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hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
dc.contributor.authorDURAND, Pierre-Luc
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
dc.contributor.authorBRÈGE, Antoine
hal.structure.identifierInstitut des corps gras [ITERG]
dc.contributor.authorCHOLLET, Guillaume
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
dc.contributor.authorGRAU, Etienne
IDREF: 187909261
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
dc.contributor.authorCRAMAIL, Henri
dc.date.accessioned2020
dc.date.available2020
dc.date.issued2018
dc.identifier.issn2161-1653
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/19801
dc.description.abstractEnFatty acids were used as precursors for the synthesis of photosensitive polycarbonate materials. In order to avoid multistep reactions, a simple and straightforward methodology toward the synthesis of photosensitive monomers has been developed. Hence, a fatty acid–based cyclic carbonate bearing an unsaturation was synthesized and subsequently polymerized in a controlled manner (Đ = 1.07) by organo-catalyzed ring-opening polymerization (ROP). A thio-cinnamate derivative was then readily synthesized via a one-pot reaction and grafted onto the polycarbonate backbone by thiol–ene reaction. The content of photoresponsive cinnamoyl moiety grafted on the polycarbonate was tunable with the reaction time. Such functionalized polycarbonates could be crosslinked (by UV irradiation at 365 nm) and partially decrosslinked (irradiated at 254 nm) and exhibit versatile properties ranging from rather tough materials to elastomeric networks with respect to the content of the photosensitive cinnamoyl moiety grafted on the polymer.
dc.language.isoen
dc.publisherWashington, D.C : American Chemical Society
dc.subject.enfatty acid
dc.subject.enpolycarbonate
dc.title.enA Simple and Efficient Approach toward Photosensitive Biobased Aliphatic Polycarbonate Materials
dc.typeArticle de revue
dc.identifier.doi10.1021/acsmacrolett.8b00003
dc.subject.halChimie/Polymères
bordeaux.journalACS Macro Letters
bordeaux.page250-254
bordeaux.volume7
bordeaux.hal.laboratoriesLaboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629*
bordeaux.issue2
bordeaux.institutionBordeaux INP
bordeaux.institutionUniversité de Bordeaux
bordeaux.peerReviewedoui
hal.identifierhal-01917959
hal.version1
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-01917959v1
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=ACS%20Macro%20Letters&rft.date=2018&rft.volume=7&rft.issue=2&rft.spage=250-254&rft.epage=250-254&rft.eissn=2161-1653&rft.issn=2161-1653&rft.au=DURAND,%20Pierre-Luc&BR%C3%88GE,%20Antoine&CHOLLET,%20Guillaume&GRAU,%20Etienne&CRAMAIL,%20Henri&rft.genre=article


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