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Cyclic voltammetric behaviour of a stable nitrogen-centred free radical, N-[(4-nitrophenyl)thio]-2,4,6-tri-tert-butylphenylaminyl

โœ Scribed by Y. Miura; A. Yamamoto; M. Kinoshita


Book ID
103064066
Publisher
Elsevier Science
Year
1984
Tongue
English
Weight
154 KB
Volume
29
Category
Article
ISSN
0013-4686

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โœฆ Synopsis


Sincecyclicvottammetry is a useful method to evaluate the electron-donor and -acceptor properties of organic and inorganic compounds, it is ofconsiderable interest to study free radicals by this electrochemicat technique. However, the free radicals which can be studied by this technique are significantly limited owing to their wellknown transient properties[l J. This problem has been overcome in part by the use of a special technique [2].

In this paper we report the cyclic voltammetric behaviour of N-[(4-nitrophenyl)thioJ-2,4,6-tri-tertbutylphenylaminyl radical (I), which is interesting as a new class of isolable nitrogen-centred free radicals[3]. NHS NO2 2 EXPERIMENTAL N-[(4-Nitrophenyl)-2,4,6-tri-tert-butylphenylaminyl radical (1) and N-[ (6nitrophenyl)thioJ-2,4,dtri-tertbutylaniline (2) were prepared by our previously reported method[3]. Cyclic voltammetry and voltammetry at a rotating * Part 22 in the series "ESR Studies of Nitrogenentred


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โœ Y. Miura; A. Tanaka ๐Ÿ“‚ Article ๐Ÿ“… 1992 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 270 KB

Thloammyls (RN%') are an interesting family of persistent nitrogen-centred free radlcals[ 1] Quite recently, we reported preparation and lsolatlon of extremely persistent nitrogen-centred free radicals, N-(arylthlo)-2,4,6-trlphenylamhno radicals (1)[2] The radicals are not destroyed by atmosphenc ox