Jump to content

Cobalt(II) iodide

From Wikipedia, the free encyclopedia
(Redirected from Cobalt diiodide)
Cobalt(II) iodide
Names
IUPAC name
Cobalt(II) iodide
Other names
cobaltous iodide, cobalt diiodide
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.035.697 Edit this at Wikidata
EC Number
  • 239-283-2
UNII
  • InChI=1S/Co.2HI/h;2*1H/q+2;;/p-2 ☒N
    Key: AVWLPUQJODERGA-UHFFFAOYSA-L ☒N
  • InChI=1/Co.2HI/h;2*1H/q+2;;/p-2
    Key: AVWLPUQJODERGA-NUQVWONBAD
  • [Co+2].[I-].[I-]
Properties
CoI2
Molar mass 312.7421 g/mol (anhydrous)
420.83 g/mol (hexahydrate)
Appearance α-form: black hexagonal crystal
β-form: yellow powder
Density α-form: 5.584 g/cm3
β-form: 5.45 g/cm3
hexahydrate: 2.79 g/cm3
Melting point α-form: 515-520 °C under vacuum
β-form: converts to α-form at 400 °C
Boiling point 570 °C (1,058 °F; 843 K)
67.0 g/100 mL[1]
+10,760·10−6 cm3/mol
Hazards
GHS labelling:
GHS07: Exclamation markGHS08: Health hazard
Warning
H302, H312, H315, H319, H332, H335
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 3: Short exposure could cause serious temporary or residual injury. E.g. chlorine gasFlammability 0: Will not burn. E.g. waterInstability 1: Normally stable, but can become unstable at elevated temperatures and pressures. E.g. calciumSpecial hazards (white): no code
3
0
1
Related compounds
Other anions
Cobalt(II) fluoride
Cobalt(II) chloride
Cobalt(II) bromide
Other cations
Nickel(II) iodide
Copper(I) iodide
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

Cobalt(II) iodide or cobaltous iodide are the inorganic compounds with the formula CoI2 and the hexahydrate CoI2(H2O)6. These salts are the principal iodides of cobalt.[2]

Synthesis

[edit]

Cobalt(II) iodide is prepared by treating cobalt powder with gaseous hydrogen iodide.[2] The hydrated form CoI2.6H2O can be prepared by the reaction of cobalt(II) oxide (or related cobalt compounds) with hydroiodic acid.

Cobalt(II) iodide crystallizes in two polymorphs, the α- and β-forms. The α-polymorph consists of black hexagonal crystals, which turn dark green when exposed to air. Under a vacuum at 500 °C, samples of α-CoI2 sublime, yielding the β-polymorph as a yellow crystals. β-CoI2 also readily absorbs moisture from the air, converting into green hydrate. At 400 °C, β-CoI2 reverts to the α-form.[2]

Structures

[edit]

The anhydrous salts adopt the cadmium halide structures.

The hexaaquo salt consists of separated [Co(H2O)6]2+ and iodide ions as verified crystallographically.[3][4]

Reactions and applications

[edit]

Anhydrous cobalt(II) iodide is sometimes used to test for the presence of water in various solvents.[5]

Cobalt(II) iodide is used as a catalyst, e.g. in carbonylations. It catalyzes the reaction of diketene with Grignard reagents, useful for the synthesis of terpenoids[6]

References

[edit]
  1. ^ Perry, Dale L.; Phillips, Sidney L. (1995), Handbook of Inorganic Compounds, San Diego: CRC Press, pp. 127–8, ISBN 0-8493-8671-3, retrieved 2008-06-03
  2. ^ a b c O. Glemser "Cobalt, Nickel" in Handbook of Preparative Inorganic Chemistry, 2nd Ed. Edited by G. Brauer, Academic Press, 1963, NY. Vol. 1. p. 1518.
  3. ^ “Structure Cristalline et Expansion Thermique de L’Iodure de Nickel Hexahydrate“ (Crystal structure and thermal expansion of nickel(II) iodide hexahydrate) Louër, Michele; Grandjean, Daniel; Weigel, Dominique Journal of Solid State Chemistry (1973), 7(2), 222-8. doi:10.1016/0022-4596(73)90157-6
  4. ^ "The crystal structure of the crystalline hydrates of transition metal salts. The structure of CoI2·6H2O" Shchukarev, S. A.; Stroganov, E. V.; Andreev, S. N.; Purvinskii, O. F. Zhurnal Strukturnoi Khimii 1963, vol. 4, pp. 63-6.<!no doi in CAS-->
  5. ^ Armarego, Wilfred L. F.; Chai, Christina L. L. (2003), Purification of Laboratory Chemicals, Butterworth-Heinemann, p. 26, ISBN 0-7506-7571-3, retrieved 2008-06-03
  6. ^ Agreda, V. H.; Zoeller, Joseph R. (1992), Acetic Acid and Its Derivatives, CRC Press, p. 74, ISBN 0-8247-8792-7, retrieved 2008-06-03