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    Synthesis, spectroscopic, and thermal properties of some azomethine complexes of Cu(II), Ni(II), and Pt(II)
    (Springer, 2012) Turkyilmaz, Murat; Onder, Alper; Baran, Yakup
    Four polydentate azomehines and their mono- and binuclear Pt(II), Cu(II), and Ni(II) complexes were synthesized and characterized. The resulting complexes were characterized by FTIR, magnetic measurements, elemental analysis, conductivity measurements, and thermal analysis. Electronic spectra and magnetic susceptibility measurements sustain the proposed distorted square-planar structures for the copper complexes. The electronic spectra display the characteristic pattern of square-planar stereochemistry for the other complexes. The thermal analyses have evidenced the thermal intervals of stability and also the thermodynamic effects that accompany them. Azomethine complexes have a similar thermal behavior for the selected metal ions. The decomposition processes as water elimination, chloride anion removal as well as degradation of the organic ligands were observed.
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    Synthesis, spectroscopic, magnetic and thermal properties of copper(II), nickel(II) and iron(II) complexes with some tetradentate ligands: Solvatochromism of iron(II)-L2
    (Elsevier Science Sa, 2012) Onder, Alper; Turkyilmaz, Murat; Baran, Yakup
    The tetradentate azomethines were prepared by condensation of 2-piperazin-1-ylethanamine, (3-morpholin-4-ylpropyl)amine with 3-methylthophene-2-carbaldehyde, salicylaldehyde and 1H-imidazole-5-carbaldehyde. The ligands were characterized based on mass, H-1 and C-13 NMR, FTIR, and elemental analyses. New complexes of ligands with copper(II), iron(II) and nickel(II) were synthesized. Metal complexes are reported and characterized by magnetic, conductivity measurements, FTIR, elemental and thermal analyses (TG-DTA). Spectral analyses show that all the ligands behave as neutral tetradentate ligands and bind to the metal via azomethine N, piperazine N, salicylaldehyde O, morpholine O, imidazole N and thiophene S. Results of magnetic measurements and thermal studies show that the geometrical structures of the nickel(II) complexes are square planar while copper(II) and iron(II) are octahedral. The thermal behaviors of these complexes show that the hydrated complexes lose the hydration water molecule in the first step, followed immediately by decomposition of the anion and ligand molecules in subsequent steps. The solvatochromic behavior of the iron(II)-(L)2 complex was investigated using the electronic spectra of 1 x 10 (3) M in four different solvents. The solvatochromism was explained in terms of MLCT transition and solvent characteristics such as polarity, nature and acceptor-donor properties. (C) 2012 Elsevier B.V. All rights reserved.