General Description
Odorless tan or off-white solid. Sinks in water.
Reactivity Profile
COPPER IODIDE has weak oxidizing or reducing powers. Redox reactions can however still occur. The majority of compounds in this class are slightly soluble or insoluble in water. If soluble in water, then the solutions are usually neither strongly acidic nor strongly basic. These compounds are not water-reactive.
Health Hazard
Inhalation causes irritation of nose and throat. Ingestion of copper salts produces violent vomiting and purging, intense pain, collapse, coma, convulsions, and paralysis. Contact with eyes or skin causes irritation.
Fire Hazard
Special Hazards of Combustion Products: Irritating hydrogen iodide or iodine vapors may form in fire.
Chemical Properties
Copper(I) iodide is naturally occurring as the white to reddishbrown mineral marshite. It is essentially insoluble in water but dissolves in complexing media such as ammonia, cyanide, and halide solutions. Copper(I) iodide is manufactured pyrometallurgically by the reaction of hot copper with iodine vapor in a process essentially identical to that for the preparation of copper(I) chloride. It has also been produced by the reaction of copper powder with methanol solutions of iodine at ambient temperatures. Copper(I) iodide is used as a feed additive and as a heat and light stabilizer in certain polymers and photographic emulsions. It is also used in cloud seeding and in the oil-drilling industry as an anticorrosion adjuvant.
Chemical Properties
Cuprous Iodide, Cu2O, cubic white crystals, practically insoluble in H2O or alcohol, soluble in NH4OH, potassium iodide, or potassium cyanide. Used in Sandmeyer’s reaction to synthesize aryl chlorides.
Purification Methods
It can be freshly prepared by dissolving an appropriate quantity of CuI in boiling saturated aqueous NaI over 30minutes. Pure CuI is obtained by cooling and diluting the solution with water, followed by filtering and washing sequentially with H2O, EtOH, EtOAc, Et2O and pentane, then drying in vacuo for 24hours [Dieter, J Am Chem Soc 107 4679 1985]. Alternatively wash it with H2O, then EtOH and finally with Et2O containing a little iodine. Traces of H2O are best removed first by heating at 110o and then at 400o. Exess of I2 is removed completely at 400o. It dissolves in Et2O if an amine is present to form the amine complex. On heating it becomes red, then black, but changes to white on cooling. It is sparingly soluble in H2O or alkali iodide solutions but readily soluble in NH3 (which absorbs CO) and in cyanide or thiosulfate solutions. [Glemser & Sauer in Handbook of Preparative Inorganic Chemistry (Ed Brauer) Academic Press Vol II p 1007 1965, Bawn & Ledwith Chem Ind (London) 1180 1957.]