Synthesis, spectral, thermal and biological properties of some novel coordination compounds of VO(IV) and biological 4[N-(4′-ethylbenzalidene) amino] antipyrine thiosemicarbazone and 4[N-(2′, 4′-dimethyl benzalidene amino] antipyrine thiosemicarbazone

Subject Areas : Journal of the Iranian Chemical Research

Surendra Prasad ¹ , Ram Kumar Agarwal ² , Hans Raj Modi ³

1 - Division of Chemical Sciences, University of South Pacific, Laucala Bay Campus, Suva, Fiji
2 - Department of Chemistry, Lajpat Rai Postgraduate College, Sahibabad-201 005 (Ghaziabad), India
3 - Department of Chemistry, Lajpat Rai Postgraduate College, Sahibabad-201 005 (Ghaziabad), India

Received: 2009-12-25 Accepted : 2009-12-24 Published : 2009-10-21

Keywords:

References:

[1] R.K. Agarwal, I. Chakraborti, Polish J. Chem. 68 (1994) 1491-1501.
[2] R.K. Agarwal, I. Chakraborti, S.K. Sharma, Polish J. Chem. 62 (1995)1085-1096.
[3] R.K. Agarwal, H. Agarwal, I. Chakraborti, Synth. React. Inorg. Met-Org. Chem. 25 (1995) 383-396.
[4] L. Singh, I. Chakraborti, N.P. Dhaka, R.K. Agarwal, Revue. Roum. Chim. 44 (1999) 119-124.
[5] L. Singh, A.K. Manglik, N.P. Dhaka, Asian J. Chem. 9 (1997) 213-217.
[6] R.K. Agarwal, S. Prasad, N. Gahlot, Turk. J. Chem. 28 (2004) 691-701.
[7] R.K. Agarwal, L. Singh, D.K. Sharma, Chim. Acta Turcica 33 (2005) 1-7.
R.K. Agarwal et al. / J. Iran. Chem. Res. 2 (2009) 173-182
182
[8] R.K. Agarwal, S. Prasad, Rev. Inorg. Chem, 26 (2006) 471-491.
[9] S. Padhye, G.B. Kauffmann, Coord. Cham. Rev. 24 (1985) 127-145.
[10] D.X. West, S.B. Padhye, P.B. Sonawane, R.C. Chikate, Asian J. Chem. Revs, 1 (1990) 125-143.
[11] M. Akbar Ali, S.E. Livingstone, Coord. Chem. Revs. 13 (1974) 101-126.
[12] M.J.M. Cam[bell, Coord. Chem. Rev. 15 (1975) 279-299.
[13] R.K. Agarwal, G.B. Singh, B. Bhushan, J. Inst. Chem. 65 (1993) 131-134.
[14] G. Durgaprasad, C.C. Patel, Indian J. Chem. 11A (1973) 1300-1305.
[15] D.N. Sathyanarayana, C.C. Patel, Indian J. Chem. 3 (1965) 486-490.
[16] A.I. Vogel, A Text Book of Quantitative analysis, Longmans Green, London, 1961.
[17] E. Kurz, G. Kober, M. Berl, Anal. Chem. 30 (1958) 1983-1986.
[18] S. Prasad, R.K. Aganwal, Trans. Metal Chem. 30 (2007) 143-149.
[19] R.K. Agarwal, G. Singh, Croat. Chem. Acta 60 (1987) 741-748.
[20] R.K. Agarwal, G. Singh, Rev. Roum. Chim. 33 (1988) 537-543.
[21] G. Shankar, R.R.P. Kumar, S.K. Ramalingam, Polyhedron 5 (1986) 991-998.
[22] R.K. Agarwal, R.K. Garg, S.K. Sindhu, J. Iran. Chem. Soc. 2 (2005) 203-211.
[23] T,S. Lane, A.Yamaguchi, A.R. James, J. Am. Chem. Soc. 80 (1958) 527-530.
[24] K. Swminathan, H.M.N.H. Irving, J. Inorg. Nucl. Chem. 26 (1964) 1291-1297.
[25] V.B. Rana, J. Inorg. Nucl. Chem. 37 (1975) 1827-1834.
[26] P.W. Sadler, J. Chem. Soc. (1961) 957-964.
[27] B. Singh, H. Mishra, J. Indian Chem. Soc. 63 (1986) 692-694.
[28] K.K. Aravindakshan, Indian J. Chem. 26A (1987) 241-246.
[29] J. Selbin, Chem. Rev. 65 (1965) 153-176.
[30] J. Selbin, Coord. Chem. Rev. 1 (1966) 293-310.
[31] B.J. Hathaway, A.E. Underhill, J. Chem. Soc. (1958) 537-544.
[32] S.K. Krishnamurthy, S. Soundararajan, Canad. J. Chem. 47 (1969) 995-1003.
[33] J.L. Burmaster, Coord. Chem. Rev. 1 (1966) 205-225.
[34] L. Sacconi, V. Campigili, Inorg. Chem. 5 (1966) 606-612.
[35] C.J. Ballhausen, H.B. Gray, Inorg. Chem. 1 (1962) 360-376.
[36] L.G. Von-Quickenborne, S.P. McGlyn, Theor. Chim. Acta 9 (1968) 390-402.
[37] D.N. Sathyanaryana, C.C. Patel, Indian J. Chem. 5 (1967) 360-368.
[38] R.K. Agarwal, G. Singh, Synth. React. Inorg. Met-Org. Chem. 16 (1986) 1183-1190.
[39] R.M. Golding, Mol. Phys. 5 (1962) 369-380.
[40] R.P. Dodge, D.H. Templeton, A. Zalkin, J. Chem. Phys. 35 (1961) 55-62.
[41] D.N. Satyanarayana, C.C. Patel, J. Inorg. Nucl. Chem. 27 (1965) 297-306.
[42] D.N. Sathyararayana, C.C. Patel, J. Inorg. Nucl. Chem. 28 (1966) 2277-2286.