Copper(I) bromide

Copper(I) bromide
Sample of copper(I) bromide
Structure of CuBr
Names
Other names
Cuprous bromide
Identifiers
CAS Number
  • 7787-70-4 checkY
3D model (JSmol)
  • Interactive image
ChemSpider
  • 22995 checkY
ECHA InfoCard 100.029.210 Edit this at Wikidata
PubChem CID
  • 24593
UNII
  • R8V209A5G0 checkY
CompTox Dashboard (EPA)
  • DTXSID6052530 Edit this at Wikidata
InChI
  • 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
Chemical formula
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)
Solubility in water
insoluble;
slightly soluble in cold water
Solubility product (Ksp)
6.27×10−9[1]
Solubility soluble in HCl, HBr, 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).
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Infobox references
Chemical compound

Copper(I) bromide is the chemical compound with the formula CuBr. This white 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 saturation than known copper(I) chloride emission.[6] Copper(I) bromide is hence an advantageous emitter in pyrotechnic flames.

Applications in organic chemistry

In the Sandmeyer reaction, CuBr is employed to convert diazonium salts into the corresponding aryl bromides:[4]

ArN+
2
+ CuBr → ArBr + N2 + Cu+

The aforementioned complex CuBr(S(CH3)2) is widely used to generate organocopper reagents.[5] Related CuBr complexes are catalysts for atom transfer radical polymerization and copper-catalyzed cross-dehydrogenative couplings (CDC).

See also

Copper(II) bromide

References

  1. ^ Rumble, John (June 18, 2018). CRC Handbook of Chemistry and Physics (99th ed.). CRC Press. pp. 5–188. ISBN 978-1138561632.
  2. ^ a b c NIOSH Pocket Guide to Chemical Hazards. "#0150". National Institute for Occupational Safety and Health (NIOSH).
  3. ^ Holleman, A. F.; Wiberg, E. "Inorganic Chemistry" Academic Press: San Diego, 2001. 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. ^ Koch, E.-C. (2015). "Spectral Investigation and Color Properties of Copper(I) Halides CuX (X=F, Cl, Br, I) in Pyrotechnic Combustion Flames". Propellants Explos. Pyrotech. 40 (6): 798–802. doi:10.1002/prep.201500231.
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  • v
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Salts and covalent derivatives of the bromide ion
HBr He
LiBr BeBr2 BBr3
+BO3
CBr4
+C
NBr3
BrN3
NH4Br
NOBr
+N
Br2O
BrO2
Br2O3
Br2O5
BrF
BrF3
BrF5
Ne
NaBr MgBr2 AlBr
AlBr3
SiBr4 PBr3
PBr5
PBr7
+P
S2Br2
SBr2
BrCl Ar
KBr CaBr2
ScBr3 TiBr2
TiBr3
TiBr4
VBr2
VBr3
CrBr2
CrBr3
CrBr4
MnBr2 FeBr2
FeBr3
CoBr2 NiBr2
NiBr42−
CuBr
CuBr2
ZnBr2 GaBr3 GeBr2
GeBr4
AsBr3
+As
+AsO3
SeBr2
SeBr4
Br2 Kr
RbBr SrBr2 YBr3 ZrBr2
ZrBr3
ZrBr4
NbBr5 MoBr2
MoBr3
MoBr4
TcBr3
TcBr4
RuBr3 RhBr3 PdBr2 AgBr CdBr2 InBr
InBr3
SnBr2
SnBr4
SbBr3
+Sb
-Sb
Te2Br
TeBr4
+Te
IBr
IBr3
XeBr2
CsBr BaBr2 * LuBr3 HfBr4 TaBr5 WBr5
WBr6
ReBr3 OsBr3
OsBr4
IrBr3
IrBr
4
PtBr2
PtBr4
AuBr
AuBr3
Hg2Br2
HgBr2
TlBr PbBr2 BiBr3 PoBr2
PoBr4
AtBr Rn
FrBr RaBr2 ** Lr Rf Db Sg Bh Hs Mt Ds Rg Cn Nh Fl Mc Lv Ts Og
 
* LaBr3 CeBr3 PrBr3 NdBr2
NdBr3
PmBr3 SmBr2
SmBr3
EuBr2
EuBr3
GdBr3 TbBr3 DyBr3 HoBr3 ErBr3 TmBr2
TmBr3
YbBr2
YbBr3
** AcBr3 ThBr4 PaBr4
PaBr5
UBr4
UBr5
NpBr3
NpBr4
PuBr3 AmBr2
AmBr3
CmBr3 BkBr3 CfBr3 EsBr2
EsBr3
Fm Md No