Title of article
Electrochemically initiated 1,4 additions: a versatile route to the determination of thiols Original Research Article
Author/Authors
Paul C. White، نويسنده , , Nathan S. Lawrence، نويسنده , , James Davis، نويسنده , , Richard G. Compton، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2001
Pages
10
From page
1
To page
10
Abstract
The electrochemical generation of quinoid intermediates and their subsequent reaction with sulphydryl thiols (RSH) have been investigated as a method by which the latter can be quantified. Nucleophilic addition of the thiol species to the electrogenerated quinoid structure leads to the production of a chemically reduced adduct whose subsequent re-oxidation at the electrode leads to an amplification of the oxidative current. This can be correlated to the concentration of thiol present within the medium. The influence of indicator composition on the nature of the analytical response has been assessed through examining the electrochemical properties of 15 derivatives and the validity of the proposed reaction pathway corroborated by comparison of the voltammetric response with computer simulations. Interference by other electroactive species (ascorbate, urate, tyrosine) and other physiological constituents (cystine, lysine) has also been assessed.
Keywords
Thiol , Analysis , Quinone , Electrode , cysteine
Journal title
Analytica Chimica Acta
Serial Year
2001
Journal title
Analytica Chimica Acta
Record number
1030718
Link To Document