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Synthesis, spectroscopic characterization and biological activities of N4O2 Schiff base ligand and its metal complexes of Co(II), Ni(II), Cu(II) and Zn(II)

[Display omitted] ► The Schiff base ligand, L is synthesized by condensation of isatin and triethylenetetramine. ► Mononuclear complexes of L have been synthesized. ► Octahedral geometry has been proposed for the complexes of L. ► L and its Cu(II) and Zn(II) complexes have been screened for antibact...

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Published in:Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy Molecular and biomolecular spectroscopy, 2012-07, Vol.93, p.86-94
Main Authors: Al-Resayes, Saud I., Shakir, Mohammad, Abbasi, Ambreen, Amin, Kr. Mohammad Yusuf, Lateef, Abdul
Format: Article
Language:English
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Summary:[Display omitted] ► The Schiff base ligand, L is synthesized by condensation of isatin and triethylenetetramine. ► Mononuclear complexes of L have been synthesized. ► Octahedral geometry has been proposed for the complexes of L. ► L and its Cu(II) and Zn(II) complexes have been screened for antibacterial activity. ► Cu(II) and Zn(II) complexes of L have been studied for in vivo analgesic activity. The Schiff base ligand, bis(indoline-2-one)triethylenetetramine (L) obtained from condensation of triethylenetetramine and isatin was used to synthesize the complexes of type, [ML]Cl2 [M=Co(II), Ni(II), Cu(II) and Zn(II)]. L was characterized on the basis of the results of elemental analysis, FT-IR, 1H and 13C NMR, mass spectroscopic studies. The stoichiometry, bonding and stereochemistries of complexes were ascertained on the basis of results of elemental analysis, magnetic susceptibility values, molar conductance and various spectroscopic studies. EPR, UV–vis and magnetic moments revealed an octahedral geometry for complexes. L and its Cu(II) and Zn(II) complexes were screened for their antibacterial activity. Analgesic activity of Cu(II) and Zn(II) complexes was also tested in rats by tail flick method. Both complexes were found to possess good antibacterial and moderate analgesic activity.
ISSN:1386-1425
DOI:10.1016/j.saa.2012.02.099