Cobalt(II) chloride refers to inorganic compounds with the formula . These compounds include anhydrous as well as several hydrates. The anhydrous form is a blue solid; the dihydrate is purple and the hexahydrate is pink. The hexahydrate is commonly used in the laboratory.
Anhydrous cobalt chloride has the cadmium chloride structure () (Rm) in which the cobalt(II) ions are octahedrally coordinated. At about 706 ðC (20 degrees below the melting point), the coordination change to tetrahedral. The vapor pressure has been reported as 7.6 mmHg at the melting point. The anhydrous salt, which is hygroscopic, sublimes under flowing hydrogen chloride. The dihydrate, CoCl<sub>2</sub>(H<sub>2</sub>O)<sub>2</sub>, is a coordination polymer. Each Co center is coordinated to four doubly bridging chloride ligands. The octahedron is completed by a pair of mutually trans aquo ligands.
Solid hexahydrate â¢6 contains the neutral molecule trans- and two molecules of water of crystallization. Claims of the formation of tri- and tetrahydrates have not been confirmed.
Cobalt chloride is fairly soluble in water. Under atmospheric pressure, the mass concentration of a saturated solution of in water is about 54% at the boiling point, 120.2 ðC; 48% at 51.25 ðC; 35% at 25 ðC; 33% at 0 ðC; and 29% at âÂÂ27.8 ðC.
Diluted aqueous solutions of contain the hexaaquo complex . Concentrated solutions are red at room temperature but become blue at higher temperatures.
The anhydrous compound can be prepared by heating the hydrated cobalt chlorides under flowing hydrogen chloride or by treating hydrated cobalt(II) acetate with acetyl chloride:
Aqueous solutions of cobalt chloride can be prepared from cobalt(II) hydroxide or cobalt(II) carbonate and hydrochloric acid according to this idealized equation:
Cooling saturated aqueous solutions yields the dihydrate between 120.2 ðC and 51.25 ðC, and the hexahydrate below 51.25 ðC. Water ice, rather than cobalt chloride, will crystallize from solutions with concentration below 29%. The monohydrate and the anhydrous forms can be obtained by cooling solutions only under high pressure, above 206 ðC and 335 ðC, respectively.
On rapid heating or in a closed container, each of the 6-, 2-, and 1- hydrates partially melts into a mixture of the next lower hydrate and a saturated solutionâÂÂat 51.25 ðC, 206 ðC, and 335 ðC, respectively. On slow heating in an open container, so that the water vapor pressure over the solid is practically zero, water evaporates out of each of the solid 6-, 2-, and 1- hydrates, leaving the next lower hydrate, at about 40ðC, 89ðC, and 125ðC, respectively. If the partial pressure of the water vapor is in equilibrium with the solid, as in a confined but not pressurized container, the decomposition occurs at about 115ðC, 145ðC, and 195ðC, respectively.
Dehydration can also be effected with trimethylsilyl chloride:
Cobalt(II) chloride is a precursor to many other cobalt compounds. The hexahydrate and the anhydrous salt are weak Lewis acids. The adducts are usually either octahedral or tetrahedral. It forms an octahedral complex with pyridine ():
With triphenylphosphine (), a tetrahedral complex results:
Salts of the anionic complex CoCl<sub>4</sub><sup>2âÂÂ</sup> can be prepared using tetraethylammonium chloride:
The tetrachlorocobaltate ion [CoCl<sub>4</sub>]<sup>2âÂÂ</sup> is the blue ion that forms upon addition of hydrochloric acid to aqueous solutions of hydrated cobalt chloride, which are pink.
Treating anhydrous cobalt chloride with hydrogen fluoride gives cobalt(II) fluoride:
Reaction of the anhydrous compound with sodium cyclopentadienide gives cobaltocene . Reaction of 1-norbornyllithium with the ÷THF produces tetrakis(1-norbornyl)cobalt(IV) â a rare example of a stable transition metal/saturated alkane compound, different products are obtained in other solvents.
Cobalt chloride is a common visual moisture indicator due to its distinct colour change when hydrated. The colour change is from some shade of blue when dry, to a pink when hydrated, although the shade of colour depends on the substrate and concentration. It is impregnated into paper to make test strips for detecting moisture in solutions, or more slowly, in air/gas. Desiccants such as silica gel can incorporate cobalt chloride to indicate when it is "spent" (i.e. hydrated).
Cobalt is essential for most higher forms of life, but more than a few milligrams each day is harmful. Although poisonings have rarely resulted from cobalt compounds, their chronic ingestion has caused serious health problems at doses far less than the lethal dose. In 1966, the addition of cobalt compounds to stabilize beer foam in Canada led to a peculiar form of toxin-induced cardiomyopathy, which came to be known as beer drinker's cardiomyopathy.
Furthermore, cobalt(II) chloride is suspected of causing cancer (i.e., possibly carcinogenic, IARC Group 2B) as per the International Agency for Research on Cancer (IARC) Monographs.
In 2005âÂÂ06, cobalt chloride was the eighth-most-prevalent allergen in patch tests (8.4%).