Organocatalytic vs. Ru-based electrochemical hydrogenation of nitrobenzene in competition with the hydrogen evolution reaction.


Journal

Dalton transactions (Cambridge, England : 2003)
ISSN: 1477-9234
Titre abrégé: Dalton Trans
Pays: England
ID NLM: 101176026

Informations de publication

Date de publication:
19 May 2020
Historique:
pubmed: 2 5 2020
medline: 2 5 2020
entrez: 2 5 2020
Statut: ppublish

Résumé

The electrochemical reduction of organic contaminants allows their removal from water. In this contribution, the electrocatalytic hydrogenation of nitrobenzene is studied using both oxidized carbon fibres and ruthenium nanoparticles supported on unmodified carbon fibres as catalysts. The two systems produce azoxynitrobenzene as the main product, while aniline is only observed in minor quantities. Although PhNO2 hydrogenation is the favoured reaction, the hydrogen evolution reaction (HER) competes in both systems under catalytic conditions. H2 formation occurs in larger amounts when using the Ru nanoparticle based catalyst. While similar reaction outputs were observed for both catalytic systems, DFT calculations revealed some significant differences related to distinct interactions between the catalytic material and the organic substrates or products, which could pave the way for the design of new catalytic materials.

Identifiants

pubmed: 32355938
doi: 10.1039/d0dt01075h
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

6446-6456

Auteurs

Alicia Moya (A)

Department of Inorganic Chemistry (module 07), Universidad Autónoma de Madrid, 28049, Madrid, Spain. ruben.mas@uam.es.

Jordi Creus (J)

Departament of Chemistry, Universitat Autònoma de Barcelona, 08193, Cerdanyola del Vallès, Barcelona, Spain. Xavier.sala@uab.cat and CNRS, LCC (Laboratoire de Chimie de Coordination), UPR8241, Université de Toulouse, UPS, INPT, F-31077 Toulouse cedex 4, France.

Nuria Romero (N)

Departament of Chemistry, Universitat Autònoma de Barcelona, 08193, Cerdanyola del Vallès, Barcelona, Spain. Xavier.sala@uab.cat.

José Alemán (J)

Department of Organic Chemistry (module 01), Universidad Autónoma de Madrid, 28049, Madrid, Spain and Institute for Advanced Research in Chemical Sciences (IAdChem), Universidad Autónoma de Madrid, 28049, Madrid, Spain.

Xavier Solans-Monfort (X)

Departament of Chemistry, Universitat Autònoma de Barcelona, 08193, Cerdanyola del Vallès, Barcelona, Spain. Xavier.sala@uab.cat.

Karine Philippot (K)

CNRS, LCC (Laboratoire de Chimie de Coordination), UPR8241, Université de Toulouse, UPS, INPT, F-31077 Toulouse cedex 4, France.

Jordi García-Antón (J)

Departament of Chemistry, Universitat Autònoma de Barcelona, 08193, Cerdanyola del Vallès, Barcelona, Spain. Xavier.sala@uab.cat.

Xavier Sala (X)

Departament of Chemistry, Universitat Autònoma de Barcelona, 08193, Cerdanyola del Vallès, Barcelona, Spain. Xavier.sala@uab.cat.

Rubén Mas-Ballesté (R)

Department of Inorganic Chemistry (module 07), Universidad Autónoma de Madrid, 28049, Madrid, Spain. ruben.mas@uam.es and Institute for Advanced Research in Chemical Sciences (IAdChem), Universidad Autónoma de Madrid, 28049, Madrid, Spain.

Classifications MeSH