Deprotonation of hexaethyl-2,4-dicarba-nido-borane(8) 2 leads first to the hexaethyl-2,4-dicarbanido-borate(1 − ) 3, and further deprotonation, using BuLi/KO t Bu, gives the hexaethyl-2,4-dicarbanido-hexaborate(2 − ) 4. The reaction of 3 with FeCl 2 affords the commo-ferracarborane [Fe(Et 6 -2,4-C 2 B 4 H) 2 ] 5, and the analogous reaction of 4 leads to the anionic sandwich complex [Fe(Et 6 -2,4-C 2 B 4 ) 2 ] 2− 6 which can be protonated to give 5. The complex 5 contains two hydrido ligands, each bridging the iron and two boron atoms. Reactions were monitored and the products were characterised by 11 B NMR spectroscopy in solution. The geometries of the carboranes, the borates (all unsubstituted and permethyl-substituted) and the iron complexes (all unsubstituted) were optimised by DFT methods [B3LYP/6-311+G(d,p) or B3LYP/6-31+G(d)], and the relevant NMR data [chemical shifts δ B)] were calculated at the same level of theory.