Silyl-substituted poly(thienylenevinylene) via heteroaromatic dehydrohalogenation polymerization

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dc.contributor.authorLee, YBko
dc.contributor.authorShim, Hong Kuko
dc.contributor.authorKo, SWko
dc.date.accessioned2013-03-04T02:31:04Z-
dc.date.available2013-03-04T02:31:04Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2003-05-
dc.identifier.citationMACROMOLECULAR RAPID COMMUNICATIONS, v.24, pp.522 - 526-
dc.identifier.issn1022-1336-
dc.identifier.urihttp://hdl.handle.net/10203/81543-
dc.description.abstractA long alkylsilyl group was attached to a thiophene ring system to overcome the instability of 2.5 bis(halomethyl) thiophene monomers, by imparting steric hindrance and electronic delocalization. The resulting stable monomer could be used directly to prepare low band gap poly(thienylenevinylene) (1.57 eV) through heteroaromatic dehydrohalogenation polymerization.-
dc.languageEnglish-
dc.publisherWILEY-V C H VERLAG GMBH-
dc.titleSilyl-substituted poly(thienylenevinylene) via heteroaromatic dehydrohalogenation polymerization-
dc.typeArticle-
dc.identifier.wosid000183719600008-
dc.identifier.scopusid2-s2.0-0038804135-
dc.type.rimsART-
dc.citation.volume24-
dc.citation.beginningpage522-
dc.citation.endingpage526-
dc.citation.publicationnameMACROMOLECULAR RAPID COMMUNICATIONS-
dc.contributor.localauthorShim, Hong Ku-
dc.contributor.nonIdAuthorLee, YB-
dc.contributor.nonIdAuthorKo, SW-
dc.type.journalArticleArticle-
dc.subject.keywordAuthordehydrohalogenation-
dc.subject.keywordAuthorGilch-
dc.subject.keywordAuthorlow band gap-
dc.subject.keywordAuthorpoly(thienylenevinylene)-
dc.subject.keywordAuthorsilicon substitution-
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