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The undissociated phenol in tyrosine will not be oxidized at +0.4 V (vs SCE) since the potential for the oxidation of phenol with various substituents is given as +0.7 − 1.65 V (vs SCE) [34 36] whereas the phenolate anion is much more easily oxidized in a 1 e− oxidation, with potentials in the range −0.5 − +0.12V (vs SCE) [34,35,37].
During methanol oxidation Pd particles were more easily oxidized than Pd(1 1 1), which reduced their activity.
This indicated that the protonation of the nitrogen atoms displays a determinant role in the voltammetric oxidation, being both prodrugs more easily oxidized than PQ protonated forms, in the order: SPQ < MPQ < PQ.
The reduction potential for hydrogen is taken by convention to be zero, and all metals with negative reduction potentials i.e., metals that are less easily reduced (more easily oxidized; e.g., zinc: Zn2+ + 2e− → Zn, − 0.763 volt)—can, in principle, displace hydrogen from a strong acid solution: Zn + 2H+ → Zn2+ + H2.
Cu atoms burst out and get more easily oxidized.
Cu atoms burst out and are more easily oxidized.
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The phenolic compounds were easily oxidized, the oxides could combine with DNA and form colloidal compounds.
LDL-cholesterol molecules are easily oxidized in a state of oxidative stress, especially the small and dense molecules.
Esters of linoleate are 49 times more reactive than oleate esters because the former contain an easily oxidized bis-allylic methylene group between the two double bonds [ 3].
These active RSH groups are easily oxidized to a sulfenic oxoform (RSOH), the initial oxidative product of cysteine.
Unfortunately, these metal chalcogenide semiconductors are easily oxidized when exposed to light, and this unfavorable situation is even more detrimental when the metal sulfide is in contact with a liquid electrolyte containing sulfur.
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