Copper cluster complex-catalyzed C–S bond formation†

IF 4.4 3区 化学 Q2 CHEMISTRY, PHYSICAL Catalysis Science & Technology Pub Date : 2024-09-26 DOI:10.1039/D4CY00968A
Nien-Chi Chang Liao, R. Sidick Basha, Bo-Hao Shih, Chia-Chun Liu, Miao-Han Wang, Po-Heng Lin and Chin-Fa Lee
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Abstract

Three distinct copper cluster complexes (A–C) containing Cu–O ligated Schiff-base ligands were synthesized and their bonding was investigated by single-crystal X-ray crystallographic studies. These complexes effectively catalyze the C–S cross coupling reaction of less reactive aliphatic thiols to synthesize thioether derivatives. This coupling reaction also tolerates well and is compatible with aryl thiols. The peculiar C(sp2)–SC(sp3) bond formation distinctly took place with high efficiency using low loading of copper cluster complex catalysts. The present report describes an alternative protocol to construct active copper cluster complexes from readily accessible, cheap and efficient ligands. These complexes are air stable, practical, easy to handle and catalyze C–S coupling reactions with good yields.

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铜簇复合物催化的 C-S 键形成†。
我们合成了三种不同的含 Cu-O 配位希夫碱配体的铜簇合物(A-C),并通过单晶 X 射线晶体学研究对它们的键合进行了研究。这些配合物能有效催化活性较低的脂肪族硫醇的 C-S 交叉偶联反应,从而合成硫醚衍生物。这种偶联反应对芳基硫醇也有很好的耐受性和兼容性。使用低负载的铜簇合物催化剂,可以高效地形成独特的 C(sp2)-SC(sp3)键。本报告介绍了一种利用易于获得、廉价而高效的配体构建活性铜簇配合物的替代方案。这些配合物空气稳定、实用、易于处理,并能以良好的产率催化 C-S 偶联反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Catalysis Science & Technology
Catalysis Science & Technology CHEMISTRY, PHYSICAL-
CiteScore
8.70
自引率
6.00%
发文量
587
审稿时长
1.5 months
期刊介绍: A multidisciplinary journal focusing on cutting edge research across all fundamental science and technological aspects of catalysis. Editor-in-chief: Bert Weckhuysen Impact factor: 5.0 Time to first decision (peer reviewed only): 31 days
期刊最新文献
Back cover Back cover Characterizing Y224 conformational flexibility in FtmOx1-catalysis using 19F NMR spectroscopy. Lanthanum-doped nickel-based composite metal oxide catalyst for hydrogenation of isophthalonitrile to produce meta-xylenediamine† IBzH (IBenzhydryl): sterically-flexible N-aliphatic N-heterocyclic carbenes (NHCs) for iron-catalyzed C(sp3)–C(sp2) cross-coupling of unactivated haloalkanes†
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