Division of Chemistry and Chemical Engineering, California Institute of Technology (USA).
Angew Chem Int Ed Engl. 2014 Aug 4;53(32):8427-31. doi: 10.1002/anie.201404078. Epub 2014 Jun 20.
The CAAC [CAAC=cyclic (alkyl)(amino)carbene] family of carbene ligands have shown promise in stabilizing unusually low-coordination number transition-metal complexes in low formal oxidation states. Here we extend this narrative by demonstrating their utility in affording access to the first examples of two-coordinate formal Fe(0) and Co(0) [(CAAC)2M] complexes, prepared by reduction of their corresponding two-coordinate cationic Fe(I) and Co(I) precursors. The stability of these species arises from the strong σ-donating and π-accepting properties of the supporting CAAC ligands, in addition to steric protection.
CAAC(环状(烷基)(氨基)卡宾)卡宾配体家族在稳定低形式氧化态下的异常低配位数过渡金属配合物方面表现出了很大的潜力。在这里,我们通过展示它们在获得首例两配位形式 Fe(0)和 Co(0)[(CAAC)2M]配合物方面的应用来扩展这一叙述,这些配合物是通过还原相应的两配位阳离子 Fe(I)和 Co(I)前体制备的。这些物种的稳定性源于支撑 CAAC 配体的强 σ-给体和 π-受体性质,以及空间位阻保护。