2014
DOI: 10.1016/j.jelechem.2013.11.015
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Study of acetylsalicylic acid electroreduction behavior at platinum electrode

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Cited by 63 publications
(26 citation statements)
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“…Within the potential range, where reduction peaks of the tested compounds appear, the supporting electrolyte (0.1 mol L -1 NaClO 4 ) shows no peaks (Fig. 2, curve 4) [22]. The voltammograms were also used in determination of half-wave potentials (E 1/2 ) of SA, ASA and AA reduction.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…Within the potential range, where reduction peaks of the tested compounds appear, the supporting electrolyte (0.1 mol L -1 NaClO 4 ) shows no peaks (Fig. 2, curve 4) [22]. The voltammograms were also used in determination of half-wave potentials (E 1/2 ) of SA, ASA and AA reduction.…”
Section: Resultsmentioning
confidence: 99%
“…redox potential, half-wave potential, reduction currents, which can be used in calculation of kinetic parameters of electrode reactions like number of exchanged electrons, transfer coefficients, rate constants of electrode reactions. These parameters are important in estimation of anti-reductive properties of drugs as well as in understanding of their reduction mechanisms [18][19][20][21][22][23].…”
Section: Introductionmentioning
confidence: 99%
“…Electrochemistry using cyclic voltammetry has been known to be used in a wide variety of applications and characterization of materials 32 – 34 . Such as determining corrosion rate of metals and quantifying compounds in a given solution 34 – 36 .…”
Section: Discussionmentioning
confidence: 99%
“…Initially, the phenoxy carboxylate radical was formed through one electron and two-proton oxidation. The phenoxy carboxylate radical underwent tautomerism and oxidation, forming 2-oxocyclohexa-3,5-dien-1-ylium carboxylate and 4-oxocyclohexa-2,5-dien-1-ylium carboxylate, which hydrolyzed to obtained 5-hydroxy-6-oxocyclohexa-1,3-dienecarboxylate and 3-hydroxy-6-oxocyclohexa-1,4-dienecarboxylate respectively, followed by the third oxidation by loss of one electron and two protons to form 5,6-dioxocyclohexa-1,3-dienecarboxylate and 3,6-dioxocyclohexa-1,4-dienecarboxylate (Scheme 1) [19][20][21][22]. In basic medium, SHAM was converted to ohydroxybenzoate ion (salicylate ion) as shown in Eq.…”
Section: Electrooxidation Of Sham In Artificial Saliva Solutionmentioning
confidence: 99%