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Recyclable anhydride catalyst for H(2)O(2) oxidation: N-oxidation of pyridine derivatives
The catalytic efficiency and recyclability of poly(maleic anhydride-alt-1-octadecene) (Od-MA) and poly(maleic anhydride-alt-1-isobutylene) (Bu-MA) were evaluated for use in the development of a metal-free, reusable catalyst for the oxidation of pyridines to pyridine N-oxides in the presence of H(2)O...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9050160/ https://www.ncbi.nlm.nih.gov/pubmed/35496532 http://dx.doi.org/10.1039/d0ra00265h |
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author | Gajeles, Ghellyn Kim, Se Mi Yoo, Jong-Cheol Lee, Kyung-Koo Lee, Sang Hee |
author_facet | Gajeles, Ghellyn Kim, Se Mi Yoo, Jong-Cheol Lee, Kyung-Koo Lee, Sang Hee |
author_sort | Gajeles, Ghellyn |
collection | PubMed |
description | The catalytic efficiency and recyclability of poly(maleic anhydride-alt-1-octadecene) (Od-MA) and poly(maleic anhydride-alt-1-isobutylene) (Bu-MA) were evaluated for use in the development of a metal-free, reusable catalyst for the oxidation of pyridines to pyridine N-oxides in the presence of H(2)O(2). The Od-MA catalyst was easily recovered via filtration with recovery yields exceeding 99.8%. The catalyst retained its activity after multiple uses and did not require any treatment for reuse. The Od-MA and H(2)O(2) catalytic system described herein is eco-friendly, operationally simple, and cost-effective; thus, it is industrially applicable. Od-MA and H(2)O(2) could potentially be used in place of percarboxylic acid as an oxidant in a wide range of oxidation reactions. |
format | Online Article Text |
id | pubmed-9050160 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90501602022-04-29 Recyclable anhydride catalyst for H(2)O(2) oxidation: N-oxidation of pyridine derivatives Gajeles, Ghellyn Kim, Se Mi Yoo, Jong-Cheol Lee, Kyung-Koo Lee, Sang Hee RSC Adv Chemistry The catalytic efficiency and recyclability of poly(maleic anhydride-alt-1-octadecene) (Od-MA) and poly(maleic anhydride-alt-1-isobutylene) (Bu-MA) were evaluated for use in the development of a metal-free, reusable catalyst for the oxidation of pyridines to pyridine N-oxides in the presence of H(2)O(2). The Od-MA catalyst was easily recovered via filtration with recovery yields exceeding 99.8%. The catalyst retained its activity after multiple uses and did not require any treatment for reuse. The Od-MA and H(2)O(2) catalytic system described herein is eco-friendly, operationally simple, and cost-effective; thus, it is industrially applicable. Od-MA and H(2)O(2) could potentially be used in place of percarboxylic acid as an oxidant in a wide range of oxidation reactions. The Royal Society of Chemistry 2020-03-03 /pmc/articles/PMC9050160/ /pubmed/35496532 http://dx.doi.org/10.1039/d0ra00265h Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Gajeles, Ghellyn Kim, Se Mi Yoo, Jong-Cheol Lee, Kyung-Koo Lee, Sang Hee Recyclable anhydride catalyst for H(2)O(2) oxidation: N-oxidation of pyridine derivatives |
title | Recyclable anhydride catalyst for H(2)O(2) oxidation: N-oxidation of pyridine derivatives |
title_full | Recyclable anhydride catalyst for H(2)O(2) oxidation: N-oxidation of pyridine derivatives |
title_fullStr | Recyclable anhydride catalyst for H(2)O(2) oxidation: N-oxidation of pyridine derivatives |
title_full_unstemmed | Recyclable anhydride catalyst for H(2)O(2) oxidation: N-oxidation of pyridine derivatives |
title_short | Recyclable anhydride catalyst for H(2)O(2) oxidation: N-oxidation of pyridine derivatives |
title_sort | recyclable anhydride catalyst for h(2)o(2) oxidation: n-oxidation of pyridine derivatives |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9050160/ https://www.ncbi.nlm.nih.gov/pubmed/35496532 http://dx.doi.org/10.1039/d0ra00265h |
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