Full metadata record
DC Field | Value | Language |
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dc.contributor.author | Cho, H.N. | - |
dc.contributor.author | Kim, S.H. | - |
dc.contributor.author | Kim, C.Y. | - |
dc.date.accessioned | 2024-01-21T21:13:54Z | - |
dc.date.available | 2024-01-21T21:13:54Z | - |
dc.date.created | 2021-09-02 | - |
dc.date.issued | 1995-01 | - |
dc.identifier.issn | 0170-0839 | - |
dc.identifier.uri | https://pubs.kist.re.kr/handle/201004/145413 | - |
dc.description.abstract | The 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.language | English | - |
dc.publisher | Springer-Verlag | - |
dc.subject | Catalysts | - |
dc.subject | Copolymerization | - |
dc.subject | Gel permeation chromatography | - |
dc.subject | Infrared spectroscopy | - |
dc.subject | Molecular weight | - |
dc.subject | Nuclear magnetic resonance spectroscopy | - |
dc.subject | Solubility | - |
dc.subject | Structure (composition) | - |
dc.subject | Synthesis (chemical) | - |
dc.subject | Thermal conductivity | - |
dc.subject | Ultraviolet spectroscopy | - |
dc.subject | Conjugated systems | - |
dc.subject | Cyclopolymerization | - |
dc.subject | Diethyl dipropargy malmonate | - |
dc.subject | Diethynylnaphthalene | - |
dc.subject | Quantitative polymer yield | - |
dc.subject | Transition metal catalysts | - |
dc.subject | Organic polymers | - |
dc.title | Synthesis and characterization of poly(1,8-diethynylnaphthalene) | - |
dc.type | Article | - |
dc.identifier.doi | 10.1007/BF00316386 | - |
dc.description.journalClass | 1 | - |
dc.identifier.bibliographicCitation | Polymer Bulletin, v.34, no.2, pp.125 - 132 | - |
dc.citation.title | Polymer Bulletin | - |
dc.citation.volume | 34 | - |
dc.citation.number | 2 | - |
dc.citation.startPage | 125 | - |
dc.citation.endPage | 132 | - |
dc.description.journalRegisteredClass | scopus | - |
dc.identifier.scopusid | 2-s2.0-0029255945 | - |
dc.type.docType | Article | - |
dc.subject.keywordPlus | Catalysts | - |
dc.subject.keywordPlus | Copolymerization | - |
dc.subject.keywordPlus | Gel permeation chromatography | - |
dc.subject.keywordPlus | Infrared spectroscopy | - |
dc.subject.keywordPlus | Molecular weight | - |
dc.subject.keywordPlus | Nuclear magnetic resonance spectroscopy | - |
dc.subject.keywordPlus | Solubility | - |
dc.subject.keywordPlus | Structure (composition) | - |
dc.subject.keywordPlus | Synthesis (chemical) | - |
dc.subject.keywordPlus | Thermal conductivity | - |
dc.subject.keywordPlus | Ultraviolet spectroscopy | - |
dc.subject.keywordPlus | Conjugated systems | - |
dc.subject.keywordPlus | Cyclopolymerization | - |
dc.subject.keywordPlus | Diethyl dipropargy malmonate | - |
dc.subject.keywordPlus | Diethynylnaphthalene | - |
dc.subject.keywordPlus | Quantitative polymer yield | - |
dc.subject.keywordPlus | Transition metal catalysts | - |
dc.subject.keywordPlus | Organic polymers | - |
dc.subject.keywordAuthor | synthesis | - |
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