Synthesis, characterization, biological activity, molecular modeling and docking studies of complexes 4-(4-hydroxy)-3-(2-pyrazine-2-carbonyl)hydrazonomethylphenyl-diazen-yl-benzenesulfonamide with manganese(II), cobalt(II), nickel(II), zinc(II) and cadmium(II)

被引:26
|
作者
Alaghaz, Abdel-Nasser M. A. [1 ]
Zayed, Mohamed E. [2 ]
Alharbi, Suliman A. [2 ]
Ammar, Reda A. A. [3 ]
Elhenawy, Ahmed [1 ,3 ]
机构
[1] Al Azhar Univ, Fac Sci, Dept Chem, Cairo 11884, Egypt
[2] King Saud Univ, Fac Sci, Dept Bot & Microbiol, Riyadh 11541, Saudi Arabia
[3] Princess Nora Bint Abdul Rahman Univ, Fac Sci, Dept Chem, Riyadh, Saudi Arabia
关键词
Azo-dye Schiffs base complexes; Electronic; IR; Molecular modeling; Biological activity; TRANSITION-METAL-COMPLEXES; SPECTROSCOPIC CHARACTERIZATION; SCHIFF; BINDING;
D O I
10.1016/j.molstruc.2014.12.041
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A new series of complexes of 4-(4-hydroxy)-3-(2-pyrazine-2-carbonyl)hydrazonomethylphenyl-diazenyl-benzenesulfonamide (HL) with Mn(II), Co(II), Ni(II), Zn(II) and Cd(II) have been prepared and characterized by different physical techniques. The IR spectra of the prepared complexes were suggested that the ligand behaves as a tri-dentate ligand through the carbonyl oxygen, azomethine nitrogen and phenolic oxygen atoms (ONO). Electronic spectra and magnetic susceptibility measurements reveal octahedral geometry for all complexes. The elemental analyses and mass spectral data have justified the ML2 composition of complexes. The EPR spectra of Mn(II), Co(II) and Ni(II) complexes support the mononuclear structure. The crystal field splitting, Racah repulsion and nephelauxetic parameters and determined from the electronic spectra of the complexes. Thermal properties and decomposition kinetics of all complexes are investigated. The geometry of the metal complexes has been optimized with the help of molecular modeling. The biological activity of these compounds against various fungi has been investigated. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:352 / 367
页数:16
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