, LANGMUIR, V15, P300 LIEBER CM, 2003, MRS BULL, V28, P486 LIU ST, 2002, NANO LETT, V2, P1055 LIU ST, 2004, NANO LETT, V4, P845 MAOZ R, 2000, ADV MATER, V12, P725 MASSART R, 1981, IEEE T MAGN, V17, P1247 MELTZER S, 2001, LANGMUIR, V17, P1713 PARK J, 2004, NAT MATER, V3, P891 PELLEGRINO T, 2005, SMALL, V1, P48 PUNTES VF, 2001, IEEE T MAGN 1, V37, P2210 PUNTES VF, 2001, SCIENCE, V291, P2115 RHEINLANDER T, 2000, MAGN ELEC SEPARATION, V10, P179 SAGIV J, 1980, J AM CHEM SOC, V102, P92 SALAITA K, 2005, J AM CHEM SOC, V127, P11283 SCHMID G, 2004, NANOPARTICLES THEORY SIMON U, 2004, NANOPARTICLES THEORY SUDFELD D, 2003, J APPL PHYS 2, V93, P7328 SUN SH, 1999, J APPL PHYS 2A, V85, P4325 SUN SH, 2000, SCIENCE, V287, P1989 TANAKA K, 2005, INT J CANCER, V116, P624 TARTAJ P, 2005, J MAGN MAGN MATER 1, V290, P28 WANG XM, 2005, J MAGN MAGN MATER, V293, P334 WHITESIDES GM, 2005, SMALL, V1, P172 WILLNER I, 2002, PURE APPL CHEM, V74, P1773 WOUTERS D, 2003, LANGMUIR, V19, P9033 WOUTERS D, 2005, ADV FUNCT MATER, V15, P938 WOUTERS D, 2005, J MATER CHEM, V15, P2353 XIA Y, 1998, ANGEW CHEM INT EDIT, V37, P550 XUE YQ, 2003, PHYS REV B, V68 ZHU XB, 2004, MRS BULL, V29, P457ISI:000236841400007IEindhoven Univ Technol, Lab Macromol Chem & Nanosci, NL-5600 MB Eindhoven, Netherlands. Univ Munich, Dept Phys, Photon & Optoelect Grp, D-80799 Munich, Germany. Ctr Nanosci, D-80799 Munich, Germany. Schubert, US, Eindhoven Univ Technol, Lab Macromol Chem & Nanosci, POB 513, NL-5600 MB Eindhoven, Netherlands. u.s.schuber l~?H7Zheng, Z. J. Azzaroni, O. Vickers, M. E. Huck, W. T. S.2006/Transfer printing water-soluble inorganic salts805-811Advanced Functional Materials166REDUCED ENVIRONMENTAL-IMPACT; DIP-PEN NANOLITHOGRAPHY; PHOTO-CROSS-LINKING; LITHOGRAPHY; FILMS; FABRICATION; TEMPLATES; CRYSTALS; PATTERNS; LAYERSArticleAprThis paper reports the first example of the fabrication of KNO3, K2CO3, CuSO4, NaOH, and mixed-inorganic-salt (KNO3 and KOH) patterns using a transfer-printing (TP) technique. The transfer quality is found to be related to the concentration of the salt solutions. By varying the immersion time, it is possible to control the heights of the raised features of the transfer-printed salts from the nanoscale to the submicrometer scale. Utilizing these inorganic salts as water-soluble masks for microfabrication is demonstrated using patterned NaOH films. The use of water as a developer solvent demonstrates the potential utility of the patterning of inorganic salts as a low-cost. simple, and, more importantly, environmentally friendly route towards accurate patterning of different materials.://000236812400010 Times Cited: 2 Cited References: AIZENBERG J, 1999, NATURE, V398, P495 AIZENBERG J, 2004, ADV MATER, V16, P1295 BALACHOVA OV, 2000, MICROELECTR J, V31, P213 BUSE K, 1998, NATURE, V393, P665 CHAE KH, 2002, J APPL POLYM SCI, V86, P1172 FELMET K, 2004, APPL PHYS LETT, V85, P3316 FU L, 2003, NANO LETT, V3, P757 GATES BD, 2005, CHEM REV, V105, P1171 HA K, 2002, ADV MATER, V14, P1614 HARNACK O, 2005, APPL PHYS LETT, V86 HAVARD JM, 1999, MACROMOLECULES, V32, P86 HU H, 2001, ADV MATER, V13, P670 JACOBS HO, 2001, SCIENCE, V291, P1763 KIM E, 1996, J AM CHEM SOC, V118, P5722 KIM JB, 2003, MACROMOL RAPID COMM, V24, P879 KIM YS, 2004, ADV MATER, V16, P581 LINDER V, 2005, SMALL, V1, P730 LOO YL, 2002, J AM CHEM SOC, V124, P7654 MEITL MA, 2004, NANO LETT, V4, P1643 ODOM TW, 1998, NATURE, V391, P62 PARK J, 2004, ADV MATER, V16, P520 SCHAPER CD, 2003, J VAC SCI TECHNOL B, V21, P2961 SCHAPER CD, 2004, J MICROLITH MICROFAB, V3, P174 SCHMID H, 1998, APPL PHYS LETT, V72, P2379 SCHUTH F, 2002, ADV MATER, V14, P629 SU M, 2002, J AM CHEM SOC, V124, P1560 TAN CH, 2004, LANGMUIR, V20, P9901 THALLADI VR, 2002, J AM CHEM SOC, V124, P3520 TOKUHISA H, 2004, LANGMUIR, V20, P1436 WANG MT, 2002, CHEM MATER, V14, P4812 WANG Z, 2003, ADV MATER, V15, P1009 XIA Y, 1998, ANGEW CHEM INT EDIT, V37, P550 ZHAO D, 1998, ADV MATER, V10, P1380ISI:000236812400010GUniv Cambridge, Dept Chem, Melville Lab Polymer Synth, Cambridge CB2 1EW, England. Univ Cambridge, Nanosci Ctr, Cambridge CB3 0FF, England. Univ Cambridge, Dept Mat Sci & Met, Cambridge CB2 3QZ, England. Zheng, ZJ, Univ Cambridge, Dept Chem, Melville Lab Polymer Synth, Lensfield Rd, Cambridge CB2 1EW, England. wtsh2@cam.ac.ukinternal-pdf://2006 AdvFuncMats Zheng Transfer Printing Water-Soluble Inorganic-2165143829/2006 AdvFuncMats Zheng Transfer Printing Water-Soluble Inorganic Salts.pdf(~?I1Basnar, B. Weizmann, Y. Cheglakov, Z. Willner, I.2006JSynthesis of nanowires using dip-pen nanolithography and biocatalytic inks713-+Advanced Materials186\AU NANOPARTICLES; METAL NANOWIRES; DNA; GROWTH; LITHOGRAPHY; INHIBITION; TEMPLATE; GOLD; TIPArticleMarGold-nanoparticle-functionalized enzymes act as "biocatalytic inks" for the generation of metallic nanowires via dip-pen nanolithography. Deposition of nanoparticle-modified oxidases or a phosphatase followed by development with their respective substrates and metal salts results in nanowires (see figure). This concept may be extended to the generation of other nanostructures via enzyme-catalyzed particle growth.://000236603700003 Times Cited: 1 Cited References: BENALI M, 2002, LANGMUIR, V18, P872 BRAUN E, 1998, NATURE, V391, P775 GINGER DS, 2004, ANGEW CHEM INT EDIT, V43, P30 HYUN J, 2004, J AM CHEM SOC, V126, P4770 KATZ E, 2004, ANGEW CHEM INT EDIT, V43, P6042 KEREN K, 2002, SCIENCE, V297, P72 KRAMER S, 2003, CHEM REV, V103, P4367 LIM JH, 2003, ANGEW CHEM INT EDIT, V42, P2309 MAO CB, 2004, SCIENCE, V303, P213 MERTIG M, 2002, NANO LETTERS, V2, P841 PAVLOV V, 2005, NANO LETT, V5, P649 RECHES M, 2003, SCIENCE, V300, P625 RICHTER J, 2001, APPL PHYS LETT, V78, P536 RIEMENSCHNEIDER L, 2005, NANO LETT, V5, P1643 SCHEIBEL T, 2003, P NATL ACAD SCI USA, V100, P4527 SU M, 2004, APPL PHYS LETT, V84, P4200 TAKEDA S, 2003, NANO LETT, V3, P1471 WEIZMANN Y, 2004, NANO LETT, V4, P787 WOUTERS D, 2004, ANGEW CHEM INT EDIT, V43, P2480 XIAO Y, 2005, CHEM-EUR J, V11, P2698 XIAO Y, 2005, LANGMUIR, V21, P5659 ZAYATS M, 2005, NANO LETT, V5, P21ISI:000236603700003Hebrew Univ Jerusalem, Inst Chem, IL-91904 Jerusalem, Israel. Willner, I, Hebrew Univ Jerusalem, Inst Chem, IL-91904 Jerusalem, Israel. willnea@vms.huji.ac.ilsinternal-pdf://2006 Adv Mat Basnar Synthesis of nanowires-3238922261/2006 Adv Mat Basnar Synthesis of nanowires.pdf ~?JGCong, Y. Fu, J. Zhang, Z. X. Cheng, Z. Y. Xing, R. B. Li, J. Han, Y. C.2006qFabrication of arrays of silver nanoparticle aggregates by microcontact printing and block copolymer nanoreactors 2737-2743"Journal of Applied Polymer Science1004block copolymers; micelles; nanoparticles SELF-ASSEMBLED MONOLAYERS; DIP-PEN NANOLITHOGRAPHY; ELECTROLESS DEPOSITION; METAL NANOPARTICLES; MICRON-SCALE; SPECTROSCOPY; MICELLES; POLYMERS; SURFACES; COLLOIDSArticleMayA combination of microcontact printing and block copolymer nanoreactors succeeded in fabricating arrays of silver nanoparticle aggregates. A complex solution of polystyrene-block-poly(4-vinylpyridine) micelles and silver salt was used as an ink to form thin films or droplets on polydimethylsiloxane stamp protrusions. After these complex aggregates were printed onto silicon substrates under controlled conditions, highly ordered arrays of disklike, dishlike, and dotlike complex aggregates were obtained. A Subsequent oxygen reactive ion etching treatment yielded arrays of silver nanoparticle aggregates. (c) 2006 Wiley Periodicals, Inc.://000236423600022 VTimes Cited: 0 Cited References: ANTONIETTI M, 1994, MACROMOLECULES, V27, P3276 BERNARD A, 2000, ADV MATER, V12, P1067 CALDERARA F, 1996, MACROMOL CHEM PHYSIC, V197, P2115 CHEN CC, 2001, ADV MATER, V13, P136 CHOI YK, 2003, J PHYS CHEM B, V107, P3340 CIEBIEN JF, 1998, NEW J CHEM, V22, P685 DICK LA, 2002, J PHYS CHEM B, V106, P853 FELDHEIM DL, 1998, CHEM SOC REV, V27, P1 FORSTER S, 1996, J CHEM PHYS, V104, P9956 FORSTER S, 1998, ADV MATER, V10, P195 FORSTER S, 2002, ANGEW CHEM INT EDIT, V41, P688 HAMLEY IW, 2003, ANGEW CHEM INT EDIT, V42, P1692 HIDBER PC, 1996, LANGMUIR, V12, P1375 JI JM, 2002, ADV MATER, V14, P41 KAMAT PV, 2002, J PHYS CHEM B, V106, P7729 KUMAR A, 1993, APPL PHYS LETT, V63, P2002 KUMAR A, 1994, LANGMUIR, V10, P1498 LEE KB, 2002, SCIENCE, V295, P1702 LEWIS LN, 1993, CHEM REV, V93, P2693 LI HW, 2002, NANO LETTERS, V2, P347 MAIER SA, 2001, ADV MATER, V13, P1501 MAO CF, 1995, J CATAL, V154, P230 MAYER ABR, 2001, POLYM ADVAN TECHNOL, V12, P96 MULVANEY P, 1996, LANGMUIR, V12, P788 MURRAY CB, 2001, MRS BULL, V26, P985 NG WK, 2002, APPL PHYS LETT, V81, P3097 NICEWARNERPENA SR, 2001, SCIENCE, V294, P137 NIE SM, 1997, SCIENCE, V275, P1102 PALACIN S, 1996, CHEM MATER, V8, P1316 PILENI MP, 2001, ADV FUNCT MATER, V13, P1501 PINER RD, 1999, SCIENCE, V283, P661 POWELL HM, 2003, LANGMUIR, V19, P9071 QIN D, 1999, ADV MATER, V11, P1433 SHIPWAY AN, 2000, CHEMPHYSCHEM, V1, P18 SHIPWAY AN, 2001, CHEM COMMUN, P2035 SOHN BH, 2001, CHEM MATER, V11, P323 SPATZ JP, 1996, ANGEW CHEM INT EDIT, V35, P1510 SPATZ JP, 2000, LANGMUIR, V16, P407 WANG MT, 2001, ADV MATER, V13, P1312 XIA YN, 1999, CHEM REV, V99, P1823 ZAMBORINI FP, 1998, J AM CHEM SOC, V120, P9700ISI:000236423600022!Chinese Acad Sci, Changchun Inst Appl Chem, Grad Sch, State Key Lab Polymer Phys & Chem, Changchun 130022, Peoples R China. Han, YC, Chinese Acad Sci, Changchun Inst Appl Chem, Grad Sch, State Key Lab Polymer Phys & Chem, 5625 Renmin St, Changchun 130022, Peoples R China. ychan@ciac.jl.cn{internal-pdf://2006_JAPS_Fabrication of arrays of silver_Cong-3608450069/2006_JAPS_Fabrication of arrays of silver_Cong.pdfh1lver Nano-0952866085\2006 JoAppPolySci Cong Fabrication of Arrays of Silver Nano.pdf*_Ζ~?KNicolau, D. V. Sawant, P. D.2005VScanning probe microscopy studies of surface-immobilised DNA/oligonucleotide molecules113-160 Immobilisation of DNA on Chips I260BerlinSpringer-Verlag BerlinATOMIC-FORCE MICROSCOPY; SINGLE DNA-MOLECULES; DIP-PEN NANOLITHOGRAPHY; SELF-ASSEMBLED MONOLAYERS; HIGHLY CONDUCTIVE NANOWIRES; OLIGONUCLEOTIDE ARRAYS; LATERAL FORCE; STRUCTURAL TRANSITIONS; BIOLOGICAL-MATERIALS; CROSSOVER MOLECULESAlthough most in vivo biomolecular recognition occurs in solution, in many practical situations (e.g., diagnostics, drug discovery and biosensing) biomolecular recognition occurs between "target" biomolecules immobilised on surfaces and "probe" complementary biomolecules approaching the surface from solution. DNA-based devices are by far the most common biomolecular and cellular planar biodevices with a still-commanding growth rate. A second, but chronologically older, interest derives from the need to understand the fundamentals of biomolecular interactions at single molecule level and in large supramolecular assemblies. Again, DNA molecules are not only essential objects of study, but also more attractive candidates as the budding blocks of artificial biomolecular devices than, e.g., proteins, because of their relative simplicity and robustness. Among the many microscopy-based techniques for the study of biomolecular interactions on surfaces, scanning probe microscopies, and especially the atomic force microscopies (AFM), are the most used because of their molecular and sub-molecular level resolution and in situ imaging capability. Apart from the high resolution mapping of surface nanotopographies, AFM can be used for the quantification and visualisation of the distribution of chemistry, hydrophobicity and local mechanical properties on surfaces, and for the fabrication of nanostructures on surfaces. The present article, which reviews from classical and latest developments regarding AFM studies of DNA molecules immobilised on surfaces, is organised along the nature of DNA aggregates on surfaces, i.e., single molecules, self-assembled layers and amorphous layers, with the last two emerging areas receiving a relatively higher emphasis. Within these three areas of application, the material is organised along the main functions of the AFM, namely imaging, probing biomolecular interactions and fabrication of nanodevices.://000236319300005 Topics in Current ChemistryTimes Cited: 0 Cited References: THOMSON ISI WEB OF K ADLEMAN LM, 1994, SCIENCE, V266, P1021 AHSAN A, 1998, BIOPHYS J, V74, P132 ALBRECHT TR, 1991, J APPL PHYS, V69, P668 ALIVISATOS AP, 1996, NATURE, V382, P609 ALLEMAND JF, 1998, P NATL ACAD SCI USA, V95, P14152 ALLEN MJ, 1997, NUCLEIC ACIDS RES, V25, P2221 AMREIN M, 1999, NANOBIOLOGY, V4, P229 ANSELMETTI D, 2000, SINGLE MOL, V1, P53 ARGAMAN M, 1997, NUCLEIC ACIDS RES, V25, P4379 BAUMANN CG, 2000, BIOPHYS J, V78, P1965 BEAKE BD, 2000, LANGMUIR, V16, P735 BEAKE BD, 2000, POLYMER, V41, P2241 BEECHER JE, 1997, POLYM MAT SCI ENG, V76, P394 BEECHER JE, 1997, POLYM MAT SCI ENG, V76, P597 BENSIMON D, 1995, PHYS REV LETT, V74, P4754 BEZANILLA M, 1994, BIOPHYS J, V67, P2454 BEZANILLA M, 1995, LANGMUIR, V11, P655 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SHLYAKHTENKO LS, 2000, NUCLEIC ACIDS RES, V28, P3472 SHLYAKHTENKO LS, 2003, ULTRAMICROSCOPY, V97, P279 SINDEN RR, 1994, DNA STRUCTURE FUNCTI SINDEN RR, 1999, AM J HUM GENET, V64, P346 SINDEN RR, 2002, J BIOSCIENCE S1, V27, P53 SINGER IL, 1993, P 20 LEED LYON S TRI SREEKUMAR A, 2001, CANCER RES, V61, P7585 STEEL AB, 2000, BIOPHYS J, V79, P975 STRICK T, 2000, PROG BIOPHYS MOL BIO, V74, P115 STRICK TR, 1996, SCIENCE, V271, P1835 STRICK TR, 1998, BIOPHYS J, V74, P2016 STRUNZ T, 1999, P NATL ACAD SCI USA, V96, P11277 SU M, 2002, J AM CHEM SOC, V124, P1560 SUN HB, 2001, ANAL CHEM, V73, P2229 TAYLOR JR, 2000, ANAL CHEM, V72, P1979 TAYLOR KA, 1999, J STRUCT BIOL, V128, P75 THOMSON NH, 1996, BIOPHYS J, V70, P2421 VESENKA J, 2002, AIP C P, V640, P109 WANG H, 1963, P S MATH THEOR AUT, P23 WANG J, 2000, NUCLEIC ACIDS RES, V28, P3011 WANG J, 2001, ANAL CHEM, V73, P2207 WATANABE H, 2001, APPL PHYS LETT, V79, P2462 WEILER J, 1996, ANAL BIOCHEM, V243, P218 WILBUR JL, 1995, LANGMUIR, V11, P825 WILLIAMS MC, 2002, ACCOUNTS CHEM RES, V35, P159 WILSON DL, 2001, P NATL ACAD SCI USA, V98, P13660 WINFREE E, 1998, NATURE, V394, P539 WINFREE E, 1998, THESIS CALTECH XIAO SJ, 2002, J NANOPART RES, V4, P313 YAN H, 2003, 9 INT M DNA BAS COMP YAN H, 2003, P NATL ACAD SCI USA, V100, P8103 YAN H, 2003, SCIENCE, V301, P1882 YANG J, 1993, J MICROSC-OXFORD, V171, P183 YANG XP, 1998, J AM CHEM SOC, V120, P9779 ZHANG M, 2002, NANOTECHNOLOGY, V13, P212 ZHOU DJ, 2002, LANGMUIR, V18, P8278 Review HEIDELBERGER PLATZ 3, D-14197 BERLIN, GERMANYISI:000236319300005Swinburne Univ Technol, BioNanoEngn Lab, Hawthorn, Vic 3122, Australia. Nicolau, DV, Swinburne Univ Technol, BioNanoEngn Lab, POB 218, Hawthorn, Vic 3122, Australia. dnicolau@swin.edu.au+~?L2Sniadecki, N. Desai, R. A. Ruiz, S. A. Chen, C. S.2006.Nanotechnology for cell-substrate interactions59-74 Annals of Biomedical Engineering341cell mechanics; cell shape; extracellular matrix; focal adhesions; integrins; mechanotransduction; micropatterning; nanotopology; Self-Assembled Monolayers (SAMs); traction forces SELF-ASSEMBLED MONOLAYERS; SMOOTH-MUSCLE-CELLS; DIP-PEN NANOLITHOGRAPHY; ATOMIC-FORCE MICROSCOPE; FOCAL ADHESIONS; TRACTION FORCES; POLY(LACTIC-CO-GLYCOLIC ACID); CYTOSKELETAL TENSION; ENDOTHELIAL-CELLS; GEOMETRIC CONTROLReviewJanIn the pursuit to understand the interaction between cells and their underlying substrates, the life sciences are beginning to incorporate micro- and nanotechnology-based tools to probe and measure cells. The development of these tools portends endless possibilities for new insights into the fundamental relationships between cells and their surrounding microenvironment that underlie the physiology of human tissue. Here, we review techniques and tools that have been used to study how a cell responds to the physical factors in its environment. We also discuss unanswered questions that could be addressed by these approaches to better elucidate the molecular processes and mechanical forces that dominate the interactions between cells and their physical scaffolds.://000236354800007 Times Cited: 1 Cited References: ABERCROMBIE M, 1971, EXP CELL RES, V67, P359 ABRAMS GA, 2000, CELL TISSUE RES, V299, P39 ABRAMS GA, 2003, UROL RES, V31, P341 ALBERTS B, 2002, MOL BIOL CELL ALENGHAT FJ, 2000, BIOCHEM BIOPH RES CO, V277, P93 ALENGHAT FJ, 2002, SCI STKE, PE6 ASHKIN A, 1987, SCIENCE, V235, P1517 BAIN CD, 1988, J AM CHEM SOC, V110, P3665 BAIN CD, 1989, J AM CHEM SOC, V111, P7155 BAIN CD, 1989, J AM CHEM SOC, V111, P7164 BALABAN NQ, 2001, NAT CELL BIOL, V3, P466 BALSS KM, 2001, J PHYS CHEM B, V105, P8970 BENINGO KA, 2001, J CELL BIOL, V153, P881 BENINGO KA, 2004, P NATL ACAD SCI USA, V101, P18024 BERNARD A, 1998, LANGMUIR, V14, P2225 BROCK A, 2003, LANGMUIR, V19, P1611 BURNS MM, 1990, SCIENCE, V249, P749 BURRIDGE K, 1996, ANNU REV CELL 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V287, C1184 HUA F, 2004, NANO LETT, V4, P2467 HUANG S, 1998, MOL BIOL CELL, V9, P3179 INGBER DE, 2003, ANN MED, V35, P564 INGBER DE, 2003, J CELL SCI, V116, P1157 INGBER DE, 2003, J CELL SCI, V116, P1397 JAMES CD, 1998, LANGMUIR, V14, P741 JEON NL, 2002, NAT BIOTECHNOL, V20, P826 JIANG GY, 2003, NATURE, V424, P334 JIANG XY, 2003, J AM CHEM SOC, V125, P2366 JIANG XY, 2005, P NATL ACAD SCI USA, V102, P975 KONG HJ, 2005, P NATL ACAD SCI USA, V102, P4300 LAURENT VM, 2005, BIOPHYS J, V89, P667 LEE GM, 1999, EXP CELL RES, V248, P294 LEE J, 1994, J CELL BIOL, V127, P1957 LEE KB, 2002, SCIENCE, V295, P1702 LEHNERT D, 2004, J CELL SCI, V117, P41 LEUNG DYM, 1976, SCIENCE, V191, P475 LI FY, 2003, BIOPHYS J 1, V84, P1252 LIEDBERG B, 1995, LANGMUIR, V11, P3821 LIN F, 2005, ANN BIOMED ENG, V33, P475 LO CM, 2000, BIOPHYS J, V79, P144 MACK PJ, 2004, AM J PHYSIOL-CELL PH, V287, C954 MANIOTIS AJ, 1997, P NATL ACAD SCI USA, V94, P849 MATTHEWS BD, 2004, BIOCHEM BIOPH RES CO, V313, P758 MCBEATH R, 2004, 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P25 SCHINDLER M, 2005, BIOMATERIALS, V26, P5624 SHIRINSKY VP, 1989, J CELL BIOL, V109, P331 SINGHVI R, 1994, SCIENCE, V264, P696 SMITH JT, 2004, LANGMUIR, V20, P8279 STOPAK D, 1985, P NATL ACAD SCI USA, V82, P2804 SUKI B, 2005, J APPL PHYSIOL, V98, P1892 TAN JL, 2003, P NATL ACAD SCI USA, V100, P1484 TAN JL, 2004, TISSUE ENG, V10, P865 TEIXEIRA AI, 2003, J CELL SCI, V116, P1881 TEIXEIRA AI, 2004, J BIOMED MATER RES A, V71, P3153 TERRAY A, 2002, SCIENCE, V296, P1841 TOLICNORRELYKKE IM, 2005, J BIOMECH, V38, P1405 UPADHYAYA A, 2004, BIOPHYS J, V86, P2923 WALPITA D, 2002, NAT REV MOL CELL BIO, V3, P137 WANG HB, 2001, P NATL ACAD SCI USA, V98, P11295 WANG N, 1993, SCIENCE, V260, P1124 WANG N, 2002, CELL MOTIL CYTOSKEL, V52, P97 XIA YN, 1998, ANNU REV MATER SCI, V28, P153 YIM EKF, 2005, BIOMATERIALS, V26, P5405 YOUSAF MN, 2001, P NATL ACAD SCI USA, V98, P5992 ZAMIR E, 2001, J CELL SCI, V114, P3583 ZLATANOVA J, 2000, PROG BIOPHYS MOL BIO, V74, P37ISI:000236354800007Univ Penn, Dept Bioengn, Philadelphia, PA 19104 USA. Johns Hopkins Univ, Dept Biomed Engn, Baltimore, MD 21205 USA. Chen, CS, Univ Penn, Dept Bioengn, Philadelphia, PA 19104 USA. cschen2@seas.upenn.eduinternal-pdf://2006 Annals of Bio Eng Sniadecki Nanotech for cell-substrate-3675604757/2006 Annals of Bio Eng Sniadecki Nanotech for cell-substrate.pdf ~?M(Lin, H. H. Kim, J. Sun, L. Crooks, R. M.20064Replication of DNA microarrays from zip code masters 3268-3272(Journal of the American Chemical Society12810IDENSITY OLIGONUCLEOTIDE ARRAYS; DIP-PEN NANOLITHOGRAPHY; MUTATIONS; BRCA1ArticleMar,This report describes a mechanical method for efficient and accurate replication of DNA microarrays from a zip code master. The zip code master is a DNA array that defines the location of oligonucleotides consisting of two parts: a code sequence, which is complementary to one or more of the zip codes, and the functional sequence, which is terminated with biotin. Following hybridization of the zip code to the code sequence, a replica surface functionalized with streptavidin is brought into conformal contact with the surface of the master. When the two surfaces are separated, the functional and code sequences are transferred to the replica, and the zip code remains on the surface of the master. Using this approach it is possible to prepare replica arrays having any configuration from a single, universal master array. Here we demonstrate that this approach can be used to replicate master arrays having up to three different sequences, that feature sizes as small as 100 mu m can be replicated, and that master arrays can be used to prepare multiple replicas.://000236035100042 Times Cited: 2 Cited References: AFFARA NA, 2003, BRIEF FUNCT GENOMICS, V2, P7 ALBRECHT C, 2003, SCIENCE, V301, P367 BLANK K, 2003, P NATL ACAD SCI USA, V100, P11356 BULLEN D, 2004, APPL PHYS LETT, V84, P789 DEMERS LM, 2002, SCIENCE, V296, P1836 FAVIS R, 2000, NAT BIOTECHNOL, V18, P561 FLAVELL AJ, 2003, NUCLEIC ACIDS RES, V31 GERRY NP, 1999, J MOL BIOL, V292, P251 GOLUB TR, 1999, SCIENCE, V286, P531 HACIA JG, 1996, NAT GENET, V14, P441 LANGE SA, 2004, ANAL CHEM, V76, P1641 LEE HJ, 2001, ANAL CHEM, V73, P5525 LIN HH, 2005, J AM CHEM SOC, V127, P11210 LOCKHART DJ, 1996, NAT BIOTECHNOL, V14, P1675 LOMBARDI S, 2004, PHARMAGENOMICS, V4, S25 MCQUAIN MK, 2003, ANAL BIOCHEM, V320, P281 OKAMOTO T, 2000, NAT BIOTECHNOL, V18, P438 PIRRUNG MC, 1997, CHEM REV, V97, P473 PIRRUNG MC, 2002, ANGEW CHEM INT EDIT, V41, P1276 STEGMAIER K, 2004, NAT GENET, V36, P257 YU AA, 2005, J AM CHEM SOC, V127, P16774 YU AA, 2005, NANO LETT, V5, P1061ISI:000236035100042Univ Texas, Dept Chem & Biochem, Austin, TX 78712 USA. Crooks, RM, Univ Texas, Dept Chem & Biochem, 1 Univ Stn,A5300, Austin, TX 78712 USA. crooks@cm.utexas.eduwinternal-pdf://2006 JACS Lin Replication of DNA microarrays-0303447573/2006 JACS Lin Replication of DNA microarrays.pdfTys-0175581764\2006 JACS Lin Replication of DNA microarrays.pdf !F~?NLee, N. K. Hong, S. H.2006RModeling collective behavior of molecules in nanoscale direct deposition processesJournal of Chemical Physics12411BDIP-PEN NANOLITHOGRAPHY; INVASION PERCOLATION; SURFACES; INK; MICAArticleMar We present a theoretical model describing the collective behavior of molecules in nanoscale direct deposition processes such as dip-pen nanolithography. We show that strong intermolecular interactions combined with nonuniform substrate-molecule interactions can produce various