Brotzel Frank, Kempf Bernhard, Singer Thomas, Zipse Hendrik, Mayr Herbert
Department Chemie und Biochemie, Ludwig-Maximilians-Universität München, Butenandtstr. 5-13 (Haus F), 81377 München, Germany.
Chemistry. 2007;13(1):336-45. doi: 10.1002/chem.200600941.
Rate and equilibrium constants for the reactions of pyridines with donor-substituted benzhydrylium ions have been determined spectrophotometrically. The correlation equation log k(20 degrees C)=s(N+E), in which s and N are nucleophile-specific parameters and E is an electrophile-specific parameter, has been used to determine the nucleophilicity parameters of various pyridines in CH(2)Cl(2) and aqueous solution and to compare them with N of other nucleophiles. It is found that the nucleophilic organocatalyst 4-(dimethylamino)pyridine (DMAP) and tertiary phosphanes have comparable nucleophilicities and carbon basicities despite widely differing Brønsted basicities. For that reason, these reactivity parameters are suggested as guidelines for the development of novel organocatalysts. The Marcus equation is employed for the determination of the intrinsic barriers of these reactions.
已通过分光光度法测定了吡啶与供体取代的二苯甲基正离子反应的速率常数和平衡常数。相关方程log k(20℃)=s(N+E)(其中s和N是亲核试剂特异性参数,E是亲电试剂特异性参数)已用于确定各种吡啶在二氯甲烷和水溶液中的亲核性参数,并将它们与其他亲核试剂的N进行比较。结果发现,尽管布朗斯特碱度差异很大,但亲核有机催化剂4-(二甲氨基)吡啶(DMAP)和叔膦具有相当的亲核性和碳碱性。因此,建议将这些反应性参数作为开发新型有机催化剂的指导原则。采用马库斯方程来确定这些反应的本征势垒。