Iron tetracarbonyl dihydride

Iron tetracarbonyl dihydride is the organometallic compound with the formula H₂Fe(CO)₄. This compound was the first transition metal hydride discovered. The complex is stable at low temperatures but decomposes rapidly at temperatures above –20 °C.^[1]

Iron tetracarbonyl dihydride

Names
Preferred IUPAC name Tetracarbonyldihydridoiron(II)[citation needed]
Other names Iron tetracarbonyl dihydride, tetracarbonyldihydroiron
Identifiers
CAS Number	12002-28-7 Y
3D model (JSmol)	Interactive image
ChemSpider	452380 N
PubChem CID	518470
InChI InChI=1S/4CO.Fe.2H/c4*1-2;;; N Key: WZSHZFPIRKSPBD-UHFFFAOYSA-N N
SMILES O=C=[FeH2](=C=O)(=C=O)=C=O
Properties
Chemical formula	FeC 4H 2O 4
Molar mass	169.901 g mol−1
Appearance	Liquid (at -20 °C)
Melting point	−70 °C (−94 °F; 203 K)
Boiling point	−20 °C (−4 °F; 253 K) (decomposes)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N verify (what is YN ?) Infobox references

Preparation

Iron tetracarbonyl dihydride was first produced by Hieber and Leutert from iron pentacarbonyl, which is first converted to HFe(CO)⁻
₄:^[2][3]

Fe(CO)₅ + 2 OH⁻ → HFe(CO)⁻
₄ + HCO⁻
₃

HFe(CO)⁻
₄ + 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.^[1][4]

Structure and properties

In iron tetracarbonyl hydride the Fe(CO)₄ group has C_2v 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.^[5] 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,^[6] the stable state for the compound has the two atoms as independent ligands.^[7]

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.^[8]

H₂Fe(CO)₄ has pK₁ of 6.8 and pK₂ of 15.^[9] The monoanion [HFe(CO)₄]⁻ has more extensive reaction chemistry because it is more stable than the dihydride.^[10][11] 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.^[12]

HFe(CO)⁻
₄ + H₂O → H₂Fe(CO)₄ + OH⁻

See also

• Potassium tetracarbonyliron hydride
• Collman's reagent

Further reading

• Tsai, J.-C.; Khan, M.A.; Nicholas, K.M. (1991). "Reduction of Coordinated Carbon Dioxide by Transition-Metal Hydrides". Organometallics. 10: 29–30. doi:10.1021/om00047a016.
• Farmery, K.; Kilner, M. (1970). "Substitution reactions of dihydridotetracarbonyliron". Journal of the Chemical Society A: 634. doi:10.1039/J19700000634.