shapes of molecular patterns including fractal-like structures. Computer simulations reveal circular and starlike patterns at low and intermediate densities of preferentially attractive surface sites, respectively. At large density of such surface sites, the molecules form a two-dimensional invasion percolation cluster. Previous experimental results showing anisotropic patterns of various chemical and biological molecules correspond to the starlike regime. (c) 2006 American Institute of Physics.://000236160000048 &Times Cited: 1 Cited References: AGARWAL G, 2003, J AM CHEM SOC, V125, P580 DELAMARCHE, 1998, J PHYS CHEM B, V102, P3324 FURUBERG L, 1988, PHYS REV LETT, V61, P2117 GINGER DS, 2004, ANGEW CHEM INT EDIT, V43, P30 HONG SH, 1999, SCIENCE, V286, P523 HONG SH, 2000, SCIENCE, V288, P1808 IVANISEVIC A, 2001, J AM CHEM SOC, V123, P7887 JANG JY, 2001, J CHEM PHYS, V115, P2721 JASCHKE M, 1995, LANGMUIR, V11, P1061 LIM JH, 2002, ADV MATER, V14, P1474 MANANDHAR P, 2003, PHYS REV LETT, V90 MANANDHAR P, 2005, LANGMUIR, V21, P3213 MCKENDRY R, 2002, NANO LETTERS, V2, P713 MICHELY T, 1993, PHYS REV LETT, V70, P3943 MYUNG S, 2005, ADV MATER, V17, P2361 PASHLEY RM, 1981, J COLLOID INTERF SCI, V83, P531 PETERSON EJ, 2004, J PHYS CHEM B, V107, P15206 PINER R, 1999, SCIENCE, V283, P29 RAO SG, 2003, NATURE, V425, P36 ROZHOK S, 2003, J PHYS CHEM B, V107, P751 SHEEHAN PE, 2002, PHYS REV LETT, V88 SU M, 2004, APPL PHYS LETT, V84, P4200 WEEKS BL, 2002, PHYS REV LETT, V88 WILKINSON D, 1983, J PHYS A-MATH GEN, V16, P3365 WILSON DL, 2001, P NATL ACAD SCI USA, V98, P13660 XU S, 1998, J AM CHEM SOC, V120, P9356 ZHANG M, 2002, NANOTECHNOLOGY, V13, P212 ZHOU HL, 2004, APPL SURF SCI, V236, P18ISI:000236160000048Sejong Univ, Dept Phys, Inst Fundamental Phys, Seoul 143743, South Korea. Seoul Natl Univ, Sch Phys, Seoul 151747, South Korea. Lee, NK, Sejong Univ, Dept Phys, Inst Fundamental Phys, Seoul 143743, South Korea. lee@sejong.ac.kr shong@phya.snu.ac.kr114711 Artn 114711internal-pdf://2006 JoChemPhysics Lee Modeling collective behavior-1293353493/2006 JoChemPhysics Lee Modeling collective behavior.pdf ~?O*Jegadesan, S. Sindhu, S. Valiyaveettil, S.2006REasy writing of nanopatterns on a polymer film using electrostatic nanolithography481-484Small24atomic force microscopy; electrostatic interactions; nanolithography; polymers; thin films DIP-PEN NANOLITHOGRAPHY; ATOMIC-FORCE MICROSCOPY; SCANNING TUNNELING MICROSCOPE; DATA-STORAGE; PROBE ARRAYS; SILICON; AFM; NANOSTRUCTURES; LITHOGRAPHY; FABRICATIONArticleApr://000235978700004 Times Cited: 0 Cited References: BINNIG G, 1999, APPL PHYS LETT, V74, P1329 BULLEN D, 2004, APPL PHYS LETT, V84, P789 BULLEN D, 2004, J MICROELECTROMECH S, V13, P594 CHOU SY, 1996, SCIENCE, V272, P85 DAGATA JA, 1990, APPL PHYS LETT, V56, P2001 FUCHS K, 1996, MACROMOLECULES, V29, P5893 GILBERT Y, 2004, MACROMOLECULES, V37, P3780 GINGER DS, 2004, ANGEW CHEM INT EDIT, V43, P30 GINGER DS, 2004, ANGEW CHEM, V116, P30 HUANG Y, 2001, SCIENCE, V291, P630 HURLEY PT, 2003, J AM CHEM SOC, V125, P11334 JANG SY, 2004, J AM CHEM SOC, V126, P9476 JEGADESAN S, 2005, ADV MATER, V17, P1282 KOLB DM, 1997, SCIENCE, V275, P1097 KULLER A, 2003, APPL PHYS LETT, V82, P3776 KUMAR A, 1995, ACCOUNTS CHEM RES, V28, P219 LEE KB, 2002, SCIENCE, V295, P1702 LIM JH, 2002, ADV MATER, V14, P1474 LYUKSYUTOV SF, 2003, APPL PHYS LETT, V83, P4405 LYUKSYUTOV SF, 2003, NAT MATER, V2, P468 MAMIN HJ, 1992, APPL PHYS LETT, V61, P1003 MASON JH, 1991, IEEE T ELECTR INSUL, V26, P318 MAYNOR BW, 2002, J AM CHEM SOC, V124, P522 MINNE SC, 1998, APPL PHYS LETT, V72, P2340 PINER RD, 1997, LANGMUIR, V13, P6864 ROZHOK S, 2004, J PHYS CHEM B, V108, P7814 SCHAFFER E, 2000, NATURE, V403, P874 SNOW ES, 1995, SCIENCE, V270, P1639 SU M, 2002, J AM CHEM SOC, V124, P1560 SUH KS, 2000, J APPL PHYS, V87, P7333 TERRIS BD, 1998, APPL PHYS A-MATE S 2, V66, S809 VETTIGER P, 2000, IBM J RES DEV, V44, P323 WOUTERS D, 2004, ANGEW CHEM INT EDIT, V43, P2480 WOUTERS D, 2004, ANGEW CHEM, V116, P2534 ZHANG M, 2002, NANOTECHNOLOGY, V13, P212ISI:000235978700004CNatl Univ Singapore, NUS Nanosci & Nanotechnol Initiat, Dept Chem, Singapore 117543, Singapore. Natl Univ Singapore, NUS Nanosci & Nanotechnol Initiat, Singapore 117542, Singapore. Valiyaveettil, S, Natl Univ Singapore, NUS Nanosci & Nanotechnol Initiat, Dept Chem, 3 Sci Dr 3, Singapore 117543, Singapore. chmsv@nus.edu.sgfile://S:\SALES\_IMPORTANT_STUFF_HERE\Bibliography_Key_Papers\all publications DPN as of 101006 Copy.Data\PDF\2006 Small Jegadesan Easy Writing of Nanopatterns-2703753023\2006 Small Jegadesan Easy Writing of Nanopatterns.pdf / ~?PAhn, Y. Hong, S. Jang, J.2006GGrowth dynamics of self-assembled monolayers in dip-pen nanolithography 4270-4273Journal of Physical Chemistry B1109\ATOMIC-FORCE MICROSCOPY; MOLECULAR-DYNAMICS; SIMULATION; DIFFUSION; SURFACES; AU(111); MODELArticleMar<Using molecular dynamics simulations, we studied the growth mechanism of self-assembled monolayers in dip-pen nanolithography. A molecule dropping from the tip kicks out a molecule sitting on the substrate, and the displaced molecule in turn kicks out a molecule next to it. This kicking propagates and finally stops when it hits the periphery of the monolayer. This monolayer growth is faster than predicted from the previous diffusion theory. Increasing the molecule-substrate binding strength enhances the molecular deposition rate and makes the monolayer well-ordered.://000235944500063 Times Cited: 0 Cited References: ALLEN MP, 1987, COMPUTER SIMULATION ALVES CA, 1992, J AM CHEM SOC, V114, P1222 BEARDMORE KM, 1998, CHEM PHYS LETT, V286, P40 BERENDSEN HJC, 1984, J CHEM PHYS, V81, P3684 BULLEN D, 2004, APPL PHYS LETT, V84, P789 DELADI S, 2004, APPL PHYS LETT, V85, P5361 DUBOIS LH, 1992, ANNU REV PHYS CHEM, V43, P437 GINGER DS, 2004, ANGEW CHEM INT EDIT, V43, P30 HAUTMAN J, 1989, J CHEM PHYS, V91, P4994 IVANISEVIC A, 2001, J AM CHEM SOC, V123, P7887 JANG JK, 2004, J CHEM PHYS, V120, P1157 JANG JY, 2001, J CHEM PHYS, V115, P2721 JANG JY, 2004, PHYS REV LETT, V92 MAHAFFY R, 1997, J PHYS CHEM B, V101, P771 MANANDHAR P, 2003, PHYS REV LETT, V90 MAYNOR BW, 2004, J AM CHEM SOC, V126, P6409 ROZHOK S, 2003, J PHYS CHEM B, V107, P751 SHEEHAN PE, 2002, PHYS REV LETT, V88 SU M, 2002, APPL PHYS LETT, V80, P4434 WEEKS BL, 2002, PHYS REV LETT, V88 WILSON DL, 2001, P NATL ACAD SCI USA, V98, P13660 ZHANG LZ, 2001, J CHEM PHYS, V114, P6869 ZHANG LZ, 2002, J CHEM PHYS, V117, P1804 ZHANG LZ, 2002, J CHEM PHYS, V117, P7342 ZHOU J, 2000, FLUID PHASE EQUILIBR, V172, P279ISI:000235944500063Pusan Natl Univ, Sch Nano Sci & Technol, Pusan 609735, South Korea. Seoul Natl Univ, Phys & Nanosyst Inst, Seoul 151747, South Korea. Jang, J, Pusan Natl Univ, Sch Nano Sci & Technol, Pusan 609735, South Korea. jkjang@pus ~?QBarsotti, R. J. Stellacci, F.2006mChemically directed assembly of monolayer protected gold nanoparticles on lithographically generated patterns962-965Journal of Materials Chemistry1610jDIP-PEN NANOLITHOGRAPHY; REACTIVE INTERMEDIATE; TEMPLATE; SURFACES; FILMS; ARCHITECTURE; CLUSTERS; LIGANDSArticleDiamine molecules were used to chemically direct the assembly of carboxylic acid terminated monolayer protected gold nanoparticles onto Au surfaces patterned with mercapto-hexadecanoic-acid by microcontact printing or dip pen nanolithography.://000235990500002 Times Cited: 0 Cited References: AKAMATSU K, 2002, J MATER CHEM, V12, P2862 BAE SS, 2005, APPL PHYS A-MATER, V80, P1305 BAIN CD, 1989, J AM CHEM SOC, V111, P321 BROUSSEAU LC, 1998, J AM CHEM SOC, V120, P7645 BRUST M, 1994, J CHEM SOC CHEM COMM, P801 CHUNG SW, 2005, SMALL, V1, P64 DEGENHART GH, 2004, LANGMUIR, V20, P6216 DEMERS LM, 2001, ANGEW CHEM INT EDIT, V40, P3071 FELDHEIM DL, 1998, CHEM SOC REV, V27, P1 GINGER DS, 2004, ANGEW CHEM INT EDIT, V43, P30 GRABAR KC, 1996, J AM CHEM SOC, V118, P1148 HE HX, 2000, LANGMUIR, V16, P3846 HONG SH, 1999, SCIENCE, V286, P523 KANG SY, 1998, LANGMUIR, V14, P226 KLEIN DL, 1996, APPL PHYS LETT, V68, P2574 KUMAR A, 1993, APPL PHYS LETT, V63, P2002 LAHIRI J, 1999, ANAL CHEM, V71, P777 LAHIRI J, 1999, LANGMUIR, V15, P2055 LI QG, 2003, LANGMUIR, V19, P166 LIU ST, 2002, NANO LETT, V2, P1055 LIU ST, 2004, NANO LETT, V4, P845 LU CH, 2004, LANGMUIR, V20, P974 MENDES PM, 2004, LANGMUIR, V20, P3766 PARK K, 1987, SCANNING MICROSCOPY, V1, P339 PINER RD, 1999, SCIENCE, V283, P661 ROZHOK S, 2003, J PHYS CHEM B, V107, P751 RUDYAK VY, 2002, TECH PHYS+, V47, P807 SHI F, 2005, LANGMUIR, V21, P1599 THELANDER C, 2001, APPL PHYS LETT, V79, P2106 XIA YN, 1998, ANGEW CHEM INT EDIT, V37, P551 YAN L, 1998, J AM CHEM SOC, V120, P6179 ZAMBORINI FP, 2003, ANAL CHIM ACTA, V496, P3 ZHANG H, 2003, NANOTECHNOLOGY, V14, P1113ISI:000235990500002MIT, Dept Mat Sci & Engn, Cambridge, MA 02139 USA. Stellacci, F, MIT, Dept Mat Sci & Engn, 77 Massachusetts Ave, Cambridge, MA 02139 USA. frstella@mit.edufile://S:\SALES\_IMPORTANT_STUFF_HERE\Bibliography_Key_Papers\all publications DPN as of 101006 Copy.Data\PDF\2006 JoMatsChem Barsotti Chemically Directed assembly.pdf~?RdLee, M. Kang, D. K. Yang, H. K. Park, K. H. Choe, S. Y. Kang, C. Chang, S. I. Han, M. H. Kang, I. C.2006Protein nanoarray on Prolinker (TM) surface constructed by atomic force microscopy dip-pen nanolithography for analysis of protein interaction 1094-1103 Proteomics64atomic force microscopy; dip-pen nanolithography; Prolinker (TM); protein nanoarray; single molecular interaction of protein CANCER; MICROARRAYS; PROTEOMICS; COMPLEX; ARRAYSArticleFebProtein nanoarrays are addressable ensembles of nano-scale protein domain on solid surfaces. This method can serve as a useful platform for ultraminiaturized bioanalysis. In this study, we investigated single molecular nanopatterning and molecular interaction of proteins that were immobilized on Prolinker (TM) surface of gold-coated silicon wafer by using dip-pen nanolithography (DPN) method. Contact force and humidity were optimized at 0.01 nN and 80%, respectively. The domain features of protein nanoarrays were developed at the contact time of 5 s. The optimized conditions for the nanoarray process were applied to create protein nanoarray using integrin alpha(v)beta(3) and angiogenin. Constructed protein nanoarrays using integrin alpha(v)beta(3) have single molecular monolayer with regular domain shape (height 15 +/- 5 nm). The changed height value due to the single molecular interaction between integrin alpha(v)beta(3) and vitronectin was approximately 30 +/- 5 nm on Prolinker (TM) surface as measured with atomic force microscopy tip. Taken together, these results suggest that protein nanoarray on Prolinker (TM) surface fabricated by well-controlled DPN process can be used to analyze single molecular interaction of protein.://000235756400002 Times Cited: 0 Cited References: BLUMEJENSEN P, 2001, NATURE, V411, P355 BOWDEN ET, 1999, ONCOGENE, V18, P4440 CELIS JE, 2003, CANCER CELL, V3, P9 CHARBONEAU L, 2002, BRIEF FUNCT GENOMICS, V1, P305 CUTLER P, 2003, PROTEOMICS, V3, P3 GE H, 2000, NUCLEIC ACIDS RES, V28, P3 HENDERSON E, 2004, MICROSC MICROANAL, V10, P1432 HONG SH, 1999, SCIENCE, V286, P523 HONG SH, 2000, SCIENCE, V288, P1808 HUFF JL, 2004, J BIOMOL SCREEN, V9, P491 IVANISEVIC A, 2001, J AM CHEM SOC, V123, P7887 KNEZEVIC V, 2001, PROTEOMICS, V1, P1271 LAL SP, 2002, DRUG DISCOV TODAY S, V7, S143 LEE KB, 2002, SCIENCE, V295, P1702 LEE KB, 2003, J AM CHEM SOC, V125, P5588 LEE Y, 2003, PROTEOMICS, V3, P2289 LEE Y, 2004, J BIOMOL SCREEN, V9, P687 LESAICHERRE ML, 2002, BIOORG MED CHEM LETT, V12, P2085 LIOTTA L, 2000, NAT REV GENET, V1, P48 MACBEATH G, 2000, SCIENCE, V289, P1760 MACBEATH G, 2002, NAT GENET S, V32, P526 MILLER JC, 2003, PROTEOMICS, V3, P56 PAWELETZ CP, 2001, ONCOGENE, V20, P1981 PINER RD, 1999, SCIENCE, V283, P661 TAKAGI J, 2002, IMMUNOL REV, V186, P111 XIONG JP, 2002, SCIENCE, V296, P151ISI:000235756400002 Chungbuk Natl Univ, Biotechnol Res Inst, Prot Chip Res Chip, Cheongju 361763, South Korea. Chungbuk Natl Univ, Dept Biochem, Cheongju 361763, South Korea. Chungbuk Natl Univ, Res Inst Ubiquitous Bioinformat Technol, Dept Semicond Engn, Cheongju 361763, South Korea. Chungbuk Natl Univ, Sch Life Sci, Dept Biol, Cheongju 361763, South Korea. Hoseo Univ, Dept Biol Sci, Asan, South Korea. Proteogen Inc, Seoul, South Korea. Kang, IC, Chungbuk Natl Univ, Biotechnol Res Inst, Prot Chip Res Chip, Cheongju 361763, South Korea. ickang@chungbuk.ac.krfile://S:\SALES\_IMPORTANT_STUFF_HERE\Bibliography_Key_Papers\all publications DPN as of 101006 Copy.Data\PDF\2006 Proteomics Lee Protein Nanoarray on Prolinker-1277512516\2006 Proteomics Lee Protein Nanoarray on Prolinker.pdf~?SoXie, X. N. Deng, M. Xu, H. Yang, S. W. Qi, D. C. Gao, X. Y. Chung, H. J. Sow, C. H. Tan, V. B. C. Wee, A. T. S.2006{Creating polymer structures of tunable electric functionality by nanoscale discharge-assisted cross-linking and oxygenation 2738-2744(Journal of the American Chemical Society1288DIP-PEN NANOLITHOGRAPHY; ATOMIC-FORCE MICROSCOPY; SCANNING PROBE LITHOGRAPHY; LIGHT-EMITTING-DIODES; SILICON SURFACES; NANO-OXIDATION; FABRICATION; CONDUCTION; FILMS; MANIPULATIONArticleMarWe report the creation of polymeric micro/nanostructures which exhibit distinct chemical and physical characteristics from the matrix poly(N-vinyl carbazole) (PVK). The structure formation is based on atomic force microscopy (AFM) facilitated cross-linking and oxygenation. The reaction of PVK with AFM lithographically induced nanoscale discharge produces raised structures in which bridge oxygen links neighboring carbazole groups. The cross-linking by bridge oxygen converts the initially insulating PVK matrix to chemically modified conducting patterns through the formation of extended pi-conjugations. A comprehensive AFM, PES (photoelectron spectroscopy), FTIR (Fourier transform infrared spectroscopy), and DFT (density functional theory) analysis is presented to address the chemophysical identity of the patterned structures. Our results demonstrate new capabilities of AFM nanolithography in generating heterogeneous functional structures in a polymer matrix.://000235787200051 wTimes Cited: 0 Cited References: ADAMEC V, 1975, J PHYS D, V8, P551 AGARWAL G, 2003, J AM CHEM SOC, V125, P580 BREDAS JL, 1983, J AM CHEM SOC, V105, P6555 DEMERS LM, 2002, SCIENCE, V296, P1836 DEMORAIS TD, 1999, ADV MATER, V11, P107 DURIG U, 2002, TRIBOL LETT, V9, P25 GEORGIEV DG, 2004, APPL PHYS LETT, V84, P4881 GILL WD, 1972, J APPL PHYS, V43, P5033 GOODBERLET JG, 2000, APPL PHYS LETT, V76, P667 HOEPPENER S, 2002, ADV MATER, V14, P1036 KIDO J, 1995, APPL PHYS LETT, V67, P2281 KING WP, 2001, APPL PHYS LETT, V78, P1300 KIY M, 2002, APPL PHYS LETT, V80, P4366 LACHAUD S, 2005, EUR PHYS J-APPL PHYS, V29, P99 LEE KB, 2002, SCIENCE, V295, P1702 LENZLINGER M, 1969, J APPL PHYS, V40, P278 LIU JF, 1997, J AM CHEM SOC, V119, P11061 LUTWYCHE MI, 2000, APPL PHYS LETT, V77, P3299 MARTINEZ RV, 2005, NANO LETT, V5, P1161 MORI G, 2005, J APPL PHYS, V97 MOULDER JF, 1995, HDB XRAY PHOTOELECTR OKADA Y, 2000, J APPL PHYS, V88, P1136 PARKER ID, 1994, J APPL PHYS, V75, P1656 POUCHERT CJ, 1981, ALDRICH LIB INFRARED SNOW ES, 1995, SCIENCE, V270, P1639 SUEZ I, 2005, NANO LETT, V5, P321 SZE SM, 1981, PHYS SEMICONDUCTOR D TELLO M, 2001, APPL PHYS LETT, V79, P424 TELLO M, 2005, ADV MATER, V17, P1480 TEO EJ, 2004, APPL PHYS LETT, V84, P3202 TU NR, 1999, J APPL PHYS, V85, P7267 TULLY DC, 1999, ADV MATER, V11, P314 TULLY DC, 2000, ADV MATER, V12, P1118 WEI YY, 2000, APPL PHYS LETT, V76, P194 XIE XN, 2004, J AM CHEM SOC, V126, P7665 XIE XN, 2005, ADV MATER, V17, P1386 XIE XN, 2005, APPL PHYS LETT, V86 XIE XN, 2005, APPL PHYS LETT, V86 XIE XN, 2005, J AM CHEM SOC, V127, P15562 YU XJ, 2005, J ELECTRON SPECTROSC, V144, P1031 ZHANG Y, 2005, J PHYS D, V36, P206 ZHANG YG, 2003, J PHYS D APPL PHYS, V36, P2006ISI:000235787200051?Natl Univ Singapore, NUSNNI, Dept Phys, Singapore 117542, Singapore. Inst High Performance Comp, Singapore 117542, Singapore. Natl Univ Singapore, Dept Engn Mech, Singapore 117576, Singapore. Xie, XN, Natl Univ Singapore, NUSNNI, Dept Phys, 2 Sci Dr 3, Singapore 117542, Singapore. nnixxn@nus.edu.sg phyweets@nus.edu.sgfile://S:\SALES\_IMPORTANT_STUFF_HERE\Bibliography_Key_Papers\all publications DPN as of 101006 Copy.Data\PDF\2006 JACS Xie Creating Polymer Structures of Tunable Electric-2852458590\2006 JACS Xie Creating Polymer Structures of Tunable Electric.pdfIF~?T{Onaran, A. G. Balantekin, M. Lee, W. Hughes, W. L. Buchine, B. A. Guldiken, R. O. Parlak, Z. Quate, C. F. Degertekin, F. L.2006XA new atomic force microscope probe with force sensing integrated readout and active tip Review of Scientific Instruments772MICROMACHINED ULTRASONIC TRANSDUCERS; OPTICAL INTERFEROMETRIC DETECTION; DIP-PEN NANOLITHOGRAPHY; SAMPLE INTERACTION; DISPLACEMENT DETECTION; TAPPING FORCE; DATA-STORAGE; MODE; SENSOR; CANTILEVERSArticleFeb?We introduce a novel probe structure for the atomic force microscope. The probe has a sharp tip placed on a micromachined membrane with an integrated displacement sensor, a diffraction-based optical interferometer. We use this probe in a microscope to directly measure the transient interaction forces between the probe tip and the sample when operating in a dynamic mode. We form images related to viscoelasticity and adhesion of the samples by recording salient features of individual tap signals. We also produce tapping mode images of sample topography an order of magnitude faster than current probe microscopes using an integrated electrostatic actuator to move the probe tip. We envision a broad range of applications for this device that range from life sciences to microelectronics. (c) 2006 American Institute of Physics.://000235664200012 Times Cited: 1 Cited References: NANOSCOPE 3100 ANCZYKOWSKI B, 1999, APPL SURF SCI, V140, P376 ANDO T, 2001, P NATL ACAD SCI USA, V98, P12468 BALANTEKIN M, 2003, PHYS REV B, V67 BALANTEKIN M, 2005, PHYS REV B, V71 BHUSHAN B, 1999, HDB MICRO NANOTRIBOL BINNIG G, 1986, PHYS REV LETT, V56, P930 BURNHAM NA, 1990, PHYS REV LETT, V64, P1931 BUSTAMANTE C, 2000, CURR OPIN STRUC BIOL, V10, P279 CHUNG SW, 2005, SMALL, V1, P64 COOPER EB, 1999, APPL PHYS LETT, V75, P3566 DEGERTEKIN FL, 2005, APPL PHYS LETT, V87 FAIN SC, 2000, APPL PHYS LETT, V76, P930 GARCIA R, 1999, PHYS REV B, V60, P4961 GIANNUZZI LA, 2005, INTRO FOCUSED ION BE GIESSIBL FJ, 2000, SCIENCE, V289, P422 GULDIKEN RO, IN PRESS IEEE T ULTR HAGLEITNER C, 2001, NATURE, V414, P293 HALL N, 2000, P IEEE ULTR S, V1, P951 HALL NA, 2002, APPL PHYS LETT, V80, P3859 HALL NA, 2003, IEEE T ULTRASON FERR, V50, P1570 HALL NA, 2004, THESIS GEORGIA I TEC HOLSCHER H, 1999, PHYS REV LETT, V83, P4780 KHURIYAKUB BT, 2000, JPN J APPL PHYS 1, V39, P2883 KNIGHT J, 2004, IEEE T ULTRASON FERR, V51, P1324 KROTIL HU, 1999, SURF INTERFACE ANAL, V27, P336 LEE W, 2004, APPL PHYS LETT, V85, P3032 LEE W, 2004, IEEE J SEL TOP QUANT, V10, P643 MARSHALL BT, 2003, NATURE, V423, P190 MCLEAN J, 2004, P IEEE ULTR S, V1, P501 MINNE SC, 1995, APPL PHYS LETT, V67, P3918 MINNE SC, 1998, APPL PHYS LETT, V73, P1742 ORALKAN O, 2002, IEEE T ULTRASON FERR, V49, P1596 PERCIN G, 2001, 6291927, US PINER RD, 1999, SCIENCE, V283, P661 POGGI MA, 2004, ANAL CHEM, V76, P3429 QUE L, 2000, J VAC SCI TECHNOL B, V18, P3450 RABE U, 2002, SURF INTERFACE ANAL, V33, P65 RODRIGUEZ TR, 2004, APPL PHYS LETT, V84, P449 RUGAR D, 2004, NATURE, V430, P329 SAHIN O, 2001, APPL PHYS LETT, V78, P2973 SAHIN O, 2004, PHYS REV B, V69 SARID D, 1994, SCANNING FORCE MICRO SARID D, 1996, J VAC SCI TECHNOL B, V14, P864 STARK M, 2002, P NATL ACAD SCI USA, V99, P8473 STARK RW, 2003, REV SCI INSTRUM, V74, P5111 SU CM, 2004, ULTRAMICROSCOPY, V100, P233 SULCHEK T, 2001, APPL PHYS LETT, V78, P1787 SULCHEK T, 2002, REV SCI INSTRUM, V73, P2928 VETTIGER P, 2002, IEEE T NANOTECHNOL, V1, P39 VIANI MB, 1999, J APPL PHYS, V86, P2258 YAMANAKA K, 1999, SURF INTERFACE ANAL, V27, P600 YARALIOGLU GG, 1998, J APPL PHYS, V83, P7405ISI:000235664200012IGeorgia Inst Technol, George W Woodruff Sch Mech Engn, Atlanta, GA 30332 USA. Georgia Inst Technol, Sch Mat Sci & Engn, Atlanta, GA 30332 USA. Stanford Univ, Edward L Ginzton Lab, Stanford, CA 94305 USA. Degertekin, FL, Georgia Inst Technol, George W Woodruff Sch Mech Engn, Atlanta, GA 30332 USA. levent.degertekin@me.gatech.edu023501 Artn 023501file://S:\SALES\_IMPORTANT_STUFF_HERE\Bibliography_Key_Papers\all publications DPN as of 101006 Copy.Data\PDF\2006 RevSciInst-3306121228\2006 RevSciInstrmts Onaran A new atomic force microscrope.pdfm~?U0Dillenback, L. M. Goodrich, G. P. Keating, C. D.2006FTemperature-programmed assembly of DNA : Au nanoparticle bioconjugates16-23 Nano Letters61DIP-PEN NANOLITHOGRAPHY; GOLD NANOPARTICLES; BUILDING-BLOCKS; NANOWIRE ARRAYS; HYBRIDIZATION; NANOSTRUCTURES; OLIGONUCLEOTIDES; NANOCRYSTALS; ORGANIZATION; SURFACEArticleJanTemperature has been used to control the order of assembly events in a solution containing three types of particles to be linked by two different sets of complementary DNA. At higher temperatures, only the duplexes having higher thermal stability were able to form. By starting at a high temperature and then cooling the sample, these more stable sequences hybridized first, followed by the less stable sequences at lower temperatures. Because of the use of thiolated DNA on Au particles, some loss and exchange of the DNA strands occurred at elevated temperatures. However, since cooperativity favors the "correct" assemblies, Au-S bond lability did not appreciably impact the order of the assembly process. Temperature programming combines the selectivity of DNA-directed assembly with the ability to control the order in which several complementary strands hybridize in a common solution and could contribute to the synthesis of more complex nanostructured materials.://000235532400004 f Times Cited: 3 Cited References: ALIVISATOS AP, 1996, NATURE, V382, P609 ANDREADIS JD, 2000, NUCLEIC ACIDS RES, V28 BLOOMFIELD VA, 2000, NUCL ACIDS STRUCTURE CAO YWC, 2002, SCIENCE, V297, P1536 CASWELL KK, 2003, J AM CHEM SOC, V125, P13914 CHUNG SW, 2005, SMALL, V1, P64 CLARIDGE SA, 2005, CHEM MATER, V17, P1628 CUI Y, 2004, NANO LETT, V4, P1093 DEMERS LM, 2000, ANAL CHEM, V72, P5535 DENG ZX, 2003, NANO LETT, V3, P1545 DENG ZX, 2005, ANGEW CHEM INT EDIT, V44, P3582 ELGHANIAN R, 1997, SCIENCE, V277, P1078 FELDHEIM