Abstract
The Co(II), Ni(II) and Cu(II) complexes of the Schiff base derived from imidazole-2-carboxaldehyde and glycylglycine were synthesized and characterized by elemental analysis, PMR, molar conductance, IR, electronic, magnetic measurements, ESR, redox properties, thermal studies, XRD and SEM. Conductance measurements indicate that the complexes are 1 : 1 electrolytes. IR data show that the ligand is tetradentate with imidazole nitrogen, azomethine nitrogen, amide nitrogen and carboxylato oxygen donor groups. Electronic spectral measurements indicate tetrahedral geometry for Co(II) and Ni(II) complexes and square-planar geometry for Cu(II). Magnetic measurements show weak ferromagnetic behavior for Co(II) and Ni(II) complexes, and paramagnetic for Cu(II) complex. The X-band ESR spectral data indicate a covalent link between metal and ligand. The complexes were found to be stabilized in unusual oxidation states of metal during electrolysis. Thermal analysis of the complexes indicate that decomposition takes place in three steps. XRD shows that Ni(II) and Cu(II) complexes have the respective crystallite size of 42 and 34 nm, while the Co(II) complex is amorphous. The surface morphology of the complexes was studied by SEM. The antimicrobial activities of the ligand and its complexes indicate that the metal complexes possess high antibacterial and antifungal activities towards the bacterial species S. aureus, E. coli, K. pneumaniae, P. vulgaris and P. aeruginosa and the fungal species A. niger, R. stolonifer, A. flavus, R. bataicola and C. albicans.
Published Version
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.