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Dinuclear Au(0) Complex Supported by Tridentate P-Mg-P Ligands
Yafei Li1, Tianze Xu1, Xinggao Ji1
1State Key Laboratory of Coordination Chemistry, Jiangsu Key Laboratory of Advanced Organic Materials, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing, 210023, China.
None:
Despite significant advances in gold chemistry, the synthesis and stabilization of gold centers in a low oxidation state, particularly dinuclear Au(0) species, remain a considerable challenge. In this work, we report the successful isolation of a novel dinuclear Au(0) complex stabilized by tridentate P-Mg-P ligands. Computational studies demonstrate that the Au(0)-Au(0) σ-bond acts as a two-electron donor to the Mg centers. Reactivity studies further revealed the complex's unprecedented ability to perform two-electron reductions on a range of substrates, akin to the behavior of well-established Mg(I) and Zn(I) dimers.
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