DL, 2002, METAL NANOPARTICLES GENOV DA, 2004, NANO LETT, V4, P153 GINGER DS, 2004, ANGEW CHEM INT EDIT, V43, P30 GOODRICH GP, 2004, LANGMUIR, V20, P10246 HAMADSCHIFFERLI K, 2002, NATURE, V415, P152 HE L, 2000, J AM CHEM SOC, V122, P9071 HERMANSON KD, 2001, SCIENCE, V294, P1082 HUANG Y, 2001, SCIENCE, V294, P1313 JIN RC, 2003, J AM CHEM SOC, V125, P1643 KANNAN B, 2004, NANO LETT, V4, P1521 KEREN K, 2003, SCIENCE, V302, P1380 KIM B, 2001, J AM CHEM SOC, V123, P7955 KIM F, 2001, J AM CHEM SOC, V123, P4360 KOVTYUKHOVA NI, 2001, J PHYS CHEM B, V105, P8762 KOVTYUKHOVA NI, 2002, CHEM-EUR J, V8, P4354 LE JD, 2004, NANO LETT, V4, P2343 LI M, 2004, J MATER CHEM, V14, P2260 LI Z, 2005, J AM CHEM SOC, V127, P11568 LOWETH CJ, 1999, ANGEW CHEM INT EDIT, V38, P1808 MANN S, 2000, ADV MATER, V12, P147 MBINDYO JKN, 2001, ADV MATER, V13, P249 MIRKIN CA, 1996, NATURE, V382, P607 MIRKIN CA, 2000, INORG CHEM, V39, P2258 MUCIC RC, 1998, J AM CHEM SOC, V120, P12674 NIEMEYER CM, 2001, ANGEW CHEM INT EDIT, V40, P4128 NIEMEYER CM, 2003, ANGEW CHEM INT EDIT, V42, P5766 NIEMEYER CM, 2003, BIOCHEM BIOPH RES CO, V311, P995 NIEMEYER CM, 2004, NANOBIOTECHNOLOGY CO ONGARO A, 2004, ADV MATER, V16, P1799 PARAK WJ, 2003, NANO LETT, V3, P33 PENA SRN, 2002, J AM CHEM SOC, V124, P7314 REICHERT J, 2000, ANAL CHEM, V72, P6025 ROSI NL, 2005, CHEM REV, V105, P1547 RYADNOV MG, 2003, J AM CHEM SOC, V125, P9388 RYAN D, 2002, J PHYS CHEM B, V106, P5371 SADASIVAN S, 2005, SMALL, V1, P103 SANDSTROM P, 2004, LANGMUIR, V20, P4182 SEEMAN NC, 1997, ACCOUNTS CHEM RES, V30, P357 SMITH PA, 2000, APPL PHYS LETT, V77, P1399 STEVENS MM, 2004, ADV MATER, V16, P915 STORHOFF JJ, 1999, CHEM REV, V99, P1849 TATON TA, 2000, SCIENCE, V289, P1757 WANG J, 2005, SMALL, V1, P1036 WANG W, 2003, J PHYS CHEM B, V107, P3400 WANG Y, 2005, NANO LETT, V5, P243 WHANG D, 2003, NANO LETT, V3, P1255 WHANG D, 2003, NANO LETT, V3, P951 WU Y, 2002, CHEM-EUR J, V8, P1260 XIA YN, 2003, ADV MATER, V15, P353 YIN YD, 2001, J AM CHEM SOC, V123, P8718 ZANCHET D, 2001, NANO LETTERS, V1, P32 ZANCHET D, 2002, J PHYS CHEM B, V106, P11758ISI:000235532400004Penn State Univ, Dept Chem, University Pk, PA 16802 USA. Keating, CD, Penn State Univ, Dept Chem, University Pk, PA 16802 USA. keating@chem.psu.edufile://S:\SALES\_IMPORTANT_STUFF_HERE\Bibliography_Key_Papers\all publications DPN as of 101006 Copy.Data\PDF\2006 Nano Letters Dillenback Temperature-programmed Assembly of DNA-3988491050\2006 Nano Letters Dillenback Temperature-programmed Assembly of DNA.pdf [~?V]Sun, S. Q. Montague, M. Critchley, K. Chen, M. S. Dressick, W. J. Evans, S. D. Leggett, G. J.2006yFabrication of biological nanostructures by scanning near-field photolithography of chloromethylphenyisiloxane monolayers29-33 Nano Letters61SELF-ASSEMBLED MONOLAYERS; DIP-PEN NANOLITHOGRAPHY; CONSTRUCTIVE NANOLITHOGRAPHY; LITHOGRAPHY; TEMPLATES; DNA; NANOPARTICLES; PATTERNS; FILMS; NANOARRAYSArticleJanWe demonstrate the fabrication of sub-100-nm DNA surface patterns by scanning near-field optical lithography using a near-field scanning optical microscope coupled to a UV laser and a chloromethylphenylsiloxane (CMPS) self-assembled monolayer (SAM). The process involves 244-nm exposure of the CMPS SAM to create nanoscale patterns of surface carboxylic acid functional groups, followed by their conversion to the N-hydroxysuccinimidyl ester and reaction of the active ester with DNA to spatially control DNA grafting with high selectivity.://000235532400006 Times Cited: 2 Cited References: BODANSZKY M, 1984, PRINCIPLES PEPTIDE S, P28 BRANDOW SL, 1997, J VAC SCI TECHNOL B, V15, P1818 BRANDOW SL, 1999, LANGMUIR, V15, P5429 BRANDOW SL, 2001, CHEM-EUR J, V7, P4495 CAO YWC, 2002, SCIENCE, V297, P1536 DRESSICK WJ, 1993, JPN J APPL PHYS PT 1, V32, P5829 DRESSICK WJ, 1999, J VAC SCI TECHNOL 1, V17, P1432 FODOR SPA, 1991, SCIENCE, V251, P767 FRESCO ZM, 2005, J AM CHEM SOC, V127, P8302 FREY BL, 1996, ANAL CHEM, V68, P3187 GEISSLER M, 2004, ADV MATER, V16, P1249 GINGER DS, 2004, ANGEW CHEM INT EDIT, V43, P30 HOEPPENER S, 2002, ADV MATER, V14, P1036 HONG BJ, 2005, LANGMUIR, V21, P4257 HUANG E, 2000, LANGMUIR, V16, P3272 KAHOLEK M, 2004, CHEM MATER, V16, P3688 KAHOLEK M, 2004, NANO LETT, V4, P373 LEE KB, 2002, SCIENCE, V295, P1702 LEE KB, 2004, NANO LETT, V4, P1869 LEGGETT GJ, 2005, ANALYST, V130, P259 LEGGETT GJ, 2005, PHYS CHEM CHEM PHYS, V7, P1107 LIU ST, 2002, NANO LETT, V2, P1055 MAOZ R, 2000, ADV MATER, V12, P424 MAOZ R, 2000, ADV MATER, V12, P725 MILLAN KM, 1993, LANGMUIR, V9, P2317 MIRANDA MA, 2001, ACCOUNTS CHEM RES, V34, P717 NAM JM, 2003, SCIENCE, V301, P1884 PARK SJ, 2002, SCIENCE, V295, P1503 PATEL N, 1997, LANGMUIR, V13, P6485 PINER RD, 1999, SCIENCE, V283, P661 SUN S, 2004, NANO LETT, V4, P1381 SUN SQ, 2002, J AM CHEM SOC, V124, P2414 SUN SQ, 2002, NANO LETT, V2, P1223 VOGEL AI, 1989, TXB PRACTICAL ORGANI, P1257ISI:000235532400006;Univ Sheffield, Dept Chem, Sheffield S3 7HF, S Yorkshire, England. Univ Leeds, Sch Phys & Astron, Leeds LS2 9JT, W Yorkshire, England. USN, Res Lab, Ctr Biomol Sci & Engn, Washington, DC 20375 USA. Leggett, GJ, Univ Sheffield, Dept Chem, Brook Hill, Sheffield S3 7HF, S Yorkshire, England. Graham.Leggett@she V~?WWRodolfa, K. T. Bruckbauer, A. Zhou, D. J. Schevchuk, A. I. Korchev, Y. E. Klenerman, D.2006hNanoscale pipetting for controlled chemistry in small arrayed water droplets using a double-barrel pipet252-257 Nano Letters62SCANNING ION-CONDUCTANCE; DIP-PEN NANOLITHOGRAPHY; CONTROLLED DEPOSITION; NANOPIPET; BIOMOLECULES; MICROSCOPY; VESICLES; MANIPULATION; DELIVERY; DNAArticleFeb:We present a new methodology which provides for the miniaturization of one of the most common tools in use in chemistry and biology laboratories today-the micropipet. We have used glass-fabricated double-barrel nanopipets to controllably produce arrayed water droplets with volumes as small as a few attoliters under an organic layer. We have addressed individual droplets and added controlled amounts of either additional volume or reagents from one of the barrels of the pipet. We demonstrate that this method can be used for miniaturized cell-free protein expression.://000235532700022 4Times Cited: 0 Cited References: BOLINGER PY, 2004, J AM CHEM SOC, V126, P8594 BRUCKBAUER A, 2002, J AM CHEM SOC, V124, P8810 BRUCKBAUER A, 2003, J AM CHEM SOC, V125, P9834 BRUCKBAUER A, 2004, J AM CHEM SOC, V126, P6508 BRUCKBAUER A, 2004, NANO LETT, V4, P1859 CHIU DT, 1999, SCIENCE, V283, P1892 FISCHER A, 2002, CHEMBIOCHEM, V3, P409 GINGER DS, 2004, ANGEW CHEM INT EDIT, V43, P30 HANSMA PK, 1989, SCIENCE, V243, P641 HE MY, 2005, APPL PHYS LETT, V87 JORGENSEN L, 2004, J PHARM SCI-US, V93, P2994 KARLSSON A, 2005, J PHYS CHEM B, V109, P1609 KATSURA S, 2001, ELECTROPHORESIS, V22, P289 KIM P, 1999, SCIENCE, V286, P2148 KORCHEV YE, 1997, BIOPHYS J, V73, P653 KOTZ KT, 2005, J AM CHEM SOC, V127, P5736 LEE KB, 2002, SCIENCE, V295, P1702 MEISTER A, 2004, APPL PHYS LETT, V85, P6260 NOMURA S, 2003, CHEMBIOCHEM, V4, P1172 RODOLFA KT, 2005, ANGEW CHEM INT EDIT, V44, P6854 SCHWARTZ JA, 2004, LAB CHIP, V4, P11 SHEVCHUK AI, 2001, BIOPHYS J, V81, P1759 STAMOU D, 2003, ANGEW CHEM INT EDIT, V42, P5580 TAHA H, 2003, APPL PHYS LETT, V83, P1041 VELEV OD, 2003, NATURE, V426, P515 YING LM, 2002, ANAL CHEM, V74, P1380 YING LM, 2005, PHYS CHEM CHEM PHYS, V7, P2859 YOGI O, 2001, ANAL CHEM, V73, P1896ISI:000235532700022Univ Cambridge, Dept Chem, Cambridge CB2 1EW, England. Univ London Imperial Coll Sci Technol & Med, Hammersmith Hosp, Div Med, London W12 0NN, England. Klenerman, D, Univ Cambridge, Dept Chem, Lensfield Rd, Cambridge CB2 1EW, England. dk10012@cam.ac.uk file://S:\SALES\_IMPORTANT_STUFF_HERE\Bibliography_Key_Papers\all publications DPN as of 101006 Copy.Data\PDF\2006 Nano Letters Rodolfa Nanoscale pipetting for controlled chemistry-2171440461\2006 Nano Letters Rodolfa Nanoscale pipetting for controlled chemistry.pdf9}?"Wei, J. H. Ginger, D. S.2007KA direct-write single-step positive etch resist for dip-pen nanotithography 2034-2037Small312Dec://000251697100008 1613-6810ISI:000251697100008Uinternal-pdf://2007_Direct write_Small_Wei-1676537601/2007_Direct write_Small_Wei.pdfJ}?#Kidambi, S. Chan, C. Lee, I.2008Tunable resistive m-dPEG acid patterns on polyelectrolyte, multilayers at physiological conditi~?YMWang, Y. H. Maspoch, D. Zou, S. L. Schatz, G. C. Smalley, R. E. Mirkin, C. A.2006hControlling the shape, orientation, and linkage of carbon nanotube features with nano affinity templates 2026-2031OProceedings of the National Academy of Sciences of the United States of America1037self-assembly; rings; structured thin films; Monte Carlo simulations SELF-ASSEMBLED MONOLAYERS; DIP-PEN NANOLITHOGRAPHY; ELECTRICAL-TRANSPORT; SCALE; FIELD; ARRAYS; ROUTE; FILMS; LOCALIZATION; TRANSISTORSArticleFebYDirected assembly of nanoscale building blocks such as single-walled carbon nanotubes (SWNTs) into desired architectures is a major hurdle for a broad range of basic research and technological applications (e.g., electronic devices and sensors). Here we demonstrate a parallel assembly process that allows one to simultaneously position, shape, and link SWNTs with sub-100-nm resolution. Our method is based on the observation that SWNTs are strongly attracted to COOH-terminated self-assembled monolayers (COOH-SAMs) and that SWINTs with lengths greater than the dimensions of a COOH-SAM feature will align along the boundary between the COOH-SAM feature and a passivating CH3-terminated SAM. By using nanopatterned affinity templates of 16-mercapto-hexadecanonic acid, passivated with 1-octadecanethiol, we have formed SWNT dot, ring, arc, letter, and even more sophisticated structured thin films and continuous ropes. Experiment and theory (Monte Carlo simulations) suggest that the COOH-SAMs localize the solvent carrying the nanotubes on the SAM features, and that van der Waals interactions between the tubes and the COOH-rich feature drive the assembly process. A mathematical relationship describing the geometrically weighted interactions between SWNTs and the two different SAMs required to overcome solvent-SWNT interactions and effect assembly is provided.://000235411600007 Times Cited: 7 Cited References: AUVRAY S, 2005, NANO LETT, V5, P451 AVOURIS P, 2002, ACCOUNTS CHEM RES, V35, P1026 BAUGHMAN RH, 2002, SCIENCE, V297, P787 COLLINS PC, 2001, SCIENCE, V292, P706 CORNELL WD, 1995, J AM CHEM SOC, V117, P5179 DUAN XJ, 2005, J AM CHEM SOC, V127, P8268 FALVO MR, 1997, NATURE, V389, P581 GAO JB, 2004, J AM CHEM SOC, V126, P16698 GATES BD, 2005, CHEM REV, V105, P1171 GINGER DS, 2004, ANGEW CHEM INT EDIT, V43, P30 HONG JM, 1998, CHEM MATER, V10, P1029 HONG SH, 1999, LANGMUIR, V15, P7897 HUANG Y, 2001, SCIENCE, V291, P630 JAVEY A, 2004, P NATL ACAD SCI USA, V101, P13408 KEREN K, 2003, SCIENCE, V302, P1380 KIM JE, 2003, J HIGH ENERGY PHYS KO H, 2005, CHEM MATER, V17, P2490 KOCABAS C, 2004, NANO LETT, V4, P2421 KONG J, 2000, SCIENCE, V287, P622 LARSEN NB, 1997, J AM CHEM SOC, V119, P3017 LAY MD, 2004, NANO LETT, V4, P603 LEE NS, 2001, DIAM RELAT MATER, V10, P265 LIANG F, 2004, NANO LETT, V4, P1257 LIU J, 1997, NATURE, V385, P780 LIU J, 1999, CHEM PHYS LETT, V303, P125 MARTEL R, 1999, NATURE, V398, P299 MEITL MA, 2004, NANO LETT, V4, P1643 MINOT ED, 2003, PHYS REV LETT, V90 PALEGROSDEMANGE C, 1991, J AM CHEM SOC, V113, P12 PINER RD, 1999, SCIENCE, V283, P661 POSTMA HWC, 2001, SCIENCE, V293, P76 RAO SG, 2003, NATURE, V425, P36 RUECKES T, 2000, SCIENCE, V289, P94 SALAITA K, 2005, SMALL, V1, P940 SANO M, 2001, SCIENCE, V293, P1299 SHEA HR, 2000, PHYS REV LETT, V84, P4441 SHVARTZMANCOHEN R, 2004, J AM CHEM SOC, V126, P14850 SNOW ES, 2005, SCIENCE, V307, P1942 TAMURA R, 2005, PHYS REV B, V71 TSUKRUK VV, 2004, PHYS REV LETT, V92 WALTERS DA, 2001, CHEM PHYS LETT, V338, P14 WU ZC, 2004, SCIENCE, V305, P1273 XIN HJ, 2003, J AM CHEM SOC, V125, P8710 XIN HJ, 2004, NANO LETT, V4, P1481 XU YQ, 2005, NANO LETT, V5, P163 YAO Z, 2000, PHYS REV LETT, V84, P2941 YU MF, 1999, NANOTECHNOLOGY, V10, P244ISI:000235411600007Northwestern Univ, Dept Chem, Evanston, IL 60208 USA. Northwestern Univ, Inst Nanotechnol, Evanston, IL 60208 USA. Rice Univ, Ctr Nanoscale Sci & Technol, Carbon Nanotechnol Lab, Houston, TX 77251 USA. Rice Univ, Dept Chem, Houston, TX 77251 USA. Rice Univ, Dept Phys, Houston, TX 77251 USA. Schatz, GC, Northwestern Univ, Dept Chem, 2145 Sheridan Rd, Evanston, IL 60208 USA. schatz@chem.northwestern.edu chadnano@northwestern.edu3065424993Slides.ppt file://S:\SALES\_IMPORTANT_STUFF_HERE\Bibliography_Key_Papers\all publications DPN as of 101006 Copy.Data\PDF\2006 PNAS Wang Controlling Shape, Orientation and Linkage of Car-3788282973\2006 PNAS Wang Controlling Shape, Orientation and Linkage of Carbon Nanotube.pdfg~?ZSeo, K. Borguet, E.2006Nanolithographic write, read, and erase via reversible nanotemplated nanostructure electrodeposition on alkanethiol-modified Au(111) in an aqueous solution 1388-1391Langmuir224SELF-ASSEMBLED MONOLAYERS; ATOMIC-FORCE MICROSCOPE; SCANNING PROBE LITHOGRAPHY; LIQUID-CRYSTALLINE PHASES; DIP-PEN NANOLITHOGRAPHY; GOLD ELECTRODES; ELECTROCHEMICAL DEPOSITION; SCALE FABRICATION; COPPER DEPOSITION; PATTERN TRANSFERArticleFeb A write, read, and erase nanolithographic method, combining in situ electrodeposition of metal nanostructures with atomic force microscopy (AFM) nanoshaving of a 1-hexadecanethiol (HDT) self-assembled monolayer (SAM) on Au(111) in an aqueous solution, is reported. The AFM tip defines the local positioning of nanotemplates via the irreversible removal of HDT molecules. Nanotemplates with lateral dimensions as narrow as 25 nm are created. The electroactive nanotemplates determine the size, shape, and position of the metal nanostructures. The potential applied to the substrate controls the amount of metal deposited and the kinetics of the deposition. Metal nanostructures can be reversibly and repeatedly electrodeposited and stripped out of the nanotemplates by applying appropriate potentials.://000235354800004 Times Cited: 0 Cited References: AMRO NA, 2000, LANGMUIR, V16, P3006 ATTARD GS, 1997, SCIENCE, V278, P838 AZZARONI O, 2003, ELECTROCHIM ACTA, V48, P3107 BARTLETT PN, 2002, PHYS CHEM CHEM PHYS, V4, P3835 BATINA N, 1992, LANGMUIR, V8, P2572 BERENZ P, 2002, J PHYS CHEM B, V106, P3673 BRUMLIK CJ, 1991, J AM CHEM SOC, V113, P3174 CAI XW, 1998, LANGMUIR, V14, P2508 CHEN L, 1994, J ELECTROCHEM SOC, V141, L43 CHIDSEY CED, 1990, LANGMUIR, V6, P682 ELLIOTT JM, 1999, CHEM MATER, V11, P3602 FASOL G, 1997, APPL PHYS LETT, V70, P2467 FAVIER F, 2001, SCIENCE, V293, P2227 FINKLEA HO, 1987, LANGMUIR, V3, P409 FOSS CA, 1994, J PHYS CHEM-US, V98, P2963 FRESCO ZM, 2004, J AM CHEM SOC, V126, P8374 GARNO JC, 2003, NANO LETT, V3, P389 GUIDUCCI C, 2004, BIOSENS BIOELECTRON, V19, P781 HAGENSTROM H, 2001, LANGMUIR, V17, P839 HE HX, 2000, LANGMUIR, V16, P3846 HOEPPENER S, 2003, NANO LETT, V3, P761 KING GM, 2005, NANO LETT, V5, P1157 KOINUMA M, 1996, SURF SCI, V358, P565 KOLB DM, 1998, ELECTROCHIM ACTA, V43, P2751 LAGRAFF JR, 1994, J PHYS CHEM-US, V98, P11246 LAGRAFF JR, 1995, J PHYS CHEM-US, V99, P10009 LI QG, 2003, LANGMUIR, V19, P166 LI QG, 2004, CHEM MATER, V16, P3402 LI WJ, 1995, LANGMUIR, V11, P4361 LI Y, 2001, J AM CHEM SOC, V123, P2105 LIU GY, 1994, LANGMUIR, V10, P367 LIU GY, 2000, ACCOUNTS CHEM RES, V33, P457 LIU JF, 2002, NANO LETT, V2, P937 LIU MZ, 2002, NANO LETTERS, V2, P863 LIU ST, 2002, NANO LETT, V2, P1055 NICEWARNERPENA SR, 2003, J PHYS CHEM B, V107, P7360 NURAJE N, 2004, J AM CHEM SOC, V126, P8088 OYAMATSU D, 1999, J ELECTROANAL CHEM, V473, P59 PATTERSON JE, 2005, J PHYS CHEM B, V109, P5045 PORTER LA, 2002, NANO LETT, V2, P1369 PORTER LA, 2003, NANO LETT, V3, P1043 PORTER MD, 1987, J AM CHEM SOC, V109, P3559 ROSI NL, 2005, CHEM REV, V105, P1547 SONDAGHUETHORST JA, 1994, APPL PHYS LETT, V64, P285 SONDAGHUETHORST JAM, 1995, LANGMUIR, V11, P4823 WALTER EC, 2003, CHEMPHYSCHEM, V4, P131 XIAO XD, 1995, LANGMUIR, V11, P1600 XU DW, 2004, NANO LETT, V4, P2223 XU S, 1997, LANGMUIR, V13, P127 XU S, 1999, LANGMUIR, V15, P7244 YANG H, 2002, CHEM MATER, V14, P1385 ZAMBORINI FP, 1998, J AM CHEM SOC, V120, P9700 ZHANG H, 2004, NANO LETT, V4, P1493 ZHU T, 1999, LANGMUIR, V15, P5197 ZOVAL JV, 1998, J PHYS CHEM B, V102, P1166ISI:000235354800004Temple Univ, Dept Chem, Philadelphia, PA 19122 USA. Borguet, E, Temple Univ, Dept Chem, Philadelphia, PA 19122 USA. eborguet@temple.edufile://S:\SALES\_IMPORTANT_STUFF_HERE\Bibliography_Key_Papers\all publications DPN as of 101006 Copy.Data\PDF\2006 Langmuir Seo Nano write read erase-2643454506\2006 Langmuir Seo Nano write read erase.pdf~?[Cho, Y. N. Ivanisevic, A.2006pMapping the interaction forces between TAR RNA and TAT peptides on GaAs surfaces using chemical force microscopy 1768-1774Langmuir224SELF-ASSEMBLED MONOLAYERS; DIP-PEN NANOLITHOGRAPHY; ACOUSTIC-WAVE SENSOR; BINDING-SPECIFICITY; PERMEABLE PEPTIDES; PROTEINS; GOLD; ALKANETHIOLS; RECOGNITION; GAAS(100)ArticleFebYThe complexation of the HIV transactivation response element (TAR) RNA with the viral regulatory protein TAT is of enormous interest for the design of new sensing and therapeutic strategies. In this work, we anchored TAT peptides on GaAs surfaces using microcontact printing. Atomic force microscopy was used to quantify the interaction between TAR RNA and model TAT peptide sequences. Different pH conditions were utilized in order to assess specific vs nonspecific interactions. AFM tips functionalized with TAR RNA molecules were used to collect adhesion maps that displayed stronger interaction with peptide sequences that contained a greater number of arginine residues. All of the studies consistently showed a pH dependence of the interaction between the surface bound peptides and the TAR RNA on the AFM tips. This work quantifies the TAR RNA/TAT peptide interaction after one of the molecules is anchored on a surface. The conclusions in this paper are consistent with previous work and demonstrate that cationic residues are responsible for the polyelectrolyte-like affinity of TAT peptides for TAR RNA.://000235354800059 Times Cited: 0 Cited References: ADLKOFER K, 2003, J PHYS CHEM B, V107, P587 AKHREMITCHEV BB, 1998, LANGMUIR, V14, P3976 BERNARD A, 1998, LANGMUIR, V14, P2225 BERNARD A, 2000, ADV MATER, V12, P1067 CALNAN BJ, 1991, SCIENCE, V252, P1167 CHO Y, 2004, J PHYS CHEM B, V108, P15223 CHO Y, 2005, J PHYS CHEM B, V109, P12731 CHO Y, 2005, J PHYS CHEM B, V109, P6225 DEMERS LM, 2002, SCIENCE, V296, P1836 ENANDER K, 2005, LANGMUIR, V21, P2480 FLORIN EL, 1994, SCIENCE, V264, P415 FUTAKI S, 2003, CURR PROTEIN PEPT SC, V4, P87 GELMAN MA, 2003, ORG LETT, V5, P3563 GOEDE K, 2004, NANO LETT, V4, P2115 GRINEVICH O, 1999, LANGMUIR, V15, P2077 HARITONGAZAL E, 2002, BIOCHEMISTRY-US, V41, P9208 HUQ I, 1997, NAT STRUCT BIOL, V4, P881 JENNINGS GK, 2003, J AM CHEM SOC, V125, P2950 KANE RS, 1999, BIOMATERIALS, V20, P2363 KIKUTA E, 2001, J AM CHEM SOC, V123, P7911 KUMAR A, 1994, LANGMUIR, V10, P1498 LAIBINIS PE, 1991, J AM CHEM SOC, V113, P7152 LONG KS, 1995, BIOCHEMISTRY-US, V34, P8885 LONG KS, 1999, BIOCHEMISTRY-US, V38, P10059 NUZZO RG, 1990, J AM CHEM SOC, V112, P558 OLSEN GL, 2005, NUCLEIC ACIDS RES, V33, P3447 PARDO L, 2003, LANGMUIR, V19, P1462 PETRONI S, 2004, APPL PHYS LETT, V85, P1039 PETROVYKH DY, 2004, LANGMUIR, V20, P429 PLASSARD C, 2005, LANGMUIR, V21, P7263 POGGI MA, 2005, ANAL CHEM, V77, P1192 POGGI MA, 2005, CHEM MATER, V17, P4289 RUNYON ST, 2003, J AM CHEM SOC, V125, P15704 SHAPORENKO A, 2003, LANGMUIR, V19, P4992 SHAPORENKO A, 2004, J PHYS CHEM B, V108, P17964 SHEEN CW, 1992, J AM CHEM SOC, V114, P1514 TASSEW N, 2002, ANAL CHEM, V74, P5313 TASSEW N, 2003, ORG BIOMOL CHEM, V1, P3268 THOREN PEG, 2004, BIOCHEMISTRY-US, V43, P3471 UKITA H, 1997, OPT REV, V4, P623 UVDAL K, 2001, LANGMUIR, V17, P2008 WANG MS, 2004, LANGMUIR, V20, P7753 WANG XF, 2004, J VAC SCI TECHNOL B, V22, P2563 WANG ZY, 2001, BIOCHEMISTRY-US, V40, P6458 WANGSAWIRAWAN ND, 2001, BIOTECHNOL PROGR, V17, P963 WHALEY SR, 2000, NATURE, V405, P665 XIA YN, 1999, CHEM REV, V99, P1823 YE S, 2003, SURF SCI, V529, P163ISI:000235354800059Purdue Univ, Dept Chem, W Lafayette, IN 47907 USA. Purdue Univ, Weldon Sch Biomed Engn, W Lafayette, IN 47907 USA. Ivanisevic, A, Purdue Univ, Dept Chem, W Lafayette, IN 47907 USA. albena@purdue.edufile://S:\SALES\_IMPORTANT_STUFF_HERE\Bibliography_Key_Papers\all publications DPN as of 101006 Copy.Data\PDF\2006 Langmuir Cho Mapping Interaction Forces TAR RNA & TAT-2577827877\2006 Langmuir Cho Mapping Interaction Forces TAR RNA & TAT.pdfK~?