Electronic Interactions in Iron- and Ruthenium-Containing Heterobimetallic Complexes: Structural and Spectroscopic Investigations

Abstract

The heterobimetallic Ru complexes Cp(CO)Ru(μ-I)(μ-dppm)PtI2 (8), Cp(CO)Ru(μ-I)(μ-dppm)PdI2 (10), and Cp(CO)RuI(μ-dppm)AuI (12) and their isoelectronic Fe analogues Cp(CO)Fe(μ-I)(μ-dppm)PtI2 (9), Cp(CO)Fe(μ-I)(μ-dppm)PdI2 (11), and Cp(CO)FeI(μ-dppm)AuI (13) were prepared by the reactions of Cp(CO)M(κ1-dppm)I (6, M = Ru; 7, M = Fe) with Pt(COD)I2, Pd(COD)I2, and AuI, respectively. All six complexes were characterized by cyclic voltammetry, IR, UV, and NMR (1H and 31P) spectroscopy, and elemental analysis. The structures of the I-bridged compounds 8−11 were determined by X-ray crystallography. Electronic interaction between the two metals is significant for the iodide-bridged compounds 8−11, as evidenced by the variation in their carbonyl stretching frequencies and UV−vis spectra, as well as in the shifts of their redox potentials in comparison to the shifts for mononuclear model compounds. In contrast, compounds 12 and 13, which have only dppm bridges, exhibit limited interactions between the two metals.