Copper(I) bromide

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Copper(I) bromide
Sample of copper(I) bromide
Structure of CuBr
Names
Other names
Cuprous bromide
Identifiers
3D model (
JSmol
)
ChemSpider
ECHA InfoCard
 100.029.210 Edit this at Wikidata
UNII
  • InChI=1S/BrH.Cu/h1H;/q;+1/p-1 checkY
    Key: NKNDPYCGAZPOFS-UHFFFAOYSA-M checkY
  • InChI=1/BrH.Cu/h1H;/q;+1/p-1
    Key: NKNDPYCGAZPOFS-REWHXWOFAY
  • Br[Cu]
Properties
CuBr
Molar mass 143.45 g/mol
Appearance white powder (see text)
Density 4.71 g/cm3, solid
Melting point 492 °C (918 °F; 765 K)
Boiling point 1,345 °C (2,453 °F; 1,618 K)
insoluble;
slightly soluble in cold water
6.27×10−9[1]
Solubility soluble in
ammonium hydroxide, acetonitrile
negligible in acetone, sulfuric acid
−49.0×10−6 cm3/mol
2.116
1.46 D
Hazards
Flash point Non-flammable
NIOSH (US health exposure limits):
PEL (Permissible)
 TWA 1 mg/m3 (as Cu)[2]
REL (Recommended)
 TWA 1 mg/m3 (as Cu)[2]
IDLH
(Immediate danger)
 TWA 100 mg/m3 (as Cu)[2]
Related compounds
Other anions
 Copper(I) chloride
Copper(I) iodide
Other cations
Silver(I) bromide
Copper(II) bromide
Mercury(I) bromide
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)

Copper(I) bromide is the

diamagnetic solid adopts a polymeric structure akin to that for zinc sulfide. The compound is widely used in the synthesis
of organic compounds and as a lasing medium in copper bromide lasers.

Preparation, basic properties, structure

The compound is white, although samples are often colored due to the presence of copper(II) impurities.[3] The copper(I) ion also oxidizes easily in air. It is commonly prepared by the reduction of cupric salts with sulfite in the presence of bromide.[4] For example, the reduction of copper(II) bromide with sulfite yields copper(I) bromide and hydrogen bromide:

2 CuBr2 + H2O + SO2−
3 → 2 CuBr + SO2−
4 + 2 HBr

CuBr is insoluble in most solvents due to its polymeric structure, which features four-coordinated, tetrahedral Cu centers interconnected by bromide ligands (ZnS structure). Upon treatment with

Lewis bases, CuBr converts to molecular adducts. For example, with dimethyl sulfide, the colorless complex is formed:[5]

CuBr + S(CH3)2 → CuBr(S(CH3)2)

In this coordination complex, the copper is two-coordinate, with a linear geometry. Other soft ligands afford related complexes. For example, triphenylphosphine gives CuBr(P(C6H5)3), although this species has a more complex structure. Thermal excitation of copper(I) bromide vapour yields a blue-violet emission which is of greater

pyrotechnic
flames.

Applications in organic chemistry

In the

aryl bromides:[4]

ArN+
2 + CuBr → ArBr + N2 + Cu+

The aforementioned complex CuBr(S(CH3)2) is widely used to generate

atom transfer radical polymerization
and copper-catalyzed cross-dehydrogenative couplings (CDC).

See also

Copper(II) bromide

References

  1. ISBN 978-1138561632
    .
  2. ^ a b c NIOSH Pocket Guide to Chemical Hazards. "#0150". National Institute for Occupational Safety and Health (NIOSH).
  3. ISBN 0-12-352651-5
    .
  4. ^ a b This report gives a procedure for generating CuBr: Hartwell, Jonathan L. (1955). "o-Chlorobromobenzene". Organic Syntheses; Collected Volumes, vol. 3, p. 185.
  5. ^ a b Jarowicki, K.; Kocienski, P. J.; Qun, L. "1,2-Metallate Rearrangement: (Z)-4-(2-Propenyl)-3-Octen-1-ol". Organic Syntheses. 79: 11; Collected Volumes, vol. 10, p. 662.
  6. doi:10.1002/prep.201500231
    .

External links

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