2013
DOI: 10.1007/s11172-013-0377-6
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Electrochemical oxidation of tetracycline on a boron doped diamond electrode within the stability potentials of water

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Cited by 8 publications
(3 citation statements)
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“…(1st) the oxidation direct of the phenolic moiety with subsequent addition of the hydroxyl group [15,[44][45][46], which can occur in two different positions, ortho and para (Scheme 1).…”
Section: Electrooxidation Of Tetracycline At the Ptnps/c/gcementioning
confidence: 99%
“…(1st) the oxidation direct of the phenolic moiety with subsequent addition of the hydroxyl group [15,[44][45][46], which can occur in two different positions, ortho and para (Scheme 1).…”
Section: Electrooxidation Of Tetracycline At the Ptnps/c/gcementioning
confidence: 99%
“…It can be seen from previous results that this reaction would lose 2 electrons and 2 protons with the subsequent addition of the hydroxyl group. 43…”
Section: Resultsmentioning
confidence: 99%
“…It can be seen from previous results that this reaction would lose 2 electrons and 2 protons with the subsequent addition of the hydroxyl group. 43 (2) Aer the transformation of electrons/protons to the hydroxyl group, the oxidation product of the rst step would produce strong intramolecular hydrogen interactions when the environment acidity was high. When the acidity of the environment decreased, the hydrogen interactions would weaken.…”
Section: Electrocatalytic Behavior and Mechanism Of Tetracyclinementioning
confidence: 99%