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Synthesis, Characterization and Spectrophotometric Determination of Vanadium(V) with Unsubstituted Cinnamoyl Hydroxamic Acid
Corresponding Author(s) : Surendra K. Rajput
Asian Journal of Chemistry,
Vol. 29 No. 2 (2017): Vol 29 Issue 2
Abstract
A series of hydroxamic acid and their derivatives play a key role in chemistry and metallochemistry in the subject of study of many synthetic experimental investigations. In this paper the synthesized compound were characterized and their structure was confirmed by standard spectroscopic method 1H NMR and IR spectrum. The determination of vanadium(V) in water and soil samples has been determined by spectrophotometric method using cinnamoyl hydroxamic acid as reagent.
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- R. Kakkar in ed.: S.P. Gupta, Theoretical Studies on Hydroxamic Acids, In: Hydroxamic Acids: A Unique Family of Chemicals with Multiple Biological Activities, Springer-Verlag, Berlin Heidelberg, pp. 19-53 (2013).
- X. Chen, L. Wang, Y. Du, Y. Wu, X. Jia, Y. Yang and B. Hong, Molecules, 16, 9178 (2011).
- S. Lee, C. Shinji, K. Ogura, M. Shimizu, S. Maeda, M. Sato, M. Yoshida, Y. Hashimoto and H. Miyachi, Bioorg. Med. Chem. Lett., 17, 4895 (2007).
- I. Perkovic, I. Butula, Z. Rajic, D. Hadjipavlou-Litina, E. Pontiki and B. Zorc, Croat. Chem. Acta, 83, 151 (2010).
- European Pharmacopoeia, Council of Europe, Stras bourf, edn 5 (2006).
- G.F. Lewis and D.J. Rader, Circ. Res., 96, 1221 (2005).
- Y. Yang, Z. Zhang, W. Jiang, L. Gao, G. Zhao, Z. Zheng, M. Wang, S. Si and B. Hong, J. Biomol. Screen., 12, 211 (2007).
- P. Bertrand, Eur. J. Med. Chem., 45, 2095 (2010).
- G. Giannini, M. Marzi, R. Pezzi, T. Brunetti, G. Battistuzzi, M.D. Marzo, W. Cabri, L. Vesci and C. Pisano, Bioorg. Med. Chem. Lett., 19, 2346 (2009).
- L.K. Gediya, P. Chopra, P. Purushottamachar, N. Maheshwari and V.C.O. Njar, J. Med. Chem., 48, 5047 (2005).
- P. Siliphaivanh, P. Harrington, D.J. Witter, K. Otte, P. Tempest, S. Kattar, A.M. Kral, J.C. Fleming, S.V. Deshmukh, A. Harsch, P.J. Secrist and T.A. Miller, Bioorg. Med. Chem. Lett., 17, 4619 (2007).
- D.J. Witter, S. Belvedere, L. Chen, J.P. Secrist, R.T. Mosley and T.A. Miller, J. Bioorg. Med. Chem. Lett., 17, 4562 (2007).
- Y. Nagaoka, T. Maeda, Y. Kawai, D. Nakashima, T. Oikawa, K. Shimoke, T. Ikeuchi, H. Kuwajima and S. Uesato, Eur. J. Med. Chem., 41, 697 (2006).
- A. Barocas, F. Baroncelli, G. Biondi and G. Grossi, J. Inorg. Nucl. Chem., 28, 2961 (1996).
- F. Baroncelli and G. Grossi, J. Inorg. Nucl. Chem., 27, 1085 (1965).
- H.R. Al-Jarrah, A.R. Al-Karaghouli, S.A. Al-Assaf and N.H. Shamon, J. Inorg. Nucl. Chem., 43, 2971 (1981).
- A.S. Gopalan, V.J. Huber, O. Zincircioglu and P.H. Smith, J. Chem. Soc. Chem. Commun., 17, 1266 (2009).
- N. Koshti, V. Huber, P. Smith and A.S. Gopalan, Tetrahedron, 50, 2657 (1994).
- V. Srilalitha, A.R.G. Prasad, V. Seshagiri and L.K. Ravindranath, Anal. Univ. Bucuresti-Chim., 19, 69 (2010).
- A. Abbaspour, S.M.M. Moosavi and R. Mirzajani, Iran. J. Sci. Tech. Trans. A., 31, 2331 (2010).
- B.K. Priya, P. Subrahmanyam, J.D. Kumar and P. Chiranjeevi, E-J. Chem., 3, 286 (2006).
