Optical and electrochemical properties of cyclometalated Pd(II) and Pt(II) complexes with a metal-metal chemical bond

Cyclometalated [M(C<^>N)(mu-(N-S))](2) complexes ((M = Pd(II), Pt(II)), (C<^>N)(-) are the deprotonated forms of 2-tolylpyridine and benzo[h]quinoline, and (N-S)(-) are pyridine-2-thiolate and benzothiazole-2-thiolate ions) are studied by H-1 NMR, IR, electronic-absorption, and emission spectroscopy, as well as by voltammetry. It is shown that the formation of the metal-metal chemical bond and the sigma (dz2) (*) orbital as a HOMO of complexes leads to the long-wavelength spin-allowed (410-512 nm) and spin-forbidden (595-673 nm) optical transitions sigma (dz2) (*) -IEuro ((C<^>N)) (*) in the absorption and phosphorescence spectra, as well as to the two-electron and successive one-electron oxidation with the formation of binuclear Pt(III) and Pd(III) complexes. The substitution of Pt(II) by Pd(II) is characterized by hypso- and bathochromic shifts of the spin-allowed and forbidden sigma (dz2) (*) -IEuro ((C<^>N)) (*) optical transitions in the absorption and phosphorescence spectra of complexes, by phosphorescence quenching of Pd(II) complexes in liquid solutions, and by an anodic shift of the oxidation potential of Pd(II) complexes compared with Pt(II) complexes.