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hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
dc.contributor.authorPINAUD, Julien
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
dc.contributor.authorKARI, Vijayakrishna
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 1 LCPO : Polymerization Catalyses & Engineering
dc.contributor.authorTATON, Daniel
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
dc.contributor.authorGNANOU, Yves
dc.date.accessioned2020
dc.date.available2020
dc.date.issued2009
dc.identifier.issn0141-8130
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/20632
dc.description.abstractEnBenzoin condensation consists in reacting two aldehyde functions through a resonance-stabilized enaminol-type intermediate called the Breslow intermediate. This communication describes for the first time the use of N-heterocyclic carbenes (NHCs) as organic catalysts for the step-growth polymerization of a bis-aldehyde monomer, namely terephtaldehyde, which leads to poly(l,4-phenylene-l-oxo-2-hydroxyethylene) referred to as polybenzoin. These NHC-catalyzed polymerizations presumably involve the formation of Breslow intermediates. The effect of the NHCs catalyst activity and of the solvent polarity on the kinetics of the polymerization and on the formation of linear and cyclic polybenzoins is discussed.
dc.language.isoen
dc.publisherElsevier
dc.subject.enN-heterocyclic carbine
dc.subject.enbenzoin condensation
dc.subject.enstep-growth polymerization
dc.subject.enBreslow intermediate
dc.subject.enorganocatalysis
dc.title.enStep-growth Polymerization of Terephtaldehyde Catalyzed by N-Heterocyclic Carbenes
dc.typeArticle de revue
dc.subject.halChimie/Polymères
bordeaux.journalInternational Journal of Biological Macromolecules
bordeaux.page4932-4936
bordeaux.volume42
bordeaux.hal.laboratoriesLaboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629*
bordeaux.issue14
bordeaux.institutionBordeaux INP
bordeaux.institutionUniversité de Bordeaux
bordeaux.peerReviewedoui
hal.identifierhal-00400016
hal.version1
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-00400016v1
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