Structural and thermal studies of some aroylhydrazone Schiff’s bases-transition metal complexes

2005 ◽  
Vol 81 (2) ◽  
pp. 339-346 ◽  
Author(s):  
H. A. El-Boraey
Author(s):  
Paresh S. More ◽  
Bipin H. Mehta

Transition metal complexes of the type ML1 [Where M= Co(II),Ni(II),Cu(II) and Zn(II), L= Schiff base of 5 nitro-salicylaldehyde and p-anisidine were characterized by using 1H NMR, TGA, Diffused reflectance and ESR spectroscopy. On the basis of above studies Co(II), Ni(II) shows tetrahedral structure, Cu(II) and Zn(II) shows square planar structure.


2011 ◽  
Vol 8 (1) ◽  
pp. 443-448 ◽  
Author(s):  
R. H. Patel ◽  
B. L. Hiran

The ligand, 2-(2-furanylmethylaminocarbonyl)benzoic acid (FMBA) and it’s transition metal complexes have been synthesized and characterized by elemental analysis, spectral studies, magnetic moments and thermal studies. The antifungal activity of all the samples was monitored against common fungi.


2007 ◽  
Vol 72 (4) ◽  
pp. 357-366 ◽  
Author(s):  
Kalagouda Gudasi ◽  
Manjula Patil ◽  
Ramesh Vadavi ◽  
Rashmi Shenoy ◽  
Siddappa Patil

A new ligand 5-[6-(5-mercapto-1,3,4-oxadiazol-2-yl)pyridin-2-yl]-1,3,4-oxadiazole- 2-thiol (L) and its Mn(II), Co(II), Ni(II), Cu(II), and Zn(II) complexes were synthesized. The authenticity of the ligand and its transition metal complexes were established by elemental analyses, conductance and magnetic susceptibility measurements, as well as spectroscopic (IR, 1H- and 13C-NMR, electronic, mass, ESR) and thermal studies. The IR and 1H-NMR spectral studies revealed the existence of the ligand in the thiol form in the solid state, whereas in the thione form in the dissolved state. The magnetic and electronic spectral studies suggest an octahedral geometry for all the complexes. The ligand acts as a tridentate ligand coordinating through the pyridine nitrogen and the nitrogen atoms (N-3' and N-3'') of the two oxadiazole rings. Antimicrobial screening of the ligand and its metal complexes were determined against the bacteria Escherichia coli and Bacillus cirroflagellosus, as well as against the fungi, Aspergillus niger and Candida albicans. .


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