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

• Published in: Dalton transactions : an international journal of inorganic chemistry 2009-04 (14), p.2510-2520
• Main Authors: Aragoni, M Carla, Arca, Massimiliano, Crespo, Miriam, Devillanova, Francesco A, Hursthouse, Michael B, Huth, Susanne L, Isaia, Francesco, Lippolis, Vito, Verani, Gaetano
• Format: Article
• Language: English
• Subjects: Computer Simulation; Crystallography, X-Ray; Models, Chemical; Models, Molecular; Molecular Structure; Nickel - chemistry; Organometallic Compounds - chemistry; Organothiophosphorus Compounds - chemistry; Quantum Theory; Sulfhydryl Compounds - chemistry; Triazines - chemistry
• ISSN: 1477-9226
• DOI: 10.1039/b819326f

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)2PS2)2] (6) Ni(II) complexes have been investigated, and the characterisation of the resulting neutral mixed complexes (2.tptz)-(6.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.tptz towards AgNO3 and CuSO4 to yield the complex [Ni(EtOpdt)(tptz)(H2O)]NO3 (7), and the dimer [(Ni(tptz)(mu-SO4)(H2O)]2.6H2O (8), respectively, is consistent with the proposed bonding models.