\<Lai, R. Y. Lee, S. H. Soh, H. T. Plaxco, K. W. Heeger, A. J.2006\Differential labeling of closely spaced biosensor electrodes via electrochemical lithography 1932-1936Langmuir224dSELF-ASSEMBLED MONOLAYERS; DIP-PEN NANOLITHOGRAPHY; DNA; GOLD; ALKANETHIOLS; FABRICATION; DESORPTIONArticleFebElectrochemical biosensors offer the promise of exceptional scalability and parallelizability. To achieve this promise, however, will require the development of new methods for the differential labeling of closely spaced electrodes with specific biomolecules such as DNA or proteins. Here we report a simple, highly selective method for passivating and differentially labeling closely separated gold electrodes with oligonucleotides or other biomolecules. Analogous to photolithography, where a light-sensitive resist is selectively removed to expose specific surfaces to further modification, we passivate gold electrodes with a self-assembled alkanethiol monolayer that protects them from modification. The monolayer is then electrochemically desorbed at relatively low potentials, allowing for the subsequent labeling of the now exposed array element with a specific sensing biomolecule. The observed passivation is highly efficient: using a C11-OH monolayer as the passivating agent, we do not observe any detectable cross-contamination of adjacent electrodes (95 mu m separation) upon labeling with a stem-loop DNA probe. Critically, the conditions employed are sufficiently gentle that depassivation reduces the DNA load on adjacent electrodes by only similar to 1%, allowing for the sequential labeling of multiple, closely spaced electrodes. This technology paves the way for labeling multiple array elements sequentially without observable cross-contamination in a fast and controlled manner.://000235354800085 Times Cited: 1 Cited References: BOKMAN CF, 2004, ANAL CHEM, V76, P2017 BRETT CMA, 2003, ELECTROANAL, V15, P557 DRUMMOND TG, 2003, NAT BIOTECHNOL, V21, P1192 EGELAND RD, 2005, NUCLEIC ACIDS RES, V33 FAN CH, 2003, P NATL ACAD SCI USA, V100, P9134 GORMAN CB, 1995, LANGMUIR, V11, P2242 HONG SH, 2000, SCIENCE, V288, P1808 HUANG Y, 2001, ANAL CHEM, V73, P1549 IMABAYASHI S, 1997, LANGMUIR, V13, P4502 KUMAR A, 1993, APPL PHYS LETT, V63, P2002 LOVE JC, 2005, CHEM REV, V105, P1103 MA FY, 2000, LANGMUIR, V16, P6188 PETERSON AW, 2001, NUCLEIC ACIDS RES, V29, P5163 PINER RD, 1999, SCIENCE, V283, P661 PORTER MD, 1987, J AM CHEM SOC, V109, P3559 RAMSAY G, 1998, NAT BIOTECHNOL, V16, P40 SCHWARTZ PV, 2002, LANGMUIR, V18, P4041 SOSNOWSKI RG, 1997, P NATL ACAD SCI USA, V94, P1119 WALLTI C, 2003, LANGMUIR, V19, P981 WANG J, 2005, ELECTROANAL, V17, P7 WIRDE M, 1999, LANGMUIR, V15, P6370 XU S, 1997, LANGMUIR, V13, P127 YANG GH, 2004, LANGMUIR, V20, P3995 YERSHOV G, 1996, P NATL ACAD SCI USA, V93, P4913 YOSAKI K, 2004, J PHYS CHEM B, V108, P6422 ZHONG CJ, 1997, J ELECTROANAL CHEM, V421, P9ISI:000235354800085Univ Calif Santa Barbara, Ctr Polymers & Organ Solids, Santa Barbara, CA 93106 USA. Univ Calif Santa Barbara, Dept Chem & Biochem, Santa Barbara, CA 93106 USA. Univ Calif Santa Barbara, Dept Phys, Santa Barbara, CA 93106 USA. Univ Calif Santa Barbara, Dept Mech Engn, Santa Barbara, CA 93106 USA. Univ Calif Santa Barbara, Biomol Sci & Engn Program, Santa Barbara, CA 93106 USA. Univ Calif Santa Barbara, Dept Mat, Santa Barbara, CA 93106 USA. Plaxco, KW, Univ Calif Santa Barbara, Ctr Polymers & Organ Solids, Santa Barbara, CA 93106 USA. file://S:\SALES\_IMPORTANT_STUFF_HERE\Bibliography_Key_Papers\all publications DPN as of 101006 Copy.Data\PDF\2006 Langmuir Lai Differential Labeling of Closely Spaced Bios-1956002879\2006 Langmuir Lai Differential Labeling of Closely Spaced Biosensor Electrodes.pdf ~?]'Moldovan, N. Kim, K. H. Espinosa, H. D.20068Design and fabrication of a novel microfluidic nanoprobe204-213)Journal of Microelectromechanical Systems151dip-pen nanolithography; microfluidics; micropipette; nanoprobe DIP-PEN NANOLITHOGRAPHY; ION TRANSFER; PROBE; MICROSCOPY; ARRAYS; TIPArticleFeb#The design and fabrication of a novel microfluidic nanoprobe system are presented. The nanoprobe consists of cantilevered ultrasharp volcano-like tips, with microfluidic capabilities consisting of microchannels connected to an on-chip reservoir. The chip possesses additional connection capabilities to a remote reservoir. The fabrication uses standard surface micromachining techniques and materials. Bulk micromachining is employed for chip release. The microchannels are fabricated in silicon nitride by a new methodology, based on edge underetching of a sacrificial layer, bird's beak oxidation for mechanically closing the edges' and deposition of a sealing layer. The design and integration of various elements of the system and their fabrication are discussed. The system is conceived mainly to work as a "nanofountain pen", i.e., a continuously writing upgrade of the dip-pen nanolithography, approach. Moreover, the new chip shows a much larger applicability area in fields such as electrochemical nanoprobes, nanoprobe-based etching, build-up tools for nanofabrication, or a probe for materials interactive analysis. Preliminary tests for writing and imaging with the new device were performed. These tests illustrate the capabilities of the new device and demonstrate possible directions for improvement.://000235453000020 Times Cited: 0 Cited References: BROWN KT, 1986, ADV MICROPIPETTE TEC BULLEN D, 2003, PROC IEEE MICR ELECT, P4 CHANDRASEKARAN S, 2003, J MICROELECTROMECH S, V12, P281 DEBOER MJ, 2000, J MICROELECTROMECH S, V9, P94 ESPINOSA HD, 2003, 60455898, US, APPL GOULD P, 2003, MAT TODAY, P34 HANSMA PK, 1989, SCIENCE, V243, P641 HONG MH, 2000, APPL PHYS LETT, V77, P2604 HONG SH, 1999, SCIENCE, V286, P523 IVANISEVIC A, 2001, J AM CHEM SOC, V123, P7887 JANG JY, 2001, J CHEM PHYS, V115, P2721 JARRELL JA, 1981, SCIENCE, V211, P277 KIM KH, 2003, MATER RES SOC S P, V782 KIM KH, 2005, SMALL, V1, P632 KLEY VB, 2000, 0042233, WO LEE KB, 2002, SCIENCE, V295, P1702 LEWIS A, 1999, APPL PHYS LETT, V75, P2689 LI Y, 2001, J AM CHEM SOC, V123, P2105 OCONNOR SD, 2002, 6501654, US OFFEREINS HL, 1992, SENSOR MATER, V3, P127 PAPAUTSKY I, 2000, IEEE T BIO-MED ENG, V47, P812 PINER RD, 1997, LANGMUIR, V13, P6864 PINER RD, 1999, SCIENCE, V283, P661 QUELLET L, 2002, 20020160561, US RANGELOW IW, 2001, J VAC SCI TECHNOL B, V19, P2723 ROZHOK S, 2003, J PHYS CHEM B, V107, P751 SHALOM S, 1992, REV SCI INSTRUM, V63, P4061 SHAO Y, 1991, J ELECTROANAL CHEM, V318, P101 SHEEHAN PE, 2002, PHYS REV LETT, V88 TAYLOR G, 1986, J ELECTROANAL CH INF, V208, P179 VETTIGER P, 2000, IBM J RES DEV, V44, P323 ZHANG M, 2002, NANOTECHNOLOGY, V13, P212ISI:000235453000020|Northwestern Univ, Evanston, IL 60208 USA. Moldovan, N, Northwestern Univ, Evanston, IL 60208 USA. espinosa@northwestern.edu file://S:\SALES\_IMPORTANT_STUFF_HERE\Bibliography_Key_Papers\all publications DPN as of 101006 Copy.Data\PDF\2006 Jo of MicroElecMech Systems Moldovan Design & Fab o-4158373188\2006 Jo of MicroElecMech Systems Moldovan Design & Fab of novel microfluid nanoprobe.pdf~?^PBhatnagar, P. Mark, S. S. Kim, I. Chen, H. Y. Schmidt, B. Lipson, M. Batt, C. A.2006@Dendrimer-scaffod-based electron-beam patterning of biomolecules315-+Advanced Materials183DIP-PEN NANOLITHOGRAPHY; SELF-ASSEMBLED MONOLAYERS; SIZED PROTEIN-PATTERNS; NANOWIRE NANOSENSORS; ALZHEIMERS-DISEASE; SOFT LITHOGRAPHY; CANCER; SURFACES; BIOSENSOR; IMMOBILIZATIONArticleFebGA layer-by-layer approach for patterning biomolecules on dendrimer scaffolds using electron-beam lithography has been developed (see Figure). A self-assembled poly(ethylene glycol) monolayer is patterned with aldehyde-terminated polyamidoamine dendrimers to allow the covalent immobilization of aminated oligonucleotide probes.://000235353700011 Times Cited: 1 Cited References: ABBOTT NL, 1992, SCIENCE, V257, P1380 ANGENENDT P, 2003, J CHROMATOGR A, V1009, P97 BENTERS R, 2001, CHEMBIOCHEM, V2, P686 BESKE OE, 2002, DRUG DISCOV TODAY S, V7, S131 BLAWAS AS, 1998, BIOMATERIALS, V19, P595 CHEN CS, 1997, SCIENCE, V276, P1425 CLARKE MF, 2004, NATURE, V432, P281 CUI HM, 2003, SCIENCE, V299, P1753 CUI Y, 2001, SCIENCE, V293, P1289 DEMERS LM, 2002, SCIENCE, V296, P1836 DUCHET J, 1997, LANGMUIR, V13, P2271 DUCHET J, 2001, COMPOS INTERFACE, V8, P177 FERRARI M, 2005, NAT REV CANCER, V5, P161 FOLCH A, 2000, ANNU REV BIOMED ENG, V2, P227 GEORGANOPOULOU DG, 2005, P NATL ACAD SCI USA, V102, P2273 GOLDFARB DL, 2004, J VAC SCI TECHNOL B, V22, P647 HAES AJ, 2005, J AM CHEM SOC, V127, P2264 ILIC B, 2000, BIOMED MICRODEVICES, V2, P317 KATZ E, 2004, ANGEW CHEM INT EDIT, V43, P6042 KOCH WH, 2004, NAT REV DRUG DISCOV, V3, P749 KRAMER S, 2003, CHEM REV, V103, P4367 LEE KB, 2002, SCIENCE, V295, P1702 LIM JH, 2003, ANGEW CHEM INT EDIT, V42, P2309 LIOTTA LA, 2003, CANCER CELL, V3, P317 MAHOROWALA AP, 2000, J VAC SCI TECHNOL 1, V18, P1411 MARKOV DA, 2004, J AM CHEM SOC, V126, P16659 MARSH RJ, 2002, COLLOID SURFACE B, V23, P31 MCDONALD JC, 2002, ACCOUNTS CHEM RES, V35, P491 OWENS J, 2004, NAT REV DRUG DISCOV, V3, P911 PATHAK S, 2004, LANGMUIR, V20, P6075 PENA DJ, 2003, LANGMUIR, V19, P9028 PIEHLER J, 2005, CURR OPIN STRUC BIOL, V15, P4 RAGHAVAN S, 2004, ADV MATER, V16, P1303 RAMANATHAN K, 2005, J AM CHEM SOC, V127, P496 SCHMIDT B, 2004, APPL PHYS LETT, V85, P4854 SIDRANSKY D, 2002, NAT REV CANCER, V2, P210 SINGH SK, 2004, NATURE, V432, P396 TAKAYAMA S, 2001, NATURE, V411, P1016 TANII T, 2004, APPL SURF SCI, V234, P102 TOKAREVA I, 2004, J AM CHEM SOC, V126, P15950 TOMALIA DA, 1990, ANGEW CHEM INT EDIT, V29, P138 TORMEN M, 2002, APPL PHYS LETT, V81, P2094 TREVISIOL E, 2003, NEW J CHEM, V27, P1713 VANDUYNE RP, 2004, SCIENCE, V306, P985 VEISEH M, 2002, LANGMUIR, V18, P6671 VOGELSTEIN B, 2004, NAT MED, V10, P789 WADUMESTHRIGE K, 1999, LANGMUIR, V15, P8580 WADUMESTHRIGE K, 2001, BIOPHYS J, V80, P1891 WANG C, 2005, ADV MATER, V17, P150 WANG WU, 2005, P NATL ACAD SCI USA, V102, P3208 WHITESIDES GM, 2001, ANNU REV BIOMED ENG, V3, P335 XIA YN, 1998, ANNU REV MATER SCI, V28, P153 ZHANG GJ, 2005, SMALL, V1, P833ISI:000235353700011Cornell Univ, Dept Biomed Engn, Ithaca, NY 14853 USA. Cornell Univ, Dept Microbiol, Ithaca, NY 14853 USA. Cornell Univ, Dept Microbiol, Ithaca, NY 14853 USA. Cornell Univ, Dept Elect & Comp Engn, Ithaca, NY 14853 USA. cab10@cornell.edufile://S:\SALES\_IMPORTANT_STUFF_HERE\Bibliography_Key_Papers\all publications DPN as of 101006 Copy.Data\PDF\2006 Adv Mat Bhatnagar Dendrimer-scaffod-based Electron Beam-2234525733\2006 Adv Mat Bhatnagar Dendrimer-scaffod-based Electron Beam.pdf ~?_ARosner, B. Duenas, T. Banerjee, D. Shile, R. Amro, N. Rendlen, J.2006cFunctional extensions of Dip Pen Nanolithography (TM) : active probes and microfluidic ink delivery S124-S130Smart Materials & Structures151/ATOMIC-FORCE MICROSCOPE; NANOSTRUCTURES; ARRAYSArticleFeb/Dip Pen Nanolithography (DPN (TM)) is an important technique for nanotechnology and a fundamental new tool for Studying the consequences of miniaturization. In this scanning probe technique a sharp tip is coated with a functional molecule (the 'ink') then brought into contact with a surface where it deposits ink via a water meniscus. The DPN process is a direct-write pattern transfer technique with nanometer resolution and is inherently general with respect to usable inks and substrates, including biomolecules such as proteins and oliconucleotides. We present functional extensions of the basic DPN process by showing multiple active probes along with the ability to load different inks onto probe tips. We present the fabrication process and characterization of thermomechanically actuated probes that use the bimorph effect to induce deflection of individual cantilevers as well as the integration of these probes with control electronics and an interface module. As an additional improvement to DPN functionality, we developed the capability to write with different inks on the probe array, permitting the fabrication of multicomponent nanodevices in one writing session. For this purpose, we fabricate passive microfluidic devices and present the microfluidic behavior and ink loading performance of these components.://000235313500021 RTimes Cited: 0 Cited References: AKAMINE S, 1992, J VAC SCI TECHNOL B, V10, P2307 ALBRECHT TR, 1990, J VAC SCI TECHNOL A, V8, P3386 BANERJEE D, 2003, MICR TOT AN SYST 7 I, V1, P57 BARONE AD, 2001, NUCLEOS NUCLEOT NUCL, V20, P525 BINNIG G, 1982, APPL PHYS LETT, V40, P178 BINNIG G, 1986, PHYS REV LETT, V56, P930 BULLEN D, 2002, MAT RES SOC P, V758 BULLEN D, 2002, SPIE SMART EL MEMS N, P17 BULLEN D, 2003, PROC IEEE MICR ELECT, P4 DEMERS LM, 2001, ANGEW CHEM INT EDIT, V40, P3069 DEMERS LM, 2002, SCIENCE, V296, P1836 FU L, 2003, NANO LETT, V3, P757 HANG M, 2001, 1 IEEE C NAN MAUI HONG SH, 1999, SCIENCE, V286, P523 HONG SH, 2000, SCIENCE, V288, P1808 KRAMER S, 2003, CHEM REV A AZ LEE KB, 2002, SCIENCE, V295, P1702 LEE KB, 2003, J AM CHEM SOC, V125, P5588 LIU J, 2002, J INORG MATER, V17, P1 MIRKIN CA, 2003, 6635311, US PINER RD, 1999, SCIENCE, V283, P661 SU M, 2003, J AM CHEM SOC, V125, P9930 ZHANG H, 2003, NANO LETT, V3, P43 ZHANG M, 2002, NANOTECHNOLOGY, V13, P212 Sp. Iss. SIISI:000235313500021NanoInk Inc, Corp Off, Chicago, IL 60607 USA. NanoInk Inc, MEMS Fabricat, Campbell, CA 95008 USA. Rosner, B, NanoInk Inc, Corp Off, 1335 Randolph St, Chicago, IL 60607 USA. file://S:\SALES\_IMPORTANT_STUFF_HERE\Bibliography_Key_Papers\all publications DPN as of 101006 Copy.Data\PDF\2006 Smart Mat&Structures Rosner Functional extensions of DPN N-4252797261\2006 Smart Mat&Structures Rosner Functional extensions of DPN Nanolithography.pdf ?~?`*Hampton, J. R. Dameron, A. A. Weiss, P. S.2006HDouble-ink dip-pen nanolithography studies elucidate molecular transport 1648-1653(Journal of the American Chemical Society1285DFORCE MICROSCOPE; NANOSTRUCTURES; FABRICATION; NANOARRAYS; GOLD; TIPArticleFebWe have investigated the transport mechanism of the inks most typically used in dip-pen nanolithography by patterning both 16-mercaptohexadecanoic acid (MHDA) and 1-octadecanethiol (ODT) on the same Au{111} substrate. Several pattern geometries were used to probe ink transport from the tip to the sample during patterning of both dots (stationary tip) and lines (moving tip). When ODT was written on top of a pre-existing MHDA structure, the ODT was observed at the outsides of the MHDA structure, and the transport rate increased. In the reverse case, the MHDA was also observed on the outsides of the previously patterned ODT features; however, the transport rate was reduced. Furthermore, the shapes of pre-existing patterns of one ink were not changed by deposition of the other ink. These results highlight the important role hydrophobicity plays, both of the substrate as well as of the inks, in determining transport properties and thereby patterns produced in dip-pen nanolithography.://000235224700059 XTimes Cited: 1 Cited References: *NANOINK, COMMUNICATION BAIN CD, 1989, J AM CHEM SOC, V111, P321 CHEUNG CL, 2003, J AM CHEM SOC, V125, P6848 GINGER DS, 2004, ANGEW CHEM INT EDIT, V43, P30 HOWARD PH, 1997, HDB PHYS PROPERTIES JASCHKE M, 1995, LANGMUIR, V11, P1061 LAIBINIS PE, 1992, J AM CHEM SOC, V114, P1990 LEE KB, 2002, SCIENCE, V295, P1702 MEYLAN WM, 1996, ENVIRON TOXICOL CHEM, V15, P100 PETERSON EJ, 2004, J PHYS CHEM B, V108, P15206 PINER RD, 1999, SCIENCE, V283, P661 RON H, 1994, LANGMUIR, V10, P4556 ROZHOK S, 2003, J PHYS CHEM B, V107, P751 SALAITA K, 2005, J AM CHEM SOC, V127, P11283 SCHWARTZ PV, 2002, LANGMUIR, V18, P4041 SHEEHAN PE, 2002, PHYS REV LETT, V88 SMITH JC, 2003, NANO LETT, V3, P883 SOUTHALL NT, 2002, J PHYS CHEM B, V106, P521 TANFORD C, 1974, J PHYS CHEM-US, V78, P2469 TANFORD C, 1980, HYDROPHOBIC EFFECT F WEEKS BL, 2002, PHYS REV LETT, V88 WEINBERGER DA, 2000, ADV MATER, V12, P1600 ZHANG H, 2003, NANO LETT, V3, P43 ZHANG H, 2003, NANOTECHNOLOGY, V14, P1113ISI:000235224700059Penn State Univ, Dept Chem, University Pk, PA 16802 USA. Penn State Univ, Dept Phys, University Pk, PA 16802 USA. Weiss, PS, Penn State Univ, Dept Chem, University Pk, PA 16802 USA. stm@psu.edufile://S:\SALES\_IMPORTANT_STUFF_HERE\Bibliography_Key_Papers\all publications DPN as of 101006 Copy.Data\PDF\2006 JACS Hampton Double-ink DPN nanlith. studies-2099152186\2006 JACS Hampton Double-ink DPN nanlith. studies.pdf ~?aPowell, T. Yoon, J. Y.2006`Fluorescent biorecognition of gold nanoparticle-IgG conjugates self-assembled on e-beam patterns106-110Biotechnology Progress221+DIP-PEN NANOLITHOGRAPHY; PROTEIN NANOARRAYSArticleJan-Feb^A new concept for line patterning of immunoglobulin G (IgG) in nanometer scale using gold nanoparticles (AuNPs) self-assembled in a nanochannel written with an electron beam is proposed and demonstrated. AuNPs are synthesized by reducing KAuCl4 with NaBH4, producing AuNPs 40-70 nm in size, where Cl- ions are capping AuNPs thus making them negatively charged and subsequently stabilized. IgG is conjugated to these AuNP's by simple adsorption. Single or multiple nanochannels are written with an electron beam using a scanning electron microscope (SEM) in a layer of poly(methyl methacrylate) (PMMA), which is spin-coated on a p-doped Si wafer. AuNPs bind into the etched nanochannel where the Si surface is exposed, while the relatively hydrophobic PMMA area repels the particles. The particles with a diameter larger than the channel width are not able to go inside of it. Anti-IgG, conjugated with fluorescein isothiocyanate (FITC), is then exposed to the patterned surface, binding specifically to the IgG-AuNP conjugates within the line patterns. These antibody-antigen bindings can be visualized with a fluorescent microscope, showing the fluorescent signal only along with the nanometer line pattern. These initial steps will lead to the formation of complex protein nanoarrays, based on the size-dependent self-assembly of AuNPs within variously sized nanopatterns.://000235244100016 YTimes Cited: 0 Cited References: BRUST M, 1994, J CHEM SOC CHEM COMM, P801 DANIEL MC, 2004, CHEM REV, V104, P293 GEISSLER M, 2004, ADV MATER, V16, P1249 HONG SH, 2000, SCIENCE, V288, P1808 LEE KB, 2002, SCIENCE, V295, P1702 LEE KB, 2003, J AM CHEM SOC, V125, P5588 LYNCH M, 2004, PROTEOMICS, V4, P1695 MINNE SC, 1998, APPL PHYS LETT, V73, P1742 PINER RD, 1999, SCIENCE, V283, P661 WHEELER AR, 2004, ANAL CHEM, V76, P4833 XU JT, 2004, BIOMED MICRODEVICES, V6, P117 YOON JY, 2003, ANAL CHEM, V75, P5097 YOON JY, 2005, AICHE J, V51, P1048ISI:000235244100016Univ Arizona, Dept Agr & Biosyst Engn, Tucson, AZ 85721 USA. Yoon, JY, Univ Arizona, Dept Agr & Biosyst Engn, Tucson, AZ 85721 USA. jyyoon@email.arizona.edu file://S:\SALES\_IMPORTANT_STUFF_HERE\Bibliography_Key_Papers\all publications DPN as of 101006 Copy.Data\PDF\2006 Biotech Progress Powell Fluorescent biorecognition of au nano-1559751241\2006 Biotech Progress Powell Fluorescent biorecognition of au nanopartilce.pdf ~?bCLim, S. K. Chun, I. S. Ban, K. S. Yoon, C. S. Kim, C. K. Kim, Y. H.2006hMono-layer of Ni100-xFex nanoparticles fabricated on a polyimide film under different curing atmospheres108-114(Journal of Colloid and Interface Science2951metallic nanoparticle; polyimide; Ni rich nanoparticle; selective reaction; XPS; H-2 atmosphere DIP-PEN NANOLITHOGRAPHY; IMIDIZATIONArticleMar)A mono-layer of nano-sized metal particles was prepared on the surface of a polyimide film by simply depositing a thin film of Ni80Fe20 on top of the polyamic acid that was spin coated onto a Si wafer. During thermal imidization of the polyamic acid film, Fe was selectively etched by reacting with the carbonyl group of the polyamic acid to leave behind uniformly distributed Ni-rich metallic particles. The average diameter of the particles was 4 nm and the particles were confined into a single layer on top of the polymer film. Moreover, it was also shown that the morphology of the nanoparticles can be substantially altered by curing the precursor film in a hydrogen atmosphere, without significantly damaging the polymer film. Thus produced nanoparticles lay exposed on top of the electrically insulating and chemically stable polymer film so that it is possible that the nanoparticles can be directly used for fabricating a nonvolatile flash memory device or as a template for building functional nano-structures. (c) 2005 Elsevier Inc. All rights reserved.://000235098700013 5Times Cited: 1 Cited References: AKAMATSU K, 2003, EUR PHYS J D, V24, P377 BRADLEY JS, 2004, NANOPARTICLES THEORY CHENITE A, 1994, J VAC SCI TECHNOL A, V12, P513 CLAUDIUS F, 2004, POLYIMIDES FUNDAMENT GHANNOUM S, 2003, LANGMUIR, V19, P4804 HOEPPENER S, 2002, ADV MATER, V14, P1036 LEE KB, 2003, J AM CHEM SOC, V125, P5588 LIM SK, 2004, J COLLOID INTERF SCI, V273, P517 LIM SK, 2004, J PHYS CHEM B, V108, P18179 LIM SK, 2005, J COLLOID INTERF SCI, V287, P501 MCKENDRY R, 2002, NANO LETTERS, V2, P713 MOULDER JF, 1995, HDB XRAY PHOTOELECTR SAMSONOV GV, 1982, OXIDE HDB SONNETT JM, 2004, POLYIMIDES FUNDAMENT, P151 YAMAZAKI K, 2003, 17 IEEE INT C MEMS, P427 ZHOU WL, 2003, J APPL PHYS 2, V93, P7340 ZHU XB, 2002, J APPL PHYS 2, V91, P7340ISI:000235098700013Hanyang Univ, Div Mat Sci & Engn, Seoul 133791, South Korea. Yoon, CS, Hanyang Univ, Div Mat Sci & Engn, Seoul 133791, South Korea. csyoon@hanyang.ac.krfile://S:\SALES\_IMPORTANT_STUFF_HERE\Bibliography_Key_Papers\all publications DPN as of 101006 Copy.Data\PDF\2006 JoColliod&InterfaceSci Lim Monolayer of Ni100xFex-3044273732\2006 JoColliod&InterfaceSci Lim Monolayer of Ni100xFex.pdf~?cDucker, R. E. Leggett, G. J.2006KA mild etch for the fabrication of three-dimensional nanostructures in gold392-393(Journal of the American Chemical Society1282SELF-ASSEMBLED MONOLAYERS; DIP-PEN NANOLITHOGRAPHY; NEAR-FIELD PHOTOLITHOGRAPHY; LITHOGRAPHY; GENERATION; SURFACES; SILICON; NANOSCALEArticleJan://000234814900006 Times Cited: 0 Cited References: ABBOTT NL, 1994, CHEM MATER, V6, P596 BAIN CD, 1987, J AM CHEM SOC, V109, P733 BIEBUYCK HA, 1997, IBM J RES DEV, V41, P159 BREWER NJ, 2005, J PHYS CHEM B, V107, P11247 BULLEN D, 2004, APPL PHYS LETT, V84, P789 COOPER E, 1999, LANGMUIR, V15, P1024 ECK W, 2000, ADV MATER, V12, P805 GINGER DS, 2004, ANGEW CHEM INT EDIT, V43, P30 HARNETT CK, 2000, APPL PHYS LETT, V76, P2466 KIM E, 1995, J ELECTROCHEM SOC, V142, P628 KRAMER S, 2003, CHEM REV, V103, P4367 KUMAR A, 1994, LANGMUIR, V10, P1498 LIU GY, 2002, P NATL ACAD SCI USA, V99, P5165 NUZZO RG, 1983, J AM CHEM SOC, V105, P4481 NUZZO RG, 1987, J AM CHEM SOC, V109, P733 PINER RD, 1999, SCIENCE, V283, P661 SUN S, 2004, NANO LETT, V4, P1381 SUN SQ, 2002, J AM CHEM SOC, V124, P2414 SUN SQ, 2002, NANO LETT, V2, P1223 SUN SQ, 2005, NANOTECHNOLOGY, V16, P1798 WEINBERGER DA, 2000, ADV MATER, V12, P1600 XIA Y, 1996, J ELECTROCHEM SOC, V143, P1070 XIA Y, 1998, ANGEW CHEM INT EDIT, V37, P550 XIA YN, 1995, CHEM MATER, V7, P2332 ZHOU DJ, 2003, ANGEW CHEM INT EDIT, V42, P4934ISI:000234814900006Univ Sheffield, Dept Chem, Sheffield S3 7HF, S Yorkshire, England. Leggett, GJ, Univ Sheffield, Dept Chem, Brook Hill, Sheffield S3 7HF, S Yorkshire, England. graham.leggett@shef.ac.ukfile://S:\SALES\_IMPORTANT_STUFF_HERE\Bibliography_Key_Papers\all publications DPN as of 101006 Copy.Data\PDF\2006 Ducker JACS Mild etch for fabrication-1724145962\2006 Ducker JACS Mild etch for fabrication.pdf F~?dINelson, B. A. King, W. P. Laracuente, A. R. Sheehan, P. E. Whitman, L. J.2006WDirect deposition of continuous metal nanostructures by thermal dip-pen nanolithographyApplied Physics Letters883CDATA-STORAGE; INK; CANTILEVERS; NANOWIRES; SURFACES; SENSORS; FILMSArticleJanWe describe the deposition of continuous metal nanostructures onto glass and silicon using a heated atomic force microscope cantilever. Like a miniature soldering iron, the cantilever tip is coated with indium metal, which can be deposited onto a surface forming lines of a width less than 80 nm. Deposition is controlled using a heater integrated into the cantilever. When the cantilever is unheated, no metal is deposited from the tip, allowing the writing to be registered to existing features on