Influence of N -Substitution on the Formation and Oxidation of NHC-CAAC-Derived Triazaalkenes.

We have studied the effect of N-substitution on the course of the reaction of imidazolium triflate. The reaction of N-heterocyclic carbene with N-tBu-substituted pyrrolinium triflate afforded 2-(pyrrolidin-2-yl)-imidazolium triflate, 3(R). Treatment of 3(R) with potassium bis(trimethylsilyl)amide (KHMDS) leads to either the dealkylation product 4 or the deprotonation product, triazaalkene 5, depending on the N-substitution at the imidazolium moiety. Density functional studies using the B3LYP/TZVP setup have been employed to explore various pathways for the dealkylation reaction and the calculated energies support the dealkylation by a large energy margin compared to the deprotonatation process. Theoretical calculations revealed that dealkylation reaction is thermodynamically more favorable than deprotonation. The triazaalkene 5 could be oxidized by AgOTf to the corresponding radical cation 6 and dication 7 in-situ. While 6 and 7 could not be isolated, the formation of the former is inferred by electron paramagnetic resonance spectroscopy and its abstraction of a H-atom to afford 3(Me). Similarly, the formation of the dication 7 is inferred by its ready elimination of isobutylene affording 8.