Iron complexes bearing new silyl-NHC bidentate ligands were synthesised by treating Fe3(CO)12 with a mixture of N-(hydrosilyl)methyl imidazolium salts and a base. These complexes showed high performance in the catalytic double hydroboration of nitrile with pinacolborane (HBpin) to produce N,N-bis(boryl)amine by a combination of UV irradiation and mild heating (60 °C). The product yields for the hydroboration of aromatic and aliphatic nitriles reached 85%-95% (NMR) using an iron complex (5 mol%). Reducing the loading amount of the iron complex to 0.5 mol% still afforded the products in high yields. An analogous ruthenium complex, which was similarly synthesised using Ru3(CO)12, showed lower activity. Stoichiometric reactions of the iron complex with nitriles afforded Fe(0)-N-silylimine complexes, which may be dormant states in nitrile hydroboration. A catalytic mechanism including Fe(0) N-silylimine species is proposed.