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N-杂环卡宾(NHC)的不对称NCN钳形单核和双核镍(II)配合物:铃木-宫浦交叉偶联反应的合成、结构及催化作用

Unsymmetrical NCN-pincer mononuclear and dinuclear nickel(ii) complexes of N-heterocyclic carbene (NHC): synthesis, structure and catalysis for Suzuki-Miyaura cross-coupling.

作者信息

Gu Shaojin, Du Jiehao, Huang Jingjing, Guo Yun, Yang Ling, Xu Weilin, Chen Wanzhi

机构信息

School of Materials Science and Engineering, Wuhan Textile University, Wuhan 430200, People's Republic of China.

Department of Chemistry, Zhejiang University, Hangzhou, 310028, People's Republic of China.

出版信息

Dalton Trans. 2017 Jan 3;46(2):586-594. doi: 10.1039/c6dt03944h.

Abstract

This report describes the synthesis and characterization of a family of unsymmetrical NCN pincer Ni(ii) complexes 2-8 with NHC-triazole arms. All of these complexes have been fully characterized by X-ray single crystal analysis, NMR spectroscopy, and elemental analysis. Complexes 2 and 4-6 were square planar with a chloride trans to the carbene carbon atoms. Complex 3 was a paramagnetic octahedral complex with its central metal surrounded by two NCN pincer ligands. Complexes 7 and 8 contain [(NHC)Ni-OH] moieties bearing a OH bridge. Both the [(NHC)Ni-OH] complexes 7 and 8 and [(NCN)Ni-Cl] complexes 2 and 4-6 were synthesized similarly via the reactions of the in situ formed Ag-NHCs from the corresponding imidazolium salts with [NiCl(PPh)]. The catalytic activities of all complexes for Suzuki-Miyaura cross-coupling were examined. Under the optimized conditions, complex 4 was active in the Suzuki-Miyaura cross-coupling reactions of aryl iodides and aryl bromides at 110 °C. Aryl chlorides were successfully coupled in the presence of triphenylphosphine as an additive.

摘要

本报告描述了一系列带有NHC-三唑臂的不对称NCN钳形Ni(ii)配合物2-8的合成与表征。所有这些配合物均已通过X射线单晶分析、核磁共振光谱和元素分析进行了全面表征。配合物2和4-6为平面正方形,氯原子与卡宾碳原子呈反式。配合物3是一种顺磁性八面体配合物,其中心金属被两个NCN钳形配体包围。配合物7和8含有带有OH桥的[(NHC)Ni-OH]部分。[(NHC)Ni-OH]配合物7和8以及[(NCN)Ni-Cl]配合物2和4-6都是通过相应咪唑盐原位形成的Ag-NHC与[NiCl(PPh)]反应类似地合成的。考察了所有配合物对铃木-宫浦交叉偶联反应的催化活性。在优化条件下,配合物4在110℃下对芳基碘化物和芳基溴化物的铃木-宫浦交叉偶联反应具有活性。在三苯基膦作为添加剂的情况下,芳基氯化物成功实现了偶联。

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