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Electrochemical oxidation of 4-tert-butylcatechol in the presence of β-cyclodextrin: Interplay between E and CE mechanisms

✍ Scribed by Mohammad Rafiee


Publisher
John Wiley and Sons
Year
2012
Tongue
English
Weight
330 KB
Volume
44
Category
Article
ISSN
0538-8066

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✦ Synopsis


Abstract

Electrochemical behavior of 4‐tert‐butylcatechol (H~2~Q) in the presence of β‐cyclodextrin (β‐CD) was studied using cyclic voltammetry and hydrodynamic voltammetry. An electrochemical model in which both H~2~Q and its oxidized form (Q) created inclusion complexes with β‐CD was proposed, and it was concluded that both free (as a result of complex‐dissociation reaction) and complex species could performed electron transfer. The heterogeneous rate constant for electron transfer of the inclusion complexes and their kinetic and thermodynamic parameters were obtained using digital simulation. © 2012 Wiley Periodicals, Inc. Int J Chem Kinet 44: 507–513, 2012


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## Abstract The oxidative C—H activation of indoles (I) with different alkenes and ketones in the presence of Ce(O‐Ac)~3~ and β‐cyclodextrin as catalytic system proceeds regioselectively in H~2~O to afford a variety of 3‐substituted indoles in good yields.