the surface. We demonstrate direct-write circuit repair by writing an electrical connection between two metal electrodes separated by a submicron gap. (c) 2006 American Institute of Physics.://000234757100055 Times Cited: 0 Cited References: ALI MB, 2002, LANGMUIR, V18, P872 CHUI BW, 1998, J MICROELECTROMECH S, V7, P69 FU L, 2003, NANO LETT, V3, P757 GARNO JC, 2003, NANO LETT, V3, P389 GINGER DS, 2004, ANGEW CHEM INT EDIT, V43, P30 GOLOVANOV V, 2005, SENSOR ACTUAT B-CHEM, V106, P563 KASIVISWANATHAN S, 1994, J APPL PHYS, V75, P2572 KING WP, 2001, APPL PHYS LETT, V78, P1300 KING WP, 2002, ASME IMECE 2002 S TH KRISHNA BR, 2000, OPT MATER, V15, P217 LI Y, 2001, J AM CHEM SOC, V123, P2105 LIM JH, 2002, ADV MATER, V14, P1474 LUDWICK MT, 1959, INDIUM DISCOVERY OCC, P770 MAYNOR BW, 2001, LANGMUIR, V17, P2575 MAYNOR BW, 2002, J AM CHEM SOC, V124, P522 NOY A, 2002, NANO LETTERS, V2, P109 PETERSON EJ, 2004, J PHYS CHEM B, V108, P15206 PINER RD, 1999, SCIENCE, V283, P661 PORTER LA, 2002, NANO LETT, V2, P1369 SHEEHAN PE, 2002, PHYS REV LETT, V88 SHEEHAN PE, 2004, APPL PHYS LETT, V85, P1589 SU M, 2002, J AM CHEM SOC, V124, P1560 SU M, 2004, APPL PHYS LETT, V84, P4200 VETTIGER P, 2002, IEEE T NANOTECHNOL, V1, P39 ZHANG H, 2004, CHEM MATER, V16, P1480 ZHANG H, 2004, NANO LETT, V4, P1493ISI:000234757100055Georgia Inst Technol, George W Woodruff Sch Mech Engn, Atlanta, GA 30332 USA. USN, Res Lab, Washington, DC 20375 USA. Nelson, BA, Georgia Inst Technol, George W Woodruff Sch Mech Engn, Atlanta, GA 30332 USA. william.king@me.gatech.edu0725394018Inserts.ppt033104 Artn 033104file://S:\SALES\_IMPORTANT_STUFF_HERE\Bibliography_Key_Papers\all publications DPN as of 101006 Copy.Data\PDF\2006 AppPhysLtrs Nelson Direct deposition of continuous metal.pdff~?e,Zhao, J. W. Kan, R. R. Zhang, Y. Chen, H. Y.2006eApplications of scanning probe microscopy in nanolithography on alkanethiol self-assembled monolayers124-130Acta Physico-Chimica Sinica221scanning probe microscopy; self-assembled monolayer; scanning tunneling microscope; atomic force microscope; nanolithography ATOMIC-FORCE MICROSCOPE; DIP-PEN NANOLITHOGRAPHY; ELECTRON-BEAM LITHOGRAPHY; TUNNELING MICROSCOPE; PATTERNS; AU(111); FABRICATION; SURFACE; FILMS; GOLDArticleJanRecent progress in the field of nanolithography of self-assembled monolayers by scanning probe microscopy (SPM), which is important in microelectronics and sensor technology, is introduced in the paper. According to the working principle, scanning probe lithography (SPL) can be classified into three categories, namely STM-based nanolithography, AFM-based nanolithography, and C-AFM-based nanolithography. SPL is a pivot of the fundamental study in the field of nanolithography for its high spatial resolution, case in fabrication and good controllability in operation. The possible application in information storage has been discussed as well.://000234824600025 Times Cited: 0 Cited References: BINNIG G, 1982, HELV PHYS ACTA, V55, P726 BINNIG G, 1986, PHYS REV LETT, V56, P930 CHIDSEY CED, 1989, J CHEM PHYS, V91, P4421 CORBITT TS, 1993, ADV MATER, V5, P935 DEMERS LM, 2001, ANGEW CHEM INT EDIT, V40, P3071 DEMERS LM, 2002, SCIENCE, V296, P1836 EIGLER DM, 1990, NATURE, V344, P524 EIGLER DM, 1991, NATURE, V352, P600 GORMAN CB, 2000, LANGMUIR, V16, P6312 GORMAN CB, 2001, LANGMUIR, V17, P6923 HONG SH, 1999, SCIENCE, V286, P523 HONG SH, 2000, SCIENCE, V288, P1808 KIM Y, 2003, J APPL PHYS, V94, P7733 KIM YT, 1992, LANGMUIR, V8, P1096 KRANZ C, 1995, ADV MATER, V7, P38 KUMAR A, 1995, ACCOUNTS CHEM RES, V28, P219 LERCEL MJ, 1994, APPL PHYS LETT, V65, P974 LERCEL MJ, 1994, J VAC SCI TECHNOL B, V12, P3663 LIU GY, 2000, ACCOUNTS CHEM RES, V33, P457 MARRIAN CRK, 1994, APPL PHYS LETT, V64, P390 MAYNOR BW, 2002, J AM CHEM SOC, V124, P522 MCKENDRY R, 2002, NANO LETTERS, V2, P713 MULLER HU, 1995, J VAC SCI TECHNOL B, V13, P2846 MULLER WT, 1995, SCIENCE, V268, P272 NIEMEYER CM, 2001, ANGEW CHEM INT EDIT, V40, P4128 PAGE CC, 1999, NATURE, V402, P47 PERKINS FK, 1994, J VAC SCI TECHNOL B, V12, P3725 PERKINS FK, 1996, APPL PHYS LETT, V68, P550 PINER RD, 1999, SCIENCE, V283, P661 POIRIER GE, 1996, SCIENCE, V272, P1145 RINGGER M, 1985, APPL PHYS LETT, V46, P832 ROSS CB, 1993, LANGMUIR, V9, P632 SALMERON M, 1992, LANGMUIR, V8, P2832 SALMERON M, 1993, LANGMUIR, V9, P3600 SCHOER JK, 1994, LANGMUIR, V10, P615 SCHOER JK, 1996, J PHYS CHEM-US, V100, P11086 SUGIMURA H, 1997, J AM CHEM SOC, V119, P9226 TARLOV MJ, 1993, J AM CHEM SOC, V115, P5305 WADUMESTHRIGE K, 1999, LANGMUIR, V15, P8580 WANO H, 2001, LANGMUIR, V17, P8224 XIA Y, 1998, ANGEW CHEM INT EDIT, V37, P550 XU LS, 1995, J VAC SCI TECHNOL B, V13, P2837 XU S, 1997, LANGMUIR, V13, P127 XU S, 1998, J AM CHEM SOC, V120, P9356 XU S, 1999, LANGMUIR, V15, P7244 YAMADA R, 2000, LANGMUIR, V16, P5523 ZHAO JW, 2001, LANGMUIR, V17, P7784 ZHAO JW, 2002, NANO LETTERS, V2, P137 ZHAO JW, 2003, APPL PHYS LETT, V83, P2034 ZHAO JW, 2004, J PHYS CHEM B, V108, P17129ISI:000234824600025 Nanjing Univ, Coll Chem & Chem Engn, Key Lab Analyt Chem Life Sci, Educ Minist China, Nanjing 210093, Peoples R China. Zhao, JW, Nanjing Univ, Coll Chem & Chem Engn, Key Lab Analyt Chem Life Sci, Educ Minist China, Nanjing 210093, Peoples R China. zhaojw@nju.edu.cninternal-pdf://2006 Acta Physico-Chimica Sinica Zhao Applcations of scanning-2437385231/2006 Acta Physico-Chimica Sinica Zhao Applcations of scanning.pdf g~?fBullen, D. Liu, C.2006?Electrostatically actuated dip pen nanolithography probe arrays504-511 Sensors and Actuators a-Physical1252jdip pen nanolithography (DPN); electrostatic actuator; atomic force microscope; nanolithography MICROSCOPYArticleJanDip pen nanolithography (DPN) is a method of creating nanoscale chemical patterns on surfaces using an atomic force microscope (AFM) probe. Until now, efforts to increase the process throughput have focused on passive multi-probe arrays and active arrays based on thermal bimetallic actuation. This paper describes the first use of electrostatic actuation to create an active DPN probe array. Electrostatic actuation offers the benefit of actuation without the probe heating required for thermal bimetallic actuation. Actuator cross talk between neighboring probes is also reduced, permitting more densely spaced probe arrays. The array presented here consists of 10 cantilever probes, where each is 120 mu m long and 20 mu m wide. Each cantilever probe is actuated by the electrostatic force between the probe and a built-in counter electrode with a 20-25 mu m gap. The tip-to-tip probe spacing, also called the array pitch, is 30 mu m. Patterns of l-octadecanethiol were created on gold surfaces to demonstrate single-probe actuation, simultaneous multi-probe actuation, and overlap of patterns from adjacent probes. The rninirnurn line width was 25 nm with an average line width of 30-40nm. (c) 2005 Elsevier B.V. All rights reserved.://000234535400057 UTimes Cited: 0 Cited References: BRUGGER J, 1994, SENSOR ACTUAT A-PHYS, V43, P339 BULLEN D, 2003, RAP PROT TECHN BOST BULLEN D, 2004, APPL PHYS LETT, V84, P789 BULLEN D, 2004, J MICROELECTROMECH S, V13, P594 CHOW EM, 2000, SENSOR ACTUAT A-PHYS, V83, P118 DEMERS LM, 2001, ANGEW CHEM INT EDIT, V40, P3069 GINGER DS, 2004, ANGEW CHEM INT EDIT, V43, P30 HONG SH, 1999, SCIENCE, V286, P523 KING WP, 2000, SOL STAT SENS ACT WO OBRIEN GJ, 2001, DES CHAR PACK MEMS M PINER RD, 1999, SCIENCE, V283, P661 SHEEHY JE, 2004, FIELD CROP RES, V88, P1 SNOW ES, 1997, P IEEE, V85, P601 WANG XF, 2003, LANGMUIR, V19, P8951 ZHANG M, 2001, P 2001 1 IEEE C NAN ZHANG M, 2001, THESIS U ILLINOIS UR ZHANG M, 2002, NANOTECHNOLOGY, V13, P212 ZOU J, 2004, J MICROMECH MICROENG, V14, P204ISI:000234535400057Univ Illinois, Micro Actuators Sensors & Syst Grp, Micro & Nanotechnol Lab, Urbana, IL 61801 USA. Liu, C, Univ Illinois, Micro Actuators Sensors & Syst Grp, Micro & Nanotechnol Lab, Urbana, IL 61801 USA. changliu@uiuc.edufile://S:\SALES\_IMPORTANT_STUFF_HERE\Bibliography_Key_Papers\all publications DPN as of 101006 Copy.Data\PDF\2006 Sens & Acts Bullen Electrostatically Dip Pen Nanolithography-1347250213\2006 Sens & Acts Bullen Electrostatically Dip Pen Nanolithography.pdf~?g;Jegadesan, S. Sindhu, S. Advincula, R. C. Valiyaveettil, S.2006Direct electrochemical nanopatterning of polycarbazole monomer and precursor polymer films: Ambient formation of thermally stable conducting nanopatterns780-786Langmuir222ATOMIC-FORCE MICROSCOPY; SCANNING TUNNELING MICROSCOPE; DIP-PEN NANOLITHOGRAPHY; ELECTROSTATIC NANOLITHOGRAPHY; NANOSTRUCTURES; SILICON; NANOFABRICATION; FABRICATION; NANOWIRES; SURFACESArticleJan The direct nanopatterning of polycarbazole on ultrathin films of a "precursor polymer" and monomer under ambient conditions is reported. In contrast to previous reports on electrochemical dip-pen nanolithography using monomer ink or electrolyte-saturated films in electrostatic nanolithography, these features were directly patterned on spin-cast films of carbazole monomer and poly(vinylcarbazole) (PVK) under room temperature and humidity conditions. Using a voltage-biased atomic force microscope (AFM) tip, electric-field-induced polymerization and cross-linking occurred with nanopatterning in these films. Different parameters, including writing speed and bias voltages, were studied to demonstrate line width and patterning geometry control. The conducting property (current- voltage (I-V) curves) of these nanopatterns was also investigated using a conducting-AFM (C-AFM) setup, and the thermal stability of the patterns was evaluated by annealing the polymer/monomer film above the glass transition (T-g) temperature of the precursor polymer. To the best of our knowledge, this is the first report in which thermally stable conducting nanopattems were drawn directly on monomer or polymer film substrates using an electrochemical nanolithography technique under ambient conditions.://000234647200038 2Times Cited: 3 Cited References: ANNIE DB, 1985, J ELECTROANAL CHEM, V189, P51 AVOURIS P, 1997, APPL PHYS LETT, V71, P285 BABA A, 2004, J PHYS CHEM B, V108, P18949 BOXLEY CJ, 2003, J PHYS CHEM B, V107, P9677 BUMM LA, 1996, SCIENCE, V271, P1705 CHEN J, 1999, SCIENCE, V286, P1550 FAN FRF, 1995, SCIENCE, V270, P1849 GAJIWALA HM, 2000, POLYMER, V41, P2009 HUANG Y, 2001, SCIENCE, V291, P630 JANG SY, 2004, J AM CHEM SOC, V126, P9476 JEGADESAN S, 2005, ADV MATER, V17, P1282 JOERN L, 2004, POLYM PREPR, V45, P783 JOHANSSON A, 2001, PHYS REV LETT, V86, P3602 JUHL S, 2004, APPL PHYS LETT, V85, P3836 KIM DY, 2000, PROG POLYM SCI, V25, P1089 KOLB DM, 1997, SCIENCE, V275, P1097 KUMAR A, 1995, ACCOUNTS CHEM RES, V28, P219 LEE M, 2004, APPL PHYS LETT, V85, P3552 LIM JH, 2002, ADV MATER, V14, P1474 LIN HN, 2002, APPL PHYS LETT, V81, P2572 LYUKSYUTOV SF, 2003, APPL PHYS LETT, V83, P4405 LYUKSYUTOV SF, 2003, NANOTECHNOLOGY, V14, P716 LYUKSYUTOV SF, 2003, NAT MATER, V2, P468 MACIT H, 2005, J APPL POLYM SCI, V96, P894 MAOZ R, 1999, ADV MATER, V11, P55 MAYNOR BW, 2002, J AM CHEM SOC, V124, P522 NIU YH, 2002, APPL PHYS LETT, V81, P634 NOY A, 2002, NANO LETTERS, V2, P109 SAILOR MJ, 1997, ADV MATER, V9, P783 SCHNEEGANS O, 2004, J PHYS CHEM B, V108, P9882 SNOW ES, 1993, APPL PHYS LETT, V63, P749 STEJSKAL J, 2002, PURE APPL CHEM, V74, P857 TARANEKAR P, 2005, MACROMOLECULES, V38, P3679 WEEKS BL, 2002, PHYS REV LETT, V88ISI:000234647200038bNatl Univ Singapore, Dept Chem, NUS Nanosci & Nanotechnol Initiat, Singapore 117543, Singapore. Univ Houston, Dept Chem, Houston, TX 77204 USA. Univ Houston, Dept Chem Engn, Houston, TX 77204 USA. Advincula, RC, Natl Univ Singapore, Dept Chem, NUS Nanosci & Nanotechnol Initiat, 3 Sci Dr 3, Singapore 117543, Singapore. chmsv@nus.edu.sg radvincula@uh.edufile://S:\SALES\_IMPORTANT_STUFF_HERE\Bibliography_Key_Papers\all publications DPN as of 101006 Copy.Data\PDF\2006 Langmuir Jegadesan Direct Electrichemical Nanpatterning-1730320959\2006 Langmuir Jegadesan Direct Electrichemical Nanpatterning.pdf ~?hfCabrini, S. Barsotti, R. J. Carpentiero, A. Businaro, L. Zaccaria, R. P. Stellacci, F. Di Fabrizio, E.2005lCross beam lithography (FIB plus EBL) and dip pen nanolithography for nanoparticle conductivity measurements 2806-2810(Journal of Vacuum Science & Technology B236 FABRICATIONArticleNov-DecFocused ion beam lithography is a very powerful technique for directly writing patterns on many substrates, it is a maskless and resistless technique that allows a very wide range of applications, providing a resolution down to 10 nm. Using a system composed by a 30 keV gallium ion beam column plus a 30 keV electron beam, nanogaps for electrical measurements of nanoparticle were fabricated with a resolution down to the nanometer scale, by exploiting FIB milling (FIBM) and electron beam lithography (EBL). Starting from prepatterned samples a square pattern reduces the width of the gold wire and a narrow line pattern opens a gap of less than 7 nm. Electrical measurements and AFM tapping mode imaging were performed on the gaps. We patterned the ends of the gold leads with dip pen nanolithography using mercapto-undecanol (MUD) to form a bond between the nanoparticle and the alcohol group attached to the gold surface. After this assembly, devices showed an increase in conductivity (10-100-fold increase). Measuring the device again one week later, we saw almost no change in conductivity, showing that we deposit a multiparticle cluster and measure its conductivity. (c) 2005 American Vacuum Society.://000234613200102 Times Cited: 0 Cited References: ANDRES RP, 1996, SCIENCE, V272, P1323 BARSOTTI RJ, 2004, LANGMUIR, V20 DEJAGER WH, 1996, MICROELECTRON ENG, V30, P353 DEMERS LM, 2002, SCIENCE, V296, P1836 DIFABRIZIO E, 2004, J PHYS-CONDENS MAT, V16, S3517 KLEIN DL, 1996, APPL PHYS LETT, V68, P2574 LIM JH, 2002, ADV MATER, V14, P1474 MCCARTY GS, 2004, NANO LETT, V4 PARK H, 1999, APPL PHYS LETT, V75, P301 PINER RD, 1999, SCIENCE, V283, P661 PORATH D, 1997, PHYS REV B, V56, P9829 VALIEV KA, 1992, PHYS SUBMICRON LITHO ZHANG H, 2003, NANO LETT, V3, P43 ZHANG H, 2003, NANOTECHNOLOGY, V14, P1113ISI:000234613200102tTASC, INFM, ELETTRA Sincrotrone Trieste, I-34017 Basovizza Trieste, Italy. MIT, Dept Mat Sci & Engn, Cambridge, MA 02139 USA. Osaka Univ, Dept Appl Phys, Osaka 5650871, Japan. Univ MAgna Graecia, I-88100 Catanzaro, Italy. Cabrini, S, TASC, INFM, ELETTRA Sincrotrone Trieste, S-S 14,Km 163-5 Area Sci Pk, I-34017 Basovizza Trieste, Italy. stefano.cabrini@elettra.trieste.itfile://S:\SALES\_IMPORTANT_STUFF_HERE\Bibliography_Key_Papers\all publications DPN as of 101006 Copy.Data\PDF\2005 Journal of VacSci&Tech Cabrini Cross beam lithography.pdf W)F~?i1Cho, N. Ryu, S. Kim, B. Schatz, G. C. Hong, S. H.2006?Phase of molecular ink in nanoscale direct deposition processesJournal of Chemical Physics12421DIP-PEN NANOLITHOGRAPHY; FORCE MICROSCOPE; ARRAYSArticleJanWe report the first observation of a phase transition in a nanoscale direct deposition process. This transition involves the melting of molecular ink layers in dip-pen nanolithography, and it is observed by measuring the temperature dependence of the growth rate of the deposited pattern. The results are interpreted using a diffusion equation approach in conjunction with a '' double-molecular-layer '' model of the adsorbed molecules on the atomic force microscope tip. The theory provides a qualitative explanation for the dependence of the pattern growth rate on solvent and adsorbed water as well as on temperature. (c) 2006 American Institute of Physics.://000234607700074 BTimes Cited: 3 Cited References: CHO Y, 2005, J PHYS CHEM B, V109, P12731 CRANK J, 1993, MATH DIFFUSION CUI Y, 2001, SCIENCE, V293, P1289 DASH JG, 1989, CONTEMP PHYS, V30, P2 FRITZ J, 2000, SCIENCE, V288, P316 JANG JY, 2001, J CHEM PHYS, V115, P2721 JASCHKE M, 1995, LANGMUIR, V11, P1061 JIANG HZ, 2005, LANGMUIR, V21, P5242 LEE KB, 2002, SCIENCE, V295, P1702 LI Z, 2003, ANGEW CHEM INT EDIT, V42, P2306 MANANDHAR P, 2003, PHYS REV LETT, V90 MAYNOR BW, 2001, LANGMUIR, V17, P2575 MILLER MM, 2001, J MAGN MAGN MATER, V225, P138 NOY A, 2002, NANO LETTERS, V2, P109 PINER RD, 1999, SCIENCE, V283, P661 PORTER LA, 2002, NANO LETT, V2, P1369 ROZHOK S, 2003, J PHYS CHEM B, V107, P751 RUDNITSKY RG, 2000, SENSOR ACTUAT A-PHYS, V83, P256 SHEEHAN PE, 2002, PHYS REV LETT, V88 TATON TA, 2000, SCIENCE, V289, P1757 WEEKS BL, 2002, PHYS REV LETT, V88 WILSON DL, 2001, P NATL ACAD SCI USA, V98, P13660 WILSON GS, 2000, CHEM REV, V100, P2693 ZHANG M, 2002, NANOTECHNOLOGY, V13, P212ISI:000234607700074Seoul Natl Univ, Dept Phys, Seoul 151747, South Korea. Northwestern Univ, Dept Chem, Evanston, IL 60208 USA. Hong, SH, Seoul Natl Univ, Dept Phys, Seoul 151747, South Korea. shong@phya.snu.ac.kr024714 Artn 024714sinternal-pdf://2006 JoChemPhys Cho Phase of molecular ink-3295765781/2006 JoChemPhys Cho Phase of molecular ink.pdfyF~?j?Chung, H. J. Xie, X. N. Sow, C. H. Bettiol, A. A. Wee, A. T. S.2006_Polymeric conical structure formation by probe-induced electrohydrodynamical nanofluidic motionApplied Physics Letters882MATOMIC-FORCE MICROSCOPY; DIP-PEN NANOLITHOGRAPHY; STABILITY; OXIDATION; FILMSArticleJanQWe report the creation of polymeric structures by atomic force microscopy (AFM) probe induced electrohydrodynamic (EHD) instability and nanofluidic flow. By biasing the AFM probe in a high field regime, single conical structure was produced on poly(methylmethacrylate) due to the initiation of strong EHD instability in the locally heated polymer melts. The pattern formation is dominated by the interplay of polymer EHD motion, polymer ablation, and AFM tip repulsion. The dependence of cone formation probability on the bending of AFM cantilevers with different stiffness was also discussed.://000234606900070 RTimes Cited: 0 Cited References: DEMERS LM, 2002, SCIENCE, V296, P1836 DESHPANDE P, 2001, APPL PHYS LETT, V79, P1688 HERMINGHAUS S, 1998, SCIENCE, V282, P916 KING WP, 2001, APPL PHYS LETT, V78, P1300 LEE KB, 2002, SCIENCE, V295, P1702 LYUKSYUTOV SF, 2003, NAT MATER, V2, P468 LYUKSYUTOV SF, 2004, PHYS REV B, V70 ODDERSHEDE L, 2000, PHYS REV LETT, V85, P1234 PEASE LF, 2003, J CHEM PHYS, V118, P3790 SCHAFFER E, 2000, NATURE, V403, P874 SCHAFFER E, 2003, ADV MATER, V15, P514 SNOW ES, 2000, APPL PHYS LETT, V76, P1782 TAYLOR GI, 1965, J FLUID MECH, V22, P1 VETTIGER P, 2002, IEEE T NANOTECHNOL, V1, P39 WU L, 2003, APPL PHYS LETT, V82, P3200 WUNDERLICH W, 1975, PHYS CONSTANT POLYME XIE XN, 2004, J AM CHEM SOC, V126, P7665 XIE XN, 2005, ADV MATER, V17, P1386ISI:000234606900070Natl Univ Singapore, NUSNNI, Singapore 117542, Singapore. Xie, XN, Natl Univ Singapore, NUSNNI, 2 Sci Dr 3, Singapore 117542, Singapore. nnixxn@nus.edu.sg phyweets@nus.edu.sg023116 Artn 023116internal-pdf://2006 AppPhysLtrs Chung Polymeric conical structure formation-3379791637/2006 AppPhysLtrs Chung Polymeric conical structure formation.pdf(1olymeric conical.pdf?|~?k%Delamarche, E. Juncker, D. Schmid, H.2005IMicrofluidics for processing surfaces and miniaturizing biological assays 2911-2933Advanced Materials1724LINKED-IMMUNOSORBENT-ASSAY; SELF-ASSEMBLED MONOLAYERS; TOTAL ANALYSIS SYSTEMS; ON-A-CHIP; CHEMICAL-ANALYSIS SYSTEM; DIP-PEN NANOLITHOGRAPHY; PROTEIN CRYSTAL-GROWTH; TUMOR-NECROSIS-FACTOR; DIRECTED LIQUID FLOW; LOW REYNOLDS-NUMBERSReviewDecThis review is an account of our efforts to develop a versatile and flexible microfluidic technology for surface-processing applications and miniaturizing biological assays The review is presented in the context of current trends in microfluidic technology and addresses some of the major challenges for confining chemical and biochemical processes on surfaces. the sealing of a microchannel with a surface, the world-to-chip interface, the displacement of liquids in small conduits, the sequential delivery of multiple solutions, the accurate patterning of surfaces, the coincident detection of various analytes, and the detection of analytes in a small and dilute sample. Our solutions to these problems include the use of reversible sealing, capillary phenomena for powering and controlling liquid transport, and non-contact microfluidics for spotting and drawing (on surfaces) with flow conditions These solutions offer many advantages over conventional techniques for handling minute amounts of liquids and may find applications in lithography, biopatterning (e.g., the patterning of biomolecules), diagnostics, drug discovery, and also cellular assays.://000234472400001 j7Times Cited: 6 Cited References: ABBOTT NL, 1995, LANGMUIR, V11, P16 ALI MF, 2003, ANAL CHEM, V75, P4732 ANDERSON JR, 2000, ANAL CHEM, V72, P3158 ANDERSSON H, 2001, ELECTROPHORESIS, V22, P249 ANGENENDT P, 2003, ANAL CHEM, V75, P4369 ATKINS PW, 1990, PHYS CHEM AUROUX PA, 2002, ANAL CHEM, V74, P2637 AYTUR T, 2002, SOL STAT SENS ACT MI BAIN CD, 1989, J AM CHEM SOC, V111, P321 BANCAUD A, 2005, ANAL CHEM, V77, P833 BARBIC M, 2001, APPL PHYS LETT, V79, P1399 BEEBE DJ, 2000, NATURE, V404, P588 BEH WS, 1999, ADV MATER, V11, P1038 BELAUBRE P, 2003, APPL PHYS LETT, V82, P3122 BENOIT V, 2001, ANAL CHEM, V73, P2412 BERLIER JE, 2003, J HISTOCHEM CYTOCHEM, V51, P1699 BERNARD A, 1998, LANGMUIR, V14, P2225 BERNARD A, 2000, ANAL CHEM, V72, P8 BERNARD A, 2001, NAT BIOTECHNOL, V19, P866 BIETSCH A, 2000, J APPL PHYS, V88, P4310 BIETSCH A, 2004, NANOTECHNOLOGY, V15, P873 BLANCHET GB, 2003, APPL PHYS LETT, V82, P463 BOUSSE L, 2001, ANAL CHEM, V73, P1207 BOUWMEESTER T, 2004, NAT CELL BIOL, V6, P97 BRODY JP, 1996, BIOPHYS J, V71, P3430 BROYLES BS, 2003, ANAL CHEM, V75, P2761 BRUCHEZ M, 1998, SCIENCE, V281, P2013 BRUCKBAUER A, 2002, J AM CHEM SOC, V124, P8810 BUECHLER KF, 1999, J CLIN LIGAND ASSAY, V22, P208 BURANDA T, 2002, ANAL CHEM, V74, P1149 BURNS JR, 2001, LAB CHIP, V1, P10 BURNS MA, 1998, SCIENCE, V282, P484 BURNS SE, 2003, MRS BULL, V11, P829 BUTLER JE, 1993, MOL IMMUNOL, V30, P1165 BUTLER JE, 1997, J MOL RECOGNIT, V10, P36 BUTLER JE, 1997, J MOL RECOGNIT, V10, P52 BUTLER JE, 2000, METHODS, V22, P4 CABRAL JT, 2004, LANGMUIR, V20, P10020 CAELEN I, 2000, LANGMUIR, V16, P9125 CESAROTADIC S, 2004, LAB CHIP, V4, P563 CHABINYC ML, 2001, ANAL CHEM, V73, P4491 CHABINYC ML, 2003, ADV MATER, V15, P1903 CHAUDHURY MK, 1992, SCIENCE, V255, P1230 CHEEK BJ, 2001, ANAL CHEM, V73, P5777 CHEN XX, 2002, ANAL CHEM, V74, P1772 CHIU DT, 1999, SCIENCE, V283, P1892 CHIU DT, 2000, P