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hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
dc.contributor.authorRADCHENKO, Alexei V.
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
dc.contributor.authorBOUCHEKIF, Hassen
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 1 LCPO : Polymerization Catalyses & Engineering
dc.contributor.authorPERUCH, Frédéric
IDREF: 152900748
dc.date.accessioned2020
dc.date.available2020
dc.date.issued2017
dc.identifier.issn0014-3057
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/20134
dc.description.abstractEnThermo-induced carbocationic polymerization of isobutyl vinyl ether (IBVE), isoprene, myrcene and ocimene is reported using triflate esters as in-situ generated single-molecule initiating system. 3-Methyl-2-butenyl triflate is used for IBVE polymerization at room temperature resulting in polymers with Mn ∼ 9500 g mol−1 and Mw/Mn ∼ 2. Triflate-ester initiated polymerization of isoprene leads to oligomers with branched and ultimately cross-linked structures. Myrcene cationic polymerization, in CH2Cl2 or cyclohexane, using 2-propenyl triflate and 1-(4-metoxyphenyl)ethyl triflate as initiators yields low molar mass oligomyrcenes with loss of olefinic protons. Ocimene cationic polymerization is reported for the first time.
dc.language.isoen
dc.publisherElsevier
dc.subject.enPolymerization
dc.subject.enCrosslinked structures
dc.subject.enOlefinic protons
dc.subject.enCationic polymerization
dc.subject.enIsobutylvinyl ether
dc.subject.enIsoprene
dc.subject.enMyrcene
dc.subject.enOcimene
dc.subject.enTriflate ester
dc.subject.enEsters
dc.subject.enEthers
dc.subject.enIn situ processing
dc.subject.enMonoterpenes
dc.subject.enOrganic compounds
dc.subject.enSingle molecule
dc.subject.enTriflates
dc.subject.enVinyl ethers
dc.subject.enCarbocationic polymerization
dc.title.enTriflate esters as in-situ generated initiating system for carbocationic polymerization of vinyl ethers, isoprene, myrcene and ocimene
dc.typeArticle de revue
dc.identifier.doi10.1016/j.eurpolymj.2017.02.001
dc.subject.halChimie/Polymères
bordeaux.journalEuropean Polymer Journal
bordeaux.page34-41
bordeaux.volume89
bordeaux.hal.laboratoriesLaboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629*
bordeaux.institutionBordeaux INP
bordeaux.institutionUniversité de Bordeaux
bordeaux.peerReviewedoui
hal.identifierhal-01473872
hal.version1
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-01473872v1
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=European%20Polymer%20Journal&rft.date=2017&rft.volume=89&rft.spage=34-41&rft.epage=34-41&rft.eissn=0014-3057&rft.issn=0014-3057&rft.au=RADCHENKO,%20Alexei%20V.&BOUCHEKIF,%20Hassen&PERUCH,%20Fr%C3%A9d%C3%A9ric&rft.genre=article


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