- S. Cakir and E. Bicher, Turk. J. Chem., 31, 223 (2007).
- K.V.K. Reddy, P. Yamini, R.K. Kumar and P. Venkateswalu, Int. J. Chem. Eng. Appl. Sci., 2, 1 (2012).
- S.K. Rajput, A. Patel and K.N. Bapat, Chem. Mater. Res., 8, 8 (2016).
References
R. Kakkar in ed.: S.P. Gupta, Theoretical Studies on Hydroxamic Acids, In: Hydroxamic Acids: A Unique Family of Chemicals with Multiple Biological Activities, Springer-Verlag, Berlin Heidelberg, pp. 19-53 (2013).
X. Chen, L. Wang, Y. Du, Y. Wu, X. Jia, Y. Yang and B. Hong, Molecules, 16, 9178 (2011).
S. Lee, C. Shinji, K. Ogura, M. Shimizu, S. Maeda, M. Sato, M. Yoshida, Y. Hashimoto and H. Miyachi, Bioorg. Med. Chem. Lett., 17, 4895 (2007).
I. Perkovic, I. Butula, Z. Rajic, D. Hadjipavlou-Litina, E. Pontiki and B. Zorc, Croat. Chem. Acta, 83, 151 (2010).
European Pharmacopoeia, Council of Europe, Stras bourf, edn 5 (2006).
G.F. Lewis and D.J. Rader, Circ. Res., 96, 1221 (2005).
Y. Yang, Z. Zhang, W. Jiang, L. Gao, G. Zhao, Z. Zheng, M. Wang, S. Si and B. Hong, J. Biomol. Screen., 12, 211 (2007).
P. Bertrand, Eur. J. Med. Chem., 45, 2095 (2010).
G. Giannini, M. Marzi, R. Pezzi, T. Brunetti, G. Battistuzzi, M.D. Marzo, W. Cabri, L. Vesci and C. Pisano, Bioorg. Med. Chem. Lett., 19, 2346 (2009).
L.K. Gediya, P. Chopra, P. Purushottamachar, N. Maheshwari and V.C.O. Njar, J. Med. Chem., 48, 5047 (2005).
P. Siliphaivanh, P. Harrington, D.J. Witter, K. Otte, P. Tempest, S. Kattar, A.M. Kral, J.C. Fleming, S.V. Deshmukh, A. Harsch, P.J. Secrist and T.A. Miller, Bioorg. Med. Chem. Lett., 17, 4619 (2007).
D.J. Witter, S. Belvedere, L. Chen, J.P. Secrist, R.T. Mosley and T.A. Miller, J. Bioorg. Med. Chem. Lett., 17, 4562 (2007).
Y. Nagaoka, T. Maeda, Y. Kawai, D. Nakashima, T. Oikawa, K. Shimoke, T. Ikeuchi, H. Kuwajima and S. Uesato, Eur. J. Med. Chem., 41, 697 (2006).
A. Barocas, F. Baroncelli, G. Biondi and G. Grossi, J. Inorg. Nucl. Chem., 28, 2961 (1996).
F. Baroncelli and G. Grossi, J. Inorg. Nucl. Chem., 27, 1085 (1965).
H.R. Al-Jarrah, A.R. Al-Karaghouli, S.A. Al-Assaf and N.H. Shamon, J. Inorg. Nucl. Chem., 43, 2971 (1981).
A.S. Gopalan, V.J. Huber, O. Zincircioglu and P.H. Smith, J. Chem. Soc. Chem. Commun., 17, 1266 (2009).
N. Koshti, V. Huber, P. Smith and A.S. Gopalan, Tetrahedron, 50, 2657 (1994).
V. Srilalitha, A.R.G. Prasad, V. Seshagiri and L.K. Ravindranath, Anal. Univ. Bucuresti-Chim., 19, 69 (2010).
A. Abbaspour, S.M.M. Moosavi and R. Mirzajani, Iran. J. Sci. Tech. Trans. A., 31, 2331 (2010).
B.K. Priya, P. Subrahmanyam, J.D. Kumar and P. Chiranjeevi, E-J. Chem., 3, 286 (2006).
S. Cakir and E. Bicher, Turk. J. Chem., 31, 223 (2007).
K.V.K. Reddy, P. Yamini, R.K. Kumar and P. Venkateswalu, Int. J. Chem. Eng. Appl. Sci., 2, 1 (2012).
S.K. Rajput, A. Patel and K.N. Bapat, Chem. Mater. Res., 8, 8 (2016).