Polymerization of 4-dimethylamino-N-propargylpyridinium bromide by transition metal catalysts

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dc.contributor.authorGal, YSko
dc.contributor.authorJin, SHko
dc.contributor.authorGui, TLko
dc.contributor.authorLee, HJko
dc.contributor.authorKim, Sang Youlko
dc.contributor.authorKim, DWko
dc.contributor.authorKo, JMko
dc.contributor.authorChun, JHko
dc.contributor.authorJang, SHko
dc.contributor.authorKim, BSko
dc.contributor.authorLee, WCko
dc.date.accessioned2013-03-04T18:02:48Z-
dc.date.available2013-03-04T18:02:48Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2003-
dc.identifier.citationJOURNAL OF MACROMOLECULAR SCIENCE-PURE AND APPLIED CHEMISTRY, v.A40, no.4, pp.401 - 413-
dc.identifier.issn1060-1325-
dc.identifier.urihttp://hdl.handle.net/10203/83551-
dc.description.abstractThe polymerization of an ionic propargyl derivative, 4-dimethylamino-N-propargylpyridinium bromide (DMAPPB), was carried out by palladium, platinum, and ruthenium chlorides. The polymerization of DMAPPB by these transition metal catalysts proceeded well to give a relatively high polymer yield. The chemical structure of the resulting polymer was characterized by such instrumental methods as elemental analysis, infrared, NMR, UV-visible spectroscopies to have conjugated polymer backbone system bearing 4-dimethylanlino-N-methylenepyridinium bromide. The polymer was soluble in DMF, DMSO, and formic acid, and found to be less hygroscopic than those of similar homologues having more smaller substituents. The resulting polymers were mostly black powders and showed the amorphous morphology.-
dc.languageEnglish-
dc.publisherMARCEL DEKKER INC-
dc.subjectCONJUGATED IONIC POLYACETYLENES-
dc.subjectTUNGSTEN-BASED CATALYSTS-
dc.subjectLIGHT-EMITTING-DIODES-
dc.subjectMETATHESIS CATALYSTS-
dc.subjectOPTICAL-PROPERTIES-
dc.subjectSIDE-CHAIN-
dc.subjectPOLY(2-ETHYNYLPYRIDINUM BROMIDE)-
dc.subjectELECTRICAL-PROPERTIES-
dc.subjectCYCLOPOLYMERIZATION-
dc.subjectDERIVATIVES-
dc.titlePolymerization of 4-dimethylamino-N-propargylpyridinium bromide by transition metal catalysts-
dc.typeArticle-
dc.identifier.wosid000182668700006-
dc.identifier.scopusid2-s2.0-0038529813-
dc.type.rimsART-
dc.citation.volumeA40-
dc.citation.issue4-
dc.citation.beginningpage401-
dc.citation.endingpage413-
dc.citation.publicationnameJOURNAL OF MACROMOLECULAR SCIENCE-PURE AND APPLIED CHEMISTRY-
dc.contributor.localauthorKim, Sang Youl-
dc.contributor.nonIdAuthorGal, YS-
dc.contributor.nonIdAuthorJin, SH-
dc.contributor.nonIdAuthorGui, TL-
dc.contributor.nonIdAuthorLee, HJ-
dc.contributor.nonIdAuthorKim, DW-
dc.contributor.nonIdAuthorKo, JM-
dc.contributor.nonIdAuthorChun, JH-
dc.contributor.nonIdAuthorJang, SH-
dc.contributor.nonIdAuthorKim, BS-
dc.contributor.nonIdAuthorLee, WC-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorpolymerization-
dc.subject.keywordAuthorconjugated polymer-
dc.subject.keywordAuthorionic polymer-
dc.subject.keywordAuthortransition metal catalyst-
dc.subject.keywordPlusCONJUGATED IONIC POLYACETYLENES-
dc.subject.keywordPlusTUNGSTEN-BASED CATALYSTS-
dc.subject.keywordPlusLIGHT-EMITTING-DIODES-
dc.subject.keywordPlusMETATHESIS CATALYSTS-
dc.subject.keywordPlusOPTICAL-PROPERTIES-
dc.subject.keywordPlusSIDE-CHAIN-
dc.subject.keywordPlusPOLY(2-ETHYNYLPYRIDINUM BROMIDE)-
dc.subject.keywordPlusELECTRICAL-PROPERTIES-
dc.subject.keywordPlusCYCLOPOLYMERIZATION-
dc.subject.keywordPlusDERIVATIVES-
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