共价键
化学
价键理论
主组元素
计算化学
债券定单
电子缺陷
价电子
结晶学
单一债券
化学键
分子轨道
原子轨道
Pi键
群(周期表)
加合物
电子
分子
粘结长度
过渡金属
物理
有机化学
晶体结构
量子力学
催化作用
出处
期刊:
日期:1989-08-01
卷期号:28 (8): 992-1007
被引量:564
标识
DOI:10.1002/anie.198909921
摘要
Abstract Textbooks of inorganic chemistry describe the formation of adducts by coordination of an electron donor to an electron acceptor, often using the amine‐boranes, X 3 N → BY 3 , as examples. In the Lewis (electron dot) formulas of the compounds, the dative bond in H 3 N → BH 3 and the covalent bond in H 3 CCH 3 are both represented by a shared electron pair. In the simple molecular orbital or valence bond models the wave functions of both electron pairs would be constructed in the same manner from the appropriate sp 3 type atomic orbitals on the bonded atoms; the difference between the covalent and the dative bond becomes apparent only after the orbital coefficients have been analyzed. This may be the reason why many structural chemists seem reluctant to distinguish between the two types of bonds. The object of this article is to remind the reader that the physiocochemical properties of covalent and dative bonds may be – and often are – quite different, and to show that a distinction between the two provides a basis for understanding the structures of a wide range of main group metal compounds.
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