том 168 издание 5 страницы 55501

Substituted o-Aminophenols as Redox-Mediators in the Thiol Oxidation to Unsymmetrical Disulfides

Тип публикацииJournal Article
Дата публикации2021-05-01
scimago Q1
wos Q2
БС1
SJR0.774
CiteScore6.1
Impact factor3.3
ISSN00134651, 19457111
Materials Chemistry
Surfaces, Coatings and Films
Electronic, Optical and Magnetic Materials
Electrochemistry
Condensed Matter Physics
Renewable Energy, Sustainability and the Environment
Краткое описание

A number of substituted o-aminophenols has been investigated as redox mediators of the thiol oxidation to disulfides. The electrooxidation of o-aminophenols leads to the corresponding o-iminobenzoquinones. These compounds react with thiols in the solution with a formation of disulfides. It was established that the use of 4,6-di-tert-butyl-2-(tert-butylamino)phenol as a redox mediator can reduce the overpotential of the thiol oxidation by 0.2–1.4 V depending on the nature of the coupling thiols. The unsymmetrical disulfides with alkyl, aryl, and heteroaryl substituents were obtained as the result of the indirect electrosynthesis.

Найдено 
Найдено 

Топ-30

Журналы

1
2
Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya
2 публикации, 22.22%
Journal of the Electrochemical Society
1 публикация, 11.11%
Chemistry Letters
1 публикация, 11.11%
Journal of Electroanalytical Chemistry
1 публикация, 11.11%
Chimica Techno Acta
1 публикация, 11.11%
ChemistrySelect
1 публикация, 11.11%
Chinese Journal of Chemistry
1 публикация, 11.11%
Chemical Engineering and Processing: Process Intensification
1 публикация, 11.11%
1
2

Издатели

1
2
Elsevier
2 публикации, 22.22%
Wiley
2 публикации, 22.22%
Pleiades Publishing
2 публикации, 22.22%
The Electrochemical Society
1 публикация, 11.11%
The Chemical Society of Japan
1 публикация, 11.11%
Ural Federal University
1 публикация, 11.11%
1
2
  • Мы не учитываем публикации, у которых нет DOI.
  • Статистика публикаций обновляется еженедельно.

Вы ученый?

Создайте профиль, чтобы получать персональные рекомендации коллег, конференций и новых статей.
Метрики
9
Поделиться
Цитировать
ГОСТ |
Цитировать
Burmistrova D. A. et al. Substituted o-Aminophenols as Redox-Mediators in the Thiol Oxidation to Unsymmetrical Disulfides // Journal of the Electrochemical Society. 2021. Vol. 168. No. 5. p. 55501.
ГОСТ со всеми авторами (до 50) Скопировать
Burmistrova D. A., Galustyan A., Smolyaninov I. V., Berberova N. T. Substituted o-Aminophenols as Redox-Mediators in the Thiol Oxidation to Unsymmetrical Disulfides // Journal of the Electrochemical Society. 2021. Vol. 168. No. 5. p. 55501.
RIS |
Цитировать
TY - JOUR
DO - 10.1149/1945-7111/abfe43
UR - https://iopscience.iop.org/article/10.1149/1945-7111/abfe43
TI - Substituted o-Aminophenols as Redox-Mediators in the Thiol Oxidation to Unsymmetrical Disulfides
T2 - Journal of the Electrochemical Society
AU - Burmistrova, Daria A.
AU - Galustyan, Andrey
AU - Smolyaninov, Ivan V.
AU - Berberova, N. T.
PY - 2021
DA - 2021/05/01
PB - The Electrochemical Society
SP - 55501
IS - 5
VL - 168
SN - 0013-4651
SN - 1945-7111
ER -
BibTex |
Цитировать
BibTex (до 50 авторов) Скопировать
@article{2021_Burmistrova,
author = {Daria A. Burmistrova and Andrey Galustyan and Ivan V. Smolyaninov and N. T. Berberova},
title = {Substituted o-Aminophenols as Redox-Mediators in the Thiol Oxidation to Unsymmetrical Disulfides},
journal = {Journal of the Electrochemical Society},
year = {2021},
volume = {168},
publisher = {The Electrochemical Society},
month = {may},
url = {https://iopscience.iop.org/article/10.1149/1945-7111/abfe43},
number = {5},
pages = {55501},
doi = {10.1149/1945-7111/abfe43}
}
MLA
Цитировать
Burmistrova, Daria A., et al. “Substituted o-Aminophenols as Redox-Mediators in the Thiol Oxidation to Unsymmetrical Disulfides.” Journal of the Electrochemical Society, vol. 168, no. 5, May. 2021, p. 55501. https://iopscience.iop.org/article/10.1149/1945-7111/abfe43.