34527-56-5Relevant articles and documents
Two-electron oxidation of N,N,N′,N′-tetramethylphenylenediamine with a chromium(v) salen complex
Chaka, Gezahegn,Bakac, Andreja
body text, p. 318 - 321 (2009/04/19)
The oxidation of tetramethylphenylenediamine (TMPD) with (salen)Cr VO+ generates initially the 2-electron product TMPD 2+, followed by the reaction with excess TMPD to yield the radical cation, TMPD+. The kineti
Mechanism and Kinetics of the Photocatalyzed Oxidation of p-Phenylenediamines by Peroxydisulfate in the Presence of Tri-2,2'-bipyridylylruthenium(II)
Nickel, Ulrich,Chen, Yao-Hong,Schneider, Siegfried,Silva, Maria I.,Burrows, Hugh D.,Formosinho, Sebastiao J.
, p. 2883 - 2888 (2007/10/02)
The autocatalytic oxidation of p-phenylenediamines with peroxydisulfate can be strongly enhanced by irradiation in the presence of tri-2.2'-bipyridylylruthenium(II).Ru(bpy)32+ acts as photosensitizer and photocatalyst.First, Ru(bpy)33+ is formed by quenching excited Ru*(bpy)32+ with S2O82-.Then the ruthenium(III) complex oxidizes p-phenylenediamine.The resulting Ru(bpy)32+ can start the cycle again.The photocatalytic oxidation of N,N-diethyl-p-phenylenediamine as well as the dark reactions were studied with stopped-flow techniques.The mechanism of this complex reaction is discussed in detail.