Abstract
The complexes [M(Hdamsm)2]X·H2O (M = Fe, X = NO3; M = Ru, X = Cl), [Ru(Hdamsm)(PPh3)2X′](X′ = Cl, Br), and [VO(Hdamsm)(acac)] (H2damsm = diacetylmonoxime Schiff base of S-methyldithiocarbazate, Hacac = acetylacetone) have been prepared and characterized by spectroscopic techniques. Their redox properties were investigated by cyclic voltammetry. The X-ray crystal structure of [Fe(Hdamsm)2]NO3.H2O has been determined and shows that the complex has a distorted octahedral geometry in which the Hdamsm behaves as a monoanionic NNS tridentate ligand coordinating via oxime nitrogen, hydrazinic imine nitrogen, and thiolate sulfur. The reactivity of these complexes toward oxidation of alcohols in the presence of t-BuOOH and H2O2 as co-oxidants is reported.
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Acknowledgments
We thank Mansoura University for a grant to one of us (A. M. F) and also National Research Centre in Cairo for the X-ray crystallographic facility.
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This paper is dedicated to Professor William (Bill) P. Griffith, for his many contributions in coordination chemistry and homogenous catalysis.
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El-Hendawy, A.M., Fayed, A.M. & Mostafa, M.R. Complexes of a diacetylmonoxime Schiff base of S-methyldithiocarbazate (H2damsm) with Fe(III), Ru(III)/Ru(II), and V(IV); catalytic activity and X-ray crystal structure of [Fe(Hdamsm)2]NO3·H2O. Transition Met Chem 36, 351–361 (2011). https://doi.org/10.1007/s11243-011-9477-z
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DOI: https://doi.org/10.1007/s11243-011-9477-z