Iron(II) bromide


Iron(II) bromide
Iron(II) bromide
IUPAC name
Iron(II) bromide
Other names
Ferrous bromide
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3D model (JSmol)
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ECHA InfoCard 100.029.244 Edit this at Wikidata
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  • DTXSID80976870 Edit this at Wikidata
  • InChI=1S/2BrH.Fe/h2*1H;/q;;+2/p-2 checkY
  • InChI=1/2BrH.Fe/h2*1H;/q;;+2/p-2
  • [Fe+2].[Br-].[Br-]
Molar mass 215.65 g mol−1
Appearance yellow-brown solid
Density 4.63 g cm−3, solid
Melting point 684 °C (1,263 °F; 957 K) (anhydrous)
27 °C (Hexahydrate)
Boiling point 934 °C (1,713 °F; 1,207 K)
117 g / 100 ml
Solubility in other solvents THF, methanol, ethanol
+13,600·10−6 cm3/mol
Rhombohedral, hP3, SpaceGroup = P-3m1, No. 164
Main hazards none
R-phrases (outdated) R20 R36/37/38
S-phrases (outdated) S26 S36
Related compounds
Other anions
Iron(II) chloride
Other cations
iron(III) bromide
Related compounds
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Iron(II) bromide is an inorganic compound with the chemical formula FeBr2. The anhydrous compound is a yellow or brownish-colored paramagnetic solid. Several hydrates of FeBr2 are also known, all being pale colored solids. It is a common precursor to other iron compounds in research laboratory, but no applications exist for this compound.


Like most metal halides, FeBr2 adopts a polymeric structure consisting of isolated metal centers cross-linked with halides. It crystallizes with the CdI2 structure, featuring close-packed layers of bromide ions, between which are located Fe(II) ions in octahedral holes.[1] The packing of the halides is slightly different from that for FeCl2, which adopts the CdCl2 motif.

Synthesis and reactions

FeBr2 is synthesized using a methanol solution of concentrated hydrobromic acid and iron powder. It adds the methanol solvate [Fe(MeOH)6]Br2 together with hydrogen gas. Heating the methanol complex in a vacuum gives pure FeBr2.[2]

FeBr2 reacts with two equivalents of tetraethylammonium bromide to give [(C2H5)4N]2FeBr4.[3] FeBr2 reacts with bromide and bromine to form the intensely colored, mixed-valence species [FeBr3Br9].[4]


FeBr2 possesses a strong metamagnetism at 4.2 K and has long been studied as a prototypical metamagnetic compound.[5][6]


  1. ^ Haberecht, J.; Borrmann, Η.; Kniep, R. (2001). "Refinement of the crystal structure of iron dibromide, FeBr2". Zeitschrift für Kristallographie - New Crystal Structures. 216 (1–4). doi:10.1524/ncrs.2001.216.14.544.
  2. ^ Winter, G. (1973). "Iron(II) Halides". Inorganic Syntheses. Inorganic Syntheses. 14. pp. 99–104. doi:10.1002/9780470132456.ch20. ISBN 9780470132456.
  3. ^ N. S. Gill, F.. B. Taylor Inorganic Syntheses 1967, volume 9, page 136-142. doi: 10.1002/9780470132401.ch37
  4. ^ Holleman, A. F.; Wiberg, E. "Inorganic Chemistry" Academic Press: San Diego, 2001. ISBN 0-12-352651-5
  5. ^ Wilkinson, M. K.; Cable, J. W.; Wollan, E. O.; Koehler, W. C. (15 January 1959). "Neutron Diffraction Investigations of the Magnetic Ordering in FeBr2, CoBr2, FeCl2, and CoCl2". Physical Review. 113 (2): 497–507. Bibcode:1959PhRv..113..497W. doi:10.1103/PhysRev.113.497.
  6. ^ Jacobs, I. S.; Lawrence, P. E. (10 December 1967). "Metamagnetic Phase Transitions and Hysteresis in FeCl2". Physical Review. 164 (2): 866–878. Bibcode:1967PhRv..164..866J. doi:10.1103/PhysRev.164.866.