化学
共价键
原子轨道
结晶学
开壳
Atom(片上系统)
电子对
之字形的
计算化学
分子轨道
路易斯酸
壳体(结构)
电子
分子
物理
量子力学
催化作用
几何学
材料科学
生物化学
数学
有机化学
计算机科学
嵌入式系统
复合材料
作者
Xinlei Yu,Dan Li,Kun Wang,Tao Xia,Chang Xu,Zhenyu Wu,Longjiu Cheng
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2021-12-29
卷期号:61 (2): 1051-1058
被引量:10
标识
DOI:10.1021/acs.inorgchem.1c03151
摘要
The nature of closed-shell AuI···AuI attraction is still a conundrum in theoretical chemistry. However, for Au2F2 with a zigzag conformation, the d10-d10 closed-shell interaction between the AuF monomers is demonstrated as a coordinate covalent bond. Chemical bonding analysis reveals that the strong AuI···AuI attraction is caused by the participation of the extraordinary active 5d orbital of Au. Based on our study, one of the 5d orbitals of the Au atom is activated to hybridize with its 6s and 6p orbitals to form hybridized dsp2 orbitals, where each Au atom is both an electron donor (Lewis base) and acceptor (Lewis Acid) in dimerization. Actually, the closed-shell AuI···AuI interaction in the zigzag conformation of Au2X2 (X = F, Cl, Br, I, or NH2) is covalent. Our results provide a rather simple but clear-cut example, where mysterious AuI···AuI attractions can be possibly explained by the covalent bond theory.
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