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Kinetic Study of Interaction of ortho-Aminophenol with Fe(III) Schiff Base Complex in Aqueous Surfactant Medium
Corresponding Author(s) : Pradyut Sarma
Asian Journal of Chemistry,
Vol. 27 No. 1 (2015): Vol 27 Issue 1
Abstract
The interaction of phenolate substrate like ortho-aminophenol with [Fe(salen)]Cl has been studied in aqueous surfactant medium. The oxygenation reaction of o-aminophenol bound [Fe(salen)]+ adduct has found to be pseudo first order. The rate constant of the oxygenation reaction has characterized in cationic, anionic and neutral surfactant medium. These rate constant values are quite encouraging. Enzyme kinetics of the oxygenation reaction has been thoroughly examined. kcat/Km value of the reaction in different surfactant medium are ranges from 7.1 × 103 to 7.9 × 103 M-1s-1 and these values support the efficiency of the enzyme. Therefore the reaction has provided a better option as model of dioxygenase enzyme.
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- G. Lin, G. Reid and T.H. Bugg, J. Am. Chem. Soc., 123, 5030 (2001); doi:10.1021/ja004280u.
- L. Que Jr. and M. Reynolds, Met. Ions Biol. Syst., 37, 505 (2000).
- M. Costas, M.P. Mehn, M.P. Jensen and L. Que, Chem. Rev., 104, 939 (2004); doi:10.1021/cr020628n.
- M.M. Taqui Khan, N.H. Khan, R.I. Kureshy, A.B. Boricha and Z.A. Shaikh, Inorg. Chim. Acta, 170, 213 (1990); doi:10.1016/S0020-1693(00)80478-8.
- 5 L. Que, R.C. Kolanczyk and L.S. White, J. Am. Chem. Soc., 109, 5373 (1987); doi:10.1021/ja00252a012.
- J.C. Moutet and A. Ourari, Electrochim. Acta, 42, 2525 (1997); doi:10.1016/S0013-4686(96)00443-4.
- M. Higuchi, Y. Hitomi, H. Minami, T. Tanaka and T. Funabiki, Inorg. Chem., 44, 8810 (2005); doi:10.1021/ic051173y.
- R. Mayilmurugan, E. Suresh and M. Palaniandavar, Inorg. Chem., 46, 6038 (2007); doi:10.1021/ic700646m.
- L. Casella, M. Gullotti, A. Pintar, L. Messori, A. Rockenbauer and M. Gyor, Inorg. Chem., 26, 1031 (1987); doi:10.1021/ic00254a014.
- M. Merkel, F.K. Müller and B. Krebs, Inorg. Chim. Acta, 337, 308 (2002); doi:10.1016/S0020-1693(02)01082-4.
- M.J. Sever and J.J. Wilker, Dalton Trans., 1061 (2004); doi:10.1039/b315811j.
- D.K. Das, C. Bhattaray and O.K. Medhi, J. Chem. Soc., Dalton Trans., 4713 (1997); doi:10.1039/a703701e.
- T. Dhanalakshmi, M. Bhuvaneshwari and M. Palaniandavar, J. Inorg. Biochem., 100, 1527 (2006); doi:10.1016/j.jinorgbio.2006.05.004.
- T. Kurahashi, K. Oda, M. Sugimoto, T. Ogura and H. Fujii, Inorg. Chem., 45, 7709 (2006); doi:10.1021/ic060650p.
- P. Sarma and O. K. Medhi, J. Surface Sci. Technol., 27, 135 (2011).
- M. Higuchi, Y. Hitomi, H. Minami, T. Tanaka and T. Funabiki, Inorg. Chem., 44, 8810 (2005); doi:10.1021/ic051173y.
- D.A. Baldwin, H.M. Marques and J.M. Pratt, J. Inorg. Biochem., 27, 245 (1986); doi:10.1016/0162-0134(86)80065-4.
- M. Velusamy, M. Palaniandavar, R.S. Gopalan and G.U. Kulkarni, Inorg. Chem., 42, 8283 (2003); doi:10.1021/ic020569w.
- D.K. Das and O.K. Medhi, J. Chem. Soc., Dalton Trans., 1693 (1998); doi:10.1039/a708732b.
- L. Que, R.C. Kolanczyk and L.S. White, J. Am. Chem. Soc., 109, 5373 (1987); doi:10.1021/ja00252a012.
- P. Mialane, L. Tchertanov, F. Banse, J. Sainton and J.-J. Girerd, Inorg. Chem., 39, 2440 (2000); doi:10.1021/ic981236v.
