Fe(II), Fe(III), Co(II), and Ni(II) chelates with three quinolinol sulfonamides have been prepared and characterized. Characterization of the solids so obtained was accomplished by elemental analysis, electronic and ir spectra, and conductivity measurements. It was found that the sulfonamide ligands act as monobasic bidentate ON donors. The bonding sites are ascertained, and the complexes were all six-coordinate assuming a distorted octahedral geometry. It was identified that the metal chelates possess enhanced antibacterial and antifungal activities relative to the free ligands

Fe(II), Fe(III), Co(II), and Ni(II) chelates with three quinolinol sulfonamides have been prepared and characterized. Characterization of the solids so obtained was accomplished by elemental analysis, electronic and ir spectra, and conductivity measurements. It was found that the sulfonamide ligands act as monobasic bidentate ON donors. The bonding sites are ascertained, and the complexes were all six-coordinate assuming a distorted octahedral geometry. It was identified that the metal chelates possess enhanced antibacterial and antifungal activities relative to the free ligands

Co(II), Ni(II) and Cu(II) complexes of some bifunctional arylidene-o-phenylenediamineSchiff bases have been prepared. Formation, stoichiometry and stability of the complexes have been tested in solution using electronic spectral measurements. Characterization of the complexes has been accomplished primarily by elemental analysis, molar conductance as well as electronic and IR spectral measurements. It is concluded that theo,o-hydroxy derivative (L 1) acts as a bivalent ONNO tetradentate ligand while the molecules of the other derivatives (L 2-L 5) are coordinated to the metal ions as bidentate NN ligands. The Cu(II)-L 1 complex is suggested to possess a tetrahedral geometry whereas the other complexes are suggested to exhibit a distarted octahedral geometry. The different bands observed in the electronic spectra of the complexes inDMF solutions have been assigned to the -*,L M CT and d-d electronic transitions.