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钌苯:一种坚固的前催化剂。

Ruthenabenzene: A Robust Precatalyst.

机构信息

Department of Chemistry, University of Illinois at Chicago, 845 W. Taylor St., Chicago, Illinois 60607, United States.

Department of Chemistry, University of Pittsburgh, 219 Parkman Avenue, Pittsburgh, Pennsylvania 15260, United States.

出版信息

J Am Chem Soc. 2021 May 19;143(19):7490-7500. doi: 10.1021/jacs.1c02237. Epub 2021 May 7.

Abstract

Metallaaromatics constitute a unique class of aromatic compounds where one or more transition metal elements are incorporated into the aromatic system, the parent of which is metallabenzene. One of the main concerns about metallabenzenes generally deals with the structural characterization related to their relative aromaticity compared to the carbon archetype. Transition metal-containing metallabenzenes are also implicated in certain catalytic processes such as alkyne metathesis polymerization; however, these transition metal-based metallaaromatic compounds have not been developed as a catalyst. Herein, we describe an effective strategy to generate diverse arrays of ruthenabenzenes and demonstrated them as an aromatic equivalent of the Grubbs-type ruthenium alkylidene catalysts. These ruthenabenzenes can be prepared via an enyne metathesis and metallotropic [1,3]-shift cascade process to form alkyne-chelated ruthenium alkylidene intermediates followed by spontaneous cycloaromatization. The aromatic nature of these complexes was confirmed by spectroscopic and X-ray crystallographic data, and the mechanistic pathways for the cycloaromatization process were studied by DFT calculations. These ruthenabenzenes display robust catalytic activity for metathesis and other transformations, which illustrates that metallabenzenes are not only compounds of structural and theoretical interests but also are a novel platform for new catalyst development.

摘要

金属芳环化合物构成了一类独特的芳香族化合物,其中一个或多个过渡金属元素被纳入芳香体系,其母体为金属苯。金属苯通常引起人们关注的一个主要问题涉及与碳原型相比其相对芳香性的结构特征。含过渡金属的金属苯还涉及某些催化过程,如炔烃复分解聚合;然而,这些基于过渡金属的金属芳环化合物尚未被开发为催化剂。在此,我们描述了一种有效的策略来生成各种钌苯,并将其证明为 Grubbs 型钌卡宾催化剂的芳香等价物。这些钌苯可以通过烯炔复分解和金属重排[1,3]-迁移级联反应来制备,形成炔烃螯合的钌卡宾中间体,然后自发环化。通过光谱和 X 射线晶体学数据证实了这些配合物的芳香性,并且通过 DFT 计算研究了环化过程的反应途径。这些钌苯对复分解和其他转化具有强大的催化活性,这表明金属苯不仅是结构和理论兴趣的化合物,而且是新催化剂开发的新平台。

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