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Studies on Synthesis and Spectral Characterization of Some Transition Metal Complexes of Azo-Azomethine Derivative of Diaminomaleonitrile
Author(s) -
C. Anitha,
C.D. Sheela,
P. Tharmaraj,
R. Shanmugakala
Publication year - 2013
Publication title -
international journal of inorganic chemistry
Language(s) - English
Resource type - Journals
eISSN - 2090-2026
pISSN - 2090-2034
DOI - 10.1155/2013/436275
Subject(s) - electron paramagnetic resonance , solvatochromism , schiff base , chemistry , molar conductivity , magnetic susceptibility , crystallography , metal , octahedral molecular geometry , scanning electron microscope , transition metal , fluorescence , ligand (biochemistry) , materials science , molecule , nuclear magnetic resonance , crystal structure , organic chemistry , biochemistry , physics , receptor , quantum mechanics , composite material , catalysis
New complexes of 2,3-bis(5-(4-chlorophenyl)diazenyl)-2-hydroxybenzylideneamino)maleonitrile (CDHBDMN) with VO(II), Mn(II), Co(II), Ni(II), Cu(II), and Zn(II) were synthesized and characterized by analytical and physicochemical techniques, that is, elemental analyses, molar conductivity, UV, IR, EPR, 1H-NMR spectra, magnetic susceptibility and also by aid of scanning electron microscopy (SEM), nonlinear optical study (NLO), fluorescence spectral studies, and solvatochromic behaviors. Electronic and magnetic susceptibility measurements of the complexes indicate square pyramidal geometry for VO(II), octahedral for Ni(II), and square planar geometry for all the other complexes. The EPR spectral data provide information about their structures on the basis of Hamiltonian parameters and the degree of covalency. These metal complexes were also tested for their antibacterial and antifungal activities to assess their inhibiting potential. Metal-mediated fluorescence enhancement is observed on complexation of the azo Schiff base ligand. The synthesized compounds were investigated for nonlinear optical properties, and the surface morphology of the Cu(II) complex was studied by scanning electron microscopy

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