Titre :

Ruthenium-catalyzed coupling reactions of co2 with c2h4 and hydrosilanes towards silyl esters

Auteur(s) :

Kirillov, Evgueni [Auteur]
Kunihiro, Kana [Auteur]
Heyte Dyshlovenko, Svetlana [Auteur]
Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
PAUL, Sébastien [Auteur]
Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Roisnel, Thierry [Auteur]
Carpentier, Jean-Francois [Auteur]

Titre de la revue :

Chemistry (Weinheim an der Bergstrasse, Germany)

Nom court de la revue :

Chemistry

Date de publication :

2020-12-30

ISSN :

1521-3765

Discipline(s) HAL :

Chimie/Catalyse

Résumé en anglais : [en]

A series of in situ-prepared catalytic systems incorporating RuII precursors and bidentate phosphine ligands has been probed in the reductive carboxylation of ethylene in the presence of triethylsilane as reductant. The ...
Lire la suite >A series of in situ-prepared catalytic systems incorporating RuII precursors and bidentate phosphine ligands has been probed in the reductive carboxylation of ethylene in the presence of triethylsilane as reductant. The catalytic production of propionate and acrylate silyl esters was evidenced by high-throughput screening (HTS) and implemented in batch reactor techniques. The most promising catalyst systems identified were made of Ru(H)(Cl)(CO)(PPh3 )3 and 1,4-bis(dicyclohexylphosphino)butane (DCPB) or 1,1'-ferrocene-diyl-bis(cyclohexylphosphine) (DCPF). A marked influence of water on the acrylate/propionate selectivity was noted. Turnover numbers [mol mol(Ru)-1 ] up to 16 for acrylate and up to 68 for propionate were reached under relatively mild conditions (20 bar, 100 °C, 0.5 mol % Ru, 40 mol % H2 O vs. HSiEt3 ). Possible mechanisms are discussed.Lire moins >

Langue :

Anglais

Audience :

Internationale

Vulgarisation :

Non

Établissement(s) :

CNRS
Centrale Lille
ENSCL
Univ. Artois
Université de Lille

Collections :

• Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181

Équipe(s) de recherche :

Valorisation des alcanes et de la biomasse (VAALBIO)

Date de dépôt :

2022-03-02T07:13:05Z