OXYHALOGEN-SULFUR CHEMISTRY - NONLINEAR OXIDATION OF 2-AMINOETHANETHIOLSULFURIC ACID (AETSA) BY BROMATE IN ACIDIC MEDIUM

Citation
J. Darkwa et al., OXYHALOGEN-SULFUR CHEMISTRY - NONLINEAR OXIDATION OF 2-AMINOETHANETHIOLSULFURIC ACID (AETSA) BY BROMATE IN ACIDIC MEDIUM, Journal of the Chemical Society. Faraday transactions, 92(22), 1996, pp. 4407-4413
Citations number
30
Categorie Soggetti
Chemistry Physical","Physics, Atomic, Molecular & Chemical
ISSN journal
09565000
Volume
92
Issue
22
Year of publication
1996
Pages
4407 - 4413
Database
ISI
SICI code
0956-5000(1996)92:22<4407:OC-NOO>2.0.ZU;2-T
Abstract
The reaction between bromate and 2-aminoethanethiolsulfuric acid, H2NC H2CH2S-SO3H (AETSA), has been studied in high acid environments. The s toichiometry in excess AETSA is BrO3- + H2NCH2CH2S-SO3H + H2O --> H2NC H2CH2SO3H + SO42- + 2H(+) + Br-. In excess BrO3- the stoichiometry is: 7BrO(3)(-) + 5H(2)NCH(2)CH(2)S-SO3H --> 5Br(H)NCH2CH2SO3H + 5SO(4)(2- ) + Br-2 + 3H(+) + H2O. The reaction displays clock reaction character istics in which there is initial quiescence followed by a sudden and r apid formation of Br-2(a). The oxidation proceeds by successive additi on of oxygen on the inner sulfur atom followed by cleavage of the S-S bond to form taurine and SO42-. The Br-2(aq) and the HOBr in solution oxidize the taurine to form a mixture of monobromotaurine and dibromot aurine. Computer simulations of a proposed 13-step reaction scheme pro duced st reasonable fit to the experimental data.