【摘要】 用量子化学DFT方法在B3LYP/3-21G*水平下研究了2-氯吡啶气相光氯化取代反应生成2,3-二氯吡啶、2,4-二氯吡啶、2,5-二氯吡啶和2,6-二氯吡啶不同产物的过渡态,并计算了活化能.结果表明,生成2,6-二氯吡啶过渡态的能量最低,所需的活化能也最低,反应优先生成2,6-二氯吡啶.生成2,6-二氯吡啶的IRC结果显示反应过程中C—H键的断裂和C—C l键的生成协同但不同步.过渡态的构型接近于产物,是一个晚期过渡态.C l原子在反应进程中是给电子的,因此,氯自由基与2-氯吡啶反应是亲核取代的SN2机理.更多还原

【Abstract】 The gas phase reaction mechanism of the photochemical chlorination of 2-chloropyridine was theoretically studied by using DFT B3LYP/3-21G~* method.The activation energy leading to 2,3-dichloropyridine,2,4-dichloropyridine,2,5-dichloropyridine and 2,6-dichloropyridine were also calculated respectively.The calculated results consistently show that the energy of transition state and the activation energy for the formation of 2,6-dichloropyridine were the lowest among the four reaction pathways.Therefore,the main product should be 2,6-dichloropyridine.The IRC result showed that the breaking of C—H and the forming of C—Cl were concerted but not synchronous.The structure of the transition state was near to 2,6-dichloropyridine,which showed that it was a late transition state.During the whole reaction processing,the Cl· acted as a nucleophilic specie,donating the electron.Therefore,S_N2 mechanism was speculated for the reaction of Cl· with 2-chloropyridine.更多还原