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This work is licensed under a Creative Commons Attribution 4.0 International License.
Synthesis, Characterization and Biological Evaluation of Schiff Base Transition Metal Complexes Derived from 4-Nitrobenzene-1,2-diamine and 5-Chloroisatin
Corresponding Author(s) : Netra Pal Singh
Asian Journal of Chemistry,
Vol. 32 No. 9 (2020): Vol 32 Issue 9, 2020
Abstract
A series of transition metal complexes of the type [MLX2], where M = Mn(II), Fe(II), Co(II), Ni(II), X = Cl–/CH3COO– and L = Schiff base derived from 4-nitrobenzene-1,2-diamine and 5-chloroisatin have been synthesized and characterized by elemental analysis, molar conductance, IR, UV-visible, magnetic moments measurement, 1H & 13C NMR and mass spectral studies. On the basis of physico-chemical studies and spectral evaluation, an octahedral geometry have been proposed for all metal(II) complexes. The antimicrobial activity of ligand and its metal complexes have been additionally screened against bacteria and fungi. Metal(II) complexes show good activity as compared to ligand towards studied microorganisms and also metal complexes checked for their catalytic properties for benzoylation of phenol.
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D. Chatterjee, S. Mukherjee and A. Mitra, J. Mol. Catal., 15, 5 (2000); https://doi.org/10.1016/S1381-1169(99)00293-9
C.M. Che and J.S. Huang, Coord. Chem. Rev., 242, 97 (2003); https://doi.org/10.1016/S0010-8545(03)00065-1
A. Rahman, M.I. Choudhary and W.J. Thomsen, Bioassay Techniques for Drug Development, Harwood Academic Publishers: The Netherlands, pp. 16-20 (2001).
G. Kumar, D. Kumar, S. Devi, R. Johari and C.P. Singh, Eur. J. Med. Chem., 45, 3056 (2010); https://doi.org/10.1016/j.ejmech.2010.03.036
B.G. Tweedy, Phytopathology, 55, 910 (1964).
X. Lin, H. Hefesha, H. Tanaka, G. Scriba and A. Fahr, Chem. Pharm. Bull. (Tokyo), 56, 1417 (2008); https://doi.org/10.1248/cpb.56.1417
L.N. Sharda and M.C. Ganorkar, Indian J. Chem., 27A, 617 (1988).
D.V. Warad, C.D. Satish, V.H. Kulkarni, C.S. Bajgur, Indian J. Chem., 39A, 415 (2000).
R. Nagar, J. Inorg. Biochem., 40, 349 (1990); https://doi.org/10.1016/0162-0134(90)80069-A
Z.H. Chohan, A. Scozzafava and C.T. Supuran, J. Enzyme Inhib. Med. Chem., 18, 259 (2003); https://doi.org/10.1080/1475636031000071817
S.K. Sengupta, O.P. Pandey, B.K. Srivastava and V.K. Sharma, Transition Met. Chem., 23, 349 (1998); https://doi.org/10.1023/A:1006986131435
G. Kumar, D. Kumar, C.P. Singh, A. Kumar and V.B. Rana, J. Serb. Chem. Soc., 75, 629 (2010); https://doi.org/10.2298/JSC090704037K