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R-NHC偶联(R = C、H、杂原子)和M-NHC键断裂在M/NHC配合物演化及催化活性物种形成中的关键作用。

The key role of R-NHC coupling (R = C, H, heteroatom) and M-NHC bond cleavage in the evolution of M/NHC complexes and formation of catalytically active species.

作者信息

Chernyshev Victor M, Denisova Ekaterina A, Eremin Dmitry B, Ananikov Valentine P

机构信息

Platov South-Russian State Polytechnic University (NPI) , Prosveschenya 132 , Novocherkassk , 346428 , Russia.

N. D. Zelinsky Institute of Organic Chemistry , Russian Academy of Sciences , Leninsky Prospect 47 , 119991 Moscow , Russian Federation.

出版信息

Chem Sci. 2020 Jun 19;11(27):6957-6977. doi: 10.1039/d0sc02629h. eCollection 2020 Jul 21.

Abstract

Complexes of metals with N-heterocyclic carbene ligands (M/NHC) are typically considered the systems of choice in homogeneous catalysis due to their stable metal-ligand framework. However, it becomes obvious that even metal species with a strong M-NHC bond can undergo evolution in catalytic systems, and processes of M-NHC bond cleavage are common for different metals and NHC ligands. This review is focused on the main types of the M-NHC bond cleavage reactions and their impact on activity and stability of M/NHC catalytic systems. For the first time, we consider these processes in terms of NHC-connected and NHC-disconnected active species derived from M/NHC precatalysts and classify them as fundamentally different types of catalysts. Problems of rational catalyst design and sustainability issues are discussed in the context of the two different types of M/NHC catalysis mechanisms.

摘要

金属与氮杂环卡宾配体(M/NHC)的配合物通常因其稳定的金属-配体骨架而被视为均相催化中的首选体系。然而,显而易见的是,即使是具有强M-NHC键的金属物种在催化体系中也会发生演变,并且M-NHC键的断裂过程对于不同的金属和NHC配体来说是常见的。本综述聚焦于M-NHC键断裂反应的主要类型及其对M/NHC催化体系活性和稳定性的影响。我们首次从源自M/NHC预催化剂的NHC连接和NHC断开的活性物种的角度考虑这些过程,并将它们归类为本质上不同类型的催化剂。在两种不同类型的M/NHC催化机制的背景下,讨论了合理催化剂设计的问题和可持续性问题。

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