Structure and Microstructure Properties of Ball Milled Fe-Zn

Nanocrystalline Fe10 %Zn and Fe30 %Zn alloys have been prepared from pure elemental powders by mechanical alloying processing in a high energy planetary ball-mill. Microstructural, structural, and magnetic characterizations of the powders were investigated by X-ray diffraction, and vibrating sample magnometer. The crystallite size reduction to the nanometer scale is accompanied by an increase in the atomic level strain. The reaction between Fe and Zn leads to the formation of a bcc Fe(Zn) solid solution with a lattice parameter close to (0.2912 nm for Fe30 %Zn and 0,2885 nm for Fe10 %Zn) after 5 h of milling. The complete dissolution of the elemental Zn powders in the a-Fe lattice gives rise to the formation of a highly disordered Fe(Zn) solid solution, where a-Fe(Zn) nanograins have a crystallite size of (229,29 Å for Fe10 %Zn (24 h) 30,09 Å for Fe30 %Zn (24 h), on prolonged milling time. The coercivity and magnetization values are 18,90 (Fe10 %Zn)Oe and 26,59 (Fe30 %Zn) emu/g, respectively, after 24 h of milling. When you are citing the document, use the following link http://essuir.sumdu.edu.ua/handle/123456789/3514

Synthesis of a Novel Zinc(II) Porphyrin Complex, Halide Ion Reception, Catalytic Degradation of Dyes, and Optoelectronic Application

This work describes the synthesis of a novel zinc(II) porphyrin complex, namely [Meso-4α-tetra-(1,2,3-triazolyl)phenylporphyrinato]zinc(II) symbolized by 4α-[Zn(TAzPP)] (4), using the click chemistry approach in the presence of copper iodide. All of the synthetic porphyrin species reported herein were fully characterized by elemental analysis, infrared spectroscopy, proton nuclear magnetic resonance, UV-visible spectroscopy, and fluorescence. To synthesize the 4α-[Zn(TAzPP)] complex (4), we produced 4α-Meso-tetra-o-nitrophenylporphyrin (H2TNO2PP) and 4α-meso-tetra-o-aminophenylporphyrin (4α-H2TNH2PP) (1) using known classic literature methods. This 4α atropisomer was converted to 4α-meso-tetra-o-azidophenylporphyrin (4α-H2TN3PP) (3) by reaction with sodium nitrite and sodium azide, and then it was metalated by Zn(II), leading to [4α-meso-tetra(2-azidophenyl)porphyrinate]zinc(II) (4α-[Zn(TN3PP)]) (3). The click chemistry synthetic method was finally used to prepare 4α-[Zn(TAzPP)] (4). This new tetracoordinated zinc(II) porphyrin complex was prepared and characterized in order to: (i) produce a receptor for anion recognition and sensing application for Cl− and Br−; (ii) study the catalytic decomposition of rhodamine B (RhB) and methyl orange (MO) dyes; and (iii) determine the electronic characteristics as a photovoltaic device. Complex (4) formed 1:1 complex stoichiometric species with chloride and bromide halides and the average association constants of the 1:1 addicts were ~ 103. The photodecomposition of RhB and MO dyes in the presence of complex (4) as a catalyst and molecular oxygen showed that complex (4) presented a photodegradation yield of approximately 70% and could be reused for five successive cycles without any obvious change in its catalytic activity. The current-voltage characteristics and impedance spectroscopy measurements of complex (4) confirmed that our zinc(II) metalloporphyrin could be used as a photovoltaic device

Synthesis of New Cobalt(III) <i>Meso</i>-Porphyrin Complex, Photochemical, X-ray Diffraction, and Electrical Properties for Photovoltaic Cells

