Thionitrosyl Complexes of Rhenium and Technetium with PPh3 and Chelating Ligands—Synthesis and Reactivity

In contrast to corresponding nitrosyl compounds, thionitrosyl complexes of rhenium and technetium are rare. Synthetic access to the thionitrosyl core is possible by two main approaches: (i) the treatment of corresponding nitrido complexes with S2Cl2 and (ii) by reaction of halide complexes with trithiazyl chloride. The first synthetic route was applied for the synthesis of novel rhenium and technetium thionitrosyls with the metals in their oxidation states “+1” and “+2”. MVNCl2 (PPh3) 2, MVNCl (PPh3) (LOMe) and MVINCl2 (LOMe) (M = Re, Tc; LOMe− = (η5-cyclopentadienyl) tris (dimethyl phosphito-P) cobaltate (III) ) complexes have been used as starting materials for the synthesis of ReII (NS) Cl3 (PPh3) 2 (1), ReII (NS) Cl3 (PPh3) (OPPh3) (2), ReII (NS) Cl (PPh3) (LOMe) + (4a), ReII (NS) Cl2 (LOMe) (5a), TcII (NS) Cl (PPh3) (LOMe) + (4b) and TcII (NS) Cl2 (LOMe) (5b). The triphenylphosphine complex 1 is partially suitable as a precursor for ongoing ligand exchange reactions and has been used for the synthesis of ReI (NS) (PPh3) (Et2btu) 2 (3a) (HEt2btu = N, N-diethyl-N′-benzoyl thiourea) containing two chelating benzoyl thioureato ligands. The novel compounds have been isolated in crystalline form and studied by X-ray diffraction and spectroscopic methods including IR, NMR and EPR spectroscopy and (where possible) mass spectrometry. A comparison of structurally related rhenium and technetium complexes allows for conclusions about similarities and differences in stability, reaction kinetics and redox behavior between these 4d and 5d transition metals.