Studying the electrochemical behavior of a smooth gold electrode in a solution of bridged 1,2,4-trioxalane in acetonitrile
- 作者: Polyakov M.V.1, Vedenyapina M.D.1, Skundin A.M.2, Yaryomenko I.A.1, Radulov P.S.1
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隶属关系:
- N. D. Zelinsky Institute of Organic Chemistry of the Russian Academy of Sciences
- A. N. Frumkin Institute of Physical Chemistry and Electrochemistry of the Russian Academy of Sciences
- 期: 卷 99, 编号 1 (2025)
- 页面: 153-160
- 栏目: ЭЛЕКТРОХИМИЯ. ГЕНЕРАЦИЯ И АККУМУЛИРОВАНИЕ ЭНЕРГИИ ИЗ ВОЗОБНОВЛЯЕМЫХ ИСТОЧНИКОВ
- ##submission.dateSubmitted##: 01.06.2025
- ##submission.datePublished##: 17.04.2025
- URL: https://clinpractice.ru/0044-4537/article/view/681878
- DOI: https://doi.org/10.31857/S0044453725010157
- EDN: https://elibrary.ru/EHQXIQ
- ID: 681878
如何引用文章
详细
The behavior of a smooth gold electrode in the medium of bridged 1,2,4-trioxalane in acetonitrile is studied by cyclic voltammetry and gravimetry methods. It is found that during the cathodic process, the reduction of the peroxide bond in the bridged 1,2,4-trioxalane molecule takes place at the electrode surface followed by the formation of a diketone moiety. During anodic oxidation, the formation of colloidal gold particles is detected.
全文:

作者简介
M. Polyakov
N. D. Zelinsky Institute of Organic Chemistry of the Russian Academy of Sciences
编辑信件的主要联系方式.
Email: SatPolyak@yandex.ru
俄罗斯联邦, Moscow, 119991
M. Vedenyapina
N. D. Zelinsky Institute of Organic Chemistry of the Russian Academy of Sciences
Email: SatPolyak@yandex.ru
俄罗斯联邦, Moscow, 119991
A. Skundin
A. N. Frumkin Institute of Physical Chemistry and Electrochemistry of the Russian Academy of Sciences
Email: SatPolyak@yandex.ru
俄罗斯联邦, Moscow, 119071
I. Yaryomenko
N. D. Zelinsky Institute of Organic Chemistry of the Russian Academy of Sciences
Email: SatPolyak@yandex.ru
俄罗斯联邦, Moscow, 119991
P. Radulov
N. D. Zelinsky Institute of Organic Chemistry of the Russian Academy of Sciences
Email: SatPolyak@yandex.ru
俄罗斯联邦, Moscow, 119991
参考
- Ann Casteel D. // Nat. Prod. Rep. 1999. V. 16. № 1. P. 55. https://doi.org/10.1039/A705725C
- Phillipson D.W., Rinehart K.L. Jr. // J. Am. Chem. Soc. 1983. V. 105. № 26. P. 7735–7736. https://doi.org/10.1039/A705725C
- Yaremenko I.A., Radulov P.S., Belyakova Y.Y. et al. // Chem. Europ. J. 2020. V. 26. № 21. P. 4734. https://doi.org/10.1002/chem.201904555
- Yaremenko I.A., Syromyatnikov M.Y., Radulov P.S. et al. // Molecules. 2020. V. 25. № 8. P. 1954. https://doi.org/10.3390/molecules25081954
- Panic G., Duthaler U., Speich B., Keiser J. // Int. J. Parasitol. Drugs Drug. Resist. 2014. V. 4. № 3. P. 185. https://doi.org/10.1016/j.ijpddr.2014.07.002
- Vil’ V.A., Yaremenko I.A., Ilovaisky A.I., Terent’ev A.O. // Synthesis and Reactions. Molecules. 2017. V. 22. № 11. P. 1881. https://doi.org/10.3390/molecules22111881
- Kiuchi F., Itano Y., Uchiyama N. et al. // J. Am. Pharm. Assoc. 2002. V. 65. № 4. P. 509. https://doi.org/10.1021/np010445g
- Wenzel D.G., Smith C.M. // J. Am. Pharm. Assoc. Am. Pharm. Assoc. 1958. V. 47. № 11. P. 792. https://doi.org/10.1002/jps.3030471109
- Herrmann L., Yaremenko I.A., Çapcı A. et al. // Chem. Med. Chem. 2022. V. 17. № 9. https://doi.org/10.1002/cmdc.202200005
- Coghi P., Yaremenko I.A., Prommana P. et al. // Ibid. 2022. V. 17. № 20. https://doi.org/10.1002/cmdc.202200328
- Slade D., Galal A.M., Gul W. et al. // Bioorg. Med. Chem. 2009. V. 17. № 23. P. 7949. https://doi.org/10.1016/j.bmc.2009.10.019
- Yaremenko I.A., Coghi P., Prommana P. et al. // Chem. Med. Chem 2020. V. 15. № 13. P. 1118–1127. https://doi.org/10.1002/cmdc.202000042
- Yaremenko I.A., Syroeshkin M.A., Levitsky D. et al. // Med. Chem. Res. 2017. V. 26. № 1. P. 170. https://doi.org/10.1007/s00044-016-1736-2
- Tiwari M.K., Chaudhary S. // Med. Res. Rev. 2020. V. 40. № 4. P. 1220. https://doi.org/10.1002/med.21657
- Uddin A., Chawla M., Irfan I. et al. // RSC Med. Chem. 2020. V. 12. № 1. P. 24. https://doi.org/10.1039/d0md00244e
