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Cuprous chloride

Copper(I) chloride
Unit cell of nantokite
Sample of copper(I) chloride
Names
IUPAC name
Copper(I) chloride
Other names
Cuprous chloride
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.028.948
EC Number 231-842-9
PubChem CID
RTECS number GL6990000
Properties
CuCl
Molar mass 98.999 g/mol
Appearance white powder, slightly green from oxidized impurities
Density 4.14 g/cm3
Melting point 423 °C (793 °F; 696 K)
Boiling point 1,490 °C (2,710 °F; 1,760 K) (decomposes)
0.047 g/L (20 °C)
1.72×10−7
Solubility insoluble in ethanol
acetone; soluble in concentrated HCl, NH4OH
Band gap 3.25 eV (300 K, direct)
-40.0·10−6 cm3/mol
1.930
Structure
Zincblende, cF20
F43m, No. 216
a = 0.54202 nm
0.1592 nm3
4
Hazards
Safety data sheet JT Baker
Harmful (Xn)
Dangerous for the environment (N)
R-phrases (outdated) R22, R50/53
S-phrases (outdated) (S2), S22, S60, S61
NFPA 704
Flammability code 0: Will not burn. E.g., water Health code 3: Short exposure could cause serious temporary or residual injury. E.g., chlorine gas Reactivity code 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g., liquid nitrogen Special hazards (white): no codeNFPA 704 four-colored diamond
Flash point Non-flammable
Lethal dose or concentration (LD, LC):
LD50 (median dose)
140 mg/kg
US health exposure limits (NIOSH):
PEL (Permissible)
TWA 1 mg/m3 (as Cu)
REL (Recommended)
TWA 1 mg/m3 (as Cu)
IDLH (Immediate danger)
TWA 100 mg/m3 (as Cu)
Related compounds
Other anions
Copper(I) bromide
Copper(I) iodide
Other cations
Copper(II) chloride
Silver(I) chloride
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
YesY  (what is YesYN ?)
Infobox references

Copper(I) chloride, commonly called cuprous chloride, is the lower chloride of copper, with the formula CuCl. The substance is a white solid sparingly soluble in water, but very soluble in concentrated hydrochloric acid. Impure samples appear green due to the presence of copper(II) chloride.

Copper(I) chloride was first prepared by Robert Boyle in the mid-seventeenth century from mercury(II) chloride ("Venetian sublimate") and copper metal:

In 1799, J.L. Proust characterized the two different chlorides of copper. He prepared CuCl by heating CuCl2 at red heat in the absence of air, causing it to lose half of its combined chlorine followed by removing residual CuCl2 by washing with water.

An acidic solution of CuCl was formerly used for analysis of carbon monoxide content in gases, for example in Hempel's gas apparatus. This application was significant during the time that coal gas was widely used for heating and lighting, during the nineteenth and early twentieth centuries.

Copper(I) chloride is produced industrially by the direct combination of copper metal and chlorine at 450–900 °C:

Cu + 0.5 Cl2 → CuCl

Copper(I) chloride can also be prepared by reducing copper(II) chloride, e.g. with sulfur dioxide:

2 CuCl2 + SO2 + 2 H2O 2 CuCl + H2SO4 + 2 HCl

Many other reducing agents can be used.

Copper(I) chloride has the cubic zincblende crystal structure at ambient conditions. Upon heating to 408 °C the structure changes to hexagonal. Several other crystalline forms of CuCl appear at high pressures (several GPa).

Copper(I) chloride is a Lewis acid, which is classified as soft according to the Hard-Soft Acid-Base concept. Thus, it tends to form stable complexes with soft Lewis bases such as triphenylphosphine:


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