- P. Sarma and O.K. Medhi, Int. J. Chem. Res., 2, 135 (2011).
- M. Pascaly, M. Duda, F. Schweppe, K. Zurlinden, F.K. Muller and B. Krebs, J. Chem. Soc., Dalton Trans., 828 (2001); doi:10.1039/B008511L.
- R. Viswanathan, M. Palaniandavar, T. Balasubramanian and T.P. Muthiah, Inorg. Chem., 37, 2943 (1998); doi:10.1021/ic970708n.
References
G. Lin, G. Reid and T.H. Bugg, J. Am. Chem. Soc., 123, 5030 (2001); doi:10.1021/ja004280u.
L. Que Jr. and M. Reynolds, Met. Ions Biol. Syst., 37, 505 (2000).
M. Costas, M.P. Mehn, M.P. Jensen and L. Que, Chem. Rev., 104, 939 (2004); doi:10.1021/cr020628n.
M.M. Taqui Khan, N.H. Khan, R.I. Kureshy, A.B. Boricha and Z.A. Shaikh, Inorg. Chim. Acta, 170, 213 (1990); doi:10.1016/S0020-1693(00)80478-8.
5 L. Que, R.C. Kolanczyk and L.S. White, J. Am. Chem. Soc., 109, 5373 (1987); doi:10.1021/ja00252a012.
J.C. Moutet and A. Ourari, Electrochim. Acta, 42, 2525 (1997); doi:10.1016/S0013-4686(96)00443-4.
M. Higuchi, Y. Hitomi, H. Minami, T. Tanaka and T. Funabiki, Inorg. Chem., 44, 8810 (2005); doi:10.1021/ic051173y.
R. Mayilmurugan, E. Suresh and M. Palaniandavar, Inorg. Chem., 46, 6038 (2007); doi:10.1021/ic700646m.
L. Casella, M. Gullotti, A. Pintar, L. Messori, A. Rockenbauer and M. Gyor, Inorg. Chem., 26, 1031 (1987); doi:10.1021/ic00254a014.
M. Merkel, F.K. Müller and B. Krebs, Inorg. Chim. Acta, 337, 308 (2002); doi:10.1016/S0020-1693(02)01082-4.
M.J. Sever and J.J. Wilker, Dalton Trans., 1061 (2004); doi:10.1039/b315811j.
D.K. Das, C. Bhattaray and O.K. Medhi, J. Chem. Soc., Dalton Trans., 4713 (1997); doi:10.1039/a703701e.
T. Dhanalakshmi, M. Bhuvaneshwari and M. Palaniandavar, J. Inorg. Biochem., 100, 1527 (2006); doi:10.1016/j.jinorgbio.2006.05.004.
T. Kurahashi, K. Oda, M. Sugimoto, T. Ogura and H. Fujii, Inorg. Chem., 45, 7709 (2006); doi:10.1021/ic060650p.
P. Sarma and O. K. Medhi, J. Surface Sci. Technol., 27, 135 (2011).
M. Higuchi, Y. Hitomi, H. Minami, T. Tanaka and T. Funabiki, Inorg. Chem., 44, 8810 (2005); doi:10.1021/ic051173y.
D.A. Baldwin, H.M. Marques and J.M. Pratt, J. Inorg. Biochem., 27, 245 (1986); doi:10.1016/0162-0134(86)80065-4.
M. Velusamy, M. Palaniandavar, R.S. Gopalan and G.U. Kulkarni, Inorg. Chem., 42, 8283 (2003); doi:10.1021/ic020569w.
D.K. Das and O.K. Medhi, J. Chem. Soc., Dalton Trans., 1693 (1998); doi:10.1039/a708732b.
L. Que, R.C. Kolanczyk and L.S. White, J. Am. Chem. Soc., 109, 5373 (1987); doi:10.1021/ja00252a012.
P. Mialane, L. Tchertanov, F. Banse, J. Sainton and J.-J. Girerd, Inorg. Chem., 39, 2440 (2000); doi:10.1021/ic981236v.
P. Sarma and O.K. Medhi, Int. J. Chem. Res., 2, 135 (2011).
M. Pascaly, M. Duda, F. Schweppe, K. Zurlinden, F.K. Muller and B. Krebs, J. Chem. Soc., Dalton Trans., 828 (2001); doi:10.1039/B008511L.
R. Viswanathan, M. Palaniandavar, T. Balasubramanian and T.P. Muthiah, Inorg. Chem., 37, 2943 (1998); doi:10.1021/ic970708n.