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hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
dc.contributor.authorRAYNAUD, Jean
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
dc.contributor.authorNA, Liu
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
dc.contributor.authorGNANOU, Yves
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 1 LCPO : Polymerization Catalyses & Engineering
dc.contributor.authorTATON, Daniel
dc.date.accessioned2020
dc.date.available2020
dc.date.created2010
dc.date.issued2010
dc.identifier.issn0024-9297
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/20531
dc.description.abstractEn1,3-Bis(di-isopropyl)imidazol-2-ylidene (1) and 1,3-bis(di-tert-butyl)imidazol-2-ylidene (2), which are N-heterocyclic carbenes (NHCs) are shown to catalyze the solution group transfer polymerization (GTP) of miscellaneous monomers in a controlled fashion at room temperature, in the presence of 1-methoxy-2-methyl-1-trimethylsiloxypropene (MTS) as initiator. The ability of seven distinct monomers, methyl methacrylate (MMA), tert-butyl acrylate (tBA), n-butyl acrylate (nBA), N,N-dimethylaminoethyl acrylate (DMAEA), N,N-dimethyl acrylamide (DMA), N,N-dimethylaminoethyl methacrylate (DMAEMA), and methacrylonitrile (MAN) to polymerize via GTP by NHC catalysis has been evaluated. The first-order kinetic plots, that is the evolution of In[M](0)/[M] versus time, systematically deviate from linearity, with the noticeable exception of GTP of DMA. A direct dependence of the rate of GTP on the concentration in MTS initiator is observed in the case of tBA carried out in THF, that is, the rate of polymerization increases with [MTS], with a first-order dependence on [MTS]. These results suggest the formation of hypervalent siliconate intermediates in NHC-induced GTP of acrylic monomers which proceeds via an associative mechanism. The nonlinear variation of In[M](0)/[M] with time in the terminal phase of the polymerization of both acrylates and methacrylates may be explained by the development of strong interactions between the NHC and pendant ester groups of poly(meth)acrylates, limiting the availability of the catalyst for chain end activation. In contrast, interactions between the NHC and amide-type units of poly(DMA) are unlikely, NHCs being not known as effective catalysts for transamidation reactions. A first-order kinetic plot with a linear variation of In[M](0)/[M] with time is thus observed for the NHC-catalyzed GTP of DMA.
dc.language.isoen
dc.publisherAmerican Chemical Society
dc.subject.enKETENE ACETALS
dc.subject.enBLOCK-COPOLYMERS
dc.subject.enMETHYL-METHACRYLATE
dc.subject.enASSOCIATIVE MECHANISM
dc.subject.enANIONIC-POLYMERIZATION
dc.subject.enDIRECT ACTIVITY EXCHANGE
dc.subject.enLIVING POLYMERIZATION
dc.subject.enCATIONIC-POLYMERIZATION
dc.subject.enRING-OPENING POLYMERIZATION
dc.subject.enEXHIBITING SLOW EQUILIBRIA
dc.title.enExpanding the Scope of Group Transfer Polymerization Using N-Heterocyclic Carbenes as Catalysts: Application to Miscellaneous (Meth)acrylic Monomers and Kinetic Investigations
dc.typeArticle de revue
dc.identifier.doi10.1021/ma101478p
dc.subject.halChimie/Polymères
bordeaux.journalMacromolecules
bordeaux.page8853-8861
bordeaux.volume43
bordeaux.hal.laboratoriesLaboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629*
bordeaux.issue21
bordeaux.institutionBordeaux INP
bordeaux.institutionUniversité de Bordeaux
bordeaux.peerReviewedoui
hal.identifierhal-00679080
hal.version1
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-00679080v1
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Macromolecules&rft.date=2010&rft.volume=43&rft.issue=21&rft.spage=8853-8861&rft.epage=8853-8861&rft.eissn=0024-9297&rft.issn=0024-9297&rft.au=RAYNAUD,%20Jean&NA,%20Liu&GNANOU,%20Yves&TATON,%20Daniel&rft.genre=article


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