Bifurcated Chalcogen Bonds Based on One σ-Hole

Saber Mehrparvar, C. Wölper, R. Gleiter, Gebhard Haberhauer
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引用次数: 1

Abstract

Chalcogen bonds are noncovalent interactions and are increasingly coming into focus for the design of complex structures in research areas such as crystal engineering, molecular recognition and catalysis. Conceptionally, chalcogen bonds can be considered as interaction between one σ-hole and one Lewis base center. Herein, we analyze the interaction between bidentate chelating ligands having two nucleophilic centers with one single σ-hole of a chalcogenazole (two-lone-pair/one-σ-hole interactions). Referring to this, we show by quantum chemical calculations and X-ray studies that three bond types are possible: in the first case, a chalcogen bond is formed between the σ-hole and only one of the Lewis base centers. In the second case, a strong bond is formed by one nucleophilic center; the second center provides only a small amount of additional stabilization. In the third case, two equivalent bonds to the σ-hole are formed by both Lewis base centers. According to the calculations the bifurcated bonds are stronger than simple chalcogen bonds and lead to a more rigid molecule arrangement in the complex.

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基于一个σ-空穴的分岔硫键
硫键是非共价相互作用,在晶体工程、分子识别和催化等研究领域的复杂结构设计中越来越受到关注。从概念上讲,硫族键可以被认为是一个σ-空穴和一个路易斯基中心之间的相互作用。在本文中,我们分析了具有两个亲核中心的双齿螯合配体与硫清唑的一个单一σ-孔之间的相互作用(两个孤对/一个σ-孔相互作用)。提到这一点,我们通过量子化学计算和X射线研究表明,有三种键类型是可能的:在第一种情况下,硫族键在σ-空穴和只有一个路易斯碱中心之间形成。在第二种情况下,一个亲核中心形成一个强键;第二中心仅提供少量的附加稳定性。在第三种情况下,σ-空穴的两个等价键是由两个路易斯基中心形成的。根据计算,分叉键比简单的硫族键更强,并导致复合物中更刚性的分子排列。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.70
自引率
0.00%
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0
审稿时长
12 weeks
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