55570-28-0Relevant articles and documents
Reaction of 2,2-diphenylquinoline-nitroxide radicals with NO-releasing SIN-1 (3-morpholinosydnonimine)
Weber,Grzesiok,Korth,Sustmann
, p. 789 - 792 (1994)
The nitroxide radicals 1 are suitable traps for nitric oxide (NO·) released from SIN-1 under aerobic conditions. Besides the stable products 2, 3, and 4, the relatively unstable nitroxides 5 are formed in this reaction, the latter decomposing to the stabl
Oxidative Dimerization of Quinolinic Nitroxides in the Presence of Trichloro- and Trifluoro- Acetic Acid. Crystal Structures of 6,6'-bis-(1-oxide-1,2,6,8a-tetrahydroquinoline)ylidene and of 2,3-Diphenylquinoline
Carloni, Patricia,Daminani, Elisabetta,Greci, Lucedio,Stipa, Pierluigi,Rizzoli, Corrado,et al.
, p. 5099 - 5108 (2007/10/02)
Quinolinic nitroxides 1a-c react with trichloro- (TCA) and trifluoro- (TFA) acetic acid to give dimers 3a-c and 4a-c as the main products.Products 3a-c are explained as arising via the intermediate formation of the radical cation 5, which forms the final