The present work describes the preparation and characterization of a new cobalt(III) porphyrin coordination compound named (chlorido)(nicotinoylchloride)[meso-tetra(para-chlorophenyl)porphyrinato]cobalt(III) dichloromethane monosolvate with the formula [CoIII(TClPP)Cl(NTC)]·CH2Cl2 (4). The single-crystal X-ray molecular structure of 4 shows very important ruffling and waving distortions of the porphyrin macrocycle. The Soret and Q absorption bands of 4 are very red-shifted as a consequence of the very distorted porphyrin core. This coordination compound was also studied by fluorescence and cyclic voltammetry. The efficiency of our four porphyrinic compounds—the H2TClPP (1) free-base porphyrin, the [CoII(TClPP)] (2) and [CoIII(TClPP)Cl] (3) starting materials, and the new Co(III) metalloporphyrin [CoIII(TClPP)Cl(NTC)]·CH2Cl2 (4)—as catalysts in the photochemical degradation was tested on malachite green (MG) dye. The current voltage of complexes 3 and 4 was also studied. Electrical parameters, including the saturation current density (Js) and barrier height (ϕb), were measured

Spectroscopic characterization, X-ray molecular structures and cyclic voltammetry study of two (piperazine) cobalt(II) meso-arylporphyin complexes. Application as a catalyst for the degradation of 4-nitrophenol

International audienceTwo new cobaltous-porphyrin complexes, namely (mu-piperazine)-bis[(meso-tetra(para-methoxyphenyl)porphyrinato)]cobalt(II) and (piperazine)[meso-tetra(para-chlorophenyl)porphyrin]cobalt(II) dichloromethane disolvate, with the formulas [{CoII(TMPP)}2(mu 2-pipz)] (complex 1) and [CoII(TClPP)(pipz)].2CH2Cl2 (complex 2), were used efficiently as catalysts in the degradation of 4-nitrophenol (4-NP) in an aqueous hydrogen peroxide solution. These cobalt(II)-pipz porphyrin complexes were characterized by a variety of spectroscopic methods including infrared, UV-visible, fluorescence, proton nuclear magnetic resonance, electron paramagnetic resonance (EPR) as well as mass spectrometry. A cyclic voltammetry investigation was also carried out on these two Co(II) metalloporphyrins. The EPR results indicate that both complexes 1 and 2 are paramagnetic low-spin (S = 1/2) cobalt(II) porphyrin complexes. Furthermore, the X-ray diffraction crystal structures of 1 and 2 were determined, and the intermolecular interactions were investigated by Hirshfeld surface analysis

New DMAP meso-arylporphyrin Magnesium(II) complex. Spectroscopic, Cyclic voltammetry and X-ray molecular structure characterization. DFT, DOS and MEP calculations and Antioxidant and Antifungal activities

International audienceThis study aims at first at the synthesis and the UV-visible, the infrared and the 1H Nuclear Magnetic Resonance spectroscopic characterizations of the 4-(dimethylamino)pyridine)[meso-tetra(para-chlorophenyl)porphyrinato]magnesium(II) with the formula [Mg(TClPP)(DMAP)].1/2C6H14 (I). The fluorescence and cyclic voltammetry studies have also been performed. The molecular structure of (I) was determined and described by single crystal X-ray diffraction analysis and Hirshfeld surfaces computational method. Complex (I) has a distorted square pyramidal geometry with a Mg__N(DMAP) distance value of 2.130 (4) Å and the average equatorial distance between the magnesium(II) central ion and the nitrogen atoms is 2.082 (3) Å. The crystal packing of our synthetic Mg(II) porphyrinic species is made by layers perpendicular to the [010] direction and the cohesion of the crystal packing is stabilized by nonconventional C–H···Cl and by C–H···Cg intermolecular interactions involving the pyrrole and phenyl rings of the porphyrin macrocycle. DFT calculations on (I) indicated an agreement with both UV-visible and IR experimental data. To gain further insights into the reactivity of (I), a density of states (DOS) and a molecular electrostatic potential (MEP) theoretical calculation were carried out. Furthermore, the antifungal and the antioxidant activities of the free base H2TClPP porphyrin, the [Mg(TClPP)] starting material and [Mg(TClPP)(DMAP)] (I) were also tested