Issue 19, 2017

Rational design of Fe catalysts for olefin aziridination through DFT-based mechanistic analysis

Abstract

Nitrene transfer reactions are increasingly used to access various kinds of amine derivatives but the underlying mechanisms have not been unraveled in most cases. Fe-catalyzed aziridination of alkenes has appeared as a promising route to aziridines which are important derivatives both per se and as intermediates in many synthetic procedures. We report the strong activity and the mechanism of di-iron catalysts for aziridination of styrenes using phenyltosyliodinane (PhI[double bond, length as m-dash]NTs). In addition, we have developed a similar mono-iron catalyst which operates under the same mechanism albeit with a reduced activity. DFT calculations were performed to investigate the structure and electronic structure of the FeIVNTs species of the latter catalyst. They suggest that the reaction pathway leading to the nitrene transfer to the olefin involves a transient charge transfer on the way to a radical intermediate, which is totally consistent with the experimental results. Moreover, these calculations identify the electron affinity (EA) of the active species as one key parameter allowing rationalization of the observations, which opens the way to improving the catalyst efficiency on a rational basis.

Graphical abstract: Rational design of Fe catalysts for olefin aziridination through DFT-based mechanistic analysis

Supplementary files

Article information

Article type
Paper
Submitted
27 6 2017
Accepted
23 8 2017
First published
12 9 2017

Catal. Sci. Technol., 2017,7, 4388-4400

Rational design of Fe catalysts for olefin aziridination through DFT-based mechanistic analysis

R. Patra, G. Coin, L. Castro, P. Dubourdeaux, M. Clémancey, J. Pécaut, C. Lebrun, P. Maldivi and J. Latour, Catal. Sci. Technol., 2017, 7, 4388 DOI: 10.1039/C7CY01283G

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