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Kinetics and Mechanism of Reaction of cis-[Cr(C2O4)2(H2O)2]– with L-Dopa in Aqueous Medium: A Comparative Antiparkinsonian Studies
Corresponding Author(s) : Sudhanshu Sekhar Rout
Asian Journal of Chemistry,
Vol. 29 No. 7 (2017): Vol 29 Issue 7
Abstract
The substitution reaction of cis-[Cr(C2O4)2(H2O)2]- with L-Dopa in aqueous medium has been studied over the range 35 £ t £ 50 °C, 3.5 £ pH £ 6.0, 5.0 × 10-3 mol dm-3 £ [L-Dopa] £ 15 × 10-3 mol dm-3, I = 0.1 mol dm-3 (KNO3). The reaction takes place via an outer sphere association between cis-[Cr(C2O4)2(H2O)2]- and L-Dopa followed by chelation. Characterization of the product was done by physico-chemical and infrared spectroscopic methods. The antiparkinsonian activity of L-Dopa was found to be less than that of the product chromium(III) complex.
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- C. Gibrat, M. Saint-Pierre, M. Bousquet, D. Levesque, C. Rouillard and F. Cicchetti, J. Neurochem., 109, 1469 (2009); https://doi.org/10.1111/j.1471-4159.2009.06072.x.
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- F. Guerrero-Romero and M. Rodriguez-Moran, Arch. Med. Res., 36, 250 (2005); https://doi.org/10.1016/j.arcmed.2005.01.004.
- J.A. Santiago and J.A. Potashkin, Neurobiol. Dis., 72, 84 (2014); https://doi.org/10.1016/j.nbd.2014.03.019.
- D.B. Shachar, N. Kahana, V. Kampel, A. Warshawsky and B.H. Youdim, Neuropharmacology, 46, 254 (2004); https://doi.org/10.1016/j.neuropharm.2003.09.005.
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- M. Szablowicz and E. Kita, Transition Met. Chem., 30, 623 (2005); https://doi.org/10.1007/s11243-005-4588-z.
- M. Pazderska-Szablowicz, A. Bialkowska and E. Kita, Transition Met. Chem., 31, 413 (2006); https://doi.org/10.1007/s11243-006-0010-8.
- B.K. Aziz and D.I. Tofiq, Int. J. Chem. Environ. Eng., 3, 34 (2012).
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- I.A. Khan, M. Sahid and Kabir-ud-Din, J. Phys.Chem., 27, 101 (1990).
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- D. Banerjee and S.D. Chaudhuri, J. Inorg. Nucl. Chem., 30, 871 (1968); https://doi.org/10.1016/0022-1902(68)80449-X.
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- A.G. MacDiarmid, Inorganic Syntheses, McGraw-Hill Book Company, New York, vol. 17, p. 149 (1979).
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References
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S.Z.A. Zaidi and N. Fatima, Eur. Chem. Bull., 3, 648 (2014); https://doi.org/10.17628/ecb.2014.3.648-653.
J.A. Santiago and J.A. Potashkin, Trends Mol. Med., 19, 176 (2013); https://doi.org/10.1016/j.molmed.2013.01.002.
F. Guerrero-Romero and M. Rodriguez-Moran, Arch. Med. Res., 36, 250 (2005); https://doi.org/10.1016/j.arcmed.2005.01.004.
J.A. Santiago and J.A. Potashkin, Neurobiol. Dis., 72, 84 (2014); https://doi.org/10.1016/j.nbd.2014.03.019.
D.B. Shachar, N. Kahana, V. Kampel, A. Warshawsky and B.H. Youdim, Neuropharmacology, 46, 254 (2004); https://doi.org/10.1016/j.neuropharm.2003.09.005.
D.K. Baral, S.S. Rout, J. Behera, S.C. Si and P. Mohanty, Transition Met. Chem., 36, 231 (2011); https://doi.org/10.1007/s11243-011-9460-8.
M. Szablowicz and E. Kita, Transition Met. Chem., 30, 623 (2005); https://doi.org/10.1007/s11243-005-4588-z.
M. Pazderska-Szablowicz, A. Bialkowska and E. Kita, Transition Met. Chem., 31, 413 (2006); https://doi.org/10.1007/s11243-006-0010-8.
