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.

Graphical abstract: Accessing chiral NHC-boranes by abstraction of C6F5 from the B(C6F5)4− weakly coordinating anion

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Article information

Article type
Communication
Submitted
05 Dec 2025
Accepted
06 May 2026
First published
03 Jun 2026
This article is Open Access
Creative Commons BY-NC license

Dalton Trans., 2026, Advance Article

Accessing chiral NHC-boranes by abstraction of C6F5 from the B(C6F5)4 weakly coordinating anion

N. Niessen, A. I. Adjieufack, N. Tumanov, J. Wouters, B. Champagne, G. Berionni and K. Bijouard, Dalton Trans., 2026, Advance Article , DOI: 10.1039/D5DT02919H

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