๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Nitration of imidazoline-n-oxide nitroxides containing the aryl nitrone group

โœ Scribed by L.B. Volodarsky; I.A. Grigor'ev; L.N. Grigor'eva; I.A. Kirilyuk


Book ID
104234024
Publisher
Elsevier Science
Year
1984
Tongue
French
Weight
230 KB
Volume
25
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

โœฆ Synopsis


sitration of 4-aryl-3-imidazoline-3-oxide nitroxyl radicals leads to 4-nitroaryl-3-imidazoline-3-oxide nitroxides via oxammonium salts formation, the nitrone group being an ortho-para orientant.

3-Imidazoline nitroxyl radicals exceed all known radicals in stability to protic and Lewis acids '. This expands the pH range of media used for


๐Ÿ“œ SIMILAR VOLUMES


Dimerization of imidazoline nitroxide ra
โœ V.I. Gulin; S.A. Dikanov; Yu.D. Tsvetkov ๐Ÿ“‚ Article ๐Ÿ“… 1990 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 455 KB

This paper reports the dimerization of imidazdine nitroxides, containing alcohol groups in the second position, in frozen toluene. The parameters of dipole-dipole interaction of electron spins in dimers were determined using 2 mm EPR spectroscopy. A geometrical model for the dimers could be obtained