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dc.rights.licenseopen
hal.structure.identifierInst Chem Technol, Dept Polymers, Prague
dc.contributor.authorHOŠŤÁLEK, Zdeněk
hal.structure.identifierInst Chem Technol, Dept Polymers, Prague
dc.contributor.authorMUNDIL, Robert
dc.contributor.authorCÍSAŘOVÁ, Ivana
hal.structure.identifierAcad Sci Czeh Republic, Inst Macromol Chem
dc.contributor.authorTRHLIKOVA, Olga
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.authorPERUCH, Frédéric
IDREF: 152900748
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
dc.contributor.authorCRAMAIL, Henri
hal.structure.identifierInst Chem Technol, Dept Polymers, Prague
dc.contributor.authorMERNA, Jan
dc.date.accessioned2020
dc.date.available2020
dc.date.issued2015
dc.identifier.issn0032-3861
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/19773
dc.description.abstractEnThe series of novel symmetric and asymmetric salphen cobalt (III) complexes with different counteranions (trichloroacetate, dinitrophenolate, pentafluorobenzoate and acetate) was synthesized and used as catalysts in copolymerization of CO2 with propylene oxide (PO) and cyclohexene oxide (CHO). Hexacoordinated structure of complexes adducts was found in solid phase. The effect of catalyst structure, temperature, CO2 pressure, catalyst/cocatalyst ratio on overall activity and selectivity was investigated. Synthesized salphen-Co (III) complexes were effective for both PO/CO2 and CHO/CO2 highly alternating copolymerization. Substitution of phenylene framework of salphen ligand by chlorine atom led to decrease of activity in PO/CO2 copolymerization. Complexes with trichloroacetate counteranion were shown to be the most active and selective in PO/CO2 copolymerization leading to poly(propylenecarbonate) with highest molar mass. On contrary, catalytic performance of salphen Co (III) complexes in CHO/CO2 copolymerization was almost independent on ligand structure and counteranion. Excellent selectivity to poly(cyclohexenecarbonate) was achieved even at 0.1 MPa CO2. MALDI-TOF analysis of polycarbonates was used to investigate the initiation step of the copolymerization.
dc.language.isoen
dc.publisherElsevier
dc.subject.enCYCLOHEXENE OXIDE
dc.subject.enSALEN COMPLEXES
dc.subject.enCobalt salphen catalyst
dc.subject.enCO2 epoxide copolymerization
dc.subject.enMALDI-TOF
dc.subject.enCO2/PROPYLENE OXIDE COPOLYMERIZATION
dc.subject.enRING-OPENING POLYMERIZATION
dc.subject.enDIIMINATE ZINC CATALYSTS
dc.subject.enCARBON-DIOXIDE
dc.subject.enALTERNATING COPOLYMERIZATION
dc.subject.enPROPYLENE-OXIDE
dc.subject.enPOLY(PROPYLENE CARBONATE)
dc.subject.enCO2/EPOXIDE COPOLYMERIZATION
dc.title.enSalphen-Co(III) complexes catalyzed copolymerization of epoxides with CO2
dc.typeArticle de revue
dc.identifier.doi10.1016/j.polymer.2015.02.018
dc.subject.halChimie/Polymères
dc.subject.halChimie/Matériaux
dc.subject.halChimie/Catalyse
dc.subject.halChimie
bordeaux.journalPolymer
bordeaux.page52-61
bordeaux.volume63
bordeaux.hal.laboratoriesLaboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629*
bordeaux.institutionBordeaux INP
bordeaux.institutionUniversité de Bordeaux
bordeaux.peerReviewedoui
hal.identifierhal-01365295
hal.version1
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-01365295v1
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Polymer&rft.date=2015&rft.volume=63&rft.spage=52-61&rft.epage=52-61&rft.eissn=0032-3861&rft.issn=0032-3861&rft.au=HOS%CC%8CT%CC%8CA%CC%81LEK,%20Zdene%CC%8Ck&MUNDIL,%20Robert&C%C3%8DSA%C5%98OV%C3%81,%20Ivana&TRHLIKOVA,%20Olga&GRAU,%20Etienne&rft.genre=article


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