Vollmer Matthew V, Xie Jing, Cammarota Ryan C, Young Victor G, Bill Eckhard, Gagliardi Laura, Lu Connie C
Department of Chemistry and Supercomputing Institute, University of Minnesota, 207 Pleasant St. SE, Minneapolis, MN, 55455, USA.
Max-Planck-Institut für chemische Energiekonversion, Stiftstraße 34-36, 45470, Mülheim an der Ruhr, Germany.
Angew Chem Int Ed Engl. 2018 Jun 25;57(26):7815-7819. doi: 10.1002/anie.201803356. Epub 2018 May 28.
Formal nickelate(-I) complexes bearing Group 13 metalloligands (M=Al and Ga) were isolated. These 17 e complexes were synthesized by one-electron reduction of the corresponding Ni →M precursors, and were investigated by single-crystal X-ray diffraction, EPR spectroscopy, and quantum chemical calculations. Collectively, the experimental and computational data support: 1) the strengthening of the Ni-M bond upon one-electron reduction, and 2) the delocalization of the unpaired spin across the Ni and M atoms. An intriguing electronic configuration is revealed where three valence electrons occupy two σ-type bonding interactions: Ni(3dz2 ) →M and σ-(Ni-M) . The latter is an unusual Ni-M σ-bonding molecular orbital that comprises primarily the Ni 4p and M np /ns atomic orbitals.
分离得到了含有第13族金属配体(M = Al和Ga)的正镍(-I)配合物。这些17电子配合物通过相应的Ni→M前体的单电子还原合成,并通过单晶X射线衍射、电子顺磁共振光谱和量子化学计算进行了研究。总体而言,实验和计算数据支持:1)单电子还原后Ni-M键的增强,以及2)未成对自旋在Ni和M原子间的离域。揭示了一种有趣的电子构型,其中三个价电子占据两个σ型键相互作用:Ni(3dz2 ) →M和σ-(Ni-M) 。后者是一种不寻常的Ni-M σ键分子轨道,主要由Ni 4p和M np/ns原子轨道组成。