B.K. Aziz and D.I. Tofiq, Int. J. Chem. Environ. Eng., 3, 34 (2012).
I.A. Khan and Kabir-Ud-Din, J. Inorg. Nucl. Chem., 43, 1082 (1981); https://doi.org/10.1016/0022-1902(81)80188-1.
I.A. Khan and Kabir-ud-Din, Indian J. Chem., 23A, 98 (1984).
I.A. Khan and M. Sahid, Indian J. Chem., 22A, 382 (1983).
S.C. Tyagi and A.A. Khan, J. Inorg. Nucl. Chem., 40, 1899 (1978); https://doi.org/10.1016/0022-1902(78)80251-6.
I.A. Khan and Kabir-ud-Din, Int. J. Chem. Kinet., 17, 1263 (1985); https://doi.org/10.1002/kin.550171203.
I.A. Khan, M. Sahid and Kabir-ud-Din, J. Phys.Chem., 27, 101 (1990).
J.K. Dei, N.N. Pasupalak and P. Mohanty, Transition Met. Chem., 22, 516 (1997); https://doi.org/10.1023/A:1018579700786.
I.A. Khan, M. Sahid and Kabir-ud-Din, J. Indian Chem. Soc., 69, 864 (1992).
D. Banerjee and S.D. Chaudhuri, J. Inorg. Nucl. Chem., 30, 871 (1968); https://doi.org/10.1016/0022-1902(68)80449-X.
G.J. Khan and Kabir-ud-Din, Proc. Indian Acad. Sci., 107, 11 (1995).
M.A. Abdullah, J. Barrett and P. O’Brien, J. Chem. Soc., Dalton Trans., 1647 (1984); https://doi.org/10.1039/dt9840001647.
B.K. Niogy and G.S. De, Proc. Ind. Acad. Sci., 92, 153 (1983).
B.K. Niogy and G.S. De, Indian J. Chem., 24A, 208 (1985).
R.E. Hamm, R.L. Johnson, R.N. Perkins and R.E. Davis, J. Am. Chem. Soc., 80, 4469 (1958); https://doi.org/10.1021/ja01550a008.
M.F. Abdel-Messih, J. Coord. Chem., 66, 1519 (2013); https://doi.org/10.1080/00958972.2013.779685.
V.C.H. Langford and H.B. Gray, Ligand Substitution Processes, W.A. Benjamin, Inc., New York, USA (1965).
A.G. MacDiarmid, Inorganic Syntheses, McGraw-Hill Book Company, New York, vol. 17, p. 149 (1979).
H.A. Adedeji, I.O. Ishola and O.O. Adeyemi, Prog. Neuropsychopharmacol. Biol. Psychiatry, 48, 245 (2014); https://doi.org/10.1016/j.pnpbp.2013.10.014.
G.M. Robinson and M.R. Smyth, Analyst, 122, 797 (1997); https://doi.org/10.1039/a701844d.
M. Sahid, I.A. Khan and Kabir-ud-Din, J. Chem. Soc., Dalton Trans., 3007 (1990); https://doi.org/10.1039/DT9900003007.
R.B. Jordan, Reaction Mechanism of Inorganic and Organometallic Systems, Oxford University Press, New York (1991).
S.K. Bhattacharyya and R. Banerjee, Polyhedron, 16, 4217 (1997); https://doi.org/10.1016/S0277-5387(97)00264-7.
I.A. Khan, M. Shahid and Kabir-ud-Din, Transition Met. Chem., 12, 393 (1987); https://doi.org/10.1007/BF01171644.
S. Mohanty, S. Anand, G.S. Brahma and P. Mohanty, J. Indian Chem. Soc., 80, 810 (2003).
J. Behera, G.S. Brahma and P. Mohanty, J. Indian Chem. Soc., 78, 125 (2001).
S.C. Dash, G.S. Brahma, R. Das, N.N. Das and P. Mohanty, Indian J. Chem., 45A, 2406 (2006).