Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/3338
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dc.contributor.authorVan Der Borght, M-
dc.contributor.authorGELAN, Jan-
dc.contributor.authorVANDERZANDE, Dirk-
dc.date.accessioned2007-11-27T15:03:41Z-
dc.date.available2007-11-27T15:03:41Z-
dc.date.issued1997-
dc.identifier.citationSYNTHETIC METALS, 84(1-3). p. 399-400-
dc.identifier.issn0379-6779-
dc.identifier.urihttp://hdl.handle.net/1942/3338-
dc.description.abstractStable methyl- and methoxy-substituted soluble precursor polymers (5a and 5b) were synthesised via a non-ionic precursor route. These precursor polymers possess a sulphoxy substituent on the ethylene segment which, can be eliminated by means of a simple thermal treatment in order to yield the conjugated polymer. The synthesis of the monomers, the precursor and the conjugated polymers is discussed briefly together with the photoluminescence properties of the latter.-
dc.language.isoen-
dc.publisherELSEVIER SCIENCE SA LAUSANNE-
dc.subject.otherpoly(phenylene vinylene) and derivatives; photoluminescence; electroluminescence-
dc.titleSynthesis of methyl- and methoxy-substituted poly(p-phenylene vinylene) via a non-ionic precursor route-
dc.typeJournal Contribution-
dc.identifier.epage400-
dc.identifier.issue1-3-
dc.identifier.spage399-
dc.identifier.volume84-
local.format.pages2-
dc.description.notesVanDerBorght, M, INST MAT RES,DIV CHEM,UNIV CAMPUS,B-3590 DIEPENBEEK,BELGIUM.-
local.type.refereedRefereed-
local.type.specifiedArticle-
dc.bibliographicCitation.oldjcatA1-
dc.identifier.doi10.1016/S0379-6779(97)80801-6-
dc.identifier.isiA1997WW43100168-
item.contributorVan Der Borght, M-
item.contributorGELAN, Jan-
item.contributorVANDERZANDE, Dirk-
item.fulltextNo Fulltext-
item.accessRightsClosed Access-
item.fullcitationVan Der Borght, M; GELAN, Jan & VANDERZANDE, Dirk (1997) Synthesis of methyl- and methoxy-substituted poly(p-phenylene vinylene) via a non-ionic precursor route. In: SYNTHETIC METALS, 84(1-3). p. 399-400.-
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