5-Chloromethyl-8-quinolinol was condensed stoichiometrically with benzotriazole in presence of potassium carbonate. The resulting 5-[1(H)-benzo triazole methylene]-8-quinolinol (BTMQ) was characterized by elemental analysis and spectral studies. The transition metal chelatesviz. Cu2+, Ni2+, Co3+, Mn2+and Zn2+of BTMQ were prepared and characterized by metal-ligand (M:L) ratio, IR and reflectance spectral studies and magnetic properties. The antifungal activity of BTMQ and its metal chelates was screened against various fungi. The results show that all these samples are good antifungal agents.
1 H NMR, 13 C NMR and IR spectroscopic techniques and reacted with transition metal salts to afford metalcontaining heterochelates. The structures of the synthesized heterochelates were characterized using elemental analyses, infrared spectra, electronic spectra, magnetic measurements, FAB mass spectrum and thermogravimetric analyses. The kinetic parameters such as order of reaction (n) and the energy of activation (E a ) are reported using the Freeman-Carroll method. The pre-exponential factor (A), the activation entropy ( S # ), the activation enthalpy ( H # ) and the free energy of activation ( G # ) were calculated. Heterochelates were also screened for their in vitro antibacterial activity against a range of Gram-positive (Bacillus substilis, Staphylococcus aureus) and Gram-negative (Escherichia coli, Serratiamarcescens) organisms.
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