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hal.structure.identifierLoker Hydrocarbon Res Inst & Dept Chem
dc.contributor.authorALBERTY, Kurt A.
hal.structure.identifierLoker Hydrocarbon Res Inst & Dept Chem
dc.contributor.authorHOGEN-ESCH, Thieo E.
hal.structure.identifierLaboratoire de Chimie des polymères organiques [LCPO]
hal.structure.identifierTeam 1 LCPO : Polymerization Catalyses & Engineering
dc.contributor.authorCARLOTTI, Stéphane
dc.date.accessioned2020
dc.date.available2020
dc.date.issued2005
dc.identifier.issn1022-1352
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/20669
dc.description.abstractEnMatching macrocyclic and linear polystyrenes (PS) were synthesized by the initiation of styrene with 2,7dimethyl-3,6-diphenyloctane dianion lithium salt followed by high dilution coupling with 1,4-bis(bromomethyl)benzene or protonation. Liquid chromatography at the critical condition shows the presence of less than 4% of linear PS impurities in the fractionated cycles. SEC studies confirm that the ratios of apparent MWs of cyclic and linear PS increase from about 0.7 to more than 0.9 as MWs decrease. Fluorescence studies show that the monomer emissions at 285 nm strongly increase with decreasing MW whereas those of the linear polymers are not significantly affected. This may be due in part to the increased rigidity of the smaller cycles that decreases the rate of radiation-less deactivation.
dc.language.isoen
dc.publisherWiley-VCH Verlag
dc.subject.encycles
dc.subject.englass transition temperature
dc.subject.enpolystyrene (PS)
dc.subject.enanionic polymerization
dc.title.enSynthesis and characterization of macrocyclic vinyl-aromatic polymers. Molecular weight-dependent glass transition temperatures and emission of macrocyclic polystyrene
dc.typeArticle de revue
dc.identifier.doi10.1002/macp.200400471
dc.subject.halChimie/Polymères
bordeaux.journalMacromolecular Chemistry and Physics
bordeaux.page1035-1042
bordeaux.volume206
bordeaux.hal.laboratoriesLaboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629*
bordeaux.issue10
bordeaux.institutionBordeaux INP
bordeaux.institutionUniversité de Bordeaux
bordeaux.peerReviewedoui
hal.identifierhal-00394380
hal.version1
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-00394380v1
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