Citation: Davood Nematollahi, Bayan Moradi, Fahimeh Varmaghani. Kinetic study of electrochemically induced Michael reaction of 1,4-dihydroxyanthraquinone with acetylacetone and benzoylacetone[J]. Chinese Chemical Letters, ;2013, 24(11): 1008-1010. shu

Kinetic study of electrochemically induced Michael reaction of 1,4-dihydroxyanthraquinone with acetylacetone and benzoylacetone

1.
a Faculty of Chemistry, Bu-Ali Sina University, Hamedan 65178-38683, Iran;
2.
b Department of Chemistry, Faculty of Science, Arak Branch, Islamic Azad University, Arak 38135-567, Iran

Corresponding author: Davood Nematollahi,
Received Date: 26 March 2013
Available Online: 16 July 2013

The electrochemical oxidation of 1,4-dihydroxyanthraquinone has been studied in the presence of acetylacetone and benzoylacetone as nucleophiles in a mixture of ethanol/water by means of cyclic voltammetry as a diagnostic technique. The results indicate the participation of electrochemically produced anthraquinone in the Michael addition reaction with acetylacetone and benzoylacetone to form the corresponding new anthraquinone derivatives. On the basis of the EC mechanism, the observed homogeneous rate constants (k_obs) of the reaction of anthraquinone with acetylacetone and benzoylacetone were estimated by comparing the experimental cyclic voltammograms with the digitally simulated results.
- 1,4-Dihydroxyanthraquinone,
- Cyclic voltammetry,
- Digital simulation,
- Acetylacetone,
- Benzoylacetone
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沈阳化工大学材料科学与工程学院沈阳 110142