Activation and selective oxy-functionalization of alkanes with metal complexes: Shilov reaction and some new aspects

Аlbert А. Shteinman
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引用次数: 22

Abstract

The quest of selective catalytic reactions for direct conversion of alkanes into valued products remains to be the most important task objective of modern chemistry and metal complex catalysis. Nowadays it is adopted that the formation of metal–alkyl intermediates (MR) is a necessary condition for activation and functionalization of alkanes on metal complexes but the mechanism of subsequent reactions of metal alkyls remain obscure, so that effective catalytic systems of this kind are still rare and uncommon. Although it is widely adopted that alkane σ-complexes (M·RH) most frequently are primary hydrocarbon intermediates in these processes, low profile in the literature is given to their reactivity and these are often considered simply just as some ‘collision complexes’. Nevertheless, theoretical and experimental studies provide more and more evidence that the СН bonds in such complexes may be markedly weakened and/or polarized, thus opening wide horizons for occurrence of subsequent direct homolytic or heterolytic reactions of alkanes. This review addresses the discussion of new routes for activation and oxygenation of saturated hydrocarbons, including those via alkane σ-complexes, without formation of metal–alkyl intermediates.

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金属配合物对烷烃的活化和选择性氧官能化:希洛夫反应及其新进展
探索烷烃直接转化为有价产物的选择性催化反应仍然是现代化学和金属络合催化的最重要的任务目标。目前人们普遍认为金属-烷基中间体(MR)的形成是金属配合物上烷烃活化和功能化的必要条件,但金属烷基后续反应的机理尚不清楚,因此此类有效的催化体系尚不多见。尽管人们普遍认为烷烃σ-配合物(M·RH)是这些过程中最常见的初级烃类中间体,但文献中对其反应性的关注较少,通常将其简单地视为一些“碰撞配合物”。然而,理论和实验研究提供了越来越多的证据表明,这些配合物中的СН键可能会明显减弱和/或极化,从而为后续烷烃的直接均解或异解反应的发生开辟了广阔的视野。本文讨论了饱和烃活化和氧化的新途径,包括通过烷烃σ-配合物活化和氧化的新途径,而不形成金属-烷基中间体。
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2.8 months
期刊介绍: The Journal of Molecular Catalysis A: Chemical publishes original, rigorous, and scholarly full papers that examine the molecular and atomic aspects of catalytic activation and reaction mechanisms in homogeneous catalysis, heterogeneous catalysis (including supported organometallic catalysis), and computational catalysis.
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