Synthesis and properties of poly[2-ethynyl-N-(p-hydroxyphenylethyl) pyridinium bromide] and poly[2-ethynyl-N-(p-hydroxyphenylethyl) pyridinium tetraphenylborate

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dc.contributor.authorGal, YSko
dc.contributor.authorJin, SHko
dc.contributor.authorLee, WCko
dc.contributor.authorKim, Sang Youlko
dc.date.accessioned2013-03-04T17:48:51Z-
dc.date.available2013-03-04T17:48:51Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2004-08-
dc.identifier.citationMACROMOLECULAR RESEARCH, v.12, no.4, pp.407 - 412-
dc.identifier.issn1598-5032-
dc.identifier.urihttp://hdl.handle.net/10203/83511-
dc.description.abstractA new hydroxyl group-containing conjugated ionic polymer, poly[2-ethynyl-N-(p-hydroxyphenylethyl)pyridinium bromide], was synthesized by the activated polymerization of 2-ethynylpyridine with p-(2-bromoethyl) phenol without any additional initiator or catalyst. The polymerization proceeded well to give a moderate yield (65%) of polymer at a reaction temparature of 90 degreesC. Another polymer, poly [2-ethynyl-N-(p-hydroxyphenylethyl)pyridinium tetraphenylborate], was readily prepared by the ion-exchange reaction of poly[2-ethynyl-N-(Phydroxyphenylethyl)pyridinium bromide] with sodium tetraphenylborate. These polymers were completely soluble in organic solvents such as DMF, DMSO, and acetone, but insoluble in water and ether. Instrumental analyses, such as NMR, IR, and UV-Vis spectroscopies, indicated that the new materials have conjugated polymer backbone systems with the designed substituents and counter anions. X-Ray diffraction analyses of the polymers indicated that they were mostly amorphous.-
dc.languageEnglish-
dc.publisherPOLYMER SOC KOREA-
dc.subjectTRANSITION-METAL CATALYSTS-
dc.subjectCONJUGATED IONIC POLYACETYLENES-
dc.subjectORGANIC CONDUCTING POLYMERS-
dc.subjectMETATHESIS POLYMERIZATION-
dc.subjectELECTRICAL-CONDUCTIVITY-
dc.subjectOPTICAL-PROPERTIES-
dc.subjectACETYLENES-
dc.subjectSALTS-
dc.titleSynthesis and properties of poly[2-ethynyl-N-(p-hydroxyphenylethyl) pyridinium bromide] and poly[2-ethynyl-N-(p-hydroxyphenylethyl) pyridinium tetraphenylborate-
dc.typeArticle-
dc.identifier.wosid000223739600012-
dc.identifier.scopusid2-s2.0-4544255410-
dc.type.rimsART-
dc.citation.volume12-
dc.citation.issue4-
dc.citation.beginningpage407-
dc.citation.endingpage412-
dc.citation.publicationnameMACROMOLECULAR RESEARCH-
dc.identifier.doi10.1007/BF03218419-
dc.contributor.localauthorKim, Sang Youl-
dc.contributor.nonIdAuthorGal, YS-
dc.contributor.nonIdAuthorJin, SH-
dc.contributor.nonIdAuthorLee, WC-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorconjugated polymer-
dc.subject.keywordAuthor2-ethynylpyridine-
dc.subject.keywordAuthorcharacterization-
dc.subject.keywordAuthorion-exchange reaction-
dc.subject.keywordAuthorsodium tetraphenylborate-
dc.subject.keywordPlusTRANSITION-METAL CATALYSTS-
dc.subject.keywordPlusCONJUGATED IONIC POLYACETYLENES-
dc.subject.keywordPlusORGANIC CONDUCTING POLYMERS-
dc.subject.keywordPlusMETATHESIS POLYMERIZATION-
dc.subject.keywordPlusELECTRICAL-CONDUCTIVITY-
dc.subject.keywordPlusOPTICAL-PROPERTIES-
dc.subject.keywordPlusACETYLENES-
dc.subject.keywordPlusSALTS-
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