Organic Salts and Merrifield Resin Supported [PM(12)O(40)](3−) (M = Mo or W) as Catalysts for Adipic Acid Synthesis

Adipic acid (AA) was obtained by catalyzed oxidation of cyclohexene, epoxycyclohexane, or cyclohexanediol under organic solvent-free conditions using aqueous hydrogen peroxide (30%) as an oxidizing agent and molybdenum- or tungsten-based Keggin polyoxometalates (POMs) surrounded by organic cations o...

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Detalles Bibliográficos
Autores principales: Pisk, Jana, Agustin, Dominique, Poli, Rinaldo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6412659/
https://www.ncbi.nlm.nih.gov/pubmed/30795615
http://dx.doi.org/10.3390/molecules24040783
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author Pisk, Jana
Agustin, Dominique
Poli, Rinaldo
author_facet Pisk, Jana
Agustin, Dominique
Poli, Rinaldo
author_sort Pisk, Jana
collection PubMed
description Adipic acid (AA) was obtained by catalyzed oxidation of cyclohexene, epoxycyclohexane, or cyclohexanediol under organic solvent-free conditions using aqueous hydrogen peroxide (30%) as an oxidizing agent and molybdenum- or tungsten-based Keggin polyoxometalates (POMs) surrounded by organic cations or ionically supported on functionalized Merrifield resins. Operating under these environmentally friendly, greener conditions and with low catalyst loading (0.025% for the molecular salts and 0.001–0.007% for the supported POMs), AA could be produced in interesting yields.
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spelling pubmed-64126592019-04-09 Organic Salts and Merrifield Resin Supported [PM(12)O(40)](3−) (M = Mo or W) as Catalysts for Adipic Acid Synthesis Pisk, Jana Agustin, Dominique Poli, Rinaldo Molecules Article Adipic acid (AA) was obtained by catalyzed oxidation of cyclohexene, epoxycyclohexane, or cyclohexanediol under organic solvent-free conditions using aqueous hydrogen peroxide (30%) as an oxidizing agent and molybdenum- or tungsten-based Keggin polyoxometalates (POMs) surrounded by organic cations or ionically supported on functionalized Merrifield resins. Operating under these environmentally friendly, greener conditions and with low catalyst loading (0.025% for the molecular salts and 0.001–0.007% for the supported POMs), AA could be produced in interesting yields. MDPI 2019-02-21 /pmc/articles/PMC6412659/ /pubmed/30795615 http://dx.doi.org/10.3390/molecules24040783 Text en © 2019 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 Article
Pisk, Jana
Agustin, Dominique
Poli, Rinaldo
Organic Salts and Merrifield Resin Supported [PM(12)O(40)](3−) (M = Mo or W) as Catalysts for Adipic Acid Synthesis
title Organic Salts and Merrifield Resin Supported [PM(12)O(40)](3−) (M = Mo or W) as Catalysts for Adipic Acid Synthesis
title_full Organic Salts and Merrifield Resin Supported [PM(12)O(40)](3−) (M = Mo or W) as Catalysts for Adipic Acid Synthesis
title_fullStr Organic Salts and Merrifield Resin Supported [PM(12)O(40)](3−) (M = Mo or W) as Catalysts for Adipic Acid Synthesis
title_full_unstemmed Organic Salts and Merrifield Resin Supported [PM(12)O(40)](3−) (M = Mo or W) as Catalysts for Adipic Acid Synthesis
title_short Organic Salts and Merrifield Resin Supported [PM(12)O(40)](3−) (M = Mo or W) as Catalysts for Adipic Acid Synthesis
title_sort organic salts and merrifield resin supported [pm(12)o(40)](3−) (m = mo or w) as catalysts for adipic acid synthesis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6412659/
https://www.ncbi.nlm.nih.gov/pubmed/30795615
http://dx.doi.org/10.3390/molecules24040783
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