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hal.structure.identifierLaboratoire de chimie de coordination [LCC]
dc.contributor.authorKALAMBLAYIL SANKARANARAYANAN, Santhosh Kumar
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 1 LCPO : Polymerization Catalyses & Engineering
dc.contributor.authorGNANOU, Yves
hal.structure.identifierLaboratoire de chimie de coordination [LCC]
dc.contributor.authorCHAMPOURET, Yohan
hal.structure.identifierLaboratoire de chimie de coordination [LCC]
dc.contributor.authorDARAN, Jean-Claude
hal.structure.identifierLaboratoire de chimie de coordination [LCC]
dc.contributor.authorPOLI, Rinaldo
dc.date.accessioned2020
dc.date.available2020
dc.date.issued2009
dc.identifier.issn0947-6539
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/20648
dc.description.abstractEnThe complex [Co-II(tmhd)(2)] (4; tmhd=2,2,6,6-tetramethylhepta-3,5-dionato) has been investigated as a mediator for controlled radical polymerization of vinyl acetate (VAc) and compared with the analogue [Co-II(acac)(2)] (1; acac=acetylacetonato). A relatively well controlled process occurs, after an induction time, with 2,2'-azobis(4-methoxyl-2.4-dimethylvaleronitrile) (V-70) as radical initiator at 30 degrees C. However, whereas the polymerization essentially stops after about six initiator half-lives in the presence of 1, it continues with a first-order rate law in the presence of 4. The successful simulation of the kinetic data shows that 4 operates simultaneously by associative (degenerative transfer, DT) and dissociative (organometallic radical polymerization., OMRP) mechanisms. The occurrence of OMRP was confirmed by an independent polymerization experiment starting from an isolated and purified [Co(tmhd)(2)](PVAc) macroinitiator. The polymer molecular weight evolves linearly with conversion in accordance with the expected values for one chain per Co atom when DT is the predominant mechanism and also during the pure OMRP process; however, observation of stagnating molecular weights at long reaction times with concomitant breakdown of the first-order rate law for monomer consumption indicates a competitive chain-transfer process catalyzed by an increasing amount of Co-II. In the presence of external donors L (water, pyridine, triethylamine) the DT pathway is blocked and the OMRP pathway is accelerated, and polymerization with complex 4 is then about five times slower than with complex 1. The reversal of relative effective OMRP rate constants k(eff) (4>1 in the absence of external donors, 4<1 in their presence) is rationalized through competitive steric effects on Co-III-C and Co-II-L bond strengths. These propositions are supported by H-1 NMR studies and by DFT calculations.
dc.language.isoen
dc.publisherWiley-VCH Verlag
dc.subject.encobalt
dc.subject.endensity functional calculations
dc.subject.enpolymerization
dc.subject.enradical reactions
dc.subject.enreaction mechanis
dc.title.enRadical Polymerization of Vinyl Acetate with Bis(tetramethylheptadionato)cobalt(II): Coexistence of Three Different Mechanisms
dc.typeArticle de revue
dc.identifier.doi10.1002/chem.200802388
dc.subject.halChimie/Polymères
bordeaux.journalChemistry - A European Journal
bordeaux.page4874-4885
bordeaux.volume15
bordeaux.hal.laboratoriesLaboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629*
bordeaux.issue19
bordeaux.institutionBordeaux INP
bordeaux.institutionUniversité de Bordeaux
bordeaux.peerReviewedoui
hal.identifierhal-00397614
hal.version1
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-00397614v1
bordeaux.COinSctx_ver=Z39.88-2004&amp;rft_val_fmt=info:ofi/fmt:kev:mtx:journal&amp;rft.jtitle=Chemistry%20-%20A%20European%20Journal&amp;rft.date=2009&amp;rft.volume=15&amp;rft.issue=19&amp;rft.spage=4874-4885&amp;rft.epage=4874-4885&amp;rft.eissn=0947-6539&amp;rft.issn=0947-6539&amp;rft.au=KALAMBLAYIL%20SANKARANARAYANAN,%20Santhosh%20Kumar&amp;GNANOU,%20Yves&amp;CHAMPOURET,%20Yohan&amp;DARAN,%20Jean-Claude&amp;POLI,%20Rinaldo&amp;rft.genre=article


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