Accessing chiral NHC-boranes by abstraction of C6F5 from the B(C6F5)4− weakly coordinating anion
Abstract
The prolonged heating of an N-heterocyclic carbene-stabilised borenium cation resulted in the abstraction of a –C6F5 group from its B(C6F5)4− counter-anion. The resulting new chiral NHC-boranes presented an unusual cis/trans isomerism around the newly formed plane. The corresponding borenium cation, due to its Lewis superacidity, is a potentially interesting new chiral organocatalyst.

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