2011
DOI: 10.1073/pnas.1104952108
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Concerted heavy-atom bond cleavage and proton and electron transfers illustrated by proton-assisted reductive cleavage of an O–O bond

Abstract: Electron transfer may be concerted with proton transfer. It may also be concerted with the cleavage of a bond between heavy atoms. All three events may also be concerted. A model is presented to analyze the kinetics of these all-concerted reactions for homogeneous or electrochemical reduction or oxidation processes. It allows the estimation of the kinetic advantage that derives from the increase of the bond-breaking driving force resulting from the concerted proton transfer. Application of the model to the ele… Show more

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Cited by 38 publications
(38 citation statements)
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“…With an ECE mechanism found theoretically implausible by digital simulations and with no evidence of a CEE mechanism, a concerted (EC) concerted E mechanism was considered. For concerted pathways not involving heavy atom bond cleavage 48 electrochemical kinetic isotope effects have been used as a diagnostic for CPET. 49 – 54 Therefore, cyclic voltammograms were obtained of 1 in the presence of sub-stoichiometric amounts of [Et 3 NH][Cl] (to permit observation of the position of 1 's reversible wave) and either 0.24 M H 2 O or 0.24 M D 2 O.…”
Section: Resultsmentioning
confidence: 99%
“…With an ECE mechanism found theoretically implausible by digital simulations and with no evidence of a CEE mechanism, a concerted (EC) concerted E mechanism was considered. For concerted pathways not involving heavy atom bond cleavage 48 electrochemical kinetic isotope effects have been used as a diagnostic for CPET. 49 – 54 Therefore, cyclic voltammograms were obtained of 1 in the presence of sub-stoichiometric amounts of [Et 3 NH][Cl] (to permit observation of the position of 1 's reversible wave) and either 0.24 M H 2 O or 0.24 M D 2 O.…”
Section: Resultsmentioning
confidence: 99%
“…The CB electrons have a potential (+0.13 V at pH 0) that is high enough for the four‐electron reduction of O 2 but insufficient for its two‐electron reduction (Figure 3 b). The H + ‐transfer‐coupled electron transfer may proceed in a concerted fashion with the OO bond cleavage to produce H 2 O 23. This reminds us of laccase with a trinuclear Cu site that catalyzes the four‐electron reduction of O 2 18.…”
Section: Obbc/ms‐bivo4‐photocatalyzed Oxidation Of Benzylamines[a]mentioning
confidence: 97%
“…[20] Indeed,m odel systems have shown the importance of PCET in chemical conversion in theoretical [21,22] ande xperimental studies. [23][24][25] For water oxidation, the removal of four electrons from two water molecules is ac rucial requirement. The removal of four protonsi se ven more difficult.…”
Section: Proton-coupled Electron Transfermentioning
confidence: 99%