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A magnetically retrievable air and moisture stable gold and palladium nanocatalyst for efficient C−C coupling reactions
In this study, we report the synthesis of a highly stable, magnetically retrievable gold and palladium nanocatalyst (AuPd@AMNPs), highly active in Suzuki cross-coupling and related homocoupling reactions. The active catalytic component in this system is palladium, which can only be stabilized in the...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7540803/ https://www.ncbi.nlm.nih.gov/pubmed/33047052 http://dx.doi.org/10.1098/rsos.200916 |
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author | Goonesinghe, Chatura Shaik, Mohamed Ratnaweera, Rivi Nalin De Silva, K. M. De Silva, Rohini M. |
author_facet | Goonesinghe, Chatura Shaik, Mohamed Ratnaweera, Rivi Nalin De Silva, K. M. De Silva, Rohini M. |
author_sort | Goonesinghe, Chatura |
collection | PubMed |
description | In this study, we report the synthesis of a highly stable, magnetically retrievable gold and palladium nanocatalyst (AuPd@AMNPs), highly active in Suzuki cross-coupling and related homocoupling reactions. The active catalytic component in this system is palladium, which can only be stabilized in the presence of gold nanoparticles. There is no significant loss of activity even after prolonged storage exposed air and moisture. The versatile nature AuPd@AMNPs is demonstrated through the selective catalysis of the homocoupling of phenylboronic acid under low concentrations of O(2) and the oxidation of phenylboronic acid to phenol under high O(2) concentrations. AuPd@AMNPs also demonstrated Ullmann-type homocoupling of 4-iodotolene with excellent yields. The magnetically retrieved catalyst could be re-used up to six times in Suzuki–Miyaura cross-coupling with consistently high activity and with a minimal loss of the noble metal species. Through these reactions we show that the gold-stabilized AuPd@AMNPs can be used as stable and recyclable palladium reservoir for multiple palladium-catalysed reactions. |
format | Online Article Text |
id | pubmed-7540803 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-75408032020-10-11 A magnetically retrievable air and moisture stable gold and palladium nanocatalyst for efficient C−C coupling reactions Goonesinghe, Chatura Shaik, Mohamed Ratnaweera, Rivi Nalin De Silva, K. M. De Silva, Rohini M. R Soc Open Sci Chemistry In this study, we report the synthesis of a highly stable, magnetically retrievable gold and palladium nanocatalyst (AuPd@AMNPs), highly active in Suzuki cross-coupling and related homocoupling reactions. The active catalytic component in this system is palladium, which can only be stabilized in the presence of gold nanoparticles. There is no significant loss of activity even after prolonged storage exposed air and moisture. The versatile nature AuPd@AMNPs is demonstrated through the selective catalysis of the homocoupling of phenylboronic acid under low concentrations of O(2) and the oxidation of phenylboronic acid to phenol under high O(2) concentrations. AuPd@AMNPs also demonstrated Ullmann-type homocoupling of 4-iodotolene with excellent yields. The magnetically retrieved catalyst could be re-used up to six times in Suzuki–Miyaura cross-coupling with consistently high activity and with a minimal loss of the noble metal species. Through these reactions we show that the gold-stabilized AuPd@AMNPs can be used as stable and recyclable palladium reservoir for multiple palladium-catalysed reactions. The Royal Society 2020-09-30 /pmc/articles/PMC7540803/ /pubmed/33047052 http://dx.doi.org/10.1098/rsos.200916 Text en © 2020 The Authors. http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/http://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Chemistry Goonesinghe, Chatura Shaik, Mohamed Ratnaweera, Rivi Nalin De Silva, K. M. De Silva, Rohini M. A magnetically retrievable air and moisture stable gold and palladium nanocatalyst for efficient C−C coupling reactions |
title | A magnetically retrievable air and moisture stable gold and palladium nanocatalyst for efficient C−C coupling reactions |
title_full | A magnetically retrievable air and moisture stable gold and palladium nanocatalyst for efficient C−C coupling reactions |
title_fullStr | A magnetically retrievable air and moisture stable gold and palladium nanocatalyst for efficient C−C coupling reactions |
title_full_unstemmed | A magnetically retrievable air and moisture stable gold and palladium nanocatalyst for efficient C−C coupling reactions |
title_short | A magnetically retrievable air and moisture stable gold and palladium nanocatalyst for efficient C−C coupling reactions |
title_sort | magnetically retrievable air and moisture stable gold and palladium nanocatalyst for efficient c−c coupling reactions |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7540803/ https://www.ncbi.nlm.nih.gov/pubmed/33047052 http://dx.doi.org/10.1098/rsos.200916 |
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