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CORRELATION BETWEEN STRUCTURE AND ELECTRICAL-CONDUCTIVITY OF SOLUBLE POLYPHENYLENES

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dc.contributor.author SIMITZIS, J en
dc.contributor.author TZEVELEKIS, D en
dc.contributor.author STAMBOULIS, A en
dc.contributor.author HINRICHSEN, G en
dc.date.accessioned 2014-03-01T01:42:03Z
dc.date.available 2014-03-01T01:42:03Z
dc.date.issued 1993 en
dc.identifier.issn 0323-7648 en
dc.identifier.uri https://dspace.lib.ntua.gr/xmlui/handle/123456789/23693
dc.subject.classification Polymer Science en
dc.subject.other PARA-TERPHENYL en
dc.subject.other BIPHENYL en
dc.title CORRELATION BETWEEN STRUCTURE AND ELECTRICAL-CONDUCTIVITY OF SOLUBLE POLYPHENYLENES en
heal.type journalArticle en
heal.language English en
heal.publicationDate 1993 en
heal.abstract Polyphenylenes were prepared by using biphenyl-AlCl3-CuCl2 according to cationic oxidative polymerization. The chlorobenzene soluble fraction was doped with 10% (w/v) solution of FeCl3, in acetonitrile. The alternating electrical conductivity, X-ray diffractograms and the FTIR-spectra of both undoped and doped polyphenylenes were measured. The proportion of the components used for the preparation of polyphenylenes strongly influences their structure as well as their conductive properties. The undoped polyphenylenes were found to be insulators, but most of them became semiconductors after doping. The increase of the alternating electrical conductivity sigma'(resulting from the real part of the admittance-vector) of the doped polyphenylenes has been explained considering the factors that influence the polyphenylenes structure: the high ratio of para/meta, the presence of both amorphous and crystalline regions, and the presence of polynuclear structures. On the other hand, the presence of aliphatic structures interrupts the conjugation system, leading to lower sigma' values. en
heal.publisher VCH PUBLISHERS INC en
heal.journalName ACTA POLYMERICA en
dc.identifier.isi ISI:A1993MN72800006 en
dc.identifier.volume 44 en
dc.identifier.issue 6 en
dc.identifier.spage 294 en
dc.identifier.epage 301 en


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