NATL ACAD SCI USA, V97, P2408 CHOI JW, 2002, LAB CHIP, V2, P27 CHRISTODOULIDES N, 2002, ANAL CHEM, V74, P3030 CLARK TJ, 2002, POINT CARE, V1, P42 CONWAY JG, 2001, J PHARMACOL EXP THER, V298, P900 CZAPLEWSKI DA, 2003, APPL PHYS LETT, V83, P4836 DARIO P, 2000, J MICROMECH MICROENG, V10, P235 DATWANI SS, 2004, LANGMUIR, V20, P4970 DEBELLEFON C, 2000, ANGEW CHEM INT EDIT, V39, P3442 DEGANS BJ, 2004, ADV MATER, V16, P203 DEGENNES PG, 2004, CAPILLARITY WETTING DELAMARCHE E, 1997, ADV MATER, V9, P741 DELAMARCHE E, 1997, SCIENCE, V276, P779 DELAMARCHE E, 1998, J AM CHEM SOC, V120, P500 DELAMARCHE E, 2001, ADV MATER, 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2003, CURR OPIN CHEM BIOL, V7, P55 ZIEZIULEWICZ TJ, 2003, TOXICOL SCI, V74, P235 ZIMMERMANN M, IN PRESS LAB CHIP ZIMMERMANN M, 2005, BIOMED MICRODEVICES, V7, P99ISI:000234472400001IBM Res GmbH, Zurich Res Lab, CH-8803 Ruschlikon, Switzerland. Delamarche, E, IBM Res GmbH, Zurich Res Lab, Saumerstr 4, CH-8803 Ruschlikon, Switzerland. emd@zurich.ibm.comfile://S:\SALES\_IMPORTANT_STUFF_HERE\Bibliography_Key_Papers\all publications DPN as of 101006 Copy.Data\PDF\2005 AdvMat Delamarche Microfluidics pr Processing Surfaces-0383756837\2005 AdvMat Delamarche Microfluidics pr Processing Surfaces.pdfK ~?l Stellacci, F.20062Towards industrial-scale molecular nanolithography15-16Advanced Functional Materials161ADIP-PEN NANOLITHOGRAPHY; DATA-STORAGE; LITHOGRAPHY; MILLIPEDE; NMEditorial MaterialJan://000234636600002 Times Cited: 0 Cited References: AUSTIN MD, 2004, APPL PHYS LETT, V84, P5299 BAILEY TC, 2002, J PHOTOPOLYM SCI TEC, V15, P481 ELEFTHERIOU E, 2003, IEEE T MAGN 1, V39, P938 GINGER DS, 2004, ANGEW CHEM INT EDIT, V43, P30 JANG JY, 2001, J CHEM PHYS, V115, P2721 KRAMER S, 2003, CHEM REV, V103, P4367 PINER RD, 1999, SCIENCE, V283, P661 SALAITA K, 2005, SMALL, V1, P940 SHEEHAN PE, 2004, APPL PHYS LETT, V85, P1589 VETTIGER P, 2002, IEEE T NANOTECHNOL, V1, P39ISI:000234636600002MIT, Dept Mat Sci & Engn, Cambridge, MA 02139 USA. Stellacci, F, MIT, Dept Mat Sci & Engn, Cambridge, MA 02139 USA. frstella@mit.eduinternal-pdf://2006 Adv Func Mat Stellacci Towards industrial-scale mol-0661960213/2006 Adv Func Mat Stellacci Towards industrial-scale molecular nanolithography.pdfXHMat Stellacci Towards industrial-scale molecular nanolithography.pdf F~?mWelle, A. M. Jacobs, H. O.2005qPrinting of organic and inorganic nanomaterials using electrospray ionization and Coulomb-force-directed assemblyApplied Physics Letters8726DIP-PEN NANOLITHOGRAPHY; PROTEIN MICROARRAYS; NANOXEROGRAPHY; NANOPARTICLES; FABRICATION; DEPOSITION; LIQUIDS; ARRAYS; CHARGE; SIZEArticleDecYThis letter reports on an additive printing process to deposit organic and inorganic nanomaterials onto desired areas on a surface. The process combines electrospray ionization with Coulomb-force-directed assembly. Electrospray ionization is used to bring the desired nanomaterial into the gas phase while carrier gas, global, and localized electric fields are used to deposit the material onto desired locations on a substrate. Albumin fluorescein isothiocyanate bovine, avidin sulforhodamine, and gold colloids were sprayed from an aqueous solution and patterned with a resolution as high as 100 nm.://000234338700091 dTimes Cited: 0 Cited References: BARRY CR, 2003, APPL PHYS LETT, V83, P5527 BARRY CR, 2003, NANOTECHNOLOGY, V14, P1057 BLANCHARD AP, 1996, BIOSENS BIOELECTRON, V11, P687 CLOUPEAU M, 1989, J ELECTROSTAT, V22, P135 CLOUPEAU M, 1994, J AEROSOL SCI, V25, P1021 FUERSTENAU SD, 2001, ANGEW CHEM INT EDIT, V40, P541 GANANCALVO AM, 1997, J AEROSOL SCI, V28, P249 JACOBS HO, 2001, SCIENCE, V291, P1763 JACOBS HO, 2002, ADV MATER, V14, P1553 KANE RS, 1999, BIOMATERIALS, V20, P2363 KWAK SK, 2004, MAT SCI ENG C-BIO S, V24, P151 LEE KB, 2002, SCIENCE, V295, P1702 LUEKING A, 1999, ANAL BIOCHEM, V270, P103 MAYER M, 2004, PROTEOMICS, V4, P2366 MOROZOV VN, 1999, ANAL CHEM, V71, P1415 MOROZOV VN, 1999, ANAL CHEM, V71, P3110 OUYANG Z, 2003, SCIENCE, V301, P1351 RODA A, 2000, BIOTECHNIQUES, V28, P492 SCHMALENBERG KE, 2004, BIOMATERIALS, V25, P1851 SHALON D, 1996, GENOME RES, V6, P639 WADUMESTHRIGE K, 2001, BIOPHYS J, V80, P1891 WIEDENSOHLER A, 1988, J AEROSOL SCI, V19, P387 ZELENY J, 1915, P CAMB PHILOS SOC, V18, P71ISI:000234338700091Univ Minnesota, Dept Elect & Comp Engn, Minneapolis, MN 55455 USA. Jacobs, HO, Univ Minnesota, Dept Elect & Comp Engn, 200 Union St SE, Minneapolis, MN 55455 USA. hjacobs@umn.edu263119 Artn 263119file://S:\SALES\_IMPORTANT_STUFF_HERE\Bibliography_Key_Papers\all publications DPN as of 101006 Copy.Data\PDF\2005 AppPhysLtrs Well-3125058821\2005 AppPhysLtrs Welle Printing of organic & inorganic.pdf~?n Antoncik, E.20051Dip-pen nanolithography: A simple diffusion model L369-L371Surface Science5991-3*surface diffusion; dip-pen nanolithographyArticleDecA simple calculation of the time dependence of the radial growth of the circles is performed within the framework of the moving boundary problem using the steady-state solution of the diffusion equation. (c) 2005 Elsevier B.V. All rights reserved.://000234132600001 Times Cited: 0 Cited References: CRANK J, 1975, MATH DIFFUSION, C13 JANG JY, 2001, J CHEM PHYS, V115, P2721 SHEEHAN PE, 2002, PHYS REV LETT, V88ISI:000234132600001Aarhus Univ, Inst Phys & Astron, DK-8000 Aarhus C, Denmark. Antoncik, E, Aarhus Univ, Inst Phys & Astron, Munkegade Bygn 520, DK-8000 Aarhus C, Denmark. isl49403@tiscali.dkfile://S:\SALES\_IMPORTANT_STUFF_HERE\Bibliography_Key_Papers\all publications DPN as of 101006 Copy.Data\PDF\2005 Surface Science Antoncik Dip-Pen Nanolithograpy.pdf O~?o*Vijaykumar, T. John, N. S. Kulkarni, G. U.2005FA resistless photolithography method for robust markers and electrodes 1475-1478Solid State Sciences712photoresist; lithography; electrode fabrication; markers; DPN METALLIC ELECTRODES; FABRICATION; CONDUCTANCE; JUNCTION; SEPARATION; TRANSPORT; MOLECULESArticleDecWe describe a method of resistless photolithography using laser for the fabrication of microscopic markers and electrodes. A single shot of laser (355 nm, 100 mJ) is used to induce local surface melting and thus transfer a pattern from the mask (TEM grid) on to the surface of silicon. With a silicon substrate pre-coated with a layer of phosphorus, the laser pulse selectively produces doped regions that are highly conducting. The electrodes and markers thus obtained are robust and can withstand harsh chemical treatments. The utility of the marker for dip-pen nanolithography is illustrated by performing gold colloid nanopatterning. (c) 2005 Elsevier SAS. All rights reserved.://000234148700005 Times Cited: 0 Cited References: BUMM LA, 1996, SCIENCE, V271, P1705 CHOU SY, 2002, NATURE, V417, P835 CHUNG SW, 2005, SMALL, V1, P1 CUI XD, 2001, SCIENCE, V294, P571 DONHAUSER ZJ, 2001, SCIENCE, V292, P2303 FISCHER PB, 1993, APPL PHYS LETT, V62, P2989 GINGER DS, 2004, ANGEW CHEM INT EDIT, V43, P30 GUILLORN MA, 2000, J VAC SCI TECHNOL B, V18, P1177 ITOUA S, 1994, NANOTECHNOLOGY, V5, P19 KERGUERIS C, 1999, PHYS REV B, V59, P12505 LI CZ, 1999, NANOTECHNOLOGY, V10, P221 LI CZ, 2000, APPL PHYS LETT, V77, P3995 LIU K, 2002, J MICHL APPL PHYS LE, V80, P5 MITAAN MM, 2001, APPL PHYS LETT, V78, P18 MITAN M, 6750124, US MORPURGO AF, 1999, APPL PHYS LETT, V74, P2084 PAL S, 2005, PHYS REV B, V71 PARK H, 1999, APPL PHYS LETT, V75, P301 PARTHASARATHY R, 2004, PHYS REV LETT, V92 REED MA, 1997, SCIENCE, V278, P252 REICHERT J, 2002, PHYS REV LETT, V88 SALOMON A, 2003, ADV MATER, V15, P1881 STEPHEN BC, 2002, NANOTECHNOLOGY, V13, P653ISI:000234148700005Jawaharlal Nehru Ctr Adv Sci Res, Chem & Phys Mat Unit, Bangalore 560064, Karnataka, India. Kulkarni, GU, Jawaharlal Nehru Ctr Adv Sci Res, Chem & Phys Mat Unit, Jakkur PO, Bangalore 560064, Karnataka, India. kulkarni@jncasr.ac.in file://S:\SALES\_IMPORTANT_STUFF_HERE\Bibliography_Key_Papers\all publications DPN as of 101006 Copy.Data\PDF\2005 Solid States Sciences Vijaykumar Resistless Photolighography Me-2465432156\2005 Solid States Sciences Vijaykumar Resistless Photolighography Method.pdf~?p8Chang, N. A. Richardson, J. J. Clem, P. G. Hsu, J. W. P.2006ZAdditive Patterning of conductors and superconductors by solution stamping nanolithography75-79Small21copper; oxides; printing; soft lithography; superconductors DIP-PEN NANOLITHOGRAPHY; THIN-FILMS; CAPILLARIES; FABRICATION; DEPOSITION; LAYERSArticleJan://000234205600011 >Times Cited: 0 Cited References: AMEMIYA N, 2004, SUPERCOND SCI TECH, V17, P1464 CLEM PG, 1997, J AM CERAM SOC, V80, P2821 FELMET K, 2004, APPL PHYS LETT, V85, P3316 FU L, 2003, NANO LETT, V3, P757 JEON NL, 1995, J MATER RES, V10, P2996 JEON NL, 1997, ADV MATER, V9, P891 KIM E, 1996, J AM CHEM SOC, V118, P5722 KIM JH, 1999, J MATER RES, V14, P1194 KITTEL C, 1996, INTRO SOLID STATE PH, P160 LANGE FF, 1996, SCIENCE, V273, P903 MARTIN CR, 2003, J PHYS CHEM B, V107, P4261 ODOM TW, 2002, LANGMUIR, V18, P5314 SCHWARTZ RW, 1997, CHEM MATER, V9, P2325 SHETH A, 1998, APPL SUPERCOND, V6, P855 SIEGAL MP, 2003, PHYSICA C, V399, P143 SU M, 2002, J AM CHEM SOC, V124, P1560 ZHANG HL, 2004, NANO LETT, V4, P1513 ZHAO XM, 1996, ADV MATER, V8, P837ISI:000234205600011Sandia Natl Labs, Albuquerque, NM 87185 USA. Hsu, JWP, Sandia Natl Labs, POB 5800,MS-1415, Albuquerque, NM 87185 USA. jwhsu@sandia.govginternal-pdf://2006_Small_Additive Patterning_Chang-2138643477/2006_Small_Additive Patterning_Chang.pdf  tterning.pdf ~?q'Garcia, R. Martinez, R. V. Martinez, J.20063Nano-chemistry and scanning probe nanolithographies29-38Chemical Society Reviews351ATOMIC-FORCE MICROSCOPE; DIP-PEN NANOLITHOGRAPHY; LOCAL OXIDATION NANOLITHOGRAPHY; SELF-ASSEMBLED MONOLAYERS; HYDROGEN-PASSIVATED SILICON; AFM FABRICATION; LITHOGRAPHY; SURFACE; NANOSTRUCTURES; PATTERNSReview~The development of nanometer-scale lithographies is the focus of an intense research activity because progress on nanotechnology depends on the capability to fabricate, position and interconnect nanometer-scale structures. The unique imaging and manipulation properties of atomic force microscopes have prompted the emergence of several scanning probe-based nanolithographies. In this tutorial review we present the most promising probe-based nanolithographies that are based on the spatial confinement of a chemical reaction within a nanometer-size region of the sample surface. The potential of local chemical nanolithography in nanometer-scale science and technology is illustrated by describing a range of applications such as the fabrication of conjugated molecular wires, optical microlenses, complex quantum devices or tailored chemical surfaces for controlling biorecognition processes.://000234096200003 o Times Cited: 2 Cited References: AVOURIS P, 1997, APPL PHYS LETT, V71, P287 BINNIG G, 1999, REV MOD PHYS, V71, P324 CAVALLINI M, 2003, APPL PHYS LETT, V83, P5286 CAVALLINI M, 2003, SCIENCE, V299, P531 CHEN CF, 2005, OPT LETT, V30, P652 CHIEN FSS, 1999, APPL PHYS LETT, V75, P2429 CLEMENT N, 2002, PHYSICA E, V13, P999 COOPER EB, 1999, APPL PHYS LETT, V75, P3566 DAGATA JA, 1990, APPL PHYS LETT, V56, P2001 DAGATA JA, 2004, J APPL PHYS, V96, P2386 DAY HC, 1993, APPL PHYS LETT, V62, P2691 FARKAS N, 2004, APPL PHYS LETT, V85, P5691 FRESCO ZM, 2004, J AM CHEM SOC, V126, P8374 FUHRER A, 2001, NATURE, V413, P822 FUIERER RR, 2002, ADV MATER, V14, P154 GARCIA R, 1999, J APPL PHYS, V86, P1898 GARCIA R, 2004, NANO LETT, V4, P1115 GARNO JC, 2003, NANO LETT, V3, P389 GEISSLER M, 2004, ADV MATER, V16, P1249 GINGER DS, 2004, ANGEW CHEM INT EDIT, V43, P30 JASCHKE M, 1995, LANGMUIR, V11, P1061 KINSER CR, 2005, NANO LETT, V5, P91 KURAMOCHI H, 2004, APPL PHYS LETT, V84, P4005 LEE W, 2002, LANGMUIR, V18, P8375 LI Y, 2001, J AM CHEM SOC, V123, P2105 LIU JF, 2004, APPL PHYS LETT, V84, P1359 LIU ST, 2004, NANO LETT, V4, P845 MAOZ R, 2000, ADV MATER, V12, P725 MARTINEZ RV, 2005, NANO LETT, V5, P1161 MATSUMOTO K, 2000, APPL PHYS LETT, V76, P239 MCKENDRY R, 2002, NANO LETTERS, V2, P713 MORI G, 2005, J APPL PHYS, V97 NYFFENEGGER RM, 1997, CHEM REV, V97, P1195 PINER RD, 1999, SCIENCE, V283, P661 QUATE CF, 1997, SURF SCI, V386, P259 SAMORI P, 2005, CHEM SOC REV, V34, P551 SHEEHAN PE, 2002, PHYS REV LETT, V88 SNOW ES, 1995, SCIENCE, V270, P1639 SNOW ES, 1998, APPL PHYS LETT, V72, P3071 SU M, 2002, APPL PHYS LETT, V80, P4434 SUEZ I, 2005, NANO LETT, V5, P321 SUGIMOTO Y, 2005, NAT MATER, V4, P156 SUGIMURA H, 2002, ADV MATER, V14, P524 TELLO M, 2001, APPL PHYS LETT, V79, P424 TELLO M, 2002, J APPL PHYS, V92, P4075 TELLO M, 2005, ADV MATER, V17, P1480 TORRES CMS, 2003, ALTERNATIVE LITHOGRA VILLARROYA M, 2004, NANOTECHNOLOGY, V15, P771 WACASER BA, 2003, APPL PHYS LETT, V82, P808 WOUTERS D, 2004, ANGEW CHEM INT EDIT, V43, P2480 XU S, 1997, LANGMUIR, V13, P127 YEUNG KL, 2004, J NANOSCI NANOTECHNO, V4, P1 YOSHINOBU T, 2003, ELECTROCHIM ACTA, V48, P3131ISI:000234096200003CSIC, Inst Microelect Madrid, Madrid 28760, Spain. Garcia, R, CSIC, Inst Microelect Madrid, Isaac Newton 8, Madrid 28760, Spain. rgarcia@imm.cnm.csic.eskinternal-pdf://2006_ChemSoc Rev_Nano-chemistry_Garcia-3447832341/2006_ChemSoc Rev_Nano-chemistry_Garcia.pdftHaemistry & scanning probe-0454540075\2006 ChemSocRev Garcia Nono-chemistry & scanning probe.pdf3~?r Dufva, M.2005'Fabrication of high quality microarrays173-184Biomolecular Engineering225-6.DNA microarrays; fabrication; immobilisation chemistry; optimisation LINKED-IMMUNOSORBENT-ASSAY; GENE-EXPRESSION PATTERNS; DIP-PEN NANOLITHOGRAPHY; DNA MICROARRAYS; HIGH-DENSITY; COVALENT ATTACHMENT; CDNA MICROARRAYS; OLIGONUCLEOTIDE MICROARRAYS; PROTEIN NANOARRAYS; OLIGODEOXYRIBONUCLEOTIDE MICROCHIPSReviewDecFabrication of DNA microarray demands that between ten (diagnostic microarrays) and many hundred thousands of probes (research or screening microarrays) are efficiently immobilised to a glass or plastic surface using a suitable chemistry. DNA microarray performance is measured by parameters like array geometry, spot density, spot characteristics (morphology, probe density and hybridised density), background, specificity and sensitivity. At least 13 factors affect these parameters and factors affecting fabrication of microarrays are used in this review to compare different fabrication methods (spotted microarrays and in situ synthesis of microarrays) and immobilisation chemistries. (C) 2005 Elsevier B.V. All rights reserved.://000234042200002 iTimes Cited: 3 Cited References: AFANASSIEV V, 2000, NUCLEIC ACIDS RES, V28, E66 ALEXANDRE I, 2001, ANAL BIOCHEM, V295, P1 ALIZADEH AA, 2000, NATURE, V403, P503 ARMSTRONG B, 2000, CYTOMETRY, V40, P102 BAO YP, 2005, NUCLEIC ACIDS RES, V33 BEIER M, 1999, NUCLEIC ACIDS RES, V27, P1970 BELLEVILLE E, 2004, J IMMUNOL METHODS, V286, P219 BENTERS R, 2002, NUCLEIC ACIDS RES, V30 CALL DR, 2001, BIOTECHNIQUES, V30, P368 CALL DR, 2001, BIOTECHNIQUES, V30, P374 CALL DR, 2001, BIOTECHNIQUES, V30, P376 CHEE M, 1996, SCIENCE, V274, P610 CHEEK BJ, 2001, ANAL CHEM, V73, P5777 CHEN JJW, 1998, GENOMICS, V51, P313 CHIU SK, 2003, BIOCHEM J, V374, P625 CHRISEY LA, 1996, NUCLEIC ACIDS RES, V24, P3031 CHU S, 1998, SCIENCE, V282, P699 CSAKI A, 2001, NUCLEIC ACIDS RES, V29 DEEGAN RD, 1997, NATURE, V389, P827 DERISI J, 1996, NAT GENET, V14, P457 DHANASEKARAN SM, 2001, NATURE, V412, P822 DIEHL F, 2001, NUCLEIC ACIDS RES, V29, E38 DOLAN PL, 2001, NUCLEIC ACIDS RES, V29 DUFVA M, 2004, BIOTECHNIQUES, V37, P286 DUFVA M, 2005, EXPERT REV PROTEOMIC, V2, P41 EDMAN CF, 1997, NUCLEIC ACIDS RES, V25, P4907 EKINS R, 1990, ANN BIOL CLIN-PARIS, V48, P655 EPSTEIN JR, 2002, ANAL CHEM, V74, P1836 EPSTEIN JR, 2003, BIOSENS BIOELECTRON, V18, P541 FERGUSON JA, 2000, ANAL CHEM, V72, P5618 FIXE F, 2004, LAB CHIP, V4, P191 FIXE F, 2004, NUCLEIC ACIDS RES, V32 FODOR SPA, 1991, SCIENCE, V251, P767 FOTIN AV, 1998, NUCLEIC ACIDS RES, V26, P1515 GEORGIADIS R, 2000, J AM CHEM SOC, V122, P3166 GUNDERSON KL, 2004, GENOME RES, V14, P870 GUNDERSON KL, 2005, NAT GENET, V37, P549 GUTMANN O, 2004, ANALYST, V129, P835 HAAB BB, 2001, GENOME BIOL, V2 HAN A, 2003, LAB CHIP, V3, P336 HAN MY, 2001, NAT BIOTECHNOL, V19, P631 HELLER MJ, 2000, ELECTROPHORESIS, V21, P157 HENRY AC, 2000, ANAL CHEM, V72, P5331 HESSNER MJ, 2003, NUCLEIC ACIDS RES, V31 HESSNER MJ, 2003, NUCLEIC ACIDS RES, V31 HONG BJ, 2005, NUCLEIC ACIDS RES, V33 HORVATH SJ, 1987, METHOD ENZYMOL, V154, P314 HUBER M, 2004, NUCLEIC ACIDS RES, V32 HUNKAPILLER M, 1984, NATURE, V310, P105 JOOS TO, 2000, ELECTROPHORESIS, V21, P2641 KHAN J, 1998, CANCER RES, V58, P5009 KHRAPKO KR, 1991, DNA SEQUENCE, V1, P375 KUMAR A, 2000, NUCLEIC ACIDS RES, V28, E71 LAUSTED C, 2004, GENOME BIOL, V5 LEBERRE V, 2003, NUCLEIC ACIDS RES, V31 LEE KB, 2002, SCIENCE, V295, P1702 LEVITBINNUN N, 2003, ANAL CHEM, V75, P1436 LINDROOS K, 2001, NUCLEIC ACIDS RES, V29, E69 LIU RH, 2003, ANAL CHEM, V75, P1911 LYNCH M, 2004, PROTEOMICS, V4, P1695 MARIE R, IN PRESS BIOSENSORS MASKOS U, 1992, NUCLEIC ACIDS RES, V20, P1675 MASKOS U, 1992, NUCLEIC ACIDS RES, V20, P1679 MENDOZA LG, 1999, BIOTECHNIQUES, V27, P778 MOORCROFT MJ, 2005, NUCLEIC ACIDS RES, V33 NAM JM, 2004, ANGEW CHEM INT EDIT, V43, P1246 NUWAYSIR EF, 2002, GENOME RES, V12, P1749 OKAMOTO T, 2000, NAT BIOTECHNOL, V18, P438 POLLACK JR, 1999, NAT GENET, V23, P41 PREININGER C, 2004, ANAL BIOCHEM, V330, P29 PROUDNIKOV D, 1998, ANAL BIOCHEM, V259, P34 REHMAN FN, 1999, NUCLEIC ACIDS RES, V27, P649 REN B, 2000, SCIENCE, V290, P2306 RICKMAN DS, 2003, NUCLEIC ACIDS RES, V31 ROGERS YH, 1999, ANAL BIOCHEM, V266, P23 SABANAYAGAM CR, 2000, NUCLEIC ACIDS RES, V28, E33 SCHENA M, 1995, SCIENCE, V270, P467 SCHENA M, 1996, P NATL ACAD SCI USA, V93, P10614 SHALON D, 1996, GENOME RES, V6, P639 SHCHEPINOV MS, 1997, NUCLEIC ACIDS RES, V25, P1155 SINGHGASSON S, 1999, NAT BIOTECHNOL, V17, P974 SOSNOWSKI RG, 1997, P NATL ACAD SCI USA, V94, P1119 STEEL AB, 1998, ANAL CHEM, V70, P4670 STEEL AB, 2000, BIOPHYS J, V79, P975 STILLMAN BA, 2000, BIOTECHNIQUES, V29, P630 STRIZHKOV BN, 2000, BIOTECHNIQUES, V29, P844 STRIZHKOV BN, 2000, BIOTECHNIQUES, V29, P850 STRIZHKOV BN, 2000, BIOTECHNIQUES, V29, P854 STROTHER T, 2000, J AM CHEM SOC, V122, P1205 STROTHER T, 2000, NUCLEIC ACIDS RES, V28, P3535 TATON TA, 2000, SCIENCE, V289, P1757 VAIDYA AA, 2004, LANGMUIR, V20, P11100 VAINRUB A, 2002, PHYS REV E 1, V66 VAINRUB A, 2003, BIOPOLYMERS, V68, P265 VASILISKOV VA, 2001, NUCLEIC ACIDS RES, V29, P2303 WADDELL E, 2000, ANAL CHEM, V72, P5907 WANG H, 2002, NUCLEIC ACIDS RES, V30 WROBEL G, 2003, NUCLEIC ACIDS RES, V31 YUEN PK, 2003, LAB CHIP, V3, P46 ZAMMATTEO N, 2000, ANAL BIOCHEM, V280, P143 ZHU H, 2001, SCIENCE, V293, P2101 ZIAUDDIN J, 2001, NATURE, V411, P107ISI:000234042200002Tech Univ Denmark, Microarray Technol Grp, Dept Micro & Nanotechnol, DK-2800 Kongens Lyngby, Denmark. Dufva, M, Tech Univ Denmark, Microarray Technol Grp, Dept Micro & Nanotechnol, Oersteds Plads,Bld 345 E, DK-2800 Kongens Lyngby, Denmark. mdu@m~?sTang, Q. Shi, S. Q. Zhou, L. M.20056Effect of surface roughness on dip-pen nanolithography 2167-2171)Journal of Nanoscience and Nanotechnology512dip-pen nanolithography; effect of surface roughness; poly(vinylidene fluoride-trifluorethylene); 1-octadecanethiol MICROSCOPY; FORCEArticleDecIn the present work, five gold thin films with various surface roughnesses were prepared by sputtering and the influence of the surface roughness of gold substrate on dip-pen nanolithography (DPN) was studied using 1-octadecanethiol (ODT) and poly(vinylidene fluoride-trifluorethylene) [P(VDF-TrFE)] as inks. It was shown that surface roughness influences both the contrast in lateral force microscopy (LFM) images and the transport rate of ink. Surfaces with less roughness give good contrast in LFM images, while rough surfaces give poor contrast. The transport rate of ink increases as the roughness decreases; however, the extent of the influence is strongly ink-dependent.://000233914500030 @Times Cited: 0 Cited References: BUNE AV, 1998, NATURE, V391, P874 DAIKHIN L, 1994, PHYS REV E, V49, P1424 GINGER DS, 2004, ANGEW CHEM INT EDIT, V43, P30 HALLMARK VM, 1987, PHYS REV LETT, V59, P2879 HSU T, 1983, ULTRAMICROSCOPY, V11, P239 KASUPKE N, 1980, SURF SCI, V92, P407 NUZZO RG, 1983, J AM CHEM SOC, V105, P4481 PINER RD, 1999, SCIENCE, V283, P661 ROSS CB, 1993, LANGMUIR, V9, P632 SHEEHAN PE, 2002, PHYS REV LETT, V88 TANG Q, 2004, J NANOSCI NANOTECHNO, V4, P948 TANG Q, 2004, SUPERLATTICE MICROST, V36, P21ISI:000233914500030Hong Kong Polytech Univ, Dept Mech Engn, Kowloon, Hong Kong, Peoples R China. Shi, SQ, Hong Kong Polytech Univ, Dept Mech Engn, Kowloon, Hong Kong, Peoples R China.)