作者:Michael Spittler、Lucas Helmecke、Constantin Czekelius
DOI:10.1002/ejoc.201800866
日期:2019.1.23
The frustrated Lewis pair‐catalyzed iodoperfluoroalkylation of olefins, its substrate activation mode, and catalyst degradation pathways are mechanistically investigated by kinetic measurements. The transformation most likely proceeds via coordination of the phosphane to the perfluoroalkyl iodide and involves radical intermediates.
通过动力学测量机制研究了受挫的路易斯对催化的烯烃碘全氟烷基化反应,其底物活化方式和催化剂降解途径。该转化最可能通过膦与全氟烷基碘的配位而进行,并涉及自由基中间体。