Abstract

The synthesis of the digermyl and germylsilyl hydronium borates 7[B(C6F5)4] and 8[B(C6F5)4] is reported. Spectroscopic (IR, NMR) and structural data supported by the results of density functional calculations indicate in both cases a symmetric or almost symmetric E–H–E′ three-center–two-electron linkage (7, E = E′ = Ge; 8, E = Si, E′ = Ge). The [B(C6F5)4]− and the [HCB11H5Br6]− salts of both cations are active in catalytic hydrodefluorination reactions of alkyl and benzyl fluorides. No significant effect of the element atom E on the determined turnover numbers was found.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call