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Mechanism of electrochemical oxidation of 1-chloro-2,2,6,6-tetramethylpiperidine
Authors:Kagan  E. Sh.  Yanilkin  V. V.  Morozov  V. I.  Nastapova  N. V.  Zhukova  I. Yu.  Kashparov  I. I.  Kashparova  V. P.
Affiliation:(1) South-Russian State Technical University (Novocherkassk Polytechnical Institute), ul. Prosveshcheniya 132, Novocherkassk, 346421, Russia;(2) Arbuzov Institute of Organic and Physical Chemistry, Kazan Research Center, Russian Academy of Sciences, ul. Arbuzova 8, Kazan, 420088, Tatarstan, Russia
Abstract:

In contrast to 2,2,6,6-tetramethylpiperidine and other aliphatic amines, at the electrochemical oxidation of 1-chloro-2,2,6,6-tetramethylpiperidine a sufficiently stable cation-radical is formed. Its formation is confirmed by the data of cyclic voltammetry and electron paramagnetic resonance. Further transformation of the cation-radical leads to the formation of 2,2,6,6-tetramethylpiperidin-1-oxyl.

Keywords:
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