“…The former is a 12‐electron Rh III fragment that binds arenes (e.g., fluorobenzene) in an η 6 ‐manner, whereas the latter is formally a 12‐electron Rh III centre with a supporting C–C σ‐bond and an agostic C–H interaction. Although the [BAr Cl2 4 ] – anion was originally reported in the open literature by Pacey as the Cs + salt,10 with a refinement in the synthesis by Serwatowski and co‐workers in 2003,11 as far as we are aware it has not been utilised in organometallic chemistry to generate and stabilise potentially reactive metal cations 12. We believe that this anion will be of use to the organometallic and catalysis communities as well as those interested in the structural determination of cationic species given its ease of preparation, attractive solubility properties, lack of anion disorder in the solid‐state, comparable coordinating properties to C 6 H 5 F and [BAr F 4 ] – , and its expedient use in synthesis.…”