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dc.contributor.authorCho, H.N.-
dc.contributor.authorKim, S.H.-
dc.contributor.authorKim, C.Y.-
dc.date.accessioned2024-01-21T21:13:54Z-
dc.date.available2024-01-21T21:13:54Z-
dc.date.created2021-09-02-
dc.date.issued1995-01-
dc.identifier.issn0170-0839-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/145413-
dc.description.abstractThe cyclopolymerization of 1,8-diethynylnaphthalene(DEN) and its copolymerization with diethyl dipropargylmalonate(DEDPM) were carried out by various transition metal catalysts. MoCl5-based catalyst was found to be very effective and gave almost a quantitative polymer yield. The resulting dark-brown homopolymer(PDEN) was partially soluble in chloroform, tetrahydrofuran, and dimethyl sulfoxide, whereas copolymer (1:1) with number avaerage molecular weight {Mathematical expression} of 2.1x104 by GPC showed good solubility in those solvents. The structure of the polymers was analysed by IR, NMR, and UV-VIS spectroscopies. From the spectral and solubility data, it is proposed that cyclized products with the conjugated system are formed. Room temperature conductivities of the I2-doped homo and copolymer were found to be about 7.5x10-3 and 5.1x10-3 S/cm, respectively. ? 1995 Springer-Verlag.-
dc.languageEnglish-
dc.publisherSpringer-Verlag-
dc.subjectCatalysts-
dc.subjectCopolymerization-
dc.subjectGel permeation chromatography-
dc.subjectInfrared spectroscopy-
dc.subjectMolecular weight-
dc.subjectNuclear magnetic resonance spectroscopy-
dc.subjectSolubility-
dc.subjectStructure (composition)-
dc.subjectSynthesis (chemical)-
dc.subjectThermal conductivity-
dc.subjectUltraviolet spectroscopy-
dc.subjectConjugated systems-
dc.subjectCyclopolymerization-
dc.subjectDiethyl dipropargy malmonate-
dc.subjectDiethynylnaphthalene-
dc.subjectQuantitative polymer yield-
dc.subjectTransition metal catalysts-
dc.subjectOrganic polymers-
dc.titleSynthesis and characterization of poly(1,8-diethynylnaphthalene)-
dc.typeArticle-
dc.identifier.doi10.1007/BF00316386-
dc.description.journalClass1-
dc.identifier.bibliographicCitationPolymer Bulletin, v.34, no.2, pp.125 - 132-
dc.citation.titlePolymer Bulletin-
dc.citation.volume34-
dc.citation.number2-
dc.citation.startPage125-
dc.citation.endPage132-
dc.description.journalRegisteredClassscopus-
dc.identifier.scopusid2-s2.0-0029255945-
dc.type.docTypeArticle-
dc.subject.keywordPlusCatalysts-
dc.subject.keywordPlusCopolymerization-
dc.subject.keywordPlusGel permeation chromatography-
dc.subject.keywordPlusInfrared spectroscopy-
dc.subject.keywordPlusMolecular weight-
dc.subject.keywordPlusNuclear magnetic resonance spectroscopy-
dc.subject.keywordPlusSolubility-
dc.subject.keywordPlusStructure (composition)-
dc.subject.keywordPlusSynthesis (chemical)-
dc.subject.keywordPlusThermal conductivity-
dc.subject.keywordPlusUltraviolet spectroscopy-
dc.subject.keywordPlusConjugated systems-
dc.subject.keywordPlusCyclopolymerization-
dc.subject.keywordPlusDiethyl dipropargy malmonate-
dc.subject.keywordPlusDiethynylnaphthalene-
dc.subject.keywordPlusQuantitative polymer yield-
dc.subject.keywordPlusTransition metal catalysts-
dc.subject.keywordPlusOrganic polymers-
dc.subject.keywordAuthorsynthesis-
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