264
Views
0
CrossRef citations to date
0
Altmetric
Research Articles

Synthesis, Magnetic Susceptibility, Thermodynamic Study and Bio-Evaluation of Transition Metal Complexes of New Schiff Base Incorporating INH Pharmacophore

, , , &
Pages 523-537 | Received 29 Jun 2021, Accepted 01 Dec 2021, Published online: 13 Dec 2021
 

Abstract

Transition metal complexes of synthesized organic ligands incorporating INH were successfully investigated by potentiometrically. The stability constants of these binary complexes were evaluated and order of stability constant found as above Zn(II) > Co(II) > Ni(II) > Mn(II) > Cu(II). Magnetic moment value clearly indicates that newly prepared transition metal complexes of N-[(E)-(2-Hydroxyphenyl)methylen]isonicotinohydrazid are paramagnetic in nature. The stability constants for complexes decrease with an increasing temperature, indicating that the composition equilibrium is exothermic in nature. Also 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 favourable. Metal complexes of organic ligand shows moderate antibacterial activity against gram positive and gram negative bacteria. It also possesses prominent antifungal activity for Nickel (II) complex. Biological evaluation results of transition metal complexes show superior pharmacological applications as compared to organic ligand.

Graphical Abstract

Acknowledgement

Authors are grateful to Dr. Maqdoom Farooqui, Principal, Dr. Rafiq Zakaria College for Women, Aurangabad, MS, India for providing necessary research facilities.

Disclosure statement

Authors state no conflict of interest.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.