866529-68-2Relevant academic research and scientific papers
Complexes of a triazine-3-thione ligand with divalent metals: Crystal structure of [CdL2DMF]2·2DMF·1/4H 2O
López-Torres, Elena,Mendiola, Ma. Antonia
, p. 1435 - 1444 (2008/10/09)
The synthesis and characterization of Cd(II), Zn(II), Pb(II), Co(III) and Ni(II) complexes of 5-methoxy-5,6-diphenyl-4,5-dihydro-2H-[1,2,4]triazine-3- thione LH2OCH3 are reported. The stoichiometry of the complexes was found to be 1:2 except for cobalt complex 4 where the ratio is 1:3. In all complexes the triazine is deprotonated and acts at least as a NS bidentate ligand. The complexes have been characterised by microanalysis, mass spectrometry, IR, multinuclear (1H, 13C and 113Cd) NMR, 13C CP/MAS NMR and magnetic susceptibility. In addition, the structure of the complex [Cd(DMF)L2] 2·2DMF·1/4H2O (1a), has been determined by X-ray diffraction. Crystallographic data show that the complex consists of a dinuclear structure, in which the ligands act as bidentate NS donors and with two of the four ligands acting as a bridge between the metal ions via the sulfur atom. According to the spectroscopic data, the same disposition is proposed for complexes 2 and 3. Complex 4 is an low spin octahedral monomeric structure with the ligand acting as a bidentate NS donor and where the metal has been oxidised to Co(III). In complex 5 the Ni(II) ion is in a square planar N 2S2 disposition, formed by two ligands. The redox behaviour of the cadmium and cobalt complexes was explored by cyclic voltammetry and shows metal-centred processes.