- Woodley C.M., Amado P.S.M., Cristiano M.L.S., O’Neill P.M. // Med. Res. Rev. 2021. V. 41. № 6. P. 3062. https://doi.org/10.1002/med.21849
- Otoguro K., Iwatsuki M., Ishiyama A. et al. //Phytochem. 2011. V. 72. № 16. P. 2024. https://doi.org/10.1016/j.phytochem.2011.07.015
- Perry T.L., Dickerson A., Khan A.A. et al. // Tetrahedron. 2001. V. 57. № 8. P. 1483. https://doi.org/10.1016/S0040-4020(00)01134-0
- Kumar M., Gehlot P.S., Parihar D. et al. // Eur. Pol. J. 2021. V. 152. https://doi.org/10.1016/j.eurpolymj.2021.110448
- Lee M., Minoura Y. // J. Chem. Soc., Faraday Trans. 1978. V. 74. № 0. P. 1726. https://doi.org/10.1039/f19787401726
- Przybysz-Romatowska M., Haponiuk J., Formela K. // Polymers. 2020. V. 12. № 1. https://doi.org/10.3390/polym12010228
- Радулов П.С., Белякова Ю.Ю., Демина А.А. и др. // Изв. АН. Сер. Хим. 2019. Т. 68. № 6. С. 1289–1292. (Radulov P.S., Belyakova Y.Y., Demina A.A. et al. // Russ. Chem. Bull. 2019. V. 68. № 6. P. 1289. https://doi.org/10.1007/s11172-019-2555-7)
- Matsumoto A., Maruoka K. // Bull. Chem. Soc. Jpn. 2020. V. 94. № 2. P. 513. https://doi.org/10.1246/bcsj.20200321
- Gemki M., Taspinar Ö., Adler A. et al. // Org. Proc. Res. Dev. 2021. V. 25. № 12. P. 2747. https://doi.org/10.1021/acs.oprd.1c00364
- Zdvizhkov A., Terent’ev A., Radulov P. et al. // Tetrahedron Lett. 2016. V. 57. № 8. https://doi.org/10.1016/j.tetlet.2016.01.061
- Rountree E.S., McCarthy B.D., Eisenhart T.T., Dempsey J.L. // Inorg. Chem. 2014. V. 53. № 19. P. 9983.
- Savéant J.-M. // Advances in Physical organic chemistry. 2000. V. 35. P. 117. https://doi.org/10.1016/s0065-3160(00)35013-4
- Magri D.C., Workentin M.S. // Org. Biomol. Chem. 2008. V. 6. № 18. P. 3354. https://doi.org//10.1039/b809356c
- Yaremenko I.A., Coghi P., Prommana P. et al. // Chem. Med. Chem. 2020. V. 15. № 13. P. 1118. https://doi.org//10.1002/cmdc.202000042
- Magri D.C., Workentin M.S. // Molecules. 2014. V. 19. № 8. P. 11999. https://doi.org//10.3390/molecules190811999
- Magri D.C., Workentin M.S. // Chemistry. 2008. V. 14. № 6. P. 1698. https://doi.org//10.1002/chem.200701740
- Веденяпина М.Д., Симакова А.П., Платонов М.М. и др. // Журн. физ. химии. 2013. Т. 87. № 3. С. 418. (Vedenyapina M.D., Simakova A.P., Platonov M.M. et al. // Russ. J. Phys. Chem. https://doi.org//10.1134/S0036024413030333)
- Magri D.C., Donkers R.L., Workentin M.S. // J. Photochem. Photobiol., A. 2001. V. 138. № 1. P. 29. https://doi.org//10.1016/S1010-6030(00)00386-5
- Stringle D.L., Magri D.C., Workentin M.S. // Chemistry. 2010. V. 16. № 1. P. 178. https://doi.org//10.1002/chem.200902023
- Веденяпина М.Д., Скундин А.М., Виль В.А. и др. // Журн. физ. химии. 2020. Т. 94. № 4. С. 624–628. (Vedenyapina M.D., Skundin A.M., Vil’ V.A. et al. // Russ. J. Phys. Chem. https://doi.org//10.1134/S0036024420040238)
- Веденяпина М.Д., Скундин А.М., Виль В.А. и др. // Журн. физ. химии. 2021. Т. 95. № 1. С. 147–151. (Vedenyapina M.D., Skundin A.M., Vil’ V.A. et al. // Russ. J. Phys. Chem. https://doi.org//10.1134/S0036024421010313)
- Веденяпина М.Д., Виль В.А., Терентьев А.О., Веденяпин А.А. // Изв. АН. Сер. Хим. 2017. Т. 66. № 11. С. 2044–2047. (Vedenyapina M.D., Vil’ V.A., Terent’ev A.O., Vedenyapin A.A. // Russ. Chem. Bull. 2017. V. 66. № 11. С. 2044.)
- Поляков М.В., Веденяпина М.Д., Скундин А.М. и др. // Журн. физ. химии. 2023. Т. 97. № 7. C. 972. https://doi.org//10.31857/S0044453723070221 (Polyakov M.V., Vedenyapina M.D., Skundin A.M. et al. // Russ. J. Phys. Chem. V. 97. P. 1438. https://doi.org//10.1134/S0036024423070221)
- Batchelor-McAuley C., Compton R.G. // J. Electroan. Chem. 2012. V. 669. P. 73. https://doi.org//10.1016/j.jelechem.2012.01.016
- Salah N., Lanez T. // Int. Lett. Chem. Phys. Astron. 2013. V. 4. P. 37.
- Поляков М.В., Веденяпина М.Д., Скундин А.М. и др. // Изв. АН. Сер. хим. 2024. Т. 74. № 4. С. 863.
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