离子对中的阳离子-阴离子缩醛键:晶体学调查与计算研究的结合

IF 3 3区 化学 Q3 CHEMISTRY, PHYSICAL Computational and Theoretical Chemistry Pub Date : 2024-11-12 DOI:10.1016/j.comptc.2024.114985
Hui Liu , Zijian Han , Yunxiang Lu , Zhijian Xu , Weiliang Zhu
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引用次数: 0

摘要

在由钙化阳离子和多种阴离子形成的盐的 X 射线晶体中,经常可以观察到阳离子-阴离子钙原键(ChBs)。在这项工作中,我们首先从剑桥结构数据库(CSD)中收集了大量由阳离子-阴离子 ChBs 组成的晶体结构。然后,我们选择了一组铬化阳离子与四种阴离子(Cl-、Br-、I- 和 NO3-)的离子配对复合物,以研究晶体结构中发现的此类相互作用。由于成键距离很短,绝对结合能相当大,这些配合物中的阳离子-阴离子 ChBs 非常强,因而具有一定程度的共价性。这些相互作用在固态和气相中都是定向的,较重的 ChB 往往具有较高的共价含量。能量分解分析表明,轨道项对阳离子和阴离子之间 ChBs 的吸引力有重要作用。
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Cation–anion chalcogen bonds in ion pairs: A combined crystallographic survey and computational investigation
Cation–anion chalcogen bonds (ChBs) have been frequently observed in the X-ray crystals of the salts formed by chalcogenated cations and a diversity of anions. In this work, we first collected a huge number of crystal structures consisting of cation–anion ChBs from the Cambridge Structural Database (CSD). Then, a set of ion-pairing complexes of chalcogenated cations with four anions (Cl, Br, I and NO3) were selected to study such interactions found in crystal structures. Owing to the much short bonding distances and the considerably large absolute binding energies, cation–anion ChBs in the complexes are very strong, leading to some degree of covalency. These interactions are directional both in solid state and in gas phase, and heavier ChBs tend to have a higher covalent content. As revealed by energy decomposition analysis, the orbital term has an important contribution to the attraction of ChBs between cations and anions.
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来源期刊
CiteScore
4.20
自引率
10.70%
发文量
331
审稿时长
31 days
期刊介绍: Computational and Theoretical Chemistry publishes high quality, original reports of significance in computational and theoretical chemistry including those that deal with problems of structure, properties, energetics, weak interactions, reaction mechanisms, catalysis, and reaction rates involving atoms, molecules, clusters, surfaces, and bulk matter.
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