Catalytic Hydrogenation of Azobenzene in the Presence of a Cuboidal Mo3S4 Cluster via an Uncommon Sulfur-Based H2 Activation Mechanism
Impacto
Scholar |
Otros documentos de la autoría: Guillamón, Eva; Oliva, Mónica; Andres, Juan; Llusar, Rosa; Pedrajas Gual, Elena; Safont Villarreal, Vicent Sixte; Algarra, Andrés G.; García Basallote, Manuel
Metadatos
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INVESTIGACIONMetadatos
Título
Catalytic Hydrogenation of Azobenzene in the Presence of a Cuboidal Mo3S4 Cluster via an Uncommon Sulfur-Based H2 Activation MechanismAutoría
Fecha de publicación
2021Editor
American Chemical SocietyISSN
2155-5435Cita bibliográfica
Guillamón, E.; Oliva, M.; Andrés, J.; Llusar, R.; Pedrajas, E.; Safont, Vicent S.; Algarra, Andres G.; Basallote, Manuel G. Catalytic Hydrogenation of Azobenzene in the Presence of a Cuboidal Mo3S4 Cluster via an Uncommon Sulfur-Based H2 Activation Mechanism. ACS Catal. 2021, 11, 2, 608–614. https://doi.org/10.1021/acscatal.0c05299Tipo de documento
info:eu-repo/semantics/articleVersión de la editorial
https://pubs.acs.org/doi/abs/10.1021/acscatal.0c05299Versión
info:eu-repo/semantics/acceptedVersionPalabras clave / Materias
Resumen
Azobenzene hydrogenation is catalyzed under moderate conditions by a cuboidal Mo3(μ3-S)(μ-S)3 diamino complex via a cluster catalysis mechanism. Dihydrogen activation by the molecular [Mo3(μ3-S)(μ-S)3Cl3(dmen)3]+ ... [+]
Azobenzene hydrogenation is catalyzed under moderate conditions by a cuboidal Mo3(μ3-S)(μ-S)3 diamino complex via a cluster catalysis mechanism. Dihydrogen activation by the molecular [Mo3(μ3-S)(μ-S)3Cl3(dmen)3]+ cluster cation takes place at the μ-S bridging atoms without direct participation of the metals in clear contrast with classical concepts. The reaction occurs with the formation of 1,2-diphenylhydrazine as an intermediate with similar appearance and disappearance rate constants. On the basis of DFT calculations, a mechanism is proposed in which formation of 1,2-diphenylhydrazine and aniline occurs through two interconnected catalytic cycles that share a common reaction step that involves H2 addition to two of the bridging sulfur atoms of the catalyst to form a dithiolate Mo3(μ3-S)(μ-SH)2)(μ-S) adduct. Both catalytic cycles have similar activation barriers, in agreement with the experimental observation of close rate constant values. Microkinetic modeling of the process leads to computed concentration–time profiles in excellent agreement with the experimental ones providing additional support to the calculated reaction mechanism. Slight modifications on the experimental conditions of the catalytic protocol in combination with theoretical calculations discard a direct participation of the metal on the reaction mechanism. The effect of the ancillary ligands on the catalytic activity of the cluster fully agrees with the present mechanistic proposal. The results herein demonstrate the capability of molybdenum sulfide materials to activate hydrogen through an uncommon sulfur based mechanism opening attractive possibilities toward their applications as catalysts in other hydrogenation processes. [-]
Publicado en
ACS Catalysis, 2021, vol. 11, no 2Entidad financiadora
Ministerio de Ciencia, Innovación y Universidades | Agencia Estatal de Investigación | Universitat Jaume I | European Regional Development Fund
Identificador de la entidad financiadora
http://dx.doi.org/10.13039/501100011033 | http://dx.doi.org/10.13039/501100011033
Código del proyecto o subvención
MICIU/ICTI2017-2020/PGC2018-094417-B-I00 | PID2019-107006GB-C22 | UJI-B2017-44 | UJI-B2019-30 | FEDER-UCA18-106840
Título del proyecto o subvención
Aproximaciones racionales para el diseño de nuevos materiales mediante la combinación de teoría y experimento | Estudios cinético-mecanísticos sobre procesos catalíticos de oxidación e hidrogenación y reacciones relacionadas
Derechos de acceso
Copyright © American Chemical Society
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info:eu-repo/semantics/openAccess
http://rightsstatements.org/vocab/InC/1.0/
info:eu-repo/semantics/openAccess
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