Potentiometric and Thermodynamic Studies of (N-[-(4-Chlorophenyl) Methylene]Nicotinohydrazide) and Its Transition Metal Complexes

Abstract

Pharmacologically active organic ligands (N-[-(4-chlorophenyl) methylene] nicotinohydrazide) synthesized through the condensation of equimolar mixture of anti-mycobacterial agent (nicotinohydrazide) with aromatic aldehyde. The reaction progress and purity of organic ligands were verified by thin layer chromatography. Formation of organic ligands was confirmed with the help of MP, IR, 1H NMR, 13C NMR and elemental analysis. Further formation of complexes of transition elements such as Mn(II), CO(II), Ni(II), Cu(II) and Zn(II) with organic ligand (Schiff base) N-[-(4-chlorophenyl)methylene] nicotinohydrazide were studied by the pH-metric technique at 25 °C, 35 °C and 45 °C in 70% (v/v)ethanol – water medium at 1 M (NaClO4) ionic strength. The stability constants of these binary complexes were evaluated and order of stability constant found as Co (II) < Mn (II) < Ni (II) < Cu (II) < Zn (II). The thermodynamic parameters associated with the complexation reactions also were calculated. It is found that the change in enthalpy (ΔH) and change in Gibb’s free energy (ΔG) were negative for all of the systems which suggested that all of the reactions were exothermic. The change in entropy (ΔS) found positive for most of the complexes which indicate in metal-ligand binding process is entropy favorable.