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Synthesis, Characterization and Biological Activity of Schiff Base Complexes of Sulfa Drug with Transition Metals
Corresponding Author(s) : V. Gomathi
Asian Journal of Chemistry,
Vol. 25 No. 4 (2013): Vol 25 Issue 4
Abstract
The Schiff base has been prepared by refluxing sulfa pyridine with 2-hydroxynaphthaldehyde in ethanolic media and then complexed with Co(II), Ni(II), Cu(II), Zn(II) and Mn(II) metal ions. The synthesized ligand and complexes were characterized by elemental analysis, molar conductances, magnetic moments, IR, 1H NMR and electronic spectral data. The spectral data of the complexes have revealed bidentate complexing nature of the Schiff base ligand through phenolic oxygen and azomethine nitrogen atoms. The antibacterial and antifungal activity of the Schiff base and its complexes have also been screened. All the metal complexes possess significant to moderate activity and the metal complexes exhibit more activity against various species compared to the Schiff base.
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- R.C. Maurya and P. Patel, Spectrosc. Lett., 32, 213 (1999).
- I. Sakiyan, E. Logoglu, S. Arsalan, N. Sari and N. Sakiyan, Biometals, 17, 115 (2004).
- K.Y. Lau, A. Mayr and K.K. Cheung, Inorg. Chim. Acta, 285, 233 (1999).
- P.P. Dholakiya and M.N. Patel, Synth. React. Inorg. Met. Org. Chem., 34, 553 (2004).
- R. Nirmal, C.R. Prakesh, K. Menakshi and P. Shanmugapandiyan, J. Young Pharm., 2, 162 (2010).
- P. Mondol, M. Banerjee, S. Jana and A. Bose, J. Young Pharmacists, 2, 169 (2010).
- E. Pontiki, D.H. Litina and A.T. Chaviara, J. Enzym. Med. Chem., 23, 1011 (2008).
- S. Kumar, D.P. Matharasi, S. Gopi, S. Sivakumar and S. Narasimhan, J. Asian Nat. Prod. Res., 12, 360 (2010).
- P.H. Wang, J.G. Keck, K.J. Lien and M.M.C. Lai, J. Med. Chem., 33, 608 (1990).
- S. Tushar, B. Baul, S. Basu, D.de Vos and A. Linden, Investig. New Drugs, 27, 419 (2008).
- W.S. Abdel-Aal, H.Y. Hassan, T. Aboul-Fadl and A.F. Youssef, Eur. J. Med. Chem., 45, 1098 (2010).
- F.M. Morad, M.M.EL, Ajaily and S. Ben Gweirif, J. Sci. Appl., 1, 72 (2007).
- A. Nishinaga, T. Yamada, H. Fujisawa and K. Ishizaki, J. Mol. Catal., 48, 249 (1988); Chem. Abstr., 111, 22902 (1989).
- H. Chakraborty, N. Paul and M.L. Rahman, Transition Met. Chem., 19, 524 (1994).
- Y.D. Zaho, D.W. Pang, Z. Zong, J.K. Cheng, Z.F. Luo, C.J. Fren, H.Y. Shen and X.C. Zhung, Huaxe Xuebao, 56, 178 (1988); Chem Abstr., 128, 252661 (1998).
- R. Sreekala, K.K. Yusuff and Mohammed, Chem. Abstr., 130, 115551 (1999).
- S. Agnihotri and K. Arora, Asian J. Chem., 22, 5125 (1999).
- S. Shrivastava, A. Kumar, Y. Pandey, S.N. Dikshit, M. Shrivastava and D.K. Agarwal, Asian J. Chem., 22, 5187 (2010).
- K.J. Boney Victory, K.U. Sherin and M.K. Muraleedharan Nair, Res. J. Pharm. Biol. Chem. Sci., 1, 324 (2010).
- H. Temel, T. Taskin and M. Sekerci, Russ. J. Inorg. Chem., 49, 347 (2004).
- D.X. West, S.B. Padhye, P.B. Sonawane and R.C. Chikte, Struct. Bonding, 76, 1 (1991).
