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Thionitrosyl radical

Dissociative ionization of [l,2,5]thiadiazolo[3,4-f][ l,2,5]thiadiazole 6 was found to be an efficient preparative route to in j// -generated thionitrosyl cyanide and its radical cation, both of which are stable and did not undergo unimolecular rearrangement under the reaction conditions. The [C,N2,S] ions were characterized by mass spectrometry (ml% 72) (see Section 10.05.3.2.2) <1997JST(418)209>. [Pg.224]

Fortunately, the —NS ligand has received only one name, thionitrosyl, which is used here. A radical name, rather than an anionic name, is used which follows the precedent set by the nitrosyl ligand itself. [Pg.118]


See other pages where Thionitrosyl radical is mentioned: [Pg.92]    [Pg.187]    [Pg.92]    [Pg.187]    [Pg.81]    [Pg.141]    [Pg.722]    [Pg.249]    [Pg.722]    [Pg.895]    [Pg.87]   


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