Direct aerobic oxidation of monoalcohol ...
Type de document :
Article dans une revue scientifique: Article original
URL permanente :
Titre :
Direct aerobic oxidation of monoalcohol and diols to acetals using tandem ru@mof catalysts
Auteur(s) :
Zhang, Songwei [Auteur]
Li, Jerry Pui Ho [Auteur]
Zhao, Jingpeng [Auteur]
Wu, Dan [Auteur]
Yuan, Biao [Auteur]
Hernandez, Willinton Yesid [Auteur]
Zhou, Wen-Juan [Auteur]
He, Tao [Auteur]
Yu, Yi [Auteur]
Yang, Yong [Auteur]
Ordomsky, Vitaly [Auteur]
Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Li, Tao [Auteur]
Li, Jerry Pui Ho [Auteur]
Zhao, Jingpeng [Auteur]
Wu, Dan [Auteur]
Yuan, Biao [Auteur]
Hernandez, Willinton Yesid [Auteur]
Zhou, Wen-Juan [Auteur]
He, Tao [Auteur]
Yu, Yi [Auteur]
Yang, Yong [Auteur]
Ordomsky, Vitaly [Auteur]

Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Li, Tao [Auteur]
Titre de la revue :
Nano research
Nom court de la revue :
Nano Res.
Date de publication :
2020-03-13
ISSN :
1998-0124
Mot(s)-clé(s) en anglais :
alcohols
aerobic oxidation
Ru nanoparticles
metal-organic framework
acetalization
aerobic oxidation
Ru nanoparticles
metal-organic framework
acetalization
Discipline(s) HAL :
Chimie/Catalyse
Résumé en anglais : [en]
The aerobic oxidation of monoalcohols and diols to acetals is an important academic and industrial challenge for the production of fine chemicals and intermediates. The existing methods usually rely on a two-step process ...
Lire la suite >The aerobic oxidation of monoalcohols and diols to acetals is an important academic and industrial challenge for the production of fine chemicals and intermediates. The existing methods usually rely on a two-step process in which alcohols are first oxidized to aldehydes over metal catalysts (Ru, Pt, Pd) and then acetalized using acids. Due to the instability of aldehydes, how to avoid over-oxidation to their respective carboxylic acids and esters is a long-standing challenge. For this reason, certain non-conjugated dialdehydes have never been successfully produced from diol oxidation. Hereby we report a Ru@metal-organic framework (MOF) tandem catalyst containing ultra-fine Ru nanoparticles (< 2 nm) for direct alcohol to acetal conversion of monoalcohol and diols with no formation of carboxylic acids. Mechanistic study reveals that the presence of Lewis acid sites in the MOF work in concert with Ru active sites to promptly convert aldehydes to acetals thereby effectively suppressing the formation of over-oxidation byproducts.Lire moins >
Lire la suite >The aerobic oxidation of monoalcohols and diols to acetals is an important academic and industrial challenge for the production of fine chemicals and intermediates. The existing methods usually rely on a two-step process in which alcohols are first oxidized to aldehydes over metal catalysts (Ru, Pt, Pd) and then acetalized using acids. Due to the instability of aldehydes, how to avoid over-oxidation to their respective carboxylic acids and esters is a long-standing challenge. For this reason, certain non-conjugated dialdehydes have never been successfully produced from diol oxidation. Hereby we report a Ru@metal-organic framework (MOF) tandem catalyst containing ultra-fine Ru nanoparticles (< 2 nm) for direct alcohol to acetal conversion of monoalcohol and diols with no formation of carboxylic acids. Mechanistic study reveals that the presence of Lewis acid sites in the MOF work in concert with Ru active sites to promptly convert aldehydes to acetals thereby effectively suppressing the formation of over-oxidation byproducts.Lire moins >
Langue :
Anglais
Audience :
Internationale
Vulgarisation :
Non
Établissement(s) :
CNRS
Centrale Lille
ENSCL
Univ. Artois
Université de Lille
Centrale Lille
ENSCL
Univ. Artois
Université de Lille
Collections :
Équipe(s) de recherche :
Catalyse pour l’énergie et la synthèse de molécules plateforme (CEMOP)
Date de dépôt :
2022-03-02T07:14:55Z