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hal.structure.identifierOsaka Municipal Tech Res Inst, Environm Technol Res Div
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
dc.contributor.authorKADOTA, Joji
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
dc.contributor.authorPAVLOVIC, Drazen
hal.structure.identifierOsaka Municipal Tech Res Inst, Environm Technol Res Div
dc.contributor.authorHIRANO, Hiroshi
hal.structure.identifierOsaka Municipal Tech Res Inst, Environm Technol Res Div
dc.contributor.authorOKADA, Akinori
hal.structure.identifierOsaka Municipal Tech Res Inst, Environm Technol Res Div
dc.contributor.authorAGARI, Yasuyuki
hal.structure.identifierInstitut des Sciences Moléculaires [ISM]
dc.contributor.authorBIBAL, Brigitte
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 1 LCPO : Polymerization Catalyses & Engineering
dc.contributor.authorDEFFIEUX, Alain
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 1 LCPO : Polymerization Catalyses & Engineering
dc.contributor.authorPERUCH, Frédéric
IDREF: 152900748
dc.date.accessioned2020
dc.date.available2020
dc.date.issued2014
dc.identifier.issn2046-2069
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/20234
dc.description.abstractEnThe acid-base catalytic system based on N,N-dimethyl-4-aminopyridine (DMAP) and a protic acid that has already been revealed to be efficient for the ring-opening polymerization (ROP) of L-lactide in solution at room temperature was tested for the same polymerization in bulk at 100 degrees C. As observed in solution, the presence of the DMAP center dot HX (X Cl, CH3SO3, CF3 SO3) salt enhanced yields. Linear and star-like polylactides with 3 and 4 branches were prepared. Polylactides were thus easily prepared reaching high molar masses (up to 75 000 g mol(-1) for linear PLLA and 140 000 g mol(-1) for star-like PLLA) with good control in less than 1 h. In all cases, the appearance of transesterification reactions was shown to occur only at very high yield. The ROP of lactones (epsilon-caprolactone and delta-valerolactone) was also investigated with the same catalytic systems in bulk conditions. In contrast to lactide polymerization, only the DMAP/DMAP center dot HOTf allowed lactone polymerization with a slower rate. However, the control over the molar masses remained very good. Block copolymers were also synthesized.
dc.language.isoen
dc.publisherRoyal Society of Chemistry
dc.subject.enACIDS
dc.subject.enCONTROLLED ROP
dc.subject.enORGANOCATALYSTS
dc.subject.enRING-OPENING POLYMERIZATION
dc.subject.enN-HETEROCYCLIC CARBENES
dc.subject.enEPSILON-CAPROLACTONE
dc.subject.enLIVING POLYMERIZATION
dc.subject.enCYCLIC ESTERS
dc.subject.enPOLYESTER SYNTHESIS
dc.subject.enBETA-BUTYROLACTONE
dc.title.enControlled bulk polymerization of L-lactide and lactones by dual activation with organo-catalytic systems
dc.typeArticle de revue
dc.identifier.doi10.1039/c4ra01239a
dc.subject.halChimie/Polymères
bordeaux.journalRSC Advances
bordeaux.page14725-14732
bordeaux.volume4
bordeaux.hal.laboratoriesLaboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629*
bordeaux.issue28
bordeaux.institutionBordeaux INP
bordeaux.institutionUniversité de Bordeaux
bordeaux.peerReviewedoui
hal.identifierhal-01368851
hal.version1
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-01368851v1
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=RSC%20Advances&rft.date=2014&rft.volume=4&rft.issue=28&rft.spage=14725-14732&rft.epage=14725-14732&rft.eissn=2046-2069&rft.issn=2046-2069&rft.au=KADOTA,%20Joji&PAVLOVIC,%20Drazen&HIRANO,%20Hiroshi&OKADA,%20Akinori&AGARI,%20Yasuyuki&rft.genre=article


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