Thin films of CuS (covellite) were deposited onto TCO (SnO 2 :F) glass by Spray Pyrolysis (SP) technique. Aqueous and water:alcohol (ethanol, 1-propanol) solutions of copper(II) chloride and thiourea with different Cu/S molar ratio have been used as precursors. The substrate temperature was varied from 185°C to 285°C. The structural and the morphological characterization of the films has been carried out by Raman spectroscopy and Scanning Electron Microscopy. The X-Ray Diffraction analysis of as-grown films showed the single-phase covellite, with hexagonal crystal structure built around three preferred orientations corresponding to (102), (103) and (110) atomic planes. The dense morphology of CuS films with large crystallites/aggregates suggest that crystal growth is the limiting step in the films deposition, at 235 °C and at 285 °C, from precursors' solution containing water or mixtures of water:alcohol as solvents. The growth of CuS thin films by spray pyrolysis is favored by increasing both the alcohol concentration and the deposition temperature.
New complexes of isonicotinoylhydrazone-9-anthraldehyde with Cu(II), Co(II) and Ni(II) have been prepared and characterized by analytical and physico-chemical techniques, such as elemental and thermal analyses, magnetic susceptibility and conductivity measurements, and electronic, EPR and IR spectral studies. The infrared spectral studies revealed the bidentate or monodentate nature of the Schiff base in the complexes; the pyridine nitrogen does not participate in the coordination. A tetrahedral geometry is suggested for the nitrate-complexes and an octahedral geometry for the others. Thermal studies support the chemical formulation of these complexes
Eight new complexes of Cu(II), Co(II), Ni(II) and Zn(II) with isonicotinic acid hydrazide (isoniazid, (INH)) and isonicotinic acid (1-naphthylmethylene) hydrazide (INNMH), having the formula of the type [M(INH)(ac)2] or [M(INNMH)(ac)2] (M = Co(II), Ni(II) and Zn(II)) and [Cu(INH)(ac)2]2, [Cu(INNMH)(ac)2]2, were synthesized and characterized. All complexes were characterized based on elemental analyses, and IR, UV-VIS-NIR and EPR spectroscopy, as well as by thermal analysis and determination of their molar conductivity and magnetic moments. The structure of INNMH was established by single crystal X-ray analysis. In all complexes, both ligands were coordinated to the metal via N and O. The complexes of Cu (II) were dimeric, with four bridges between acetate ions and Cu(II).
Complexes of Cu(II), Ni(II), Co(II) with the 9-anthraldehyde isonicotinoyl hydrazone ligand (HL1) and the 3,5-di-tert-butyl-4-hydroxybenzaldehyde isonicotinoyl hydrazone ligand (H2L2) were synthesized by the template method. The complexes were characterized by analytical analysis, IR, UV-Vis and ESR spectroscopy, magnetic measurements, conductometry and thermal analysis and the two ligands by 1H-NMR spectroscopy. From the elemental analysis, 1:2 (metal:ligand) stoichiometry for the complexes of Cu(II), Ni(II) with the ligands HL1 and H2L2 and 1:1 (metal:ligand) stoichiometry for the complex of Co(II) with the ligand HL1 are proposed. The molar conductance data showed that the complexes are non-electrolytes. The magnetic susceptibility results coupled with the electronic and ESR spectra suggested a distorted octahedral geometry for the complexes Ni(II)/HL1, Ni(II)/H2L2 and Cu(II)/H2L2, a tetrahedral stereochemistry for the complex Cu/HL1 and a square-planar geometry for the complex Co/HL1. The IR spectra demonstrated the bidentate coordination of the ligands HL1 and H2L2 by the O=C amide oxygen and the azomethine nitrogen, as well as monodentate coordination of the ligand HL1 by the azomethine nitrogen in the Cu(II)complex. The antibacterial activity of the ligands and their metallic complexes were tested against Staphylococcus aureus, Escherichia coli and Klebsiella pneumoniae.
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