Soluble polyimides with trifluoromethyl pendent groups

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dc.contributor.authorKim, Sun Dalko
dc.contributor.authorLee, Sanghwako
dc.contributor.authorHeo, Jaewonko
dc.contributor.authorKim, Sang Youlko
dc.contributor.authorChung, Im Sikko
dc.date.accessioned2014-08-27T02:45:15Z-
dc.date.available2014-08-27T02:45:15Z-
dc.date.created2013-11-06-
dc.date.created2013-11-06-
dc.date.issued2013-10-
dc.identifier.citationPOLYMER, v.54, no.21, pp.5648 - 5654-
dc.identifier.issn0032-3861-
dc.identifier.urihttp://hdl.handle.net/10203/187407-
dc.description.abstractUnsymmetrical and symmetrical diamine monomers containing trifluoromethyl groups, 2-trifluoro methyl-4,4'-diaminodiphenyl sulfide and 2,2'-bis(trifluoromethyl)-4,4'-diamino-diphenyl sulfide, were synthesized from 2-chloro-5-nitrobenzotrifluoride as a starting material in two steps, respectively. Diamine monomers were polymerized with PMDA, BPDA, BTDA, and ODPA using a solution imidization method with N-methyl-2-pyrrolidone as a solvent at 190 degrees C to obtain the corresponding polyimides. They had inherent viscosities that ranged from 0.54 to 0.71 dL/g in N-methyl-2-pyrrolidone at 30 C. All of the synthesized polyimides showed good solubility in polar aprotic solvents and phenolic solvents regardless of the number of trifluoromethyl groups. The 5% weight loss temperatures of the polyimides are in the range of 534-561 degrees C in nitrogen, and 505-542 C in air. The Tg values and the thermal expansion coefficients of these polymers are in the range of 234-325 degrees C and in the range of 47.4 63.2 ppm/degrees C, respectively. Also, all of the synthesized polyimides have relatively low refractive indices (around 1.6) and birefringence (below 0.36). Published by Elsevier Ltd.-
dc.languageEnglish-
dc.publisherELSEVIER SCI LTD-
dc.subjectAROMATIC-SUBSTITUTION REACTION-
dc.subjectNITRO DISPLACEMENT REACTION-
dc.subjectPOLY(BIPHENYLENE OXIDE)S-
dc.subjectUNSYMMETRICAL DIAMINE-
dc.subjectFLUORINATED POLYIMIDES-
dc.subjectRELATIVE PERMITTIVITY-
dc.subjectPOLY(ARYLENE ETHER)S-
dc.subjectREFRACTIVE-INDEXES-
dc.subjectCYANO GROUPS-
dc.subjectFREE-VOLUME-
dc.titleSoluble polyimides with trifluoromethyl pendent groups-
dc.typeArticle-
dc.identifier.wosid000326204200025-
dc.identifier.scopusid2-s2.0-84885023400-
dc.type.rimsART-
dc.citation.volume54-
dc.citation.issue21-
dc.citation.beginningpage5648-
dc.citation.endingpage5654-
dc.citation.publicationnamePOLYMER-
dc.identifier.doi10.1016/j.polymer.2013.08.057-
dc.embargo.liftdate9999-12-31-
dc.embargo.terms9999-12-31-
dc.contributor.localauthorKim, Sang Youl-
dc.contributor.nonIdAuthorKim, Sun Dal-
dc.contributor.nonIdAuthorLee, Sanghwa-
dc.contributor.nonIdAuthorHeo, Jaewon-
dc.contributor.nonIdAuthorChung, Im Sik-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorTrifluoromethyl groups-
dc.subject.keywordAuthorPolyimides-
dc.subject.keywordAuthorHigh performance polymers-
dc.subject.keywordPlusAROMATIC-SUBSTITUTION REACTION-
dc.subject.keywordPlusNITRO DISPLACEMENT REACTION-
dc.subject.keywordPlusPOLY(BIPHENYLENE OXIDE)S-
dc.subject.keywordPlusUNSYMMETRICAL DIAMINE-
dc.subject.keywordPlusFLUORINATED POLYIMIDES-
dc.subject.keywordPlusRELATIVE PERMITTIVITY-
dc.subject.keywordPlusPOLY(ARYLENE ETHER)S-
dc.subject.keywordPlusREFRACTIVE-INDEXES-
dc.subject.keywordPlusCYANO GROUPS-
dc.subject.keywordPlusFREE-VOLUME-
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