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hal.structure.identifierUniv Liege, Dept Chem, CERM
dc.contributor.authorCORDELLA, Daniela
hal.structure.identifierUniv Liege, Dept Chem, CERM
dc.contributor.authorKERMAGORET, Anthony
hal.structure.identifierUniv Liege, Dept Chem, CERM
dc.contributor.authorDEBUIGNE, Antoine
hal.structure.identifierUniv Liege, Dept Chem, CERM
dc.contributor.authorJÉRÔME, Christine
hal.structure.identifierUniv Basque Country UPV EHU, Joxe Mari Korta Ctr, POLYMAT
dc.contributor.authorMECERREYES, David
hal.structure.identifierUniv Basque Country UPV EHU, Joxe Mari Korta Ctr, POLYMAT
dc.contributor.authorISIK, Mehmet
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 1 LCPO : Polymerization Catalyses & Engineering
dc.contributor.authorTATON, Daniel
hal.structure.identifierUniv Liege, Dept Chem, CERM
dc.contributor.authorDETREMBLEUR, Christophe
dc.date.accessioned2020
dc.date.available2020
dc.date.issued2015
dc.identifier.issn0024-9297
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/20239
dc.description.abstractEnThe organometallic-mediated radical polymerization (OMRP) of N-vinyl-3-alkylimidazolium-type monomers, featuring the bis(trifluoromethylsulfonyl)imide counter-anion (Tf2N-) in the presence of Co(acac)(2) as controlling agent, is reported. Polymerizations of monomers with methyl, ethyl, and butyl substituents are fast, reaching high monomer conversion in ethyl acetate as solvent at 30 degrees C, and afford structurally well-defined hydrophobic poly(ionic liquid)s (PILs) of N-vinyl type. Block copolymer synthesis is also achieved by sequential OMRP of N-vinyl-3-alkyldazolium salts carrying different alkyl chains and different counteranions (Tf2N- or Br-). These block copolymerizations are carried out at 30 degrees C, either under homogeneous solution in methanol or in a biphasic medium consisting of a mixture of ethyl acetate and water. Unprecedented PIL-b-PIL block copolymers are thus prepared under these conditions. However, anion exchange occurs at the early stage of the growth of the second block. Finally, diblock copolymers generated in the biphasic medium can be readily coupled by addition of isoprene, forming all PIL-based and symmetrical ABA-type triblock copolymers in a one-pot process. Such a direct block copolymerization method, involving vinylimidazolium monomers bearing different alkyl chains, thus opens new opportunities in the precision synthesis of all PIL-based block copolymers of tunable properties.
dc.language.isoen
dc.publisherAmerican Chemical Society
dc.subject.enSEPARATION
dc.subject.enMETATHESIS
dc.subject.enCONDUCTIVITY
dc.subject.enPERFORMANCE
dc.subject.enPOLYMERIZED IONIC LIQUIDS
dc.subject.enFRAGMENTATION CHAIN TRANSFER
dc.subject.enVINYL-ACETATE
dc.subject.enRAFT POLYMERIZATION
dc.subject.enANION-EXCHANGE
dc.subject.enELECTROLYTES
dc.title.enAll Poly(ionic liquid)-Based Block Copolymers by Sequential Controlled Radical Copolymerization of Vinylimidazolium Monomers
dc.typeArticle de revue
dc.identifier.doi10.1021/acs.macromol.5b01013
dc.subject.halChimie/Polymères
bordeaux.journalMacromolecules
bordeaux.page5230-5243
bordeaux.volume48
bordeaux.hal.laboratoriesLaboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629*
bordeaux.issue15
bordeaux.institutionBordeaux INP
bordeaux.institutionUniversité de Bordeaux
bordeaux.peerReviewedoui
hal.identifierhal-01366538
hal.version1
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-01366538v1
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Macromolecules&rft.date=2015&rft.volume=48&rft.issue=15&rft.spage=5230-5243&rft.epage=5230-5243&rft.eissn=0024-9297&rft.issn=0024-9297&rft.au=CORDELLA,%20Daniela&KERMAGORET,%20Anthony&DEBUIGNE,%20Antoine&J%C3%89R%C3%94ME,%20Christine&MECERREYES,%20David&rft.genre=article


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