In this Communication, we report an intramolecular C-H bond amination reaction of a dipyrromethene ferrous complex with organic azides. Monitoring of the spectral changes (variable temperature NMR and UV-vis) of the FeII complex reveals no buildup of an intermediate during conversion of the starting material into the nitrene-inserted product. The rate-determining step appears to be azide addition to the 14-electron FeII complex, hinting at the potential that these and related platforms may have to effect atom and group-transfer processes.Chemistry and Chemical BiologyVersion of Recor
Is data on this page outdated, violates copyrights or anything else? Report the problem now and we will take corresponding actions after reviewing your request.