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可持续的碳质纳米材料负载钯作为用于铃木-宫浦偶联的高效无配体多相催化剂。

Sustainable carbonaceous nanomaterial supported palladium as an efficient ligand-free heterogeneouscatalyst for Suzuki-Miyaura coupling.

作者信息

Shetty Apoorva, Sunil Dhanya, Rujiralai Thitima, P Maradur Sanjeev, N Alodhayb Abdullah, Hegde Gurumurthy

机构信息

Department of Chemistry, CHRIST (Deemed to Be University) Hosur Road Bangalore 560029 India.

Centre for Advanced Research and Development (CARD), CHRIST (Deemed to Be University) Hosur Road Bangalore 560029 India

出版信息

Nanoscale Adv. 2024 Apr 10;6(9):2516-2526. doi: 10.1039/d4na00116h. eCollection 2024 Apr 30.

Abstract

A novel ligand-free heterogeneous catalyst was synthesized pyrolysis of pods to produce carbon nanospheres (SS-CNSs), which served as a carbon support for immobilizing palladium nanoparticles through an reduction technique (Pd/SS-CNS). The SS-CNSs effectively integrated 3% of Pd on their surfaces with no additional activation procedures needed. The nanomaterials obtained underwent thorough characterization employing various techniques such as FT-IR, XRD, FE-SEM, TEM, EDS, ICP-AES, and BET. Subsequently, the efficiency of this Pd/SS-CNS catalyst was assessed for the synthesis of biaryl derivatives Suzuki coupling, wherein different boronic acids were coupled with various aryl halides using an environmentally benign solvent mixture of EtOH/HO and employing only 0.1 mol% of Pd/SS-CNS. The catalytic system was conveniently recovered through centrifugation and demonstrated reusability without any noticeable decline in catalytic activity. This approach offers economic viability, ecological compatibility, scalability, and has the potential to serve as an alternative to homogeneous catalysis.

摘要

通过对豆荚进行热解合成了一种新型无配体多相催化剂,以制备碳纳米球(SS-CNSs),通过一种简单的还原技术将其作为碳载体用于固定钯纳米颗粒(Pd/SS-CNS)。SS-CNSs在其表面有效整合了3%的钯,无需额外的活化程序。使用FT-IR、XRD、FE-SEM、TEM、EDS、ICP-AES和BET等各种技术对所得纳米材料进行了全面表征。随后,评估了这种Pd/SS-CNS催化剂在铃木偶联反应中合成联芳基衍生物的效率,其中使用EtOH/H₂O的环境友好型溶剂混合物,仅使用0.1 mol%的Pd/SS-CNS,使不同的硼酸与各种芳基卤化物偶联。该催化体系通过离心方便地回收,并且显示出可重复使用性,催化活性没有任何明显下降。这种方法具有经济可行性、生态兼容性、可扩展性,并且有潜力作为均相催化的替代方法。

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