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以氮杂环卡宾与1,2,5-碲二唑配合物为例的给体-受体相互作用中的键合本质

Nature of Bonding in Donor-Acceptor Interactions Exemplified by Complexes of N-Heterocyclic Carbenes with 1,2,5-Telluradiazoles.

作者信息

Pushkarevsky Nikolay A, Petrov Pavel A, Grigoriev Denis S, Smolentsev Anton I, Lee Lucia M, Kleemiss Florian, Salnikov Georgy E, Konchenko Sergey N, Vargas-Baca Ignacio, Grabowsky Simon, Beckmann Jens, Zibarev Andrey V

机构信息

Nikolaev Institute of Inorganic Chemistry, Siberian Branch, Russian Academy of Sciences, 630090, Novosibirsk, Russia.

Department of Natural Sciences, Novosibirsk State University, 630090, Novosibirsk, Russia.

出版信息

Chemistry. 2017 Aug 16;23(46):10987-10991. doi: 10.1002/chem.201703018. Epub 2017 Jul 31.

Abstract

Comprehensive structural, spectroscopic, and quantum chemical analyses of new donor-acceptor complexes between N-heterocyclic carbenes and 1,2,5-telluradiazoles and a comparison with previously known complexes involving tellurenyl cations showed that the dative C-Te bonds cannot be solitarily described with only one Lewis formula. Canonical Lewis formulas that denote covalency and arrows emphasizing ionicity complement each other in varying extents. Evaluation of the relative weights of these resonance forms requires proper bonding description with a well-balanced toolbox of analytical methods. If for conciseness only, one resonance form is used, it must be the most significant one according to the analytical evaluation. If unclear, all significant resonance forms should be displayed.

摘要

对新型氮杂环卡宾与1,2,5-碲二唑之间的供体-受体配合物进行全面的结构、光谱和量子化学分析,并与先前已知的涉及碲烯阳离子的配合物进行比较,结果表明,配位C-Te键不能仅用一个路易斯公式单独描述。表示共价性的标准路易斯公式和强调离子性的箭头在不同程度上相互补充。评估这些共振形式的相对权重需要使用一套平衡良好的分析方法进行适当的键合描述。如果仅为简洁起见使用一种共振形式,则根据分析评估它必须是最重要的一种。如果不清楚,则应显示所有重要的共振形式。

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