作者:P. Miles、H. Suschitzky
DOI:10.1016/s0040-4020(01)99291-9
日期:1962.1
Decomposition of acylarylnitrosamines in benzene produces not only free radicals as is well recognized, but also intermediate ion pairs. The generality of this dual mechanism is experimentally demonstrated by use of nucleophilically activated fluorine as a ‘label’. The appearance of acylfluoride in the reaction products from fluorine substituted acylarylnitrosamines is interpreted.
苯中的酰基芳基亚硝胺的分解不仅产生众所周知的自由基,而且还会产生中间离子对。通过使用亲核活化的氟作为“标记”,实验证明了这种双重机理的普遍性。解释了在氟取代的酰基芳基亚硝胺的反应产物中酰基氟的出现。