ABSTRACT
[Mn(H2dapsox)Cl(H2O)]ClċH2O (1) and Zn(H2dapsox)-(H2O)2]Cl2ċH2O (2) were synthesized from 2,6-diacetylpyridine (dap), oxamic acid hydrazide (sox) and MnCl2ċ4H2O or ZnCl2ċ2H2O in 1:2:1 molar ratio, employing a template approach. Based on elemental analyses, molar conductivity and magnetic susceptibility data, IR, 1H and 13C NMR and EA spectra, as well as thermal analyses (DSC and TG), a pentagonal-bipyramidal (PBP) geometry for the complexes was determined. Symmetrically coordinated 2′,2′″-(2,6-pyridindiyldiethylidene)dioxamohydrazide (H2dapsox) is located as a pentadentate ligand in the equatorial plane. The stability of the 3d metal complexes having the PBP geometry is discussed. It was found that Co(II) and Mn(II) produce the most stable complexes of this type, while the Zn(II) complex of the same geometry is much less stable.
ACKNOWLEDGMENT
This work was supported by the Ministry for Science and Technology of the Republic of Serbia.