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dc.rights.licenseopen
hal.structure.identifierTeam 1 LCPO : Polymerization Catalyses & Engineering
dc.contributor.authorRADCHENKO, Alexei
hal.structure.identifierTeam 1 LCPO : Polymerization Catalyses & Engineering
dc.contributor.authorGRANGE, Jérémie
hal.structure.identifierTeam 1 LCPO : Polymerization Catalyses & Engineering
dc.contributor.authorVAX, Amelie
hal.structure.identifierSociété Michelin
dc.contributor.authorJEAN-BAPTISTE-DIT-DOMINIQUE, François
hal.structure.identifierSociété Michelin
dc.contributor.authorMATMOUR, Rachid
hal.structure.identifierTeam 2 LCPO : Biopolymers & Bio-sourced Polymers
dc.contributor.authorGRELIER, Stéphane
hal.structure.identifierTeam 1 LCPO : Polymerization Catalyses & Engineering
dc.contributor.authorPERUCH, Frédéric
IDREF: 152900748
dc.date.accessioned2020
dc.date.available2020
dc.date.issued2019
dc.identifier.issn1759-9954
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/19572
dc.description.abstractEnThe synthesis of polypeptide hybrids by controlled/living ring-opening polymerization of N-carboxyanhydrides (NCA) using Schreiner′s thiourea catalyst and amino-alcohol terminated poly(1,4-cis-isoprene)s as initiators was demonstrated for γ-benzyl-ʟ-glutamate (BLG) and ε-tert-butyloxycarbonyl-ʟ-lysine (BLL) NCAs. One-pot synthesis of amino-alcohol terminated macroinitiators from heterotelechelic keto/aldehyde polyisoprene by reductive amination of carbonyl(s) was presented. Selection of amines allowed to obtain mono-, di-and tri-functional macroinitiators that were used for the synthesis of polyisoprene-polypeptide hybrids of different architecture: AB, BAB, AB2, BAB2, CBABC. Due to the living character of the polymerization, the molar mass of the polypeptide blocks could be controlled by the monomer to initiator ratio (6000<Mn<44000 g/mol), while sequential monomer addition allowed the synthesis of a pentablock terpolymer: poly(BLG-b-BLL-b-isoprene-b-BLL-b-BLG)
dc.language.isoen
dc.publisherRoyal Society of Chemistry - RSC
dc.title.enFacile synthesis of 1,4-cis-polyisoprene–polypeptide hybrids with different architectures
dc.typeArticle de revue
dc.identifier.doi10.1039/c9py00241c
dc.subject.halChimie/Polymères
bordeaux.journalPolymer Chemistry
bordeaux.page2456-2468
bordeaux.volume10
bordeaux.hal.laboratoriesLaboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629*
bordeaux.issue19
bordeaux.institutionBordeaux INP
bordeaux.institutionUniversité de Bordeaux
bordeaux.peerReviewedoui
hal.identifierhal-02136046
hal.version1
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-02136046v1
bordeaux.COinSctx_ver=Z39.88-2004&amp;rft_val_fmt=info:ofi/fmt:kev:mtx:journal&amp;rft.jtitle=Polymer%20Chemistry&amp;rft.date=2019&amp;rft.volume=10&amp;rft.issue=19&amp;rft.spage=2456-2468&amp;rft.epage=2456-2468&amp;rft.eissn=1759-9954&amp;rft.issn=1759-9954&amp;rft.au=RADCHENKO,%20Alexei&amp;GRANGE,%20J%C3%A9r%C3%A9mie&amp;VAX,%20Amelie&amp;JEAN-BAPTISTE-DIT-DOMINIQUE,%20Fran%C3%A7ois&amp;MATMOUR,%20Rachid&amp;rft.genre=article


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