Iron tetracarbonyl dihydride

Iron tetracarbonyl dihydride was first produced by Hieber and Leutert from iron pentacarbonyl, which is first converted to HFe(CO): :Fe(CO)5 + 2 OH− → HFe(CO) + HCO :HFe(CO) + H+ → H2Fe(CO)4 Since the compound is thermally labile and sensitive to light, ideal conditions in 1930's Munich called for winter nights. The early method was called the "polar night synthesis." As recommended by Hieber and Leutert, the compound can be purified by trap-to-trap distillation. == Structure and properties ==

In iron tetracarbonyl hydride the Fe(CO)4 group has C2v molecular symmetry with a geometry intermediate between octahedral and tetrahedral. Viewed as an octahedral complex, the hydride ligands are cis. Viewed as a tetrahedral Fe(CO)4 complex, the hydrides occupy adjacent faces of the tetrahedron. Although the structure of tetracarbonyliron with the hydrogen atoms bound as a single H2 ligand has been proposed as an intermediate in some rearrangement reactions, the stable state for the compound has the two atoms as independent ligands. == Reactions ==

Iron tetracarbonyl dihydride undergoes rapid ligand substitutions by phosphorus ligands: :H2Fe(CO)4 + PPh3 → H2Fe(CO)3PPh3 The substitution mechanism is proposed to entail transient formation of a 16e− formyl intermediate. H2Fe(CO)4 has pK1 of 6.8 and pK2 of 15. The Potassium tetracarbonyliron hydride|monoanion [HFe(CO)4]− has more extensive reaction chemistry because it is more stable than the dihydride. The monoanion is an intermediate in the homogeneous iron-carbonyl-catalyzed water-gas shift reaction (WGSR). The slow step in the WGSR is the proton transfer from water to the iron hydride anion. :HFe(CO) + H2O → H2Fe(CO)4 + OH− ==See also==