Homoleptic ruthenium(II) complexes bearing imidazol(in)ium-2-dithiocarboxylate ligands: synthesis, characterization, and redox properties.

Five cationic ruthenium(II) chelates with the generic formula [Ru(SC·NHC)](PF) were readily obtained upon cleavage of the [RuCl(-cymene)] dimer with representative imidazol(in)ium-2-dithiocarboxylate zwitterions (NHC·CS) in the presence of KPF. The homoleptic complexes were fully characterized by various analytical techniques and the molecular structure of one of them was determined by single-crystal X-ray diffraction analysis. As expected, it featured an octahedral RuS core surrounded by three imidazol(in)ium rings and their nitrogen substituents. The robustness of the Ru-S bonds combined with the chelate effect of the κ-,'-dithiocarboxylate units and the steric protection imparted by bulky 1,3-diarylimidazol(in)ium groups most likely accounted for the outstanding stability of these species in solution. Cyclic voltammetry showed that the five homoleptic complexes featured characteristic waves for a monoelectronic redox process corresponding to the Ru/Ru couple with values ranging between 0.97 and 1.27 V Ag/AgCl. This half-wave potential was clearly dependent on the nature of their ancillary ligands as the evolution of the values roughly paralleled the basicity sequence of the NHCs used to prepare them, in line with the trends observed when monitoring the chemical shifts of the CS unit on C NMR spectroscopy and the CS asymmetric stretching vibration wavenumbers on IR spectroscopy.