Browsing by Author "Malik, Azad"
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Item Bis(piperidinedithiocarbamato)pyridinecadmium(II) as a Single-Source Precursor for the Synthesis of CdS Nanoparticles and Aerosol-Assisted Chemical Vapour Deposition (AACVD) of CdS thin films(2014) Lewis, David J.; Revaprasadu, Neerish; Mlowe, Sixberth; Malik, Azad; Mubofu, Egid B.; O'Brien, Paul; Raftery, JamesThe synthesis and single-crystal X-ray structure of bis(piperidinedithiocarbamato)pyridinecadmium(II), [Cd(S2C(NC5H10))2(NC5H5)] are reported and its use as a precursor for the synthesis of hexagonal CdS nanoparticles and CdS thin films is presented. Thermogravimetric analysis (TGA) of this complex showed clean decomposition in two steps to give CdS. Thermolysis of the complex in hexadecylamine at different temperatures in the range 190 ¬ 270 °C gave CdS nanostructures including nanorods and oval shaped particles. The band gap of the as-synthesized CdS nanoparticles varied as the temperature was increased. CdS thin films with optical direct band gaps of ca. 2.4 eV were deposited by aerosol-assisted chemical vapour deposition (AACVD) in the temperature range 350 to 450 oC using the same precursor. Powder X-ray diffraction (p-XRD) patterns of CdS nanoparticles and thin films confirmed the hexagonal phase of CdS.Item The Synthesis, Spectroscopy and X-ray Single Crystal Structure of Catena-[(μ-anacardato)-copper(II)bipyridine][Cu2{(μ-O2CC6H3(o-OH)(o-C15H31)}4(NC5H5)2](2013-08) Malik, Azad; O'Brien, Paul; Tuna, Floriana; Pritchard, Robin G.; Buchweishaija, Joseph; Kimambo, Elianaso; Mubofu, Egid B.Hydrogenation of crude anacardic acid gave a transparent crystalline product on recrystallization. When reacted with copper nitrate in the presence of pyridine it produced green crystals of a pyridine adduct of a dimeric copper(ii) anacardate with the copper acetate structure. The X-ray single crystal structures of both anacardic acid and the copper complex were determined. Magnetic studies have confirmed strong antiferromagnetic coupling between copper(ii) centre in the dimer. The exchange coupling constant was determined to be J = -324 cm(-1). The EPR spectra of the polycrystalline product are consistent with spin S = 1. The zero-field splitting parameter and g tensor values are |D| = 0.36 cm(-1), g|| = 2.36 and g⊥ = 2.06.