Complexation of cobalt (II) with new Schiff base and amide ligands

Main Article Content

Jihan Hameed Abdulameer
Lamyaa Salih Mahdi
Mosa Jaafar Mosa

Keywords

cobalt II complexes, amide ligands, Schiff base ligands, binuclear complexes

Abstract

Two complexes of cobalt (II) were prepared in this research with new Schiff base and amide ligand. by using a common condensation reaction between benzidine with 4- hydroxy-3-methox benzaldehyde to prepare a first ligand while the other ligand was prepared between 4-chlorobenzoicacid and 1,4-diamino benzene. Both ligands have been added to Cobalt II yielded two complexes of Co+2. FT-IR, UV-Vis and H1NMR techniques were used to identify all of these compounds in addition to measure the molar conductivity of complexes, at end all the evidences proved that formation of complexes with sp3d2 hybridization and octahedral geometry. After the incubation period at 37 °C for 24 h, the biological behavior of the binding produced with its antibacterial compounds against (Staphylococcus aureus and Escherichia coli) at different concentrations (10, 50 and 200) ppm was examined. The results showed that the performance of the prepared compounds was better in resisting and reducing the growth of bacteria tested at high concentrations.

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References

1. R. B. Hoffman and A. john, "Organic Chemistry", 2nd edition., Wiley & sons, 2004.
2. H.M. Hassan, P. Omid and J. Christoph, Z. Naturforsch. C Biosci., 62, 717 – 720, 2007.
3. M. A. Ashraf, K. Mahmood and Abdul Wajid. International Conference on Chemistry and Chemical Process. V10, 2011.
4. D.R. Williams, Chem. Rev., 72, 203, 1972.
5. Campos, J.R. Anacona and M.M. Campos-Vallette, Mian group Met. chem., 22, 283, 1999.
6. N. Sari, S. Arslan, E. Logoglu and I. Sakiyan, G.U.J. Sci, 16, 283, 2003.
7. M. Verma, S.N. Pandeya, K N. Singh, J P. Stabler and Acta Pharm., 54, 49, 2004.
8. R. M. Laniganan and T. D. Sheppard, Eur. J. Org. Chem., 7453–7465, 2013.
9. P .Rajput, A. Sharma, J. Pharmacol. Med. Chem., 2, 2, 2018.
10. D. J. Constable, P. J. Dunn and J. D. Hayler, Green Chem., 9, 5, 411-20, 2007.
11. J.S . Carey, D. Laffan and C. Thomson, Org. Biomol. Chem.;4,12, 337-47., 2006.
12. S. Roy and G.W. Gribble, Tetrahedron, 68, 9867-9923, 2012.
13. M. Opanasenko , M. Shamzhy and M. Lamač , , Čejka J.Catal. Today, 204, 94-100, 2013.
14. M. J. Mosa, J. H. Abdulameer and L.S. Mahdi. Journal of Global Pharma Technology, 10,9, 403-411, 2017.
15. M.P.Sathisha, U.N.Shetti and V.K.Revakar, Euro. J. of Medi. Chem., 43,11, 2338-2346, 2008.
16. J. H. Abdulameer. , S. Kudair and M. J. Mosa, IOP Conf. Series: Materials Science and Engineering, 571, 2019.
17. K.M. Hayder , Journal of the Taiwan Institute of Chemical Engineers, 46, 74–81, 2015.
18. A.R. Kennedy, M.O. Okoth and D. Walsh, Metal –organic comp. , 67, 8 , 1138, 2011.
19. K.M. Hayder, H.H. M., M. J. Mosa , Iranian Journal of Catalysis 4 (3), 195-203, 2014.