~?tIYu, A. A. Savas, T. Cabrini, S. diFabrizio, E. Smith, H. I. Stellacci, F.2005rHigh resolution printing of DNA feature on poly(methyl methacrylate) substrates using supramolecular nano-stamping 16774-16775(Journal of the American Chemical Society12748MDIP-PEN NANOLITHOGRAPHY; MOLECULAR PRINTBOARDS; LITHOGRAPHY; PROTEINS; METALSArticleDec://000233759200013 vTimes Cited: 5 Cited References: AULETTA T, 2004, ANGEW CHEM INT EDIT, V43, P369 BERNARD A, 2001, NAT BIOTECHNOL, V19, P866 BRUININK CM, 2005, CHEM-EUR J, V11, P3988 CASE MA, 2003, NANO LETT, V3, P425 CHOU SY, 1996, J VAC SCI TECHNOL B, V14, P4129 CUI Y, 2001, SCIENCE, V293, P1289 DEMERS LM, 2002, SCIENCE, V296, P1836 FIXE F, 2004, NUCLEIC ACIDS RES, P32 LIN HH, 2005, J AM CHEM SOC, V127, P11210 LOVE JC, 2005, CHEM REV, V105, P1103 RENAULT JP, 2002, ANGEW CHEM INT EDIT, V41, P2320 XIA YN, 1998, ANGEW CHEM INT EDIT, V37, P551 YU AA, 2005, NANO LETT, V5, P1061ISI:000233759200013MIT, Ctr Mat Sci & Engn, Cambridge, MA 02139 USA. MIT, Elect Res Lab, Cambridge, MA 02139 USA. Lab TASC Statale 14, I-34012 Trieste, Italy. Univ Magna Graecia, Bionem Lab, I-88100 Catanzaro, Italy. Stellacci, F, MIT, Ctr Mat Sci & Engn, Cambridge, MA 02139 USA. frstella@mit.edufile://S:\SALES\_IMPORTANT_STUFF_HERE\Bibliography_Key_Papers\all publications DPN as of 101006 Copy.Data\PDF\2005 JACS Yu High Resolution Printing of DNA Feature-0389500766\2005 JACS Yu High Resolution Printing of DNA Feature.pdf ~?u*Hampton, J. R. Dameron, A. A. Weiss, P. S.2005DTransport rates vary with deposition time in dip-pen nanolithography 23118-23120Journal of Physical Chemistry B10949>FORCE MICROSCOPE; NANOSTRUCTURES; FABRICATION; NANOARRAYS; TIPLetterDecJBy patterning with dip-pen nanolithography using tip dwell times ranging from 15 s to 2 h over a period of 19 h, we show that the transport rate for smaller patterns is different than for larger ones. This transport behavior is found for both I-octadecanethiol (ODT) and 16-mercaptohexadecanoic acid (MHDA) inks on gold substrates. Additionally, MHDA shows an overall decrease in transport rate as a function of total writing time during such experiments. These results indicate that measurements with short dwell times are insufficient to determine transport rates for larger features.://000233864300003 Times Cited: 1 Cited References: *NANOINK, COMMUNICATION CHEUNG CL, 2003, J AM CHEM SOC, V125, P6848 GINGER DS, 2004, ANGEW CHEM INT EDIT, V43, P30 JANG JY, 2001, J CHEM PHYS, V115, P2721 JASCHKE M, 1995, LANGMUIR, V11, P1061 LEE KB, 2002, SCIENCE, V295, P1702 MANANDHAR P, 2003, PHYS REV LETT, V90 PETERSON EJ, 2004, J PHYS CHEM B, V108, P15206 PINER RD, 1999, SCIENCE, V283, P661 ROZHOK S, 2003, J PHYS CHEM B, V107, P751 SCHWARTZ PV, 2002, LANGMUIR, V18, P4041 SHEEHAN PE, 2002, PHYS REV LETT, V88 SMITH JC, 2003, NANO LETT, V3, P883 WEEKS BL, 2002, PHYS REV LETT, V88 WEINBERGER DA, 2000, ADV MATER, V12, P1600 ZHANG H, 2003, NANO LETT, V3, P43 ZHANG H, 2003, NANOTECHNOLOGY, V14, P1113ISI:000233864300003Penn State Univ, Dept Chem, University Pk, PA 16802 USA. Penn State Univ, Dept Phys, University Pk, PA 16802 USA. Weiss, PS, Penn State Univ, Dept Chem, University Pk, PA 16802 USA. stm@psu.edufile://S:\SALES\_IMPORTANT_STUFF_HERE\Bibliography_Key_Papers\all publications DPN as of 101006 Copy.Data\PDF\2005 JPC Hampton Transport Rates Vary w disposition.pdf$w ~?v,He, L. Z. Dexter, A. F. Middelberg, A. P. J.2006&Biomolecular engineering at interfaces989-1003Chemical Engineering Science613$biomolecule; protein; interface; analysis; self-assembly; processing DIP-PEN NANOLITHOGRAPHY; SELF-ASSEMBLED MONOLAYERS; SUM-FREQUENCY GENERATION; LANGMUIR-BLODGETT-FILMS; BY-LAYER CONSTRUCTION; CELL-ADHESION; SINGLE-MOLECULE; THIN-FILMS; HEXADECANE/WATER INTERFACE; FLUORESCENCE SPECTROSCOPYReviewFebQA broad review of technologically focused work concerning biomolecules at interfaces is presented. The emphasis is on developments in interfacial biomolecular engineering that may have a practical impact in bioanalysis, tissue engineering, emulsion processing or bioseparations. We also review methods for fabrication in an attempt to draw out those approaches that may be useful for product manufacture, and briefly review methods for analysing the resulting interfacial nanostructures. From this review we conclude that the generation of knowledge and-innovation at the nanoscale far exceeds our ability to translate this innovation into practical outcomes addressing a market need, and that significant technological challenges exist. A particular challenge in this translation is to understand how the structural properties of biomolecules control the assembled architecture, which in turn defines product performance, and how this relationship is affected by the chosen manufacturing route. This "structure-architecture-process-performance (SAPP)" interaction problem is the familiar laboratory scale-up challenge in disguise. A further challenge will be to interpret biomolecular self- and directed-assembly reactions using tools of chemical reaction engineering, enabling rigorous manufacturing optimization of self-assembly laboratory techniques. We conclude that many of the technological problems facing this field are addressable using tools of modem chemical and biomolecular engineering, in conjunction with knowledge and skills from the underpinning sciences. (c) 2005 Elsevier Ltd. All rights reserved.://000233814600009 Times Cited: 4 Cited References: ABAD LW, 2002, ANAL BIOCHEM, V310, P107 ANZAI J, 1998, ANAL CHEM, V70, P811 ANZAI J, 1999, LANGMUIR, V15, P221 AOTA S, 1994, J BIOL CHEM, V269, P24756 ARNOLD M, 2004, CHEMPHYSCHEM, V5, P383 BALABUSHEVITCH NG, 2001, BIOTECHNOL BIOENG, V76, P207 BARRAUD A, 1985, THIN SOLID FILMS, V134, P195 BAYLEY H, 2001, NATURE, V413, P226 BECK JS, 1992, J AM CHEM SOC, V114, P10834 BERNARD A, 1998, LANGMUIR, V14, P2225 BLODGETT KB, 1935, J AM CHEM SOC, V57, P1007 BLODGETT KB, 1937, PHYS REV, V51, P964 BLODGETT KB, 1939, PHYS REV, V55, P391 BOS MA, 2001, ADV COLLOID INTERFAC, V91, P437 BRAHA O, 1997, CHEM BIOL, V4, P497 BRUCHEZ M, 1998, SCIENCE, V281, P2013 CANNIZZARO SM, 1998, BIOTECHNOL BIOENG, V58, P529 CARUSO F, 1998, SCIENCE, V282, P1111 CARUSO F, 2000, LANGMUIR, V16, P1485 CASCAOPEREIRA LG, 2003, LANGMUIR, V19, P2349 CASTNER DG, 2002, SURF SCI, V500, P28 CHAN WCW, 1998, SCIENCE, V281, P2016 CHEN DH, 2004, PROCESS BIOCHEM, V39, 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NISTOR C, 2002, ANALYST, V127, P1076 OGAWA T, 1996, AM LAB, V28, P171 PARKINSON EL, 2004, COLLOID SURFACE B, V39, P23 PETKOV JT, 2000, LANGMUIR, V16, P3703 PETRALLIMALLOW T, 1993, J PHYS CHEM-US, V97, P1383 PIERSCHBACHER MD, 1984, NATURE, V309, P30 PINER RD, 1999, SCIENCE, V283, P661 REYES CD, 2003, J BIOMED MATER RES A, V65, P511 RICH RL, 2003, J MOL RECOGNIT, V16, P351 ROBERTS C, 1998, J AM CHEM SOC, V120, P1648 ROCO MC, 2001, SOCIAL IMPLICATIONS RONCO C, 2002, KIDNEY INT S80, V61, S126 ROWLEY JA, 1999, BIOMATERIALS, V20, P45 RUOSLAHTI E, 1987, SCIENCE, V238, P491 SACKMANN E, 1996, SCIENCE, V271, P43 SACKMANN E, 2000, TRENDS BIOTECHNOL, V18, P58 SARIKAYA M, 2004, ANNU REV MATER RES, V34, P373 SATRIANO C, 2003, MAT SCI ENG C-BIO S, V23, P779 SCHENA M, 1995, SCIENCE, V270, P467 SCHMIDT A, 1992, BIOPHYS J, V63, P1385 SCHWARZ A, 1998, LANGMUIR, V14, P5526 SINGHGASSON S, 1999, NAT BIOTECHNOL, V17, P974 STEVENS MM, 2004, LANGMUIR, V20, P7747 SUN Y, 1998, BIOTECHNOL BIOENG, V58, P58 SWALEN JD, 1987, LANGMUIR, V3, P932 TALHAM DR, 2004, CHEM REV, V104, P5479 TAMERLER C, 2003, PROG ORG COAT, V47, P267 TASHIRO K, 1989, J BIOL CHEM, V264, P16174 TCHOLAKOVA S, 2003, LANGMUIR, V19, P5640 TCHOLAKOVA S, 2004, LANGMUIR, V20, P7444 THESS A, 2002, J BIOL CHEM, V277, P36321 THOMPSON NL, 1993, EUR BIOPHYS J BIOPHY, V22, P367 TIRRELL M, 2003, UNSOLVED PORBLEMS NA, P63 UETZ P, 2000, NATURE, V403, P623 VACASSY R, 1997, SEP PURIF TECHNOL, V12, P243 WANG J, 1996, ANAL CHEM, V68, P2629 WANG J, 2003, J AM CHEM SOC, V125, P9914 WANG J, 2004, J PHYS CHEM B, V108, P3625 WATANABE T, 1999, ANAL CHIM ACTA, V386, P69 WEISENHORN AL, 1992, ULTRAMICROSCOPY, V42, P1125 WEISS S, 2000, NAT STRUCT BIOL, V7, P724 WHITESIDES GM, 2002, SCIENCE, V295, P2418 WILLIAMS A, 1997, COLLOID SURFACE A, V125, P189 WILLIAMS CT, 2002, SURF SCI, V500, P545 XU GF, 2001, P NATL ACAD SCI USA, V98, P3652 YAN L, 1998, J AM CHEM SOC, V120, P6179 YE SX, 2003, LANGMUIR, V19, P1515 YE SX, 2004, LANGMUIR, V20, P5897 YOON JJ, 2004, BIOMATERIALS, V25, P5613 ZHANG X, 2004, J NANOPART RES, V6, P125 ZHANG ZP, 2005, BIOMATERIALS, V26, P47 ZHUANG XW, 2000, SCIENCE, V288, P2048 ZHUANG XW, 2003, CURR OPIN STRUC BIOL, V13, P88ISI:000233814600009Univ Queensland, Sch Engn, Ctr Biomol Engn, St Lucia, Qld 4072, Australia. Middelberg, APJ, Univ Queensland, Sch Engn, Ctr Biomol Engn, St Lucia, Qld 4072, Australia. a.middelberg@uq.edu.ausinternal-pdf://2006 CES He Biomolecular Eng at Interfaces-2877724437/2006 CES He Biomolecular Eng at Interfaces.pdfT ^aces-2284932410\2006 CES He Biomolecular Eng at Interfaces.pdf.~?w#Chen, J. M. Liao, S. W. Tsai, Y. C.2005hElectrochemical synthesis of polypyrrole within PMMA nanochannels produced by AFM mechanical lithography11-17Synthetic Metals1551conducting polymers; polypyrrole; nanowires; electropolymerization; AFM lithography ATOMIC-FORCE-MICROSCOPE; DIP-PEN NANOLITHOGRAPHY; SCANNING-TUNNELING-MICROSCOPY; CONDUCTING POLYMERS; MICROELECTRONIC DEVICES; AQUEOUS-SOLUTIONS; C-60 MOLECULES; FABRICATION; NANOSTRUCTURES; NANOWIRESArticleOct'A novel approach for the fabrication of polypyrrole nanowires via electropolymerization within poly(methyl methacrylate) (PMMA) nanochannels on an indium tin oxide (ITO) substrate is reported. The nanochannels width and depth obtained by atomic force microscopy (AFM) mechanical lithography on PMMA coated ITO substrate are about 150 and 35 nm. The nanochannels act as templates for electropolymerization of polypyrrole nanowires. The morphology of PMMA nanochannels and polypyrrole nanowires were investigated by AFM. The polypyrrole nanowires are around 350 nm in width and 20 mu m in length. The conducting properties of polypyrrole nanowires were identified by AFM with a conducting tip (CT-AFM). The AFM current image shows that the current difference can be distinguished between doped polypyrrole nanowires and PMMA thin film. The present methodology demonstrates the feasibility and effectiveness of electropolymerization of polypyrrole nanowires within PMMA nanochannels produced by AFM mechanical lithography. (C) 2005 Elsevier B.V. All rights reserved.://000233652300002 H Times Cited: 0 Cited References: ANDRIEUX CP, 1991, J PHYS CHEM-US, V95, P10158 ASAVAPIRIYANONT S, 1984, J ELECTROANAL CH INF, V177, P229 BAUR C, 1998, NANOTECHNOLOGY, V9, P360 BEH WS, 1999, ADV MATER, V11, P1038 BETON PH, 1995, APPL PHYS LETT, V67, P1075 BINNIG G, 1982, PHYS REV LETT, V49, P57 BINNIG G, 1986, PHYS REV LETT, V56, P930 BOUCHIAT V, 1996, APPL PHYS LETT, V69, P3098 CAMPBELL PM, 1995, APPL PHYS LETT, V66, P1388 CUBERES MT, 1996, APPL PHYS LETT, V69, P3016 DAI HJ, 1998, APPL PHYS LETT, V73, P1508 DELEEUW DM, 1997, SYNTHETIC MET, V87, P53 FONTAINE PA, 1998, J APPL PHYS, V84, P1776 FORZANI ES, 2004, NANO LETT, V4, P1785 HONG SH, 1999, SCIENCE, V286, P523 HSU JH, 2004, J VAC SCI TECHNOL B, V22, P2768 HU S, 1998, J VAC SCI TECHNOL B, V16, P1983 HU S, 1998, J VAC SCI TECHNOL B, V16, P2822 JAHROMI S, 2002, CHEMPHYSCHEM, V8, P693 JANG SY, 2004, J AM CHEM SOC, V126, P9476 JEROME C, 1998, ANGEW CHEM INT EDIT, V37, P2488 JEROME C, 2004, SYNTHETIC MET, V142, P207 JOO J, 2003, SYNTHETIC MET 1, V135, P7 KLEHN B, 1999, J APPL PHYS, V85, P3897 KUNZE U, 1999, ADV MATER, V11, P1473 LEE KB, 2002, SCIENCE, V295, P1702 LI Y, 2001, J AM CHEM SOC, V123, P2105 LIVACHE T, 1998, CLIN CHIM ACTA, V278, P171 MAGNO R, 1997, APPL PHYS LETT, V70, P1855 MAMIN HJ, 1992, APPL PHYS LETT, V61, P1003 MAMIN HJ, 1996, APPL PHYS LETT, V69, P433 MARTIN CR, 1996, CHEM MATER, V8, P1739 MAYNOR BW, 2002, J AM CHEM SOC, V124, P522 PARK JW, 2001, SYNTHETIC MET, V117, P119 PARK SW, 1995, APPL PHYS LETT, V67, P2415 PINER RD, 1999, SCIENCE, V283, P661 RAJESH SS, 2004, J APPL POLYM SCI, V93, P927 ROCCO AM, 1996, ELECTROCHIM ACTA, V41, P2805 SHIN MC, 1996, BIOSENS BIOELECTRON, V11, P161 SHIRAKAWA H, 1977, J CHEM SOC CHEM COMM, P579 SINGH S, 2004, ANAL CHIM ACTA, V502, P144 SNOW ES, 1994, APPL PHYS LETT, V64, P1932 SOH HT, 2001, SCANNING PROBE LITHO SOHN LL, 1995, APPL PHYS LETT, V67, P1552 SOMANI P, 2000, ACTA MATER, V48, P2859 TSAU LM, 1994, APPL PHYS LETT, V64, P2133 TULLY DC, 1999, ADV MATER, V11, P314 UANG YM, 2003, BIOSENS BIOELECTRON, V19, P141 WILDER K, 1998, APPL PHYS LETT, V73, P2527 ZENG K, 2000, ANAL CHEM, V72, P2211ISI:000233652300002Natl Chung Hsing Univ, Dept Chem Engn, Taichung 402, Taiwan. Tsai, YC, Natl Chung Hsing Univ, Dept Chem Engn, Taichung 402, Taiwan. yctsai@dragon.nchu.edu.twfile://S:\SALES\_IMPORTANT_STUFF_HERE\Bibliography_Key_Papers\all publications DPN as of 101006 Copy.Data\PDF\2005 Syn Metals Chen Electrochem syn polypyrrole PMMA-1635152165\2005 Syn Metals Chen Electrochem syn polypyrrole PMMA.pdf~?x,Ding, L. Li, Y. Chu, H. B. Li, X. M. Liu, J.2005LCreation of cadmium sulfide nanostructures using AFM dip-pen nanolithography 22337-22340Journal of Physical Chemistry B10947SCANNING TUNNELING MICROSCOPE; SELF-ASSEMBLED MONOLAYERS; NANOMETER-SCALE; PROBE LITHOGRAPHY; FORCE MICROSCOPE; FILM DEPOSITION; SURFACE; ARRAYS; INK; ADSORPTIONArticleDec#A dip-pen nanolithography (DPN) process capable of depositing nanoscaled structures of semiconducting US materials was developed by careful control of the reaction speed between the precursors. The new development expanded the scope of the powerful DPN process and provided more insight in the deposition mechanism. Features ranging from several hundreds of nanometers to sub-50 nanometers were generated and characterized. The effects of the surface property of the substrate, the relative humidity, the translating rate, and the temperature were systematically investigated. X-ray photoelectron spectroscopy (XPS) was used to verify the chemical composition of the patterns. In principle, this simple and convenient method should be applicable to deposit various metal sulfides on suitable substrates.://000233684500038 Times Cited: 0 Cited References: BERGMAN AA, 1998, LANGMUIR, V14, P6785 BULLEN D, 2004, APPL PHYS LETT, V84, P789 BUTLER EA, 1958, ANAL CHEM, V30, P1379 CHOU SY, 2001, MRS BULL, V26, P512 CHRISEY LA, 1996, NUCLEIC ACIDS RES, V24, P3031 CROMMIE MF, 1993, SCIENCE, V262, P218 DEMERS LM, 2002, SCIENCE, V296, P1836 DREXLER KE, 1986, ENGINES CREATION COM DUAN X, 2003, MOL NANOELECTRONICS, P199 DUCKER WA, 1999, LANGMUIR, V15, P160 EIGLER DM, 1990, NATURE, V344, P524 FALVO MR, 1999, NATURE, V397, P236 GINGER DS, 2004, ANGEW CHEM INT EDIT, V43, P30 GUNDIAH G, 2004, APPL PHYS LETT, V84, P5341 HANG SH, 2000, SCIENCE, V288, P1808 HONG SH, 1999, SCIENCE, V286, P523 IM HJ, 2000, MACROMOLECULES, V33, P9606 IVANISEVIC A, 2001, J AM CHEM SOC, V123, P7887 JASCHKE M, 1995, LANGMUIR, V11, P1061 KRAMER S, 2003, CHEM REV, V103, P4367 LEE KB, 2002, SCIENCE, V295, P1702 LI Y, 1999, CHEM MATER, V11, P3433 LI Y, 2001, J AM CHEM SOC, V123, P2105 LIM JH, 2002, ADV MATER, V14, P1474 LIU GY, 2000, ACCOUNTS CHEM RES, V33, P457 LU JH, 2004, J AM CHEM SOC, V126, P11136 MAOZ R, 2000, ADV MATER, V12, P424 MAYNOR BW, 2001, LANGMUIR, V17, P2575 MAYNOR BW, 2002, J AM CHEM SOC, V124, P522 MCKENDRY R, 2002, NANO LETTERS, V2, P713 MO YW, 1993, SCIENCE, V261, P886 MORIGUCHI I, 1999, CHEM MATER, V11, P1603 NICOLAU DV, 1998, LANGMUIR, V14, P1927 NYFFENEGGER RM, 1997, CHEM REV, V97, P1195 PETERSON EJ, 2004, J PHYS CHEM B, V108, P15206 PINER RD, 1999, SCIENCE, V283, P661 PORTER LA, 2002, NANO LETT, V2, P1369 QUATE CF, 1997, SURF SCI, V386, P259 ROZHOK S, 2003, J PHYS CHEM B, V107, P751 SCHWARTZ PV, 2002, LANGMUIR, V18, P4041 SHEEHAN PE, 2002, PHYS REV LETT, V88 SHEEHAN PE, 2004, APPL PHYS LETT, V85, P1589 SU M, 2002, J AM CHEM SOC, V124, P1560 THOMAS PJ, 2004, J MATER CHEM, V14, P625 WALLRAFF GM, 1999, CHEM REV, V99, P1801 WEEKS BL, 2002, J PHYS REV LETT, V88 WILSON DL, 2001, P NATL ACAD SCI USA, V98, P13660 XIA Y, 1998, ANGEW CHEM INT EDIT, V37, P550 YAMAGUCHI K, 1998, J PHYS CHEM B, V102, P9677 ZHANG H, 2003, NANOTECHNOLOGY, V14, P1113ISI:000233684500038 Peking Univ, Coll Chem & Mol Engn, Key Lab Phys & Chem Nanodevices, Beijing 100871, Peoples R China. Duke Univ, Dept Chem, Durham, NC 27708 USA. Li, Y, Peking Univ, Coll Chem & Mol Engn, Key Lab Phys & Chem Nanodevices, Beijing 100871, Peoples R China. yanli@pku.edu.cn jliu@chem.duke.edu4059397478Inserts.pptfile://S:\SALES\_IMPORTANT_STUFF_HERE\Bibliography_Key_Papers\all publications DPN as of 101006 Copy.Data\PDF\2005 JPC Ding Cadmium sulfide Nanostructures-1505322026\2005 JPC Ding Cadmium sulfide Nanostructures.pdf~?y0Choi, H. J. Kim, N. H. Chung, B. H. Seong, G. H.2005wMicropatterning of biomolecules on glass surfaces modified with various functional groups using photoactivatable biotin60-66Analytical Biochemistry3471photobiotin; photoactivation; micropatterning; immobilization; DNA hybridization DIP-PEN NANOLITHOGRAPHY; MICROFLUIDIC CHANNELS; IMMOBILIZATION; CHEMISTRY; MECHANISM; PROTEINSArticleDecBiomolecule patterning by photolithographic methods has considerable advantages because a large number of different biomolecules can be assembled on a spatial area by a combinatorial method and complex biomolecule patterning can be created in situ in closed environments such as microfluidic channels. Here, a photobiotin was used as the photoactivatable reagent to create patterned arrays of biomolecules. The variability of photobiotin deposition on glass substrates modified with a variety of materials having carboxyl, lysine, aldehyde, amine groups, and BSA (bovine serum albumin) was characterized by subsequent derivatization with Cy3-labeled streptavidin. The fluorescence images of the photobiotin patterned glass surfaces showed that the BSA/aldehyde-coated glass could be considered as the most appropriate substrate to immobilize photobiotin, in view of the homogeneous immobilization of biomolecules with high density in defined regions and the reduction of nonspecific binding to the surface. In streptavidin equilibrium adsorption assays, the maximum amount of streptavidin-Cy3 bound to the BSA/aldehyde-coated glass surface continued to rise with increasing streptavidin-Cy3 concentration until 12.0 mu g/mL was reached and the surface then became saturated. Also, a line array of biotin-labeled single-strand probe DNAs was created on the BSA/aldehyde-coated glass by photolysis of photobiotin through a slit-type mask and biotin/streptavidin/biotin chemistry, extended to a quantitative measurement of the concentrations of target DNA. The results of target DNA analysis showed linearity over a wide range from 0.5 ng/mL to 5 mu g/mL and were reproducible. (c) 2005 Elsevier Inc. All rights reserved.://000233698400008 nTimes Cited: 0 Cited References: AGARWAL G, 2003, J AM CHEM SOC, V125, P7408 BERNARD A, 2001, ANAL CHEM, V73, P8 BROOKS SA, 1999, ANAL CHEM, V71, P2558 BROOKS SA, 2000, ANAL CHEM, V72, P3253 BRUCKBAUER A, 2004, J AM CHEM SOC, V126, P6508 CHEN CS, 1997, SCIENCE, V276, P1425 DEMERS LM, 2002, SCIENCE, V296, P1836 DONTHA N, 1997, ANAL CHEM, V69, P2619 FLEMING SA, 1995, TETRAHEDRON, V51, P12479 FODOR SPA, 1991, SCIENCE, V251, P767 HENGSAKUL M, 1996, BIOCONJUGATE CHEM, V7, P249 HOLDEN MA, 2004, ANAL CHEM, V76, P1838 IDDON B, 1979, ANGEW CHEM, V18, P900 KIM EE, 1991, J MOL BIOL, V218, P449 MICHEL R, 2002, LANGMUIR, V18, P3281 PRITCHARD DJ, 1995, ANAL CHEM, V67, P3605 SEONG GH, 2002, ANAL CHEM, V74, P3372 SEONG GH, 2002, J AM CHEM SOC, V124, P13360 SU XD, 2002, BIOCHEM BIOPH RES CO, V290, P962 WHITESIDES GM, 2001, ANNU REV BIOMED ENG, V3, P335 WILCHEK M, 1990, METHOD ENZYMOL, V184, P5 WILDE LM, 2001, ANALYST, V126, P195 WILLNER I, 2000, ANGEW CHEM INT EDIT, V39, P1180 YE T, 2005, J PHYS CHEM B, V109, P9927ISI:000233698400008Korea Res Inst Biosci & Biotechnol, Bionanotechnol Res Ctr, Taejon 305600, South Korea. Hanyang Univ, Dept Appl Chem, Ansan 425791, South Korea. Chung, BH, Korea Res Inst Biosci & Biotechnol, Bionanotechnol Res Ctr, Taejon 305600, South Korea. chungbh@kribb.re.kr ghseong@hanyang.ac.krfile://S:\SALES\_IMPORTANT_STUFF_HERE\Bibliography_Key_Papers\all publications DPN as of 101006 Copy.Data\PDF\2005 AnalBiochem Choi Micropatterning of biomolecules-3366562341\2005 AnalBiochem Choi Micropatterning of biomolecules.pdf~?z2Lee, S. W. Sanedrin, R. G. Oh, B. K. Mirkin, C. A.2005kNanostructured polyelectrolyte multilayer organic thin films generated via parallel dip-pen nanolithography2749-+Advanced Materials1722SELF-ASSEMBLED MONOLAYERS; LAYER POLYMER-FILMS; SELECTIVE DEPOSITION; NANOPARTICLE PROBES; GOLD NANOPARTICLES; CHARGED SURFACES; ARRAYS; ADSORPTION; TEMPLATES; DNAArticleNovPolyelectrolyte multilayer (PEM) organic thin films with diameters ranging from 80 to 200 nm can be generated from dip-pen nanolithography (DPN) fabricated templates. Through the use of multi-pen AFM cantilever probes, parallel fabrication of PEM features with nanoscale resolution can be achieved. This demonstrates the versatility of the parallel DPN approach and its applicability to building nano-/microscale structures in conjunction with a layer-by-layer method.://000233651600021 D Times Cited: 2 Cited References: BARBUCCI R, 2003, J MATER SCI-MATER M, V14, P721 BOGUNIAKUBIK K, 2002, BIOSYSTEMS, V65, P123 BULLEN D, 2004, APPL PHYS LETT, V84, P789 CAO YW, 2001, J AM CHEM SOC, V123, P7961 CHEUNG CL, 2003, J AM CHEM SOC, V125, P6848 CHOU SY, 2001, MRS BULL, V26, P512 CLARK SL, 1997, MACROMOLECULES, V30, P7237 CLARK SL, 1998, ADV MATER, V10, P1515 CLARK SL, 1999, ADV MATER, V11, P1031 CUTLER CA, 2002, ADV MATER, V14, P684 DECHER G, 1991, MAKROMOL CHEM-M SYMP, V46, P321 DECHER G, 1997, SCIENCE, V277, P1332 DELONGCHAMP DM, 2003, CHEM MATER, V15, P1165 DELONGCHAMP DM, 2003, CHEM MATER, V15, P1575 DEMERS LM, 2002, SCIENCE, V296, P1836 ELGHANIAN R, 1997, SCIENCE, V277, P1078 GINGER DS, 2004, ANGEW CHEM INT EDIT, V43, P30 GROSDEMANGE CP, 1991, J AM CHEM SOC, V113, P12 HAMMOND PT, 1995, MACROMOLECULES, V28, P7569 HAMMOND PT, 1999, CURR OPIN COLLOID IN, V4, P430 HAMMOND PT, 2004, ADV MATER, V16, P1271 HONG SH, 1999, SCIENCE, V286, P523 HONG SH, 2000, SCIENCE, V288, P1808 HUCK WTS, 1999, LANGMUIR, V15, P6862 ICHINOSE I, 1996, CHEM LETT, P257 JIANG XP, 2000, LANGMUIR, V16, P8501 JIANG XP, 2001, ADV MATER, V13, P1669 JIN RC, 2001, SCIENCE, V294, P1901 KHOPADE AJ, 2002, BIOMACROMOLECULES, V3, P1154 KIDAMBI S, 2004, J AM CHEM SOC, V126, P16286 KIDAMBI S, 2004, J AM CHEM SOC, V126, P4697 KUMAR A, 1994, SCIENCE, V263, P60 LEE KB, 2002, SCIENCE, V295, P1702 LI LS, 2002, CHEM MATER, V14, P1159 LI XM, 2003, J AM CHEM SOC, V125, P4279 LIM JH, 2002, ADV MATER, V14, P1474 LIM JH, 2003, ANGEW CHEM INT EDIT, V42, P2309 LIU GY, 2000, ACCOUNTS CHEM RES, V33, P457 LIU XG, 2005, SCIENCE, V307, P1763 LVOV Y, 1995, J CHEM SOC CHEM COMM, P2313 MAYNOR BW, 2002, J AM CHEM SOC, V124, P522 MENDELSOHN JD, 2003, BIOMACROMOLECULES, V4, P96 MULLER WT, 1995, SCIENCE, V268, P272 NYAMJAV D, 2004, CHEM MATER, V16, P5216 PARK J, 2004, ADV MATER, V16, P520 PARK SJ, 2002, SCIENCE, V295, P1503 PINER RD, 1999, SCIENCE, V283, P661 PRIME KL, 1993, J AM CHEM SOC, V115, P10714 SALAITA K, 2005, SMALL, V1, P940 SCHLENOFF JB, 1998, ADV MATER, V10, P347 SERVICE RF, 2002, SCIENCE, V298, P2322 SMITH JC, 2003, NANO LETT, V3, P883 SU M, 2002, J AM CHEM SOC, V124, P1560 TATON TA, 2000, SCIENCE, V289, P1757 WALLRAFF GM, 1999, CHEM REV, V99, P1801 WILSON DL, 2001, P NATL ACAD SCI USA, V98, P13660 XIA Y, 1998, ANGEW CHEM INT EDIT, V37, P550 XIA YN, 1999, CHEM REV, V99, P1823 YU M, 2005, J MATER CHEM, V15, P649 ZHANG H, 2002, ADV MATER, V14, P1472 ZHANG M, 2002, NANOTECHNOLOGY, V13, P212 ZHU HG, 2003, BIOMACROMOLECULES, V4, P378 ZOU J, 2003, APPL PHYS LETT, V83, P581ISI:000233651600021Northwestern Univ, Dept Chem, Evanston, IL 60208 USA. Northwestern Univ, Inst Nanotechnol, Evanston, IL 60208 USA. Mirkin, CA, Northwestern Univ, Dept Chem, 2145 Sheridan Rd, Evanston, IL 60208 USA. chadnano@northwestern.edufile://S:\SALES\_IMPORTANT_STUFF_HERE\Bibliography_Key_Papers\all publications DPN as of 101006 Copy.Data\PDF\2005 AdvMat Lee Nanostructured Polyelectrolyte Films via Parallet DPN-1009907780\2005 AdvMat Lee Nanostructured Polyelectrolyte Films via Parallet DPN.pdf ~?