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Synthesis,Crystal Structure,and Electrochemistry of Iron and Cobalt Complexes Supported by a Pentadentate Amine‐bis(phenolate) Ligand
Authors:Xiao‐Wei Song  Chang Guo  Chang‐Neng Chen
Affiliation:1. Anhui Province Key Laboratory of Optoelectronic and Magnetism Functional Materials, Key Laboratory of Functional Coordination Compounds of Anhui Higher Education Institutes, Anqing Normal University, Anqing, Anhui, P. R. China;2. State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, Fujian, P. R. China
Abstract:The pentadentate amine‐bis(phenolate) ligand 6,6′‐(dipyridin‐2‐ylmethylazanediyl)bis(methylene)bis(2,4‐dimethylphenol) (H2L) was prepared and characterized. This ligand readily coordinates with FeIII or CoIII ions, and the resulting complexes [FeIIILCl] ( 1 ) and [CoIIIL(H2O)]Cl ( 2 ) were characterized by elemental analysis. X‐ray structural studies show that the ligand in complexes 1 and 2 acts as a pentadentate ligand, leaving one coordination side of the transition metal available for exogenous ligands such as chloride ion ( 1 ) or water ( 2 ) ligand, and the central metal atoms are hexacoordinate in a similar distorted octahedral arrangement. Electrochemical studies reveal that each of the complexes exhibits multiple redox processes in the potential window investigated. Complex 1 shows one reversible oxidative event at 0.32 V and one quasi‐reversible reduction event at –1.03 V, while the complex 2 displays one reversible oxidative event at 0.18 V and one quasi‐reversible reduction at –0.64 V.
Keywords:Cobalt  Iron  Pentadentate amine‐bis(phenolate) ligand  Structure elucidation
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