化学
轨道杂交
原子轨道
化学键
Atom(片上系统)
分子轨道
价电子
价(化学)
结晶学
镧系元素
协调数
分子
原子序数
电子
计算化学
原子物理学
离子
分子轨道理论
物理
有机化学
量子力学
计算机科学
嵌入式系统
作者
Dongfeng Xue,Congting Sun,Xiaoyan Chen
标识
DOI:10.1002/cjoc.201700425
摘要
Both the bonding mode and geometry can serve as the chemical bonding nature of central cation, which is essentially determined by the atomic orbital‐hybridization. In this work, we focus on the possible chemical bonding scheme of central cations on the basis of a quantitative analysis of electron domain of an atom. Starting from the hybridization of outer atomic orbitals that are occupied by valence electrons, we studied the possible orbital hybridization scheme of atoms in the periodic table and the corresponding coordination number as well as possible molecular geometries. According to distinct hybrid orbital sets, the chemical bonding of central cations can be classified into three typical types, resulting in the cations with a variety of coordination numbers ranging from 2 to 16. Owing to different hybridization modes, the highest coordination number of cations in IA and IIA groups is larger than that in IB‐VIIIB groups, and the coordination number of lanthanide elements is most abundant. We also selected NaNO 3 , Fe( NO 3 ) 3 • 9H 2 O , Zn( NO 3 ) 2 • 6H 2 O , Y( NO 3 ) 3 • 3H 2 O , and La( NO 3 ) 3 • 6H 2 O as examples to confirm the direct relationship between chemical bonding characteristics and orbital hybrid set by IR spectra. The present study opens the door to reveal the chemical bonding nature of atoms on the basis of hybridization and will provide theoretical guides in structural design at an atomic level.
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