晶体工程
化学
卤化物
卤素
超分子化学
背景(考古学)
卤键
氢键
从头算
计算化学
量子化学
从头算量子化学方法
卤化氢
结晶学
无机化学
晶体结构
物理化学
分子
有机化学
古生物学
烷基
生物
作者
Lee Brammer,E.A. Bruton,Paul Sherwood
摘要
The similarities and differences between the behavior of carbon-bound and terminal metal-bound halogens and halide ions as potential hydrogen bond acceptors has been extensively investigated through examination of many thousands of interactions present in crystal structures. Halogens in each of these environments are found to engage in hydrogen bonding, and geometric preferences for these interactions have been established. Notably, typical H···X−M angles are markedly different for X = F than for X = Cl, Br, I. Furthermore, there are significant parallels between the behavior of moderately strong hydrogen bond acceptors X−M and the much weaker acceptors X−C. The underlying reasons for the observed geometric preferences have been established by ab initio molecular orbital calculations using suitable model systems. The results are presented within the context of their potential applications in crystal engineering and supramolecular chemistry, including relevance to nucleation in halogenated solvents. The broader implications of the results in areas such as halocarbon coordination chemistry, binary metal halide solid-state chemistry, and the study of weakly coordinating anions are also discussed.
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