Self-protonation upon the electroreduction of 2- and 4-nitrophenylhydroxylamines in aprotic media

Self-protonation upon the electroreduction of 2- and 4-nitrophenylhydroxylamines in aprotic media Full article

Journal

Mendeleev Communications
ISSN: 1364-551X , E-ISSN: 0959-9436

Output data

Year: 2009, Volume: 19, Number: 5, Pages: 258-259 Pages count : 2 DOI: 10.1016/j.mencom.2009.09.008

Authors

Syroeshkin Mikhail A. ¹ , Mendkovich Andrei S. ¹ , Mikhalchenko Ludmila V. ¹ , Rusakov Alexander I. ¹ , Gul’tyai Vadim P. ¹

Affiliations

1	N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 119991 Moscow, Russian Federation

Cyclic voltammetry and controlled potential electrolysis were used to show that radical anions of 2- and 4-nitrophenylhydroxylamines electrochemically generated in a 0.1 M Bu4NClO4 solution in DMF undergo protonation with the starting compounds (self-protonation) followed by the formation of the corresponding nitroanilines.

Syroeshkin M.A. , Mendkovich A.S. , Mikhalchenko L.V. , Rusakov A.I. , Gul’tyai V.P.
Self-protonation upon the electroreduction of 2- and 4-nitrophenylhydroxylamines in aprotic media
Mendeleev Communications. 2009. V.19. N5. P.258-259. DOI: 10.1016/j.mencom.2009.09.008 WOS Scopus OpenAlex

Web of science:	WOS:000271368800008
Scopus:	2-s2.0-70349318336
OpenAlex:	W2040590514

DB	Citing
OpenAlex	8
Scopus	9
Web of science	8