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由索烃配位的铜(I)催化的交叉脱氢C-O偶联反应。

Cross dehydrogenative C-O coupling catalysed by a catenane-coordinated copper(i).

作者信息

Zhu Lihui, Li Jiasheng, Yang Jun, Au-Yeung Ho Yu

机构信息

Department of Chemistry, The University of Hong Kong Pokfulam Road Hong Kong P. R. China

State Key Laboratory of Synthetic Chemistry, The University of Hong Kong Pokfulam Road Hong Kong P. R. China.

出版信息

Chem Sci. 2020 Nov 1;11(48):13008-13014. doi: 10.1039/d0sc05133k.

Abstract

Catalytic activity of copper(i) complexes supported by phenanthroline-containing catenane ligands towards a new C(sp)-O dehydrogenative cross-coupling of phenols and bromodicarbonyls is reported. As the phenanthrolines are interlocked by the strong and flexible mechanical bond in the catenane, the active catalyst with an open copper coordination site can be revealed only transiently and the stable, coordinatively saturated Cu(i) pre-catalyst is quickly regenerated after substrate transformation. Compared with a control Cu(i) complex supported by non-interlocked phenanthrolines, the catenane-supported Cu(i) is highly efficient with a broad substrate scope, and can be applied in gram-scale transformations without a significant loss of the catalytic activity. This work demonstrates the advantages of the catenane ligands that provide a dynamic and responsive copper coordination sphere, highlighting the potential of the mechanical bond as a design element in transition metal catalyst development.

摘要

据报道,含菲咯啉的索烃配体负载的铜(I)配合物对酚类和溴代二羰基化合物的新型C(sp)-O脱氢交叉偶联反应具有催化活性。由于菲咯啉在索烃中通过强而灵活的机械键相互锁定,具有开放铜配位位点的活性催化剂只能短暂显现,并且在底物转化后稳定的、配位饱和的Cu(I)预催化剂会迅速再生。与由非互锁菲咯啉负载的对照铜(I)配合物相比,索烃负载的Cu(I)具有高效性和广泛的底物范围,并且可以应用于克级转化而不会显著损失催化活性。这项工作证明了索烃配体的优势,即提供动态且响应性的铜配位环境,突出了机械键作为过渡金属催化剂开发中设计元素的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81dd/8163234/20bf31374aa4/d0sc05133k-f1.jpg

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