Reaction pathways of 2,2,2-trifluoroethylamine and n-butylamine with [Ru(bpy)2(NO)Cl]2+
作者:Florencia Di Salvo、Alejandro Crespo、Darı́o A. Estrin、Fabio Doctorovich
DOI:10.1016/s0040-4020(02)00382-4
日期:2002.5
The reaction of [Ru(bpy)2(NO)Cl]2+ with 2,2,2-trifluoroethylamine produced [Ru(bpy)2(NO)Cl]+ by electron transfer and a number of organic compounds formed via nucleophilic substitution of the intermediate 2,2,2-trifluoroethyldiazonium ion (free or coordinated). Density functional theory computed results suggest that stabilization of the trifluoroethyldiazonium ion by complexation is much larger than
[Ru(bpy)2(NO)Cl] 2+与2,2,2-三氟乙胺的反应通过电子转移产生[Ru(bpy)2(NO)Cl] +,并通过亲核取代形成许多有机化合物中间体2,2,2-三氟乙基重氮离子(游离的或配位的)。密度泛函理论计算结果表明,通过络合作用稳定的三氟乙基重氮离子比对应于丁基离子的稳定度大得多,这与没有观察到源自CF 3 CH 2 +的重排产物的事实相符。