Mixed aza-thia crowns containing the 1,10-phenanthroline subunit. Substitution reactions in [NiL(MeCN)][BF4](2) {L=2,5,8-trithia[9](2,9)-1,10-phenanthrolinophane}

The substitution reactions of the co-ordinated acetonitrile molecule in [Ni L(MeCN)][BF4](2) 1 (L = 2,5,8-trithia-[9](2,9)-1,10-phenanthrolinophane) wi th different anionic and neutral ligands L' [Cl-, Br-, I-, CN-, SCN-, H2O, pyridine (py), aniline tan), 1, 3-dimethyl-4-imidazoline-2-thione (etu) or 1,3-dimethyl-4-imidazoline-2-selone (eseu)] have been studied by using elec tronic spectroscopy. While the reaction with all the anionic ligands is qua ntitative, for the neutral ones an equilibrium takes place; the correspondi ng equilibrium constants have been determined in MeCN at 25 degrees C. The complex cations [NiL(L')]((2 - n)+) (n = 0 for neutral and 1 for anionic li gands) have also been isolated in the solid state, mainly as BF4- salts and the compounds [NiL(H2O)[ClO4](2) . H2O, [NiL(Cl)]Cl . H2O, [NiL(SCN)]BF4 . MeNO2, [NiL(eseu)][BF4](2) and [NiL(py)][BF4](2) have been characterized b y X-ray diffraction studies. In these complexes a distorted octahedral geom etry is achieved at the Ni-II with five sites occupied by the macrocyclic l igand L and the sixth by the appropriate ligand L'. The electrochemistry of all the prepared compounds has been studied by cyclic voltammetry. In part icular the reductive cyclic voltammetry of 1 in acetonitrile shows a quasi- reversible one-electro n reduction wave near E-1(1/2) = - 1.0 V vs. Fc/Fc(). Electrochemical reduction by con trolled-potential electrolysis at this potential in the presence of the axial ligand PMe3 and investigation of the reduced product by ESR spectroscopy confirm the reduction process to be me tal based and to correspond to the formation of the [(NiL)-L-I](+) species.