Abstract

The chelating behavior of 2,6-diacetylpyridine bis(2-aminobenzoylhydrazone) (H 2dapa) towards manganese(II), cadmium(II) and oxovanadium(IV) ions has been studied by elemental analyses, conductance measurements, magnetic properties and spectral (IR, 1H NMR, UV–Vis and EPR) studies. The IR spectral studies suggest the pentadentate nature of the ligand with pyridine nitrogen, two azomethine nitrogens and two carbonyl oxygen atoms as the ligating sites. Six coordinate structure for [VO(H 2dapa)]SO 4 · H 2O and seven coordinate structures for [Mn(H 2dapa)(Cl)(H 2O)]Cl · 2H 2O and [Cd(H 2dapa)Cl 2] · H 2O complexes have been proposed. Pentagonal bipyramidal geometry for [Mn(H 2dapa)(Cl)(H 2O)]Cl · 2H 2O and [Cd(H 2dapa)(Cl 2)] · H 2O complexes was confirmed by single crystal analysis. The X-band EPR spectra of the oxovanadium(IV) and manganese(II) complexes in the polycrystalline state at room (300 K) and also at liquid nitrogen temperature (77 K) were recorded and their salient features are reported.

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