{!Li, B. Zhang, Y. Hu, J. Li, M. Q.2005VFabricating protein nanopatterns on a single DNA molecule with Dip-pen nanolithography312-315Ultramicroscopy1051-4atomic force microscopy (AFM); Dip-pen nanolithography (DPN); single DNA molecules; protein nanoarray ATOMIC-FORCE MICROSCOPY; MANIPULATION; NANOMANIPULATION; AFMArticleNov^Positioning proteins onto single DNA molecules is of great importance for basic research in biology as well as direct applications in nanotechnology. Herein, the generality of an atomic force microscopy (AFM)-based Dip-pen nanolithography (DPN) approach is explored and extended to fabricate protein nanopatterns along a single DNA molecule. Important procedures are presented, including a modified molecular combing method for DNA stretching and DPN for depositing protein "ink". This approach is able to check resulting pattern by AFM at real time and in situ. (c) 2005 Elsevier B.V. All rights reserved.://000233317300044 Times Cited: 0 Cited References: BENNINK ML, 1999, CYTOMETRY, V36, P200 BENSIMON A, 1994, SCIENCE, V265, P2096 FOTIADIS D, 2002, MICRON, V33, P385 FUJIHIRA M, 1976, CHEM LETT, P875 HU J, 2002, NANO LETTERS, V2, P55 HURLEY PT, 2003, J AM CHEM SOC, V125, P7408 HYUN J, 2004, J AM CHEM SOC, V126, P4770 JUNG H, 2003, J AM CHEM SOC, V125, P12096 KOJIMA H, 1994, P NATL ACAD SCI USA, V91, P12962 LI B, 1999, NUCL SCI TECH, V10, P134 LI B, 2003, CHINESE SCI BULL, V48, P673 LIPHARDT J, 2001, SCIENCE, V292, P733 LYUBCHENKO Y, 1993, P NATL ACAD SCI USA, V90, P2137 OESTERHELT F, 2000, SCIENCE, V288, P143 PINER RD, 1999, SCIENCE, V283, P661 SEVERIN M, 2004, NANO LETT, V4, P577 SHLYAKHTENKO LS, 2000, NUCLEIC ACIDS RES, V28, P3472 SU M, 2002, APPL PHYS LETT, V80, P4434 TAKEDA S, 2003, NANO LETT, V3, P1471 THALHAMMER S, 1997, J STRUCT BIOL, V119, P232 ZHANG Y, 2000, PROBE MICROSC, V2, P31ISI:000233317300044Chinese Acad Sci, Shanghai Inst Appl Phys, Shanghai 201800, Peoples R China. Shanghai Jiao Tong Univ, Bio X Sci Res Ctr, Shanghai 200030, Peoples R China. Li, MQ, Chinese Acad Sci, Shanghai Inst Appl Phys, Shanghai 201800, Peoples R China. junhu22@hotmail.com liminqian@hotmail.com2649990246Inserts.pptfile://S:\SALES\_IMPORTANT_STUFF_HERE\Bibliography_Key_Papers\all publications DPN as of 101006 Copy.Data\PDF\2005 Ultramicroscopy Li Positioning Protein onto single DNA molecules.pdf K~?|6Binder, W. H. Kluger, C. Straif, C. J. Friedbacher, G.2005RDirected nanoparticle binding onto microphase-separated block copolymer thin films 9405-9410Macromolecules3823MULTIVALENT SUPRAMOLECULAR INTERACTIONS; DIP-PEN NANOLITHOGRAPHY; MONODISPERSE NANOCRYSTALS; MOLECULAR PRINTBOARDS; ORGANIZATION; ASSEMBLIES; TEMPLATESArticleNov://000233225600003 yTimes Cited: 3 Cited References: AULETTA T, 2004, ANGEW CHEM INT EDIT, V43, P369 BARON R, 2005, ANGEW CHEM INT EDIT, V44, P4010 BHAT RR, 2003, NANOTECHNOLOGY, V14, P1145 BINDER HW, IN PRESS CURR ORG CH BINDER WH, 2004, MACROMOLECULES, P9321 BINDER WH, 2005, ANGEW CHEM INT EDIT, P5172 BOAL AK, 2000, NATURE, V404, P746 BOAL AK, 2004, CHEM MATER, V16, P3252 BOCKSTALLER MR, 2005, ADV MATER, V17, P1331 CHIU JJ, 2005, J AM CHEM SOC, V127, P5036 CHUNG SW, 2005, SMALL, V1, P64 CRESPOBIEL O, 2005, J AM CHEM SOC, V127, P7594 DEMERS LM, 2002, SCIENCE, V296, P1836 KOLB HC, 2001, ANGEW CHEM INT EDIT, V40, P2004 KWART H, 1952, J AM CHEM SOC, V74, P3094 LIN Y, 2005, NATURE, V434, P55 MAHALINGAM V, 2004, LANGMUIR, V20, P11756 MAURY P, 2005, ADV FUNCT MATER, V15, P451 MINELLI C, 2004, COLLOID POLYM SCI, V282, P1274 MINELLI C, 2005, LANGMUIR, V21, P7080 MISNER MJ, 2003, ADV MATER, V15, P221 MURRAY CB, 2000, ANNU REV MATER SCI, V30, P545 ROGACH AL, 2002, ADV FUNCT MATER, V12, P653 SHENHAR R, IN PRESS ADV MAT SOHN BH, 2003, J AM CHEM SOC, V125, P6368 STORHOFFF JJ, 2002, LANGMUIR, V18, P6666 THOMPSON RB, 2001, SCIENCE, V292, P2469 YEH SW, 2004, MACROMOL RAPID COMM, V25, P1679 YEH SW, 2005, MACROMOLECULES, V38, P6559 ZIRBS R, 2005, LANGMUIR, V21, P8414ISI:0002332256000033Vienna Tech Univ, Inst Appl Synthet Chem, Div Macromol Chem, A-1060 Vienna, Austria. Vienna Tech Univ, Inst Chem Technol & Analyt, A-1060 Vienna, Austria. Binder, WH, Vienna Tech Univ, Inst Appl Synthet Chem, Div Macromol Chem, Getreidemarkt 9-163-MC, A-1060 Vienna, Austria. wbinder@mail.zserv.tuwien.ac.atfile://S:\SALES\_IMPORTANT_STUFF_HERE\Bibliography_Key_Papers\all publications DPN as of 101006 Copy.Data\PDF\2005 Macromolecules Binder Directed Nanoparticle Binding-0374608738\2005 Macromolecules Binder Directed Nanoparticle Binding.pdf ~?}+Su, M. Pan, Z. X. Dravid, V. P. Thundat, T.2005ELocally enhanced relative humidity for scanning probe nanolithography 10902-10906Langmuir2124DIP-PEN NANOLITHOGRAPHY; SELF-ASSEMBLED MONOLAYERS; FORCE MICROSCOPY; NANOMETER-SCALE; AIR; LITHOGRAPHY; INK; NANOSTRUCTURES; SURFACES; METALSArticleNovThe formation of a water meniscus between a sharp tip and a solid surface is one of the prevailing requirements for scanning probe microscope (SPM)-based lithographies, such as dip-pen nanolithography (DPN) and conductive tip induced oxidation. The water meniscus functions as a medium for the oxidation of or mass transfer to the solid surface. Here we report a simple, efficient, and effective approach to enhance the local relative humidity and thus increase the size of the water meniscus by bringing a water-containing capillary tube to the proximity of the tip-surface contact area. The enhancement in local relative humidity is confirmed via an increase in the measured tip-surface adhesion forces and the widths of DPN generated parallel lines. Compared to the global control of relative humidity for the whole lithography system, the short distance between the "water reservoir" and the tip-surface contact area enables rapid increase in the local vapor pressure of water, less perturbation, and minimal erosion to the state-of-the-art electronics. As a result, most scanning probe lithography experiments at high relative humidity can now be performed in a reasonable time frame.://000233371200002 kTimes Cited: 0 Cited References: DEMERS LM, 2002, SCIENCE, V296, P1836 FRISBIE CD, 1994, SCIENCE, V265, P2071 GINGER DS, 2004, ANGEW CHEM INT EDIT, V43, P30 GRIGG DA, 1992, J VAC SCI TECHNOL A, V10, P680 ISRAELACHVILI JN, 1992, INTERMOLECULAR SURFA IVANISEVIC A, 2002, J AM CHEM SOC, V124, P11997 KRAMER S, 2003, CHEM REV, V103, P4367 LIU GY, 2000, ACCOUNTS CHEM RES, V33, P457 MAOZ R, 2000, ADV MATER, V12, P424 MAYNOR BW, 2001, LANGMUIR, V17, P2575 NOY A, 2002, NANO LETTERS, V2, P109 NYFFENEGGER RM, 1997, CHEM REV, V97, P1195 PARKER AR, 2001, NATURE, V414, P33 PINER RD, 1997, LANGMUIR, V13, P6864 PINER RD, 1999, SCIENCE, V283, P661 ROZHOK S, 2003, J PHYS CHEM B, V107, P751 SHEEHAN PE, 2004, APPL PHYS LETT, V85, P1589 SU M, 2002, APPL PHYS LETT, V80, P4434 THUNDAT T, 1993, SURF SCI LETT, V294, L939 WANG R, 1997, NATURE, V388, P431 WEINBERGER DA, 2000, ADV MATER, V12, P1600 WILDER K, 1997, J VAC SCI TECHNOL B, V15, P1811 XU L, 1998, SURF SCI, V407, P251 ZAMBORINI FP, 1998, J AM CHEM SOC, V120, P9700ISI:000233371200002 Oak Ridge Natl Lab, Div Life Sci, Oak Ridge, TN 37831 USA. Northwestern Univ, Dept Mat Sci & Engn, Evanston, IL 60208 USA. Northwestern Univ, Int Inst Nanotechnol, Evanston, IL 60208 USA. Su, M, Oak Ridge Natl Lab, Div Life Sci, Oak Ridge, TN 37831 USA. sum1@ornl.govfile://S:\SALES\_IMPORTANT_STUFF_HERE\Bibliography_Key_Papers\all publications DPN as of 101006 Copy.Data\PDF\2005 Langmuir Su Locally enhanced relative humidity-4110272846\2005 Langmuir Su Locally enhanced relative humidity.pdfi~?~FRodolfa, K. T. Bruckbauer, A. Zhou, D. J. Korchev, Y. E. Klenerman, D.2005RTwo-component graded deposition of biomolecules with a double-barreled nanopipette 6854-6859'Angewandte Chemie-International Edition4442DNA; nanotechnology; nanowriting; proteins; scanning probe microscopy DIP-PEN NANOLITHOGRAPHY; SCANNING ION-CONDUCTANCE; PROTEIN NANOSTRUCTURES; DNA; IMMOBILIZATION; MICROSCOPY; DELIVERY; SURFACESArticle://000233142900007 xTimes Cited: 2 Cited References: 2004, WORLD PRECISION INST, V98 AGARWAL G, 2003, J AM CHEM SOC, V125, P580 AGARWAL G, 2003, J AM CHEM SOC, V125, P7408 BRUCKBAUER A, 2002, J AM CHEM SOC, V124, P8810 BRUCKBAUER A, 2003, J AM CHEM SOC, V125, P9834 DEMERS LM, 2001, ANGEW CHEM INT EDIT, V40, P3071 DEMERS LM, 2001, ANGEW CHEM, V113, P3161 GINGER DS, 2004, ANGEW CHEM INT EDIT, V43, P30 HANSMA PK, 1989, SCIENCE, V243, P641 HONG SH, 1999, SCIENCE, V286, P523 HONG SH, 2000, SCIENCE, V288, P1808 JIANG XY, 2005, ANAL CHEM, V77, P2338 KIM KH, 2005, SMALL, V1, P632 KORCHEV YE, 1997, BIOPHYS J, V73, P653 LEE KB, 2003, J AM CHEM SOC, V125, P5588 LOCKHART DJ, 2000, NATURE, V405, P827 MACBEATH G, 2000, SCIENCE, V289, P1760 PINER RD, 1999, SCIENCE, V283, P661 SEEMAN NC, 2003, NATURE, V421, P427 SHEVCHUK AI, 2001, BIOPHYS J, V81, P1759 TAHA H, 2003, APPL PHYS LETT, V83, P1041 WILSON DS, 2003, ANGEW CHEM, V115, P510 YING LM, 2002, ANAL CHEM, V74, P1380 ZHOU D, 2003, NANO LETT, V3, P1517 ZHOU DJ, 2003, LANGMUIR, V19, P10557ISI:000233142900007Univ Cambridge, Dept Chem, Cambridge CB2 1EW, England. Univ London Imperial Coll Sci & Technol, Div Med, London W12 0NN, England. Klenerman, D, Univ Cambridge, Dept Chem, Lensfield Rd, Cambridge CB2 1EW, England. dk10012@cam.ac.uk file://S:\SALES\_IMPORTANT_STUFF_HERE\Bibliography_Key_Papers\all publications DPN as of 101006 Copy.Data\PDF\2005 AngeChemie Rodolfa Two Component Graded Deposition of Biomolecul-0795522893\2005 AngeChemie Rodolfa Two Component Graded Deposition of Biomolecules.pdf TF~?0Banerjee, D. Amro, N. A. Disawal, S. Fragala, J.2005@Optimizing microfluidic ink delivery for dip pen nanolithography=Journal of Microlithography Microfabrication and Microsystems42dip pen nanolithography (DPN); deep reactive ion etching (DRIE); reactive ion etching (RIE); volume-of-fluids (VOF) method; microfluidics; lab-on-a-chip; capillary flow; scanning probe lithographyArticleApr-JunIn Dip Pen Nanolithography (TM) (DPN (TM)) ultrasharp tips coated with chemical compounds (or "ink") are in contact with a surface to produce submicron sized features. There is a need to deliver multiple inks to an array of closely spaced tips (or "pens"). This work demonstrates the design optimization, fabrication process development, process optimization, and testing of a microfluidic ink delivery apparatus (called "inkwells") for simultaneously coating an array of DPN pens with single or multiple inks. The objective of this work is to deliver between four and ten different inks from reservoirs into an appropriately spaced microwell array. The tips of the multipen array are coated with the same or different inks by dipping them into the microwell array. The reservoirs, microwells, and their connecting microchannels were etched in silicon wafers using deep reactive ion etching. Fluid actuation was achieved by capillary flow (wicking). The optimum layouts for different applications were selected with respect to the volume requirement of different inks, the efficacy of ink-well filling, prevention of bubble formation, and the ease of operation (such as dipping and writing) with a parallel array of pens. (c) 2005 Society of Photo-Optical Instrumentation Engineers.://000232841900015 Times Cited: 0 Cited References: BARONE AD, 2001, NUCLEOS NUCLEOT NUCL, V20, P525 DEMERS LM, 2002, SCIENCE, V296, P1836 MILLS AF, 1995, HEAT MASS TRANSFER PINER RD, 1999, SCIENCE, V283, P661 WHITE FM, 1994, FLUID MECHISI:000232841900015NanoInk Inc, Microfabricat Grp, Campbell, CA 95008 USA. NanoInk Inc, Corp Off, Chicago, IL 60607 USA. Banerjee, D, Texas A&M Univ, Dept Mech Engn, College Stn, TX 77843 USA.023014 Artn 023014file://S:\SALES\_IMPORTANT_STUFF_HERE\Bibliography_Key_Papers\all publications DPN as of 101006 Copy.Data\PDF\2005 JoMicrolith,fab,Sys Banerjee Optimizing microfluidic ink.pdf ~?Wang, X. F. Liu, C.2005;Multifunctional probe array for nano patterning and imaging 1867-1872 Nano Letters510>DIP-PEN NANOLITHOGRAPHY; SOFT LITHOGRAPHY; MICROSCOPE; INK; AUArticleOctThis letter reports the design, fabrication, and testing of a multifunctional scanning probe array for nanoscale imaging and patterning. The probe array consists of multiple cantilever probes, with each probe being able to perform a dedicated function such as scanning probe lithography (e.g., dip pen nanolithography and scanning probe contact printing) or scanning probe microscopy (e.g., atomic force microscopy and lateral force microscopy). The bending states of each probe can be controlled by using an integrated thermal electric actuator so that it is possible to engage any individual probe(s) independently for writing or imaging purposes. The multifunctional probe array is therefore capable of performing a rich variety of operations with minimal chemical crosstalk and high registration accuracy. It will eliminate the need for probe chip exchanges and increase the operational efficiency. The probe tips in a given array may be made of different materials. Further, the tip and cantilever may be made of different materials for a given probe. In this work, we focus on the development of a probe array consisting of dip pen nanolithography probes, scanning probe contact printing probes (of various tip sizes), and scanning probe microscopy probes.://000232623700002 Times Cited: 1 Cited References: BULLEN D, 2004, J MICROELECTROMECH S, V13, P594 EIGLER DM, 1990, NATURE, V344, P524 GARDENIERS JGE, 1998, J APPL PHYS, V83, P7844 GINGER DS, 2004, ANGEW CHEM INT EDIT, V43, P30 HONG SH, 1999, SCIENCE, V286, P523 KOVACS GTA, 1998, MICROMACHINED TRANSD KRAMER S, 2003, CHEM REV, V103, P4367 LI Y, 2001, J AM CHEM SOC, V123, P2105 MAYNOR BW, 2001, LANGMUIR, V17, P2575 NYFFENEGGER RM, 1997, CHEM REV, V97, P1195 PINER RD, 1999, SCIENCE, V283, P661 QUATE CF, 1997, SURF SCI, V386, P259 RYU KS, 2004, J MICROELECTROMECH S, V13, P568 SCHOER JK, 1996, J PHYS CHEM-US, V100, P11086 WANG XF, 2003, LANGMUIR, V19, P8951 WANG XF, 2004, J VAC SCI TECHNOL B, V22, P2563 WEGSCHEIDER S, 1995, THIN SOLID FILMS, V264, P264 WHITESIDES GM, 2001, ANNU REV BIOMED ENG, V3, P335 XIA YN, 1998, ANNU REV MATER SCI, V28, P153 ZHANG H, 2004, NANO LETT, V4, P1649 ZOU J, 2004, J MICROMECH MICROENG, V14, P204ISI:000232623700002Univ Illinois, Micro & Nanotechnol Lab, Urbana, IL 61801 USA. Liu, C, Univ Illinois, Micro & Nanotechnol Lab, 208 N Wright St, Urbana, IL 61801 USA. changliu@uiuc.edufile://S:\SALES\_IMPORTANT_STUFF_HERE\Bibliography_Key_Papers\all publications DPN as of 101006 Copy.Data\PDF\2005 Nano Letters Wang Multifunctional Probe Array for Nano-3418162525\2005 Nano Letters Wang Multifunctional Probe Array for Nano.pdf [~?!Barry, C. R. Gu, J. Jacobs, H. O.2005hCharging process and coulomb-force-directed printing of nanoparticles with sub-100-nm lateral resolution 2078-2084 Nano Letters510DIP-PEN NANOLITHOGRAPHY; GAS-PHASE; ARRAYS; SCALE; NANOXEROGRAPHY; MANIPULATION; NANOFABRICATION; PARTICLES; SURFACES; CONTRASTArticleOctsThis article reports on a new charging process and Coulomb-force-directed assembly of nanoparticles onto charged surface areas with sub-100-nm resolution. The charging is accomplished using a flexible nanostructured thin silicon electrode. Electrical nanocontacts have been created as small as 50 nm by placing the nanostructured electrode onto an electret surface. The nanocontacts have been used to inject charge into 50 nm sized areas. Nanoparticles were assembled onto the charge patterns, and a lateral resolution of 60 nm has been observed for the first time. A comparison of the nanoparticle patterns with the surface potential distribution recorded by Kelvin probe force microscopy (KFM) revealed a mismatch in the lateral resolution. One possible explanation is that nanoparticles may visualize charge patterns at a sub60-nm length scale that is not well resolved using KFM.://000232623700043 Times Cited: 3 Cited References: BARRY CR, 2003, APPL PHYS LETT, V83, P5527 BARRY CR, 2003, NANOTECHNOLOGY, V14, P1057 BAUR C, 1998, NANOTECHNOLOGY, V9, P360 BRAUN E, 1998, NATURE, V391, P775 BULLEN D, 2004, APPL PHYS LETT, V84, P789 CHOTHIA C, 1975, NATURE, V256, P705 CUI Y, 2004, NANO LETT, V4, P1093 DABROWSKI MJ, 1998, CHEM BIOL, V5, P689 DEGANS BJ, 2004, ADV MATER, V16, P203 DING Y, 2005, P 2005 NSF DMII GRAN FUDOUZI H, 2001, J NANOPART RES, V3, P193 HUANG Y, 2002, ANAL CHEM, V74, P3362 JACKSON JD, 1975, CLASSICAL ELECTRODYN JACOBS HO, 1997, ULTRAMICROSCOPY, V69, P39 JACOBS HO, 1998, J APPL PHYS, V84, P1168 JACOBS HO, 1999, SURF INTERFACE ANAL, V27, P361 JACOBS HO, 2001, SCIENCE, V291, P1763 JACOBS HO, 2002, ADV MATER, V14, P1553 JEON S, 2004, ADV MATER, V16, P1369 KRINKE TJ, 2001, APPL PHYS LETT, V78, P3708 LI D, 2005, NANO LETT, V5, P913 LOO YL, 2002, APPL PHYS LETT, V81, P562 MAGDASSI S, 2003, LANGMUIR, V19, P939 MAZUR K, 1997, J PHYS D APPL PHYS, V30, P1383 MESQUIDA P, 2001, ADV MATER, V13, P1395 MUELLER T, 1995, NUOVO CIMENTO SOC D, V17, P425 NAUKOKS N, 2005, MICROELECTRON ENG, V78, P31 NIEMEYER CM, 2001, COLLOID POLYM SCI, V279, P68 ODOM TW, 2002, LANGMUIR, V18, P5314 PERLMAN MM, 1973, ELECTRETS CHARGE STO PINER RD, 1999, SCIENCE, V283, P661 RAO SG, 2003, NATURE, V425, P36 VELEV OD, 2003, NATURE, V426, P515 WINNINGHAM TA, 1998, SURF SCI, V406, P221 WRIGHT WMD, 1998, NANOTECHNOLOGY, V9, P133 XIA YN, 1999, CHEM REV, V99, P1823 YELLEN BR, 2004, ADV MATER, V16, P111ISI:000232623700043Univ Minnesota, Dept Elect & Comp Engn, Minneapolis, MN 55455 USA. Jacobs, HO, Univ Minnesota, Dept Elect & Comp Engn, 200 Union St SE, Minneapolis, MN 55455 USA. hjacobs@umn.edu file://S:\SALES\_IMPORTANT_STUFF_HERE\Bibliography_Key_Papers\all publications DPN as of 101006 Copy.Data\PDF\2005 Nano Letters Barry Charging Process Coulomb-force Directed Asse-3021694245\2005 Nano Letters Barry Charging Process Coulomb-force Directed Assembly.pdf ~?/Myung, S. Lee, M. Kim, G. T. Ha, J. S. Hong, S.2005[Large-scale "surface-programmed assembly" of pristine vanadium oxide nanowire-based devices2361-+Advanced Materials1719^DIP-PEN NANOLITHOGRAPHY; WALLED CARBON NANOTUBES; TRANSISTORS; FABRICATION; TEMPLATES; SENSORSArticleOct"Surface-programmed assembly" is presented as a technique (see Figure) to achieve high-precision assembly and alignment of a large number of pristine V2O5 nanowires on solid substrates. Positively charged surface molecular patterns guide the assembly and alignment of negatively charged V2O5 nanowires on solid substrates. Large-scale assembly Of V2O5 nanowire-based transistors is demonstrated and their gating effects are confirmed.://000232625900015 Times Cited: 10 Cited References: ANCONA MG, 2003, NANO LETT, V3, P135 BACHTOLD A, 2001, SCIENCE, V294, P1317 CHANG YJ, 2004, APPL PHYS LETT, V84, P5392 COFFEY DC, 2005, J AM CHEM SOC, V127, P4564 COMINI E, 2002, APPL PHYS LETT, V81, P1869 CUI Y, 2001, SCIENCE, V293, P1289 DAI HJ, 1996, NATURE, V384, P147 GAO JB, 2004, J AM CHEM SOC, V126, P16698 HEO YW, 2004, APPL PHYS LETT, V85, P2274 HUANG Y, 2001, SCIENCE, V291, P630 JUNGFENG J, 2005, ADV MATER, V17, P764 KRUSINELBAUM L, 2004, NATURE, V431, P672 LIU J, 1999, CHEM PHYS LETT, V303, P125 LIVAGE J, 1991, CHEM MATER, V3, P578 MANANDHAR P, 2003, PHYS REV LETT, V90 MARTEL R, 1998, APPL PHYS LETT, V73, P2447 MUSTER J, 2000, ADV MATER, V12, P420 NURAJE N, 2004, J AM CHEM SOC, V126, P8088 NYAMJAV D, 2003, ADV MATER, V15, P1805 PINER RD, 1999, SCIENCE, V283, P661 RAO SG, 2003, NATURE, V425, P36 SNOW ES, 2005, SCIENCE, V307, P1942 SORDAN R, 2001, APPL PHYS LETT, V79, P2073 STAR A, 2004, ADV MATER, V16, P2049 XIA YN, 1995, J AM CHEM SOC, V117, P3274 ZHANG Y, 1998, SCIENCE, V281, P973 ZHANG YG, 2001, APPL PHYS LETT, V79, P3155 ZHENG GF, 2004, ADV MATER, V16, P1890ISI:000232625900015)Seoul Natl Univ, Phys & Nanosyst Inst, Seoul 151742, South Korea. Korea Univ, Dept Elect Engn, Seoul 136701, South Korea. Korea Univ, Dept Chem & Biol Engn, Seoul 136701, South Korea. Hong, S, Seoul Natl Univ, Phys & Nanosyst Inst, NS50 Shilim Dong, Seoul 151742, South Korea. shong@phya.snu.ac.krfile://S:\SALES\_IMPORTANT_STUFF_HERE\Bibliography_Key_Papers\all publications DPN as of 101006 Copy.Data\PDF\2005 AdvMats Myung Large-scale surface-programmed assembly.pdf_~?KGroll, J. Albrecht, K. Gasteier, P. Riethmueller, S. Ziener, U. Moeller, M.2005PNanostructured ordering of fluorescent markers and single proteins on substrates 1782-1787 Chembiochem610molecular recognition; monolayers; nanostructures; protein adsorption; single molecules MICROARRAY SUPPORT MATERIALS; SELF-ASSEMBLED MONOLAYERS; DIP-PEN NANOLITHOGRAPHY; IMMOBILIZED PROTEINS; ENERGY-TRANSFER; GOLD SURFACES; ARRAYS; NANOPARTICLES; FABRICATION; TECHNOLOGYArticleOctHighly ordered hexagonal nanopatterns of gold clusters on glass substrates were used as anchoring points for the specific attachment of fluorescence dyes and proteins labeled with fluorescence dyes. Thiol- or disulfide-containing linker molecules were used for the binding to the gold dots. In order to ensure specific binding on the gold dots only, the surface area in between the dots was protected against unspecific adsorption. For the attachment of polar low-molecular-weight fluorescence dyes, an octadecyltri-chlorosilane self-assembled monolayer was prepared on the surface in between the gold dots, whereas a layer prepared from star-shaped poly(ethylene oxide-stat-propylene oxide) prepolymers was used to prevent unspecific adsorption of proteins between the gold dots. Fluorescence microscopy proved the specific binding of the dyes as well as of the proteins. Scanning force microscopy studies show that each gold dot is only capable of binding one protein. at a time.://000232570100012 Times Cited: 1 Cited References: AMIRGOULOVA EV, 2004, CHEMPHYSCHEM, V5, P552 ANGENENDT P, 2002, ANAL BIOCHEM, V309, P253 ANGENENDT P, 2003, J CHROMATOGR A, V1009, P97 ARNOLD M, 2004, CHEMPHYSCHEM, V5, P383 CHANCE RR, 1978, ADV CHEM PHYS, V37, P1 DREXHAGE KH, 1966, BER BUNSEN PHYS CHEM, V70, P1179 DREXHAGE KH, 1974, P