Neutral mesoionic carbenes (MICs) based on a 1,2,3-triazole core have had a strong impact on various branches of chemistry such as homogeneous catalysis, electrocatalysis, and photochemistry/photophysics. We present here the first general synthesis of anionic mesoionic carbenes (anMICs) based on a 1,2,3-triazole core and a borate backbone. The free anMIC is stable in solution under an inert atmosphere at low temperatures, and can be stored for several weeks. Analysis of donor properties shows that these anMICs are extremely strong σ-donors, bypassing the donor properties of strong donors such as MICs, NHCs, anionic NHCs and N-heterocyclic olefins. The room temperature conversion of the free anMICs leads to three equally interesting compound classes: an amide-coordinated borane based on a MIC-borane backbone, a polymeric triazolide and an amide-coordinated metallo-MIC-borane. The metallo-MIC-borane is an interesting precursor for the synthesis of further amide-coordinated MIC-borane compounds. Quantum chemical calculations have been used to elucidate the mechanism of transformation of the anMICs. Gold(I) complexes of the anMIC ligands are potent catalysts for the hydroamination of alkynes without the need for any additional reagents. We thus introduce three new categories of mesoionic compounds here with potential for different branches of chemistry and beyond.
