Jump to content

Cobalt(II) cyanide

From Wikipedia, the free encyclopedia
Cobalt(II) cyanide
Names
IUPAC name
Cobalt(II) cyanide
Other names
cobaltous cyanide
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.008.028 Edit this at Wikidata
UNII
  • InChI=1S/2CN.Co/c2*1-2;/q2*-1;+2 checkY
    Key: CWZOMTYLSNXUEL-UHFFFAOYSA-N checkY
  • InChI=1/2CN.Co/c2*1-2;/q2*-1;+2
    Key: CWZOMTYLSNXUEL-UHFFFAOYAR
  • [Co+2].[C-]#N.[C-]#N
Properties
Co(CN)2
Molar mass 110.968 g/mol (anhydrous)
147.00 g/mol (dihydrate)
165.02 g/mol (trihydrate)
Appearance deep-blue powder
hygroscopic (anhydrous)
reddish-brown powder (dihydrate)
Density 1.872 g/cm3 (anhydrous)
Melting point 280 °C (536 °F; 553 K) (anhydrous)
insoluble[1]
Solubility dihydrate
degraded with dissolution by NaCN, KCN, NH4OH, HCl
+3825·10−6 cm3/mol
Related compounds
Other anions
Cadmium chloride,
Cadmium iodide
Other cations
Zinc cyanide,
Calcium cyanide,
Magnesium cyanide
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) cyanide is the inorganic compound with the formula Co(CN)2. It is coordination polymer that has attracted intermittent attention over many years in the area of inorganic synthesis and homogeneous catalysis.

Uses

[edit]

Cobalt(II) cyanide has been used as a precursor to dicobalt octacarbonyl.[2]

Preparation and structure

[edit]

The trihydrate salt is obtained as a reddish-brown precipitate by adding two equivalents of potassium cyanide to a cobalt salt solution:[3]

CoCl2(H2O)6 + 2 KCN → Co(CN)2 + 2 KCl + 6 H2O

With excess cyanide, the red brown dicyanide dissolves to give pentacyanocobaltate.[4]

Solid cobalt(II) cyanide is a coordination polymer consisting of cobalt ions linked by cyanide units in a cubic arrangement, each such cobalt atom having octahedral geometry, and an additional cobalt atom in half of the cubic cavities.[5] That is, the structure is actually Co[Co(CN)3]2 in a zeolite-like structure. It forms hydrates and other inclusion complexes by having substances diffuse into the cavities that do not contain the cobalt atoms.[5]

References

[edit]
  1. ^ Lide, David R., ed. (2006). CRC Handbook of Chemistry and Physics (87th ed.). Boca Raton, FL: CRC Press. ISBN 0-8493-0487-3.
  2. ^ Sternberg, Heinz W.; Wender, Irving; Orchin, Milton; Lynch Jr., M. A.; Sesny, W. J. (1957). "Cobalt Tetracarbonyl Hydride". Inorganic Syntheses. Inorganic Syntheses. Vol. 5. pp. 192–195. doi:10.1002/9780470132364.ch55. ISBN 9780470132364.
  3. ^ Bigelow, John H.; Bailar Jr., John C. (1946). "Potassium Hexacyanocobaltate(III)". Inorganic Syntheses. Inorganic Syntheses. Vol. 2. pp. 225–227. doi:10.1002/9780470132333.ch72. ISBN 9780470132333.
  4. ^ Kwiatek, Jack (1968). "Reactions Catalyzed by Pentacyanocobaltate(II)". Catalysis Reviews. 1: 37–72. doi:10.1080/01614946808064700.
  5. ^ a b Weiss, Armin; Rothenstein, W. (1963). "Cobalt(II) Cyanide, its Three-Demensional Frame-work Structure and Zeolitic Compounds". Angewandte Chemie International Edition. 2 (7): 396. doi:10.1002/anie.196303962.