Kinetics and mechanism of oxidation of L-cysteine and DL-methionine by morpholinium chlorochromate in aqueous acidic medium

Bijaylaxmi Mohanty, J. Behera, P. Mohanty, S. Acharya, A. K. Patnaik, S. P. Das
2011 Zenodo  
P.G. Department of Chemistry, Utkal University, Bhubaneswar-751 004, Orissa, India biMMT, Bhubaneswar, Orissa, India P.G. Department of Chemistry, Khallikote (Autonomous) College, Berhampur-760 001, Orissa, India E-mail : ajaypattanaik_kumar@yahoo.co.in P.G. Department of Chemistry, Ravenshaw University, Cuttack-753 003, Orissa, India Manuscript received 25 November 2010. revised 09 March 2011, accepted 17 March 2011 The kinetics of the redox reaction of MCC (morpholinium chlorochromate) with
more » ... cysteine and DL-methionine have been studied over the range 2.0 ≤ 103 [amino acid]T ≤ 6.0, 0.1 ≤ [H+] ≤ 0.25, 0.1 ≤ I ≤ 0.8 mol dm-3 and 293 K ≤ T ≤ 313 K in aqueous perchlorate medium. The redox reaction showed first order dependence in [amino acid] r and [MCC]T. The main products of the reaction were cystine and methionine sulfoxide respectively. The activation parameters ΔH# (kJ moi-1) and ΔS1 (JK-1 moi-1) for the redox reactions of L-cysteine and DL-methionine for k1 and k2 paths are found to be 44.82 ± 9.1, 54.11 ± 7.1, 26.69 ± 9.0, 60.64 ± 12.24 and -243.05 ± 29.8, -268.29 ± 23.4 and -206.62 ± 30.3, -319.83 ± 40.43 respectively. The valus of ΔH# and ΔS# were both favourable for electron transfer processes. Negative ΔS# indicates the ordered transition state for the redox reactions.
doi:10.5281/zenodo.5790631 fatcat:mvhjnizvyrcddkzuqyhgqfacm4