作者:Claudio Tonelli、Vito Tortelli
DOI:10.1016/0022-1139(93)02945-b
日期:1994.5
perfluoroalkanes in the presence of molecular halogens (Cl2, Br2, I2) has been studied. The clear-cut cleavage of the most hindered carbon-carbon bond and the trapping by halogens of the intermediate radicals so formed account for the product distribution. Kinetic measurements support a mechanism based on homolytic rupture of the perfluoroalkanes as the rate-determining step, followed by the fast reaction
研究了一些高度支化的全氟烷烃在分子卤素(Cl 2,Br 2,I 2)存在下的热分解。如此阻碍形成的最受阻碍的碳-碳键的清楚裂解和卤素的捕集导致了产物的分布。动力学测量结果支持了一种机制,该机制基于全氟烷烃的均相断裂作为速率确定步骤,然后是中间体与卤素的快速反应。