Investigation on the reactivity of dithiophosphonato/dithiophosphato NiII complexes towards 2,4,6-tris-2-pyridyl-1,3,5-triazine: developments and new perspectives

The reactions between tptz and differently substituted dithiophosphonato [Ni(ROpdt)(2)] [ROpdt = (RO)(4-MeOC6H4) PS2-; R = Et (2); Pr (3); i-Pr (4); Bu (5)] and dithiophosphato [Ni((EtO)(2)PS2)(2)] (6) Ni-II complexes have been investigated, and the characterisation of the resulting neutral mixed complexes (2 center dot tptz)-(6 center dot tptz) is reported. In all these complexes, tptz forces one of the two dithiophosphonato/dithiophosphato ligands to behave as a monodentate ligand, a coordination mode rarely found in analogous Ni-II phosphorodithioato complexes. A comparison has been performed between the Ni-S bond distances of the new complexes and those of isologous dithiophosphonato, dithiophosphato and dithiophosphito Ni-II square-planar complexes, and of their penta-and hexa-coordinated adducts. The results, also supported by DFT calculations, are discussed and explained in terms of the structural trans-effect (STE). The reactivity of 2 center dot tptz towards AgNO3 and CuSO4 to yield the complex [Ni(EtOpdt)(tptz)(H2O)] NO3 (7), and the dimer [(Ni(tptz)(mu-SO4)(H2O)](2)center dot 6H(2)O (8), respectively, is consistent with the proposed bonding models.