Williams D L
Department of Chemistry, University of Durham, United Kingdom.
Nitric Oxide. 1997;1(6):522-7. doi: 10.1006/niox.1997.0159.
The reagents capable of effecting electrophilic and free radical nitrosation are briefly reviewed, together with the appropriate mechanisms, and in the light of these findings the possibilities of peroxynitrite/peroxynitrous acid acting as a nitrosating species are considered. The conclusion is that it is not to be expected that conventional direct nitrosation would occur. However, the very low yields of some nitrosation products can be accounted for in terms of nitrosation via the nitrogen oxide decomposition products of peroxynitrite. Thus NO could react with a radical substrate, or be converted to N2O3 (a well-known nitrosating species), whereas NO2 if formed can nitrosate via N2O4. A short post-script is added reviewing the Cu+-mediated reaction of S-nitrosothiols, generating (at low [thiol]) nitric oxide.
本文简要综述了能够引发亲电亚硝化反应和自由基亚硝化反应的试剂及其相应机理,并基于这些研究结果探讨了过氧亚硝酸根/过氧亚硝酸作为亚硝化剂的可能性。结论是,传统的直接亚硝化反应不太可能发生。然而,某些亚硝化产物的极低产率可以通过过氧亚硝酸根分解产生的氮氧化物进行亚硝化来解释。因此,一氧化氮可以与自由基底物反应,或转化为三氧化二氮(一种著名的亚硝化剂),而如果生成二氧化氮,则可以通过四氧化二氮进行亚硝化。最后补充了一个简短的后记,回顾了铜离子介导的S-亚硝基硫醇反应,(在低[硫醇]浓度下)生成一氧化氮。