Abstract
A rapid, sensitive and accurate method for the determination of substituted oxadiazol
(I&II) has been developed based on the reduction of electroactive group (-C=S) at
hanging mercury electrode by using square wave voltammetric technique. The reduction
peaks obtained at –0.028 and –0.172 V Vs Ag/AgC1 fir compounds I & II respectively at
pH 2 in Britton – Robinson buffer are recommended for the trace determination of these
compounds. Regression analysis on standard curve indicated a linear relationship
between peak current and concentration over the rang 1.2 × 10-6–2.5 × 10-5 M with a
correlation coefficient of more than 0.98.
(I&II) has been developed based on the reduction of electroactive group (-C=S) at
hanging mercury electrode by using square wave voltammetric technique. The reduction
peaks obtained at –0.028 and –0.172 V Vs Ag/AgC1 fir compounds I & II respectively at
pH 2 in Britton – Robinson buffer are recommended for the trace determination of these
compounds. Regression analysis on standard curve indicated a linear relationship
between peak current and concentration over the rang 1.2 × 10-6–2.5 × 10-5 M with a
correlation coefficient of more than 0.98.