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hal.structure.identifierDepartment of Colloid Chemistry [Potsdam]
dc.contributor.authorKUZMICZ, Danuta
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
dc.contributor.authorCOUPILLAUD, Paul
hal.structure.identifierDepartment of Colloid Chemistry [Potsdam]
dc.contributor.authorMEN, Yongjun
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 1 LCPO : Polymerization Catalyses & Engineering
dc.contributor.authorVIGNOLLE, Joan
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
dc.contributor.authorVENDRAMINETTO, Giordano
hal.structure.identifierDepartment of Colloid Chemistry [Potsdam]
dc.contributor.authorAMBROGI, Martina
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 1 LCPO : Polymerization Catalyses & Engineering
dc.contributor.authorTATON, Daniel
hal.structure.identifierDepartment of Colloid Chemistry [Potsdam]
dc.contributor.authorYUAN, Jiayin
dc.date.accessioned2020
dc.date.available2020
dc.date.issued2014
dc.identifier.issn0032-3861
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/20195
dc.description.abstractEnIonic liquid-functionalized mesoporous polymeric networks with specific surface area up to 935 m(2)/g have been successfully synthesized one pot by solvothermal copolymerization of divinylbenzene and monomeric ionic liquids. The as-obtained polymers exhibit a monolithic structure featuring large pore volumes, an abundant mesoporosity and an adjustable content of ionic liquids. The effect of the reaction conditions on the pore structure has been studied in detail. These poly(ionic liquid)-based porous networks (PILPNs) have then been employed as precursors in two distinct applications, namely organo-catalysis and production of microporous carbon monoliths. Selected organocatalyzed reactions, including carbonatation of propylene oxide by cycloaddition with carbon dioxide, benzoin condensation, and cyanosilylation of benzaldehyde have been readily triggered by PILPNs acting as crosslinked polymer-supported (pre)catalysts. The two latter reactions required the prior deprotonation of the imidazolium salt units with a strong base to successfully generate polymer-supported N-heterocyclic carbenes, referred to as poly(NHC)s. Facile recycling and reuse of polymer-supported (pre)catalysts was achieved by simple filtration owing to the heterogeneous reaction conditions. Furthermore, PILPNs could be easily converted into microporous carbon monoliths via CO2 activation. (C) 2014 Elsevier Ltd. All rights reserved.
dc.language.isoen
dc.publisherElsevier
dc.subject.enCO2
dc.subject.enFACILE PREPARATION
dc.subject.enPOROUS POLYMERS
dc.subject.enDIOXIDE
dc.subject.enPoly(ionic liquid)
dc.subject.enMesoporous polymer
dc.subject.enN-Heterocyclic carbene
dc.subject.enN-HETEROCYCLIC CARBENES
dc.subject.enPOLYMERIC IONIC LIQUIDS
dc.subject.enSOLID BASE CATALYSTS
dc.subject.enHYDROGEN CARBONATES
dc.subject.enEFFICIENT SYNTHESIS
dc.subject.enTRANSESTERIFICATION
dc.title.enFunctional mesoporous poly(ionic liquid)-based copolymer monoliths: From synthesis to catalysis and microporous carbon production
dc.typeArticle de revue
dc.identifier.doi10.1016/j.polymer.2014.04.032
dc.subject.halChimie/Polymères
bordeaux.journalPolymer
bordeaux.page3423-3430 SI
bordeaux.volume55
bordeaux.hal.laboratoriesLaboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629*
bordeaux.issue16
bordeaux.institutionBordeaux INP
bordeaux.institutionUniversité de Bordeaux
bordeaux.peerReviewedoui
hal.identifierhal-01373031
hal.version1
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-01373031v1
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Polymer&rft.date=2014&rft.volume=55&rft.issue=16&rft.spage=3423-3430%20%20SI&rft.epage=3423-3430%20%20SI&rft.eissn=0032-3861&rft.issn=0032-3861&rft.au=KUZMICZ,%20Danuta&COUPILLAUD,%20Paul&MEN,%20Yongjun&VIGNOLLE,%20Joan&VENDRAMINETTO,%20Giordano&rft.genre=article


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