On the Edge of the Known: Extremely Electron-Rich (Di)Carboranyl Phosphines

The syntheses of the first B9-connected carboranylphosphines (B9-Phos) featuring two carboranyl moieties as well as access to B9-Phos ligands with bulky electron-donating substituents, previously deemed unattainable, is reported. The electrochemical properties of the B9-Phos ligands were investigated, revealing the ability of the mesityl derivatives to form stabilized phosphoniumyl radical cations. The B9-Phos ligands display an extremely electron-releasing character surpassing that of alkyl phosphines and commonly used N-heterocyclic carbenes. This is demonstrated by their very small Tolman electronic parameters (TEPs) as well as extremely low P-Se coupling constants. Cone angles and buried volumes attest to the high steric demand exerted by the (di)carboranyl phosphines. The dicarboranyl phosphine Au-I complexes show superior catalytic performance in the hydroamination of alkynes compared to the monocarboranyl phosphine analogs.

Automated summary

The synthesis of B9-Phos ligands with two carboranyl moieties and bulky electron-donating substituents, previously deemed unattainable, is reported. The electrochemical properties of B9-Phos ligands were investigated, showing the ability of mesityl derivatives to form stabilized phosphoniumyl radical cations. The B9-Phos ligands possess a highly electron-releasing character surpassing that of alkyl phosphines and commonly used N-heterocyclic carbenes.