State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, 345 Lingling Road, Shanghai, 200032, P.R. China.
State Key Laboratory of Fine Chemicals, School of Chemical Engineering, Dalian University of Technology, Dalian, 11602, P.R. China.
Angew Chem Int Ed Engl. 2017 Mar 1;56(10):2720-2724. doi: 10.1002/anie.201611162. Epub 2017 Jan 27.
N-Heterocyclic carbene based pincer ligands bearing a central silyl donor, [CSiC] , have been envisioned as a class of strongly σ-donating ligands that can be used for synthesizing electron-rich transition-metal complexes for the activation of inert bonds. However, this type of pincer ligand and complexes thereof have remained elusive owing to their challenging synthesis. We herein describe the first synthesis of a CSiC pincer ligand scaffold through the coupling of a silyl-NHC chelate with a benzyl-NHC chelate induced by one-electron oxidation in the coordination sphere of a cobalt complex. The monoanionic CSiC ligand stabilizes the Co dinitrogen complex [(CSiC)Co(N )] with an unusual coordination geometry and enables the challenging oxidative addition of E-H bonds (E=C, N, O) to Co to form Co complexes. The structure and reactivity of the cobalt(I) complex are ascribed to the unique electronic properties of the CSiC pincer ligand, which provides a strong trans effect and pronounced σ-donation.
基于 N-杂环卡宾的钳形配体带有一个中心硅供体 [CSiC],被设想为一类强 σ-供体配体,可用于合成富电子过渡金属配合物以活化惰性键。然而,由于其合成具有挑战性,这类钳形配体及其配合物仍然难以捉摸。我们在此描述了通过在钴配合物的配位球中单电子氧化诱导的硅基-NHC 螯合物与苄基-NHC 螯合物的偶联,首次合成了 CSiC 钳形配体支架。单阴离子 CSiC 配体稳定了 Co 二氮配合物 [(CSiC)Co(N2)],具有不寻常的配位几何形状,并使具有挑战性的 E-H 键(E=C、N、O)的氧化加成反应能够在 Co 上形成 Co 配合物。钴 (I) 配合物的结构和反应性归因于 CSiC 钳形配体的独特电子特性,它提供了强的反式效应和显著的 σ-供体。