Yan Bai
Shanxi Teachers University
6 Papers
11 Citations
Yan Bai is an academic researcher from Shanxi Teachers University. The author has contributed to research in topics: Covalent bond & Vicinal. The author has an hindex of 2, co-authored 6 publications.
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Papers
CO oxidation on the heterodinuclear tantalum–nickel monoxide carbonyl complex anions
Jumei Zhang,Jumei Zhang,Ya Li,Yan Bai,Gang Li,Dong Yang,Huijun Zheng,Jinghan Zou,Xiangtao Kong,Hongjun Fan,Zhiling Liu,Ling Jiang,Hua Xie +12 more
TL;DR: In this article, the authors provided new insight into the composition-selective mechanism of CO oxidation on heteronuclear metal complexes, of which the composition be tailored to fulfill the desired chemical behaviors.
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Unsaturated binuclear homoleptic nickel carbonyl anions Ni2(CO)n− (n = 4–6) featuring double three-center two-electron Ni–C–Ni bonds
TL;DR: Despite the absence of direct multiple Ni-Ni bonds, the two nickel atoms in Ni2(CO)n- (n = 4-6) complexes are joined by two bridging carbonyl ligands via the sharing three-center two-electron Ni-C-Ni bond in turn to achieve the ( 16,16), (16,18), and eventually the favored (18,18) configurations.
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Multicenter electron-sharing σ-bonding in the AgFe(CO)4- complex.
Zhiling Liu,Yan Bai,Ya Li,Jing He,Qingyang Lin,Lina Hou,Hai-Shun Wu,Fu-Qiang Zhang,Jianfeng Jia,Hua Xie,Zichao Tang +10 more
TL;DR: The bonding analyses revealed a peculiar decentralized bonding situation, where the silver atom is covalently bonded to both the iron center and the vicinal carbon atoms in the form of an electron-sharing σ bond.
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Triply Carbonyl-Bridged Ni2(CO)5 Featuring Triple Three-Center Two-Electron Ni-C-Ni Bonds Instead of Ni≡Ni Triple Bond.
TL;DR: The elaborate analyses manifest that the tribridged Ni2(CO)5 features triple three-center two-electron Ni-C-Ni bonds instead of Ni≡Ni triple bond, which is comparable to the intermetallic distance anticipated for the triple bond.
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Dative versus electron-sharing bonding in the isoelectronic argon compounds ArR+ (R = CH3, NH2, OH, and F)
Zhiling Liu,Jing He,Ya Li,Yan Bai,Qingyang Lin,Yurong Guo,Fu-Qiang Zhang,Hai-Shun Wu,Jianfeng Jia +8 more
TL;DR: In this article, a computational investigation of the isoelectronic ArR+ (R = CH3, NH2, OH, and F) species has been performed, and the ground states of all four complexes are determined to be the lowest singlet isomers.
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