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hal.structure.identifierInstitut des Sciences Moléculaires [ISM]
dc.contributor.authorALSARRAF, Jérôme
hal.structure.identifierInstitut des Sciences Moléculaires [ISM]
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
dc.contributor.authorAMMAR, Yacine Ait
hal.structure.identifierInstitut des Sciences Moléculaires [ISM]
dc.contributor.authorROBERT, Frédéric
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.authorCLOUTET, Eric
IDREF: 151048681
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 2 LCPO : Biopolymers & Bio-sourced Polymers
dc.contributor.authorCRAMAIL, Henri
hal.structure.identifierInstitut des Sciences Moléculaires [ISM]
dc.contributor.authorLANDAIS, Yannick
dc.date.accessioned2020
dc.date.available2020
dc.date.issued2012
dc.identifier.issn0024-9297
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/20465
dc.description.abstractEnA systematic survey of basic/nucleophilic organocatalysts for the polyaddition in bulk of polyols, PEG-600, and PTMO-650, to isophorone diisocyanate (IPDI) has been performed. Guanidines were shown to be very efficient catalysts for the urethane linkage formation. Bicyclic penta-alkylated guanidines such as MTBD led to polyurethane molecular weight and dispersity that are in the range of those observed with tin-based catalysts such as DBTDL. Tetra-alkylated guanidine such as TBD was shown to be a weaker catalyst as compared to pentaalkylated guanidines, as a result of its high reactivity toward isocyanate, resulting in the formation of a less nucleophilic urea. Although the mechanism has not yet been firmly established, these experiments suggest that a nucleophilic-catalysis mechanism, involving the attack of one of the nitrogen of the guanidine onto the unsaturated system of the isocyanate, should not be totally ruled out with such strong Bronsted base catalysts.
dc.language.isoen
dc.publisherAmerican Chemical Society
dc.subject.enACTIVATION
dc.subject.enISOCYANATES
dc.subject.enLACTIDE
dc.subject.enCO2
dc.subject.enORGANIC CATALYSTS
dc.subject.enLIVING POLYMERIZATION
dc.subject.enCATALYTIC MECHANISMS
dc.subject.enRING-OPENING POLYMERIZATION
dc.subject.enN-HETEROCYCLIC CARBENES
dc.title.enCyclic Guanidines as Efficient Organocatalysts for the Synthesis of Polyurethanes
dc.typeArticle de revue
dc.identifier.doi10.1021/ma2026258
dc.subject.halChimie/Polymères
bordeaux.journalMacromolecules
bordeaux.page2249-2256
bordeaux.volume45
bordeaux.hal.laboratoriesLaboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629*
bordeaux.issue5
bordeaux.institutionBordeaux INP
bordeaux.institutionUniversité de Bordeaux
bordeaux.peerReviewedoui
hal.identifierhal-00758513
hal.version1
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-00758513v1
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Macromolecules&rft.date=2012&rft.volume=45&rft.issue=5&rft.spage=2249-2256&rft.epage=2249-2256&rft.eissn=0024-9297&rft.issn=0024-9297&rft.au=ALSARRAF,%20J%C3%A9r%C3%B4me&AMMAR,%20Yacine%20Ait&ROBERT,%20Fr%C3%A9d%C3%A9ric&CLOUTET,%20Eric&CRAMAIL,%20Henri&rft.genre=article


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