Abstract

Two monomeric cobalt(II) complexes, [CoL(N3)]ClO4 (1) and CoL(N3)2 (2), where L is tris((3,5-dimethylpyrazol-yl) methyl) amine, were synthesized and their crystal structures were determined by X-ray diffraction technique. Complex 1 is five coordinated with one azide nitrogen atom and four nitrogen atoms of the tris((3,5-dimethyipyrazol-1-yl)-methyl) amine ligand, and the metal center is in distorted trigonal bipyramidal environment. Complex 2 is six coordinated distorted octahedron with the two azide nitrogen atoms and four nitrogen donors of the tris((3,5-dimethylpyrazol-l-yl)-methyl) amine ligand. The solution behaviors of the title complexes have been further investigated by UV-Vis, and 1H NMR analysis. It is found that the formation of 1 and 2 depends on the molar ratio of the azide ion to metal salt and ligand. Complex 1 attached with one aside group is more stable and easy to generate than complex 2 incorporated with two azide groups, and the reasons were well discussed.

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