Two-electron reduction of carbene-supported 9-bromo-9-borafluorenes with excess KC8 , Na, or Li-naphthalenide affords six N-heterocyclic carbene (NHC)- or cyclic(alkyl)(amino) carbene (CAAC)-stabilized borafluorene anions (3-8)-the first isolated and structurally authenticated examples of the elusive 9-carbene-9-borafluorene monoanion. The electronic structure, bonding, and aromaticity of the boracyclic anions were comprehensively investigated via computational studies. Compounds 5 and 8 react with metal halides via salt elimination to give new B-E (E=Au, Se, Ge)-containing materials (9-12). Upon reaction with diketones, the carbene ligand cleanly dissociates from 5 or 8 to yield new B-O containing spirocycles (13-14) that cannot be easily obtained using "normal" valent borafluorene compounds. Collectively, these results support the notion that carbene-stabilized monoanionic borafluorenes may serve as a new platform for the one-step construction of higher-value boracyclic materials.
Keywords: borafluorene; boron; boryl anions; carbenes; nucleophilic substitution.
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