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hal.structure.identifierEcole nationale supérieure de chimie, polymères et materiaux de strasbourg (ECPM)
dc.contributor.authorBALLY, Florence
hal.structure.identifierEcole nationale supérieure de chimie, polymères et materiaux de strasbourg (ECPM)
dc.contributor.authorISMAILOVA, Esma
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 4 LCPO : Polymer Materials for Electronic, Energy, Information and Communication Technologies
dc.contributor.authorBROCHON, Cyril
hal.structure.identifierEcole nationale supérieure de chimie, polymères et materiaux de strasbourg (ECPM)
dc.contributor.authorSERRA, Christophe A.
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 4 LCPO : Polymer Materials for Electronic, Energy, Information and Communication Technologies
dc.contributor.authorHADZIIOANNOU, Georges
dc.date.accessioned2020
dc.date.available2020
dc.date.issued2011
dc.identifier.issn0024-9297
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/20434
dc.description.abstractEnHighly branched polymethacrylates have recently offered new perspectives in lithographic performance and drug delivery. The control of branching remains yet challenging and requires fundamental investigation to consider new applications. Therefore, an advanced study of the formation mechanism of branched polymers synthesized by self-condensing vinyl copolymerization (SCVCP) of a methacrylic AB* inimer, 2-(2-bromoisobutyryloxy)ethyl methacrylate (BIEM), with methyl methacrylate (MMA) via atom transfer radical polymerization (ATRP) has been performed. Evidence of branched structures was obtained with a conventional GPC apparatus equipped with a multiangle light scattering detector and detailed (1)H NMR analyses. A three-step reaction scheme is suggested according to the dependence of molecular weight with conversion. Controlled radical polymerization mainly occurs until moderate conversions, with the participation of inimer as chain initiator. Then the polymerization of small macromolecules, through consumption of polymerizable moiety, dramatically increases the molecular weight of polymer. Finally, a loss of control partially due to thermal decomposition of residual comonomers occurs at high conversion. This mechanistic methodology will allow, with adequate reaction process, the one-step preparation of controlled branched macromolecular architectures leading to functional materials.
dc.language.isoen
dc.publisherAmerican Chemical Society
dc.subject.enMETHACRYLATE
dc.subject.enPOLYELECTROLYTES
dc.subject.enPOLYACRYLATES
dc.subject.enCONDENSING VINYL POLYMERIZATION
dc.subject.enHYPERBRANCHED POLYMERS
dc.subject.enDENDRITIC MACROMOLECULES
dc.subject.enDESIGNING DENDRIMERS
dc.subject.enMOLECULAR-PARAMETERS
dc.subject.enDRUG-DELIVERY
dc.subject.enCOPOLYMERIZATION
dc.title.enMechanistic study of Atom Transfer Radical Polymerization in the Presence of an Inimer: Toward Highly Branched Controlled Macromolecular Architectures through One-Pot Reaction
dc.typeArticle de revue
dc.identifier.doi10.1021/ma2011443
dc.subject.halChimie/Polymères
bordeaux.journalMacromolecules
bordeaux.page7124-7131
bordeaux.volume44
bordeaux.hal.laboratoriesLaboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629*
bordeaux.issue18
bordeaux.institutionBordeaux INP
bordeaux.institutionUniversité de Bordeaux
bordeaux.peerReviewedoui
hal.identifierhal-00817471
hal.version1
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-00817471v1
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