Issue 48, 2022

Aromaticity-enhanced reactivity of geminal frustrated Lewis pairs

Abstract

The presence of a cyclopropenimine moiety as the Lewis base partner in geminal frustrated Lewis pairs greatly enhances the reactivity of the system towards the activation of small molecules. This is mainly due to an increase of the aromaticity strength of this fragment during the activation reaction which results in a significant gain of stability ultimately leading to low barrier and high exergonic transformations.

Graphical abstract: Aromaticity-enhanced reactivity of geminal frustrated Lewis pairs

Supplementary files

Article information

Article type
Communication
Submitted
08 Apr 2022
Accepted
19 May 2022
First published
19 May 2022

Chem. Commun., 2022,58, 6801-6804

Aromaticity-enhanced reactivity of geminal frustrated Lewis pairs

J. J. Cabrera-Trujillo and I. Fernández, Chem. Commun., 2022, 58, 6801 DOI: 10.1039/D2CC02013K

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