|
This article is cited in 4 scientific papers (total in 4 papers)
Acid-catalysed degradation of the organomercury intermediates of pentafluorophenylmercury bromide reduction near a mercury electrode
V. A. Kurmaza, A. B. Ershlerb a Institute of Problems of Chemical Physics, Russian Academy of Sciences, Chernogolovka, Moscow Region, Russian Federation
b A.N. Frumkin Institute of Physical Chemistry and Electrochemistry, Russian Academy of Sciences, Moscow, Russian Federation
Abstract:
The acid-catalysed protolysis of intermediates, formed either during one-electron reduction of substituted arylmercury salt (C6F5HgBr) or by the adsorption of bis(arylalkynyl)mercury compound [(PhC≡C)2Hg] on a Hg electrode has been found in lowacidic media (3 < pH < 6), whereas it was not observed in alkylmercury salt (PrnHgOAc).
Citation:
V. A. Kurmaz, A. B. Ershler, “Acid-catalysed degradation of the organomercury intermediates of pentafluorophenylmercury bromide reduction near a mercury electrode”, Mendeleev Commun., 16:4 (2006), 234–237
Linking options:
https://www.mathnet.ru/eng/mendc3602 https://www.mathnet.ru/eng/mendc/v16/i4/p234
|
|