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吡啶单亚胺钼羰基配合物对 CO2 的还原:CO2 的协同金属-配体结合。

Reduction of CO2 by Pyridine Monoimine Molybdenum Carbonyl Complexes: Cooperative Metal-Ligand Binding of CO2.

机构信息

Joint Center for Artificial Photosynthesis, Division of Chemistry and Chemical Engineering, California Institute of Technology, 1200 East California Boulevard, Pasadena, CA 91125 (USA).

Department of Chemistry and Biochemistry, University of California, San Diego, 9500 Gilman Drive MC 0358, La Jolla, California 92093 (USA).

出版信息

Chemistry. 2015 Jun 1;21(23):8497-503. doi: 10.1002/chem.201500463. Epub 2015 Apr 29.

Abstract

[((Ar) PMI)Mo(CO)4 ] complexes (PMI=pyridine monoimine; Ar=Ph, 2,6-di-iso-propylphenyl) were synthesized and their electrochemical properties were probed with cyclic voltammetry and infrared spectroelectrochemistry (IR-SEC). The complexes undergo a reduction at more positive potentials than the related [(bipyridine)Mo(CO)4 ] complex, which is ligand based according to IR-SEC and DFT data. To probe the reaction product in more detail, stoichiometric chemical reduction and subsequent treatment with CO2 resulted in the formation of a new product that is assigned as a ligand-bound carboxylate, ( iPr 2PhPMI)Mo(CO)3 (CO2 ) , by NMR spectroscopic methods. The CO2 adduct ( iPr 2PhPMI)Mo(CO)3 (CO2 ) could not be isolated and fully characterized. However, the C-C coupling between the CO2 molecule and the PDI ligand was confirmed by X-ray crystallographic characterization of one of the decomposition products of ( iPr 2PhPMI)Mo(CO)3 (CO2 ) .

摘要

[((Ar) PMI)Mo(CO)4 ] 配合物(PMI=吡啶单亚胺;Ar=Ph,2,6-二异丙基苯基)被合成,并通过循环伏安法和红外光谱电化学(IR-SEC)研究了它们的电化学性质。根据 IR-SEC 和 DFT 数据,这些配合物的还原电位比相关的 [(bipyridine)Mo(CO)4 ] 配合物更正,这是配体为基础的。为了更详细地研究反应产物,化学计量还原并用 CO2 处理会导致形成一种新的产物,通过 NMR 光谱方法将其指定为配体结合的羧酸盐 ( iPr 2PhPMI)Mo(CO)3 (CO2 ) 。CO2 加合物 ( iPr 2PhPMI)Mo(CO)3 (CO2 ) 不能被分离并进行完全表征。然而,通过 X 射线晶体学对 ( iPr 2PhPMI)Mo(CO)3 (CO2 ) 的一种分解产物的表征,确认了 CO2 分子与 PDI 配体之间的 C-C 偶联。

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