- J.H. Chohan and M.M. Naseer, Appl. Organomet. Chem., 21, 728 (2007).
- R.C. Maurya, P. Patel and S. Rajput, Synth. React. Inorg. Met.-Org. Chem., 33, 801 (2003).
- J.H. Deshmukh and M.N. Deshpande, Asian J. Chem., 22, 5961 (2010).
- V.L. Chavan and B.H. Mehta, Asian J. Chem., 22, 5976 (2010)
References
R.C. Maurya and P. Patel, Spectrosc. Lett., 32, 213 (1999).
I. Sakiyan, E. Logoglu, S. Arsalan, N. Sari and N. Sakiyan, Biometals, 17, 115 (2004).
K.Y. Lau, A. Mayr and K.K. Cheung, Inorg. Chim. Acta, 285, 233 (1999).
P.P. Dholakiya and M.N. Patel, Synth. React. Inorg. Met. Org. Chem., 34, 553 (2004).
R. Nirmal, C.R. Prakesh, K. Menakshi and P. Shanmugapandiyan, J. Young Pharm., 2, 162 (2010).
P. Mondol, M. Banerjee, S. Jana and A. Bose, J. Young Pharmacists, 2, 169 (2010).
E. Pontiki, D.H. Litina and A.T. Chaviara, J. Enzym. Med. Chem., 23, 1011 (2008).
S. Kumar, D.P. Matharasi, S. Gopi, S. Sivakumar and S. Narasimhan, J. Asian Nat. Prod. Res., 12, 360 (2010).
P.H. Wang, J.G. Keck, K.J. Lien and M.M.C. Lai, J. Med. Chem., 33, 608 (1990).
S. Tushar, B. Baul, S. Basu, D.de Vos and A. Linden, Investig. New Drugs, 27, 419 (2008).
W.S. Abdel-Aal, H.Y. Hassan, T. Aboul-Fadl and A.F. Youssef, Eur. J. Med. Chem., 45, 1098 (2010).
F.M. Morad, M.M.EL, Ajaily and S. Ben Gweirif, J. Sci. Appl., 1, 72 (2007).
A. Nishinaga, T. Yamada, H. Fujisawa and K. Ishizaki, J. Mol. Catal., 48, 249 (1988); Chem. Abstr., 111, 22902 (1989).
H. Chakraborty, N. Paul and M.L. Rahman, Transition Met. Chem., 19, 524 (1994).
Y.D. Zaho, D.W. Pang, Z. Zong, J.K. Cheng, Z.F. Luo, C.J. Fren, H.Y. Shen and X.C. Zhung, Huaxe Xuebao, 56, 178 (1988); Chem Abstr., 128, 252661 (1998).
R. Sreekala, K.K. Yusuff and Mohammed, Chem. Abstr., 130, 115551 (1999).
S. Agnihotri and K. Arora, Asian J. Chem., 22, 5125 (1999).
S. Shrivastava, A. Kumar, Y. Pandey, S.N. Dikshit, M. Shrivastava and D.K. Agarwal, Asian J. Chem., 22, 5187 (2010).
K.J. Boney Victory, K.U. Sherin and M.K. Muraleedharan Nair, Res. J. Pharm. Biol. Chem. Sci., 1, 324 (2010).
H. Temel, T. Taskin and M. Sekerci, Russ. J. Inorg. Chem., 49, 347 (2004).
D.X. West, S.B. Padhye, P.B. Sonawane and R.C. Chikte, Struct. Bonding, 76, 1 (1991).
J.H. Chohan and M.M. Naseer, Appl. Organomet. Chem., 21, 728 (2007).
R.C. Maurya, P. Patel and S. Rajput, Synth. React. Inorg. Met.-Org. Chem., 33, 801 (2003).
J.H. Deshmukh and M.N. Deshpande, Asian J. Chem., 22, 5961 (2010).
V.L. Chavan and B.H. Mehta, Asian J. Chem., 22, 5976 (2010)