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hal.structure.identifierInstitut Charles Sadron [ICS]
hal.structure.identifierInst Le Bel, Lab Chim Metaux & Catalyse
dc.contributor.authorPELASCINI, Frédéric
hal.structure.identifierInstitut Charles Sadron [ICS]
hal.structure.identifierTeam 1 LCPO : Polymerization Catalyses & Engineering
dc.contributor.authorPERUCH, Frédéric
IDREF: 152900748
hal.structure.identifierInstitut Charles Sadron [ICS]
dc.contributor.authorLUTZ, Pierre Joseph
hal.structure.identifierInst Le Bel, Lab Chim Metaux & Catalyse
dc.contributor.authorWESOLEK, Marcel
hal.structure.identifierInst Le Bel, Lab Chim Metaux & Catalyse
dc.contributor.authorKRESS, Jacky
dc.date.accessioned2020
dc.date.available2020
dc.date.issued2005
dc.identifier.issn0014-3057
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/20642
dc.description.abstractEnIn the present paper, the synthesis of new pyridine bis(imine) ligands modified with halogens (Cl, Br, CF3) or alkyl groups (Heptyl, tert-butyl, Phenyl,...) is reported. When coordinated with iron or cobalt dichloride, they yielded complexes which were associated to methylaluminoxane (MAO) to achieve the polymerization of ethylene. It was shown that cobalt catalysts are generally more sensitive to the ligand substitutions than the iron ones. The addition of a chlorine atom on the ligand frame is generally unfavorable. On the contrary, the presence of a bromine atom seems more favorable. Phenyl rings lead to almost completely inactive catalysts, probably because of a too weak coordination to the metal. It was also demonstrated that a mono-substitution of the aryl groups with an electron-withdrawing group (-CF3) is sufficient to yield polymers, whereas, considering the bulkiness of this substituent only, oligomers would have been expected
dc.language.isoen
dc.publisherElsevier
dc.subject.encobalt
dc.subject.enpyridine bis(imine)
dc.subject.enethylene polymerization
dc.subject.eniron
dc.title.enPyridine bis(imino) iron and cobalt complexes for ethylene polymerization: influence of the aryl imino substituents
dc.typeArticle de revue
dc.identifier.doi10.1016/j.eurpolymj.2004.12.004
dc.subject.halChimie/Polymères
bordeaux.journalEuropean Polymer Journal
bordeaux.page1288-1295
bordeaux.volume41
bordeaux.hal.laboratoriesLaboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629*
bordeaux.issue6
bordeaux.institutionBordeaux INP
bordeaux.institutionUniversité de Bordeaux
bordeaux.peerReviewedoui
hal.identifierhal-00397966
hal.version1
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-00397966v1
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