19329-77-2Relevant academic research and scientific papers
Reactions of nitrosoarenes with nitrogen monoxide (nitric oxide) and nitrogen dioxide: Formation of diarylnitroxides
Astolfi, Paola,Carloni, Patricia,Damiani, Elisabetta,Greci, Lucedio,Marini, Milvia,Rizzoli, Corrado,Stipa, Pierluigi
, p. 3279 - 3285 (2008)
Nitrosoarenes react with nitrogen monoxide (nitric oxide) at room temperature and in aprotic media to afford the corresponding diarylnitroxides by the intermediate formation of N-nitrosoarylnitroxides. However, these latter spin adducts, in contrast with literature reports, have never been detected by us. N-nitrosophenylnitroxide is obtained only in the oxidation of the ammonium salt of N-nitrosophenylhydroxylamine (cupferron) with trace amounts of lead tetraacetate. However, it evolves with time to diphenylnitroxide, as demonstrated by following the reaction course in the ESR cavity. On a macroscale level, the reaction between nitrosobenzene and nitric oxide leads to the formation of N-nitrosodiphenylamine, 4-nitro-N-nitrosodiphenylamine, 4-nitrodiphenylamine and 4,4′-dinitrodiphenylamine, in addition to diphenylnitroxide. Diarylnitroxides are also obtained when nitrosoarenes react with small amounts of nitrogen dioxide; the mechanism of this reaction is proposed and discussed. The structure of 4-nitro-N-nitrosodiphenylamine was determined by X-ray analysis. Wiley-VCH Verlag GmbH & Co. KGaA, 2008.
