Characterization and antifungal study of genuine oxovanadium(IV) mixed-ligand complexes with schiff bases

Polish Journal of Chemistry

Volumn 79, Issue 12, 2005, Pages 1843-1851

  Parekh, H M ^a   Pansuriya, P B ^a   Patel, M N ^a  

^a SARDAR PATEL UNIVERSITY   (India)

Author keywords

Antifungal activity; Fungicides; Octahedral geometry; Oxovanadium(IV) complexes; Schiff bases

Indexed keywords

EID: 31544436345     PISSN: 01375083     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (32)

1. Jones R.D., Summerville D.A. and Basolo F., Chem. Rev., 79, 139 (1979).
2. Henrici-Olive G. and Olive S., The Chemistry of the Catalysed Hydrogenation of Carbon Monoxide, Springer, Berlin, 1984, p. 152.
3. Dugas H. and Penney C., Bioorganic Chemistry, Springer, NY, 1981, p. 435.
4. Margerum J.D. and Miller L.J., Photochromism, Interscience, Wiley, 1971, p. 569.
5. Sakurai H., Fujisawa Y., Fujimoto S., Yasui H. and Takuno T., J. Trace Elem. Exp. Med., 12, 393 (1999).
6. Sharif E., Spielman S., Nachliel L., Khamaisi M., Bar-On H. and Ziv E., Diabetes/Metabolism Res. Rev., 17, 55 (2001).
7. Allegretti Y., Ferrer E.G., Gonzalez Baro A.C. and Williams P.A.M., Polyhedron, 20, 387 (2000).
8. Thompson K.H., McNeill J.H. and Orvig C., Chem. Rev., 99, 2561 (1999).
9. Patel N.H., Parekh H.M. and Patel M.N., Trans. Met. Chem., 30, 13 (2005).
10. th Ed., Longman, London, 1989.
11. Dholakiya P.P. and Patel M.N., Synth. React. Inorg. Met.-Org. Chem., 32, 819 (2002).
12. Panchal P.K., Patel D.H. and Patel M.N., Synth. React. Inorg. Met.-Org. Chem., 34, 1223 (2004).
13. th Ed., D. Van Nostrand Company, Inc., New Jersey, Vol. I, 1211, 1962.
14. Freedman H.H., J. Am. Chem. Soc., 83, 2900 (1961).
15. Madhu N.T. and Radhakrishnan P.K., Trans. Met. Chem., 25, 287 (2000).
16. Singh N.K., Kushawaha S.K., Srivastava A. and Sodhi A., Synth. React. Inorg. Met.-Org. Chem., 32, 1758 (2002).
17. Tarafder M.T.H., Miah M.A.J., Bose R.N. and Ali A.M., J. Inorg. Nucl. Chem., 43, 1351 (1981).
18. Li Y.T., Yan C.W., Xu C.S. and Liao D.Z., Synth. React. Inorg. Met.-Org. Chem., 30, 1069 (2000).
19. Singh R.V. and Tandon J.P., Synth. React. Inorg. Met.-Org. Chem., 9, 137 (1979).
20. El-Saied F.A., Ayad M.I. and Aly S.A., Trans. Met. Chem., 18, 279 (1993).
21. Pandya B.R., Menon S.K. and Agrawal Y.K., Synth. React. Inorg. Met.-Org. Chem., 34, 1291 (2004).
22. rd Ed., Wiley Interscience, NY, 1977, p. 292.
23. Köksal H., Tümer M. and Serin S., Synth. React. Inorg. Met.-Org. Chem., 26, 1577 (1996).
24. Zamian J.R., Dockal E.R., Castellano G. and Oliva G., Polyhedron, 14, 1283 (1995).
25. Dutta S.K., Edward, Tiekink A.T. and Chaudhury M., Polyhedron, 16, 1863 (1997).
26. Ballhausen C.J. and Gray H.B., Inorg. Chem., 1, 111 (1962).
27. Kuska H.A. and Yang P., Inorg. Chem., 13, 1090 (1974).
28. Atlas R.M., Manual of Industrial Microbiology and Biotechnology., 2nd Ed., ASM Press, Washington DC, 1999, p. 1.
29. Chauhan J.B., Subramanian R.B. and Sanyal P.K., Indian J. Environ. Toxicol., 12, 22 (2002).
30. Anjaneyula Y. and Rao R.P., Synth. React. Inorg. Met.-Org. Chem., 16, 257 (1986).
31. Tweedy B.G., Phytopathology, 55, 910 (1964).
32. Dharmaraj N., Viswanathamurthi P. and Natarajan K., Trans. Met. Chem., 26, 105 (2001).