Carbonylative Suzuki-Miyaura cross-coupling by immobilized Ni@Pd NPs supported on carbon nanotubes

Nan, L. and Yalan, C. and Jixiang, L. and Dujuan, O. and Wenhui, D. and Rouhi, J. and Mustapha, M. (2020) Carbonylative Suzuki-Miyaura cross-coupling by immobilized Ni@Pd NPs supported on carbon nanotubes. RSC Advances, 10 (47). pp. 27923-27931. ISSN 20462069

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Abstract

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. This journal is © The Royal Society of Chemistry.

Item Type: Article
Additional Information: cited By 46
Uncontrolled Keywords: Composite structures; Core shell nanoparticles; Green manufacturing; Nanocatalysts; Precious metals; Synthesis (chemical), Carbonylative cross-coupling; Catalytic performance; Catalytic reduction; External magnetic field; Phenylboronic acids; Reaction mixture; Structural composites; Suzuki-Miyaura cross-coupling, Carbon nanotubes
Depositing User: Mr Ahmad Suhairi UTP
Date Deposited: 10 Nov 2023 03:27
Last Modified: 10 Nov 2023 03:27
URI: https://khub.utp.edu.my/scholars/id/eprint/12912

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