Cadmium chloride

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Cadmium chloride
Cadmium chloride hemipentahydrate
General
Molecular formula CdCl2
Molar mass 183.316 g/mol
Appearance white solid, hygroscopic
CAS number [10108-64-2]
Properties
Density and phase 4.08 g/cm3, solid
Solubility in water 140 g/100 ml (20 °C)
Solubility in methanol 1.7 g/100 ml
Solubility in acetone insoluble
Melting point 564 °C
Boiling point 960 °C
Structure
Coordination
geometry
 ?
Crystal structure rhombohedral
Hazards
MSDS External MSDS
EU classification Highly toxic (T+)
Carc. Cat. 2
Muta. Cat. 2
Repr. Cat. 2
Dangerous for
the environment (N)
R-phrases R45, R46, R60, R61, R25,
R26, R48/23/25, R50/53
S-phrases S53, S45, S60, S61
Flash point non-flammable
Supplementary data page
Structure and
properties
n, εr, etc.
Thermodynamic
data
Phase behaviour
Solid, liquid, gas
Spectral data UV, IR, NMR, MS
Related compounds
Other anions Cadmium fluoride
Cadmium bromide
Cadmium iodide
Other cations Zinc chloride
Mercury(II) chloride
Except where noted otherwise, data are given for
materials in their standard state (at 25 °C, 100 kPa)
Infobox disclaimer and references

Cadmium chloride is a white crystalline compound of cadmium and chlorine, with the formula CdCl2. It is a hygroscopic solid which is highly soluble in water and slightly soluble in alcohol. Although it is considered to be ionic, it has considerable covalent character to its bonding. The crystal structure for cadmium chloride described below, a 2D layer lattice, is often used as a reference for describing other crystal structures.

Contents

[edit] Crystal structure

Cadmium chloride crystal structure
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Cadmium chloride crystal structure

Cadmium chloride forms crystals with cubic symmetry. The structure is based on the sodium chloride crystal structure, but with half of the metal ions removed (the "missing" ions are shown as hatched light blue balls in the drawing). The resultant structure consists of a layered lattice. This same basic structure is found in many other salts and minerals, particularly those where there is some degree of covalent bonding, such as in manganese(II) chloride, cobalt(II) chloride or magnesium chloride.

[edit] Chemical properties

Cadmium chloride has a high solubility in water, and it dissociates into ions. A certain amount of hydrolysis to species such as [CdOH(H2O)x]+ may occur. The high solubility may be due in part to formation of complex ions such as in Cd2+ CdCl42− (CdCl2 is a Lewis acid). With excess chloride ion in water or acetonitrile it forms mainly CdCl3 and the tetrahedral anion, CdCl42−:

CdCl2(aq) + 2 Cl(aq) → CdCl42−(aq)

With large cations it is possible to produce trigonal bipyramidal CdCl53−.

[edit] Preparation

Anhydrous cadmium chloride can be prepared by the action of anhydrous chlorine or hydrogen chloride gas on heated cadmium metal.

Cd(s) + 2 HCl(g) → CdCl2(s) + H2(g)

Hydrochloric acid may be used to make hydrated CdCl2 from the metal, or alternatively from cadmium oxide or cadmium carbonate.

[edit] Uses

Cadmium chloride is used for the preparation of cadmium sulfide, used as "Cadmium Yellow", a brilliant yellow pigment which is stable to heat and sulfide fumes.

CdCl2(aq) + H2S(g) → CdS(s) + 2 HCl(aq)

In the laboratory, anhydrous CdCl2 can be used for the preparation of organocadmium compounds of the type R2Cd where R = aryl or primary alkyl. These were once used in the synthesis of ketones from acyl chlorides (see below), however they have largely been supplanted by organocopper compounds which are much less toxic.

CdCl2 + 2 RMgX → R2Cd + MgCl2 + MgX2

R2Cd + R'COClR'COR + CdCl2

Cadmium chloride is also used for electroplating.

[edit] References

  1. N. N. Greenwood, A. Earnshaw, Chemistry of the Elements, 2nd ed., Butterworth-Heinemann, Oxford, UK, 1997.
  2. Handbook of Chemistry and Physics, 71st edition, CRC Press, Ann Arbor, Michigan, 1990.
  3. The Merck Index, 7th edition, Merck & Co, Rahway, New Jersey, USA, 1960.
  4. D. Nicholls, Complexes and First-Row Transition Elements, Macmillan Press, London, 1973.
  5. A. F. Wells, 'Structural Inorganic Chemistry, 5th ed., Oxford University Press, Oxford, UK, 1984.
  6. J. March, Advanced Organic Chemistry, 4th ed., p. 723, Wiley, New York, 1992.

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