Sn(II) oxadiazole Schiff bases
1359
References
[1] D.N. Dhar, C.L. Taploo. J. Sci. Ind. Res., 41, 501 (1982).
[2] N. Hou, L.J. Xu, Y.H. Pao. Medline, 27, 732 (1992).
[3] S.N. Pandeya, D.S. Ram, G. Nath, E.D. Cleri. Arzneimittel Forschung, 50, 55 (2000).
[4] H. Pavlov, D.J. Litina, A.A. Geronikaki. Drug Des. Discov., 15, 199 (1997).
[5] S.K. Sridhar, A. Ramesh. Biol. Pharm. Bull., 24, 1149 (2001).
[6] C. Deliwala. J. Med. Chem., 49, 450 (1971).
[7] B. Dash, M. Patra, S. Paraharaj. Indian J. Med. Chem., 19, 894 (1980).
[8] B.S. Holla, B. Veerendra, M.K. Shivananda, B. Poojary. Eur. J. Med. Chem., 38, 759 (2003).
[9] A.D. Garnovskii, A.L. Nivorozhkin, V.L. Minkin. Coord. Chem. Rev., 126, 1 (1993).
[10] A.M. Khedr, N.A. El-Wakiel, S. Jadon, V. Kumar. J. Coord. Chem., 64, 851 (2011).
[11] P.A. Vigato, S. Tamburini. Coord. Chem. Rev., 248, 1717 (2004).
[12] E.S. Claudio, H.A. Godwin, J.S. Magyar. Progr. Inorg. Chem., 51, 1 (2003).
[13] N. Nimitsiriwat, V.C. Gibson, E.L. Marshall, M.R. Elsegood. Dalton Trans., 3710 (2009).
[14] C.-Y. Qi, Z.-X. Wang. J. Polym. Sci. A: Polym. Chem., 44, 4621 (2006).
[15] A.I. Vogel. A Text Book of Quantitative Inorganic Analysis, Longmans, London (1969).
[16] CS Chem 3D Ultra Molecular Modeling and Analysis, Cambridge. Available online at:
[17] R.C. Maurya, S. Rajput. J. Mol. Struct., 794, 24 (2006).
[18] B.K. Singha, H.K. Rajourb, A. Prakasha, N. Bhojakc. Global J. Inorg. Chem., 1, 65 (2010).
[19] A.W. Bauer, W.M. Kirby, C. Sherris, M. Turck. Am. J. Clin. Path., 45, 493 (1966).
[20] M.A. Pfaller, L. Burmeister, M.A. Bartlett, M.G. Rinaldi. J. Clin. Microbiol., 26, 1437 (1988).
[21] National Committee for Clinical Laboratory Standards. Performance Antimicrobial Susceptibility of
Flavobacteria, Vol. 41 (1997).
[22] National Committee for Clinical Laboratory Standards. Reference Method for Broth Dilution Antifungal
Susceptibility Testing of Conidium-forming Filamentous Fungi: Proposed Standard M38-A, NCCLS,
Wayne, PA, USA (2002).
[23] National Committee for Clinical Laboratory Standards. Method for Antifungal Disk Diffusion
Susceptibility Testing of Yeast: Proposed Guideline M44-P, NCCLS, Wayne, PA, USA (2003).
[24] National Committee for Clinical Laboratory Standards. Methods for Dilution Antimicrobial
Susceptibility Tests for Bacteria that Grow Aerobically. Approved standard M7-A3, NCCLS, Villanova,
PA (1993).
[25] L.D. Liebowitz, H.R. Ashbee, E.G.V. Evans, Y. Chong, N. Mallatova, M. Zaidi, D. Gibbs. Diagn.
Microbiol. Infect. Dis., 4, 27 (2001).
[26] M.J. Matar, L. Ostrosky-Zeichner, V.L. Paetznick, J.R. Rodriguez, E. Chen, J.H. Rex. Antimicrob.
Agents Chemother., 47, 1647 (2003).
[27] R.L. Vale, M.M. Borges, L.E.S. DeSandro, G.E. Gilmarra. Inverse Probl. Sci. Eng., 14, 511 (2006).
[28] B.K. Singh, P. Mishra, B.S. Garg. Transition Met. Chem., 32, 603 (2007).
[29] A.M. Khedr, D.F. Draz. J. Coord. Chem., 63, 1418 (2010).
[30] K. Nakamoto. Infrared Spectra of Inorganic and Coordination Compounds, Wiley-Interscience,
New York (1970).
[31] B. Murukan, S.K. Bhageerethi, M. Kochukittan. J. Coord. Chem., 60, 1607 (2007).
[32] A. Hatzidumitrious, C.A. Bolos. Polyhedron, 17, 1779 (1998).
[33] M.J. Kharodawala, A.K. Rana. Synth. React. Inorg. Met.-Org. Nano-Met. Chem., 33, 1483 (2003).
[34] A. Varshney, J.P. Tandon, A.J. Crowe. Polyhedron, 5, 739 (1986).
[35] B. Wang, H. Ma. Synth. React. Inorg. Met. Org. Chem., 34, 1009 (2004).
[36] R.M. Issa, A.M. Khedr, H. Rizk. J. Chin. Chem. Soc., 55, 875 (2008).
[37] M.E. Moustafa, E.H. El-Mossalamy, A.S. Amin. Monatsh. Chem., 126, 901 (1995).
[38] D.N. Kumar, B.S. Garg. Spectrochim. Acta A, 64, 141 (2006).
[39] A.P. Mishra, M. Khare, S.K. Gautam. Synth. React. Inorg. Met-Org. Chem., 32, 1485 (2002).
[40] A.P. Mishra, R.K. Mishra, S.P. Shrivastava. J. Serb. Chem. Soc., 74, 523 (2009).
[41] B.K. Singh, P. Mishra, B.S. Garg. Main Group Chem., 5, 163 (2006).
[42] M.A. Phaniband, S.D. Dhumwad. Transition Met. Chem., 32, 1117 (2007).