Patterned polymer growth on silicon surfaces using microcontact printing and surface-initiated polymerization

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dc.contributor.authorJeon, NLko
dc.contributor.authorChoi, Insungko
dc.contributor.authorWhitesides, GMko
dc.contributor.authorKim, NYko
dc.contributor.authorLaibinis, PEko
dc.contributor.authorHarada, Yko
dc.contributor.authorFinnie, KRko
dc.contributor.authorGirolami, GSko
dc.contributor.authorNuzzo, RGko
dc.date.accessioned2009-11-19T08:13:21Z-
dc.date.available2009-11-19T08:13:21Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued1999-12-
dc.identifier.citationAPPLIED PHYSICS LETTERS, v.75, no.26, pp.4201 - 4203-
dc.identifier.issn0003-6951-
dc.identifier.urihttp://hdl.handle.net/10203/12927-
dc.description.abstractPatterned polymer films were grown on SiO2/Si surfaces by a process starting with microcontact printing (mu CP) of octadecyltrichlorosilane (OTS), formation of a monolayer derived from norbornenyl trichlorosilane (Nbn-SiCl3) in areas not protected by OTS, activation of the surfaces derived from Nbn-SiCl3 with a ruthenium catalyst, and surface-initiated ring-opening metathesis polymerization of derivatives of norbornene by the catalytically active ruthenium species. These patterned polymer films were successfully used as reactive ion etching resists. The combination of mu CP and surface-initiated polymerization makes possible molecular-level control of polymer composition and thickness in both lateral and vertical directions: the smallest patterned lateral features were 2 mu m lines; this width was determined by the features of the stamp used in mu CP and is not the intrinsic limit of the method. The thickness of the polymer film was, typically, 5-100 nm and could be controlled by monomer concentration and reaction time. (C) 1999 American Institute of Physics. [S0003-6951(99)01052-9].-
dc.languageEnglish-
dc.language.isoen_USen
dc.publisherAMER INST PHYSICS-
dc.subjectMETATHESIS POLYMERIZATION-
dc.subjectGOLD-
dc.subjectALKANETHIOLS-
dc.subjectFILMS-
dc.titlePatterned polymer growth on silicon surfaces using microcontact printing and surface-initiated polymerization-
dc.typeArticle-
dc.identifier.wosid000084504700052-
dc.identifier.scopusid2-s2.0-0011300548-
dc.type.rimsART-
dc.citation.volume75-
dc.citation.issue26-
dc.citation.beginningpage4201-
dc.citation.endingpage4203-
dc.citation.publicationnameAPPLIED PHYSICS LETTERS-
dc.identifier.doi10.1063/1.125582-
dc.embargo.liftdate9999-12-31-
dc.embargo.terms9999-12-31-
dc.contributor.localauthorChoi, Insung-
dc.contributor.nonIdAuthorJeon, NL-
dc.contributor.nonIdAuthorWhitesides, GM-
dc.contributor.nonIdAuthorKim, NY-
dc.contributor.nonIdAuthorLaibinis, PE-
dc.contributor.nonIdAuthorHarada, Y-
dc.contributor.nonIdAuthorFinnie, KR-
dc.contributor.nonIdAuthorGirolami, GS-
dc.contributor.nonIdAuthorNuzzo, RG-
dc.type.journalArticleArticle-
dc.subject.keywordPlusMETATHESIS POLYMERIZATION-
dc.subject.keywordPlusGOLD-
dc.subject.keywordPlusALKANETHIOLS-
dc.subject.keywordPlusFILMS-
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