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

被引:27
|
作者
Zhu, Lihui [1 ]
Li, Jiasheng [1 ]
Yang, Jun [1 ]
Au-Yeung, Ho Yu [1 ,2 ]
机构
[1] Univ Hong Kong, Dept Chem, Pokfulam Rd, Hong Kong, Peoples R China
[2] Univ Hong Kong, State Key Lab Synthet Chem, Pokfulam Rd, Hong Kong, Peoples R China
关键词
TRANSFER RADICAL-ADDITION; ASYMMETRIC CATALYSIS; ROTAXANE; PHENOLS; LIGANDS; RING; COMPLEXES; DESIGN; CHEMISTRY; BONDS;
D O I
10.1039/d0sc05133k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Catalytic activity of copper(i) complexes supported by phenanthroline-containing catenane ligands towards a new C(sp(3))-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.
引用
收藏
页码:13008 / 13014
页数:8
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