Rhodium Complexes Non-Covalently Bound to Cyclodextrins: Novel Water-Soluble Supramolecular Catalysts for the Biphasic Hydroformylation of Higher Olefins

Autor: Benoît Sueur, André Mortreux, Mathieu Sauthier, Hervé Bricout, Sébastien Tilloy, Yves Castanet, Loïc Leclercq, Eric Monflier
Přispěvatelé: Laboratoire de Physico-Chimie des Interfaces et Applications, Centre National de la Recherche Scientifique (CNRS), Unité de Catalyse et Chimie du Solide - UMR 8181 (UCCS), Centrale Lille Institut (CLIL)-Université d'Artois (UA)-Centrale Lille-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Université de Lille, Université d'Artois (UA)-Centrale Lille-Institut de Chimie du CNRS (INC)-Université de Lille-Centre National de la Recherche Scientifique (CNRS)
Rok vydání: 2005
Předmět:
Zdroj: Chemistry-A European Journal
Chemistry-A European Journal, Wiley-VCH Verlag, 2005, 11, pp.6228-6236. ⟨10.1002/chem.200500337⟩
Chemistry-A European Journal, 2005, 11, pp.6228-6236. ⟨10.1002/chem.200500337⟩
ISSN: 1521-3765
0947-6539
Popis: A new class of cationic alpha-cyclodextrins bearing 2-hydroxy-3-trimethylammoniopropyl groups has been synthesised. We investigated their efficiency as mass-transfer promoters in a biphasic hydroformylation reaction catalysed by a rhodium trisulfonated triphenylphosphine system. These cationic alpha-cyclodextrins greatly increased the reaction rate, the chemoselectivity, and, surprisingly, the linear-to-branched aldehyde ratio. We attributed this unexpected enhancement of the linear-to-branched aldehyde ratio to the in situ formation of new catalytic supramolecular species obtained by ion-exchange between the catalyst ligand and the cationic alpha-cyclodextrins.
Databáze: OpenAIRE