Highly regio-selective hydroformylation ...
Type de document :
Article dans une revue scientifique
URL permanente :
Titre :
Highly regio-selective hydroformylation of biomass derived eugenol using aqueous biphasic Rh/TPPTS/CDs as a greener and recyclable catalyst
Auteur(s) :
Jagtap, Samadhan A. [Auteur]
Monflier, Eric [Auteur]
Unité de Catalyse et Chimie du Solide - UMR 8181 [UCCS]
Ponchel, Anne [Auteur]
Unité de Catalyse et Chimie du Solide - UMR 8181 [UCCS]
Bhanage, Bhalchandra M. [Auteur]
Monflier, Eric [Auteur]
Unité de Catalyse et Chimie du Solide - UMR 8181 [UCCS]
Ponchel, Anne [Auteur]
Unité de Catalyse et Chimie du Solide - UMR 8181 [UCCS]
Bhanage, Bhalchandra M. [Auteur]
Titre de la revue :
Molecular Catalysis
Numéro :
436
Pagination :
157-163
Date de publication :
2017-07
Discipline(s) HAL :
Chimie/Catalyse
Résumé en anglais : [en]
A Rh/TPPTS catalyzed aqueous biphasic hydroformylation of eugenol was performed in an aqueous medium in the presence of different modified cyclodextrins. The internal olefin such as anethole shows high selectivity towards ...
Lire la suite >A Rh/TPPTS catalyzed aqueous biphasic hydroformylation of eugenol was performed in an aqueous medium in the presence of different modified cyclodextrins. The internal olefin such as anethole shows high selectivity towards the branched aldehydes (78%) where as terminal alkene like eugenol shows high selectivity towards the linear aldehydes (87%). The various reaction parameters such as effect of syngas pressure, time, temperature, catalyst precursor and loading have been studied. The high activity and high selectivity towards the linear aldehydes is due to the steric crowding of methyl group present in RAME-β-cyclodextrins. The effect of ratio of Rh/TPPTS/RAME-β-CD were also studied for the hydroformylation of eugenol. Moreover, this catalytic system was recycled up to four consecutive cycles without loss in its catalytic activity and selectivity.Lire moins >
Lire la suite >A Rh/TPPTS catalyzed aqueous biphasic hydroformylation of eugenol was performed in an aqueous medium in the presence of different modified cyclodextrins. The internal olefin such as anethole shows high selectivity towards the branched aldehydes (78%) where as terminal alkene like eugenol shows high selectivity towards the linear aldehydes (87%). The various reaction parameters such as effect of syngas pressure, time, temperature, catalyst precursor and loading have been studied. The high activity and high selectivity towards the linear aldehydes is due to the steric crowding of methyl group present in RAME-β-cyclodextrins. The effect of ratio of Rh/TPPTS/RAME-β-CD were also studied for the hydroformylation of eugenol. Moreover, this catalytic system was recycled up to four consecutive cycles without loss in its catalytic activity and selectivity.Lire moins >
Langue :
Anglais
Audience :
Internationale
Vulgarisation :
Non
Établissement(s) :
ENSCL
CNRS
Centrale Lille
Univ. Artois
Université de Lille
CNRS
Centrale Lille
Univ. Artois
Université de Lille
Collections :
Équipe(s) de recherche :
Catalyse et chimie supramoléculaire (CASU)
Date de dépôt :
2019-09-25T14:05:26Z