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Sonogashira和Negishi偶联反应中中间体和过渡态的模型化合物:大型异双金属配合物中的键比计算化学预测的更弱。

Model Compounds for Intermediates and Transition States in Sonogashira and Negishi Coupling: - Bonds in Large Heterobimetallic Complexes Are Weaker than Computational Chemistry Predicts.

作者信息

Oeschger Raphael J, Bissig Raphael, Chen Peter

机构信息

Laboratorium für Organische Chemie, ETH Zürich, CH-8093 Zürich, Switzerland.

出版信息

J Am Chem Soc. 2022 Jun 15;144(23):10330-10343. doi: 10.1021/jacs.2c01641. Epub 2022 May 31.

DOI:10.1021/jacs.2c01641
PMID:35639626
Abstract

We report an experimental study, with accompanying DFT calculations, on a series of heterobimetallic complexes with Pd(II) and Cu(I), Ag(I), or Au(I). The isolable pincer complexes are models for the intermediates and transition state for the transmetalation step in Sonogashira and Negishi coupling reactions, among which, according to the DFT calculations, only the transition state has the two metal centers within bonding distance. Furthermore, we report a substituted version of an analogous heterobimetallic complex in which a competing dissociation sets an upper-bound on the strength of the - metal-metal bond. Analysis of the structures in the solid state and in solution, and the competitive dissociation experiment in the gas phase, indicate that the dispersion-corrected DFT method used in the study appears to overestimate the strength of the metal-metal interaction, thus distorting the shape of the computed potential energy surface systematically for transmetalation.

摘要

我们报告了一项实验研究,并辅以密度泛函理论(DFT)计算,该研究针对一系列含有钯(II)与铜(I)、银(I)或金(I)的异双金属配合物展开。可分离的钳形配合物是Sonogashira和Negishi偶联反应中金属转移步骤的中间体和过渡态模型,其中,根据DFT计算,只有过渡态的两个金属中心处于键距范围内。此外,我们报告了一种类似异双金属配合物的取代形式,其中竞争性解离为金属 - 金属键的强度设定了上限。对固态和溶液中的结构分析以及气相中的竞争性解离实验表明,该研究中使用的色散校正DFT方法似乎高估了金属 - 金属相互作用的强度,从而系统性地扭曲了计算得到的金属转移势能面的形状。

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