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Selective Styrene Oxidation to Benzaldehyde over Recently Developed Heterogeneous Catalysts

The selective oxidation of styrene under heterogeneous catalyzed conditions delivers environmentally friendly paths for the production of benzaldehyde, an important intermediate for the synthesis of several products. The present review explores heterogeneous catalysts for styrene oxidation using a v...

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Autores principales: Andrade, Marta A., Martins, Luísa M. D. R. S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8002843/
https://www.ncbi.nlm.nih.gov/pubmed/33802853
http://dx.doi.org/10.3390/molecules26061680
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author Andrade, Marta A.
Martins, Luísa M. D. R. S.
author_facet Andrade, Marta A.
Martins, Luísa M. D. R. S.
author_sort Andrade, Marta A.
collection PubMed
description The selective oxidation of styrene under heterogeneous catalyzed conditions delivers environmentally friendly paths for the production of benzaldehyde, an important intermediate for the synthesis of several products. The present review explores heterogeneous catalysts for styrene oxidation using a variety of metal catalysts over the last decade. The use of several classes of supports is discussed, including metal–organic frameworks, zeolites, carbon materials and silicas, among others. The studied catalytic systems propose as most used oxidants tert-butyl hydroperoxide, and hydrogen peroxide and mild reaction conditions. The reaction mechanism proceeds through the generation of an intermediate reactive metal–oxygen species by catalyst-oxidant interactions. Overall, most of the studies highlight the synergetic effects among the metal and support for the activity and selectivity enhancement.
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spelling pubmed-80028432021-03-28 Selective Styrene Oxidation to Benzaldehyde over Recently Developed Heterogeneous Catalysts Andrade, Marta A. Martins, Luísa M. D. R. S. Molecules Review The selective oxidation of styrene under heterogeneous catalyzed conditions delivers environmentally friendly paths for the production of benzaldehyde, an important intermediate for the synthesis of several products. The present review explores heterogeneous catalysts for styrene oxidation using a variety of metal catalysts over the last decade. The use of several classes of supports is discussed, including metal–organic frameworks, zeolites, carbon materials and silicas, among others. The studied catalytic systems propose as most used oxidants tert-butyl hydroperoxide, and hydrogen peroxide and mild reaction conditions. The reaction mechanism proceeds through the generation of an intermediate reactive metal–oxygen species by catalyst-oxidant interactions. Overall, most of the studies highlight the synergetic effects among the metal and support for the activity and selectivity enhancement. MDPI 2021-03-17 /pmc/articles/PMC8002843/ /pubmed/33802853 http://dx.doi.org/10.3390/molecules26061680 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Andrade, Marta A.
Martins, Luísa M. D. R. S.
Selective Styrene Oxidation to Benzaldehyde over Recently Developed Heterogeneous Catalysts
title Selective Styrene Oxidation to Benzaldehyde over Recently Developed Heterogeneous Catalysts
title_full Selective Styrene Oxidation to Benzaldehyde over Recently Developed Heterogeneous Catalysts
title_fullStr Selective Styrene Oxidation to Benzaldehyde over Recently Developed Heterogeneous Catalysts
title_full_unstemmed Selective Styrene Oxidation to Benzaldehyde over Recently Developed Heterogeneous Catalysts
title_short Selective Styrene Oxidation to Benzaldehyde over Recently Developed Heterogeneous Catalysts
title_sort selective styrene oxidation to benzaldehyde over recently developed heterogeneous catalysts
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8002843/
https://www.ncbi.nlm.nih.gov/pubmed/33802853
http://dx.doi.org/10.3390/molecules26061680
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