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Electrochemical Reduction of G3-Factor Endoperoxide and Its Methyl Ether: Evidence for a Competition between Concerted and Stepwise Dissociative Electron Transfer

✍ Scribed by Fadia Najjar; Christiane André-Barrès; Michel Baltas; Corinne Lacaze-Dufaure; David C. Magri; Mark S. Workentin; Théodore Tzédakis


Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
162 KB
Volume
13
Category
Article
ISSN
0947-6539

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✦ Synopsis


Abstract

The reduction of the bicyclic G‐factor endoperoxides G3 and G3Me was studied in N,N‐dimethylformamide using cyclic voltammetry and convolution analysis. Electron transfer leads to irreversible cleavage of the OO bond. Detailed analysis of the voltammetry curves reveals a non‐linear dependence on the transfer coefficient indicating a mechanistic transition from a stepwise mechanism to one with more concerted character with increasing potential. By using quantum calculations to estimate the OO bond dissociation energies, the experimental data was used to evaluate the standard reduction potentials and other pertinent thermochemical information.