A Well-Defined Anionic Dicopper(I) Monohydride Complex that Reacts like a Cluster

被引:13
作者
Bienenmann, Roel L. M. [1 ]
Schanz, Alexandra J. [1 ]
Ooms, Pascale L. [1 ]
Lutz, Martin [2 ]
Broere, Daniel L. J. [1 ]
机构
[1] Univ Utrecht, Fac Sci, Debye Inst Nanomat Sci, Organ Chem & Catalysis, Univ Weg 99, NL-3584 CG Utrecht, Netherlands
[2] Univ Utrecht, Fac Sci, Bijvoet Ctr Biomol Res, Struct Biochem, Univ Weg 99, NL-3584 CG Utrecht, Netherlands
关键词
Copper Hydrides; Dinuclear Complexes; Expanded Pincer; Homogeneous Catalysis; Hydrosilylation; COPPER(I) HYDRIDE; CARBON-DIOXIDE; HYDROSILYLATION; REACTIVITY; MECHANISM; CONVENIENT;
D O I
10.1002/anie.202202318
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Low-nuclearity copper hydrides are rare and few well-defined dicopper hydrides have been reported. Herein, we describe the first example of a structurally characterized anionic dicopper hydride complex. This complex does not display typical reactivity associated with low-nuclearity copper hydrides, such as alcoholysis or insertion reactions. Instead, its stoichiometric and catalytic reactivity is akin to that of copper hydride clusters. The distinct reactivity is ascribed to the robust dinuclear core that is bound tightly within the dinucleating ligand scaffold.
引用
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页数:5
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