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Portugaliae Electrochimica Acta
Print version ISSN 0872-1904
Port. Electrochim. Acta vol.26 no.5 Coimbra 2008
Study of 'Transition State' with Applied Potential [Mn Sulfonamides Cephalothin] System
M.S. Parihar and F. Khan*
Electrochemical Laboratory, Department of Chemistry, Dr. H.S. Gour University, Sagar-4700 003, M. P. India
Received 11 September 2007; accepted 13 May 2008
Abstract
Kinetic parameters and stability constants of [Mn sulfonamides cephalothin] system were reported at pH = 7.30 ± 0.01 in 1.0 M NaCO4 at 25 ºC. The sulfonamides were sulfadiazine, sulfisoxazoe, sulfamethaxyzoe, sulfamethazine, sulfathiazoe, sulfacetamide and sulfaniamide as primary ligands, and cephalothin as secondary ligand. Values of transfer coefficient (α) varied from (0.41 to 0.59), showing that transition state behaves between oxidant and reductant response to applied potential and it adjusts itself in such a way that the transition state is located midway between dropping mercury electrode and solution interface. The rate constants (k) varied from 3.61 x 10-3 cm.sec.-1 to 9.93 x 10-3 cm.sec.-1, confirming that the electrode processes were quasi reversible. Small changes in potential not only affect the rate of the electrochemical reaction, but also strongly affect the rate constant. Values of stability constants (og β) varied from 1.75 to 9.13, showing that these drugs or their complexes could be used against Mn toxicity.
Keywords: electrode kinetics in [Mn sulfonamides cephalothin] system.
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References
1. S. Bellu and M. Rizzotto, Quim. Nova 30(5) (2007) 1136. [ Links ]
2. L. S. Goodman and Gimans, The Pharmacological Basis of Therapeutics, 11th ed., The McGraw-Hill Co., New York, 2006.
3. F. Martinez, C.M. Avila and A. Gomez, J. Braz. Chem. Soc. 14(5) (2003) 803.
4. A. Cleasby, A. Wonacott, T. Skarzynski, R.E. Hubbard, G.J. Davies, A.E. Proudfoot, A.E. Bernard, M.A. Payton, T.N. Well, Nature Struct. Biol. 3 (1996) 470.
5. A. Mastrolorenzo and C.T. Supuran, Metal Based Drug 7 (2000) 49.
6. L. Meites, Polarographic Technique, 2nd ed., Interscience Publishers, New York, 1965, p. 62.
7. P.J. Gellings, Z. Elektrochem. 66 (1962) 477; Ber. Bun. Physik. Chem. 67 (1963) 799.
8. D. Deford and D.N. Hume, J. Am. Chem. Soc. 73 (1951) 5321.
9. W.B. Schaap and D. L. McMaster, J. Am. Chem. Soc. 83 (1961) 4699.
10. R.C. Kapoor, B.S. Aggarwal, Principles of Polarography, 1st ed., Wiley Eastern Limited, New Delhi, 1991, p. 40.
11. A.E. Martell, Chemistry of Metal Chelate Compounds, 2nd ed., Prentice Hall Inc., America, 1953, p. 134.
12. F. Khan, J. Chin. Chem. Soc. 52 (2005) 569.
13. R. Tamamushi and N.Z. Tanaka, Phys. Chem. New Folge 39 (1963) 117.
14. R. Tamamushi, K. Ishibashi and N.Z. Tanaka, Phys. Chem. New Folge 35 (1962) 211.
15. P.W. Atkins, Physical Chemistry, W.H. Freeman and Co., San Francisco, 1978, p. 959.
16. F. Khan, J. Chin. Chem. Soc. 54 (2007) 673.
* Corresponding author. E-mail address: faridkhan58@yahoo.com