Electrochemically initiated transformation of 4-nitrophenylhydroxylamine into 4,4′-dinitroazobenzene

Electrochemically initiated transformation of 4-nitrophenylhydroxylamine into 4,4′-dinitroazobenzene Full article

Journal

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

Output data

Year: 2011, Volume: 21, Number: 1, Pages: 26-28 Pages count : 3 DOI: 10.1016/j.mencom.2011.01.011

Authors

Syroeshkin Mikhail A. ¹ , Mikhalchenko Ludmila V. ¹ , Leonova Marina Yu. ¹ , Mendkovich Andrei S. ¹ , Rusakov Alexander I. ² , Gul’tyai Vadim P. ¹

Affiliations

1	N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 119991 Moscow, Russian Federation
2	P. G. Demidov Yaroslavl State University, 150000 Yaroslavl, Russian Federation

Based on controlled potential electrolysis and cyclic voltammetry, the chain reaction of 4,4′-dinitroazobenzene formation was shown to be initiated during the electrochemical reduction of 4-nitrophenylhydroxylamine in DMF.

Syroeshkin M.A. , Mikhalchenko L.V. , Leonova M.Y. , Mendkovich A.S. , Rusakov A.I. , Gul’tyai V.P.
Electrochemically initiated transformation of 4-nitrophenylhydroxylamine into 4,4′-dinitroazobenzene
Mendeleev Communications. 2011. V.21. N1. P.26-28. DOI: 10.1016/j.mencom.2011.01.011 WOS Scopus OpenAlex

Web of science:	WOS:000288411500011
Scopus:	2-s2.0-79951507356
OpenAlex:	W2039538405

DB	Citing
OpenAlex	10
Scopus	9
Web of science	9