Cargando…
Carbonylative Suzuki–Miyaura cross-coupling by immobilized Ni@Pd NPs supported on carbon nanotubes
In this study, a novel carbon nanotube (CNT) based nanocatalyst (Ni@Pd/CNT) was synthesized by modifying CNTs using Ni@Pd core–shell nanoparticles (NPs). Ni@Pd/CNT was used in catalytic carbonylative cross-coupling between 4-iodoanisole and phenylboronic acid. The Ni@Pd NPs possessed a magnetic nick...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9055625/ https://www.ncbi.nlm.nih.gov/pubmed/35519106 http://dx.doi.org/10.1039/d0ra03915b |
_version_ | 1784697454690566144 |
---|---|
author | Nan, Liu Yalan, Cai Jixiang, Li Dujuan, Ouyang Wenhui, Duan Rouhi, Jalal Mustapha, Mazli |
author_facet | Nan, Liu Yalan, Cai Jixiang, Li Dujuan, Ouyang Wenhui, Duan Rouhi, Jalal Mustapha, Mazli |
author_sort | Nan, Liu |
collection | PubMed |
description | In this study, a novel carbon nanotube (CNT) based nanocatalyst (Ni@Pd/CNT) was synthesized by modifying CNTs using Ni@Pd core–shell nanoparticles (NPs). Ni@Pd/CNT was used in catalytic carbonylative cross-coupling between 4-iodoanisole and phenylboronic acid. The Ni@Pd NPs possessed a magnetic nickel (Ni) core with a palladium (Pd) structural composite shell. Thus, the use of Ni had led to a reduced consumption of Pd without sacrificing the overall catalytic performance, simultaneously making it reusable as it could be conveniently recovered from the reaction mixture by using an external magnetic field. Immobilization of the Ni@Pd NPs on carbon nanotubes not only prevented their aggregation, but also significantly enhanced the accessibility of the catalytically active sites. The abovementioned approach based on carbon nanotubes and Ni@Pd NPs provided a useful platform for the fabrication of noble-metal-based nanocatalysts with easy accessibility and low cost, which may allow for an efficient green alternative for various catalytic reductions. |
format | Online Article Text |
id | pubmed-9055625 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90556252022-05-04 Carbonylative Suzuki–Miyaura cross-coupling by immobilized Ni@Pd NPs supported on carbon nanotubes Nan, Liu Yalan, Cai Jixiang, Li Dujuan, Ouyang Wenhui, Duan Rouhi, Jalal Mustapha, Mazli RSC Adv Chemistry In this study, a novel carbon nanotube (CNT) based nanocatalyst (Ni@Pd/CNT) was synthesized by modifying CNTs using Ni@Pd core–shell nanoparticles (NPs). Ni@Pd/CNT was used in catalytic carbonylative cross-coupling between 4-iodoanisole and phenylboronic acid. The Ni@Pd NPs possessed a magnetic nickel (Ni) core with a palladium (Pd) structural composite shell. Thus, the use of Ni had led to a reduced consumption of Pd without sacrificing the overall catalytic performance, simultaneously making it reusable as it could be conveniently recovered from the reaction mixture by using an external magnetic field. Immobilization of the Ni@Pd NPs on carbon nanotubes not only prevented their aggregation, but also significantly enhanced the accessibility of the catalytically active sites. The abovementioned approach based on carbon nanotubes and Ni@Pd NPs provided a useful platform for the fabrication of noble-metal-based nanocatalysts with easy accessibility and low cost, which may allow for an efficient green alternative for various catalytic reductions. The Royal Society of Chemistry 2020-07-27 /pmc/articles/PMC9055625/ /pubmed/35519106 http://dx.doi.org/10.1039/d0ra03915b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Nan, Liu Yalan, Cai Jixiang, Li Dujuan, Ouyang Wenhui, Duan Rouhi, Jalal Mustapha, Mazli Carbonylative Suzuki–Miyaura cross-coupling by immobilized Ni@Pd NPs supported on carbon nanotubes |
title | Carbonylative Suzuki–Miyaura cross-coupling by immobilized Ni@Pd NPs supported on carbon nanotubes |
title_full | Carbonylative Suzuki–Miyaura cross-coupling by immobilized Ni@Pd NPs supported on carbon nanotubes |
title_fullStr | Carbonylative Suzuki–Miyaura cross-coupling by immobilized Ni@Pd NPs supported on carbon nanotubes |
title_full_unstemmed | Carbonylative Suzuki–Miyaura cross-coupling by immobilized Ni@Pd NPs supported on carbon nanotubes |
title_short | Carbonylative Suzuki–Miyaura cross-coupling by immobilized Ni@Pd NPs supported on carbon nanotubes |
title_sort | carbonylative suzuki–miyaura cross-coupling by immobilized ni@pd nps supported on carbon nanotubes |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9055625/ https://www.ncbi.nlm.nih.gov/pubmed/35519106 http://dx.doi.org/10.1039/d0ra03915b |
work_keys_str_mv | AT nanliu carbonylativesuzukimiyauracrosscouplingbyimmobilizednipdnpssupportedoncarbonnanotubes AT yalancai carbonylativesuzukimiyauracrosscouplingbyimmobilizednipdnpssupportedoncarbonnanotubes AT jixiangli carbonylativesuzukimiyauracrosscouplingbyimmobilizednipdnpssupportedoncarbonnanotubes AT dujuanouyang carbonylativesuzukimiyauracrosscouplingbyimmobilizednipdnpssupportedoncarbonnanotubes AT wenhuiduan carbonylativesuzukimiyauracrosscouplingbyimmobilizednipdnpssupportedoncarbonnanotubes AT rouhijalal carbonylativesuzukimiyauracrosscouplingbyimmobilizednipdnpssupportedoncarbonnanotubes AT mustaphamazli carbonylativesuzukimiyauracrosscouplingbyimmobilizednipdnpssupportedoncarbonnanotubes |