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Mendeleev Communications, 2012, Volume 22, Issue 2, Pages 111–113
DOI: https://doi.org/10.1016/j.mencom.2012.03.021
(Mi mendc2758)
 

This article is cited in 4 scientific papers (total in 4 papers)

Electrochemical reduction and radical anions of benzo[b]thioxanthene-6,11,12-trione and thioxanthene-1,4,9-trione

N. V. Vasilieva, I. G. Irtegova, V. A. Loskutov, L. A. Shundrin

N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russian Federation
Full-text PDF (784 kB) Citations (4)
Abstract: The electrochemical reduction of benzo[b]thioxanthene-6,11,12-trione and thioxanthene-1,4,9-trione in DMSO, MeCN and HMPA is an EE process, which is characterized by two separate one electron reversible peaks on cyclic voltammograms, first peak retains reversibility in DMSO–H2O mixtures, corresponding radical anions were obtained by one electron reduction of the above compounds and characterized by EPR and DFT calculations at the (U)B3LYP/6-31+G* level of theory.
Keywords: thioxanthenes, electrochemical reduction, cyclic voltammetry, radical anions.
Document Type: Article
Language: English


Citation: N. V. Vasilieva, I. G. Irtegova, V. A. Loskutov, L. A. Shundrin, “Electrochemical reduction and radical anions of benzo[b]thioxanthene-6,11,12-trione and thioxanthene-1,4,9-trione”, Mendeleev Commun., 22:2 (2012), 111–113
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  • https://www.mathnet.ru/eng/mendc2758
  • https://www.mathnet.ru/eng/mendc/v22/i2/p111
  • This publication is cited in the following 4 articles:
    1. I. K. Shundrina, I. A. Os'kina, D. S. Odintsov, A. A. Gismatulin, I. A. Azarov, L. A. Shundrin, V. A. Gritsenko, “Octafluorobiphenyl-4,4'-diyl 9-oxothioxanthene-1,4-diyl polyether – a promising material for organic film based memristors: synthesis, memristive effect and charge transport mechanism”, Mendeleev Commun., 34:5 (2024), 667–669  mathnet  crossref
    2. Danila S. Odintsov, Irina A. Os'kina, Irina G. Irtegova, Leonid A. Shundrin, “Electrochemical Reduction of 1H‐Thioxanthene‐1,4,9‐trione and 3‐Methyl‐1H‐thioxanthene‐1,4,9‐trione – Representatives of a New Class of Heterocycles Related to Thioxanthenone”, Eur J Org Chem, 26:33 (2023)  crossref
    3. Nuno R. Candeias, Alexander Efimov, Comprehensive Heterocyclic Chemistry IV, 2022, 512  crossref
    4. N. V. Vasilieva, I. G. Irtegova, V. A. Loskutov, L. A. Shundrin, “Redox properties and radical anions of 2-substituted thioxanthen-9-ones and their 2-methyl S-oxide derivatives”, Mendeleev Commun., 23:6 (2013), 334–336  mathnet  crossref
    Citing articles in Google Scholar: Russian citations, English citations
    Related articles in Google Scholar: Russian articles, English articles
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