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含第15族供体(Y = N、P和As)与第14族受体(M = Si、Ge、Sn和Pb)的准金属氮杂环蕃中的配位键合

Dative Bonding in Quasimetallatranes Containing Group 15 Donors (Y = N, P, and As) and Group 14 Acceptors (M = Si, Ge, Sn, and Pb).

作者信息

Bakry Aamy A, Fanelli Matthew G, Zeldin Martel, Donald Kelling J, Parish Carol A

机构信息

Department of Chemistry, Gottwald Center for the Sciences, University of Richmond, Richmond, Virginia 23173, United States.

出版信息

Inorg Chem. 2024 Sep 30;63(39):18005-18015. doi: 10.1021/acs.inorgchem.4c02532. Epub 2024 Sep 20.

Abstract

Metallatranes and their analogous fused ring [3.3.0] bicyclic compounds, quasimetallatranes, have emerged as fascinating molecular systems with intriguing structural, bonding, and conformational properties. We present a comprehensive investigation aimed at unraveling the nature of dative bonding and exploring the conformational flexibility of these compounds. We extensively characterize the dative bond between the metal center and the electron pair donor, using a range of modeling techniques. Our analyses involve structural optimizations, molecular orbital examinations, and covalency ratio calculations, which provide a thorough understanding of the bonding interactions responsible for the stability of these systems. The results confirmed the presence of dative bonds, supported by the close proximity between the metal and the electron-donating group, and the observation of overlapping electron density. Our studies reveal a correlation between the size of the electron-donor and the coordinating metal atom, and the strength of the dative interaction, as indicated by the bond length and the Wiberg bond indices. This bond strength, in turn, influences the conformational preferences adopted by these compounds. This investigation sheds light on the fundamental aspects of the fused ring [3.3.0] bicyclic quasimetallatrane compounds and offers valuable insights into their unique properties.

摘要

金属氮杂环蕃及其类似的稠环[3.3.0]双环化合物——准金属氮杂环蕃,已成为具有引人入胜的结构、键合和构象性质的迷人分子体系。我们开展了一项全面研究,旨在阐明配位键的本质并探索这些化合物的构象灵活性。我们使用一系列建模技术,广泛地表征了金属中心与电子对供体之间的配位键。我们的分析包括结构优化、分子轨道研究和共价比计算,这些能让我们深入了解对这些体系稳定性起作用的键合相互作用。结果证实了配位键的存在,其依据是金属与供电子基团之间的紧密接近以及电子密度重叠的观察结果。我们的研究揭示了供电子体和配位金属原子的大小与配位相互作用强度之间的相关性,这由键长和维伯格键指数表明。反过来,这种键强会影响这些化合物所采用的构象偏好。这项研究阐明了稠环[3.3.0]双环准金属氮杂环蕃化合物的基本方面,并为其独特性质提供了有价值的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4cd/11445729/2a81b46454ba/ic4c02532_0001.jpg

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