Synthesis of dihydroxy poly(ethylene-co-butadiene) via metathetical depolymerization: Kinetic and mechanistic aspects
PERUCH, Frédéric
Laboratoire de Chimie des Polymères Organiques [LCPO]
Team 1 LCPO : Polymerization Catalyses & Engineering
Laboratoire de Chimie des Polymères Organiques [LCPO]
Team 1 LCPO : Polymerization Catalyses & Engineering
CARLOTTI, Stéphane
Laboratoire de Chimie des Polymères Organiques [LCPO]
Team 1 LCPO : Polymerization Catalyses & Engineering
Voir plus >
Laboratoire de Chimie des Polymères Organiques [LCPO]
Team 1 LCPO : Polymerization Catalyses & Engineering
PERUCH, Frédéric
Laboratoire de Chimie des Polymères Organiques [LCPO]
Team 1 LCPO : Polymerization Catalyses & Engineering
Laboratoire de Chimie des Polymères Organiques [LCPO]
Team 1 LCPO : Polymerization Catalyses & Engineering
CARLOTTI, Stéphane
Laboratoire de Chimie des Polymères Organiques [LCPO]
Team 1 LCPO : Polymerization Catalyses & Engineering
Laboratoire de Chimie des Polymères Organiques [LCPO]
Team 1 LCPO : Polymerization Catalyses & Engineering
DEFFIEUX, Alain
Laboratoire de Chimie des Polymères Organiques [LCPO]
Team 1 LCPO : Polymerization Catalyses & Engineering
< Réduire
Laboratoire de Chimie des Polymères Organiques [LCPO]
Team 1 LCPO : Polymerization Catalyses & Engineering
Langue
en
Article de revue
Ce document a été publié dans
Polymer. 2008, vol. 49, n° 23, p. 4935-4941
Elsevier
Résumé en anglais
We investigate the synthesis of dihydroxytelechelic poly(ethylene-co-1,3-butadiene) via metathetical depolymerization of the corresponding high molar mass copolymers in the presence of first generation Grubbs catalyst and ...Lire la suite >
We investigate the synthesis of dihydroxytelechelic poly(ethylene-co-1,3-butadiene) via metathetical depolymerization of the corresponding high molar mass copolymers in the presence of first generation Grubbs catalyst and butene diacetate as functionalizing chain transfer agent, followed by hydrolysis of the acetoxy chain ends. Formation of telechelic oligomers is complicated by a fast back-biting reaction leading to cyclohexene and macrocycles production. The thermodynamically favored formation of unsaturated six membered ring results from the presence of 1,7-dienic unsaturations in the starting copolymer. Macrocycles also rapidly and almost quantitatively form in the first reaction stage. Opportunely they can re-open in the presence of functionalizing transfer agent, owing that the later is introduced in molar excess with respect to the macrocycle, finally yielding linear dihydroxytelechelic oligomers.< Réduire
Mots clés en anglais
metathesis
poly(ethylene-co-butadiene)
depolymerization
Origine
Importé de halUnités de recherche