Abstract
Treatment of 2-phenyl-1,3-bis(selenocyanate)propane with Fe3(CO)12 yielded the expected diiron diselenolato complex [(μ-SeCH2)2CHC6H5]Fe2(CO)6 (1). Reaction of complex 1 with bis(diphenylphosphine)methane (dppm) in refluxing xylene gave an intra-molecular phosphine bridging complex [(μ-SeCH2)2CHC6H5]Fe2(CO)4(μ-dppm) (2), while reaction of complex 1 with 1,1′-bis(diphenylphosphino)ferrocene (dppf) in the presence of the decarbonylating agent Me3NO afforded an inter-molecular phosphine bridging tetrairon complex {[(μ-SeCH2)2CHC6H5]Fe2(CO)5}2(μ, κ 1, κ 1-dppf) (3). All three complexes were characterized by physical–chemical and spectroscopic methods and for complexes 2 and 3 by X-ray crystallography. Their electrochemical behaviors, especially in the presence of HBF4 for 2, were investigated by cyclic voltammetry.
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Li, CG., Cui, MJ., Xue, F. et al. Phenyl-functionalized diiron diselenolato complexes with intra- or inter-molecular bridging bidentate phosphine ligands. Transition Met Chem 40, 493–500 (2015). https://doi.org/10.1007/s11243-015-9940-3
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DOI: https://doi.org/10.1007/s11243-015-9940-3