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Updated: Dec 18, 2025

Characterizing Lewis Pairs Using Titration Coupled with In Situ Infrared Spectroscopy
Published on: February 20, 2020
Lewis Acidity and Basicity: Another Measure of Carbene Reactivity
Trent H Stein1, Monica Vasiliu1, Anthony J Arduengo1
1Department of Chemistry and Biochemistry, The University of Alabama, Tuscaloosa, Alabama 35487-0336, United States.
Abstract:
The structural and energetic reactivities of various carbenes are evaluated against a standard electrophile (proton) and a standard nucleophile (fluoride). The proton and fluoride affinities of the carbenes studied provide an increased understanding of reactivity modes and mechanisms. General classification of carbenic reactivity as a singlet nucleophilic carbene or a singlet electrophilic carbene is facilitated by this present study, and a need for further classification means along the border between electrophilic and nucleophilic reactivity is considered. The results are based on electronic structure calculations at the composite correlated molecular orbital theory G3MP2 level.
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