Square wave voltammetric investigations on 2,2-Dimethyl-1,3-dioxan-5-phenylazo-4,6-dione

Publication date: Available online 17 July 2015 Source:Egyptian Journal of Basic and Applied Sciences Author(s): A.M.A. Helmy, A. Fekri, M.M. Shahba The mostly advanced polarographic mode of measurement, square wave (SW), was applied for studying reduction of for 2,2-Dimethyl-1,3-dioxan-4,6-dione (Meldrum acid) and its 5-phenyl-azo substituent in 40% v/v ethanolic universal buffer (pH~ 2–12). At more negative potentials, a 2e pH-dependent wave (dEp/dpH = 31 mv) was assigned to one carbonyl group, while at more positive potentials a 4e pH-dependent wave (dEp/dpH = 71 mv) was assigned to the azomethine group. Based on the polarographic data and acid-base pKa values were determined spectrophotometrically. The reduction mechanism pathway was suggested. The azomethine group proved to be in the azo form since the nitro group of the p-NO2 derivative is reduced at a more negative potential than the azomethine linkage. Fair Ep-σ correlation was obtained with positive p values (~0.2–0.3), indicating that the substituents facilitate the reduction process at the dropping electrode.
Source: Egyptian Journal of Basic and Applied Sciences - Category: Science Source Type: research
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