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Copper(I) chloride

From Wikipedia, the free encyclopedia
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)
8127933
ChEBI
ChemSpider
DrugBank
ECHA InfoCard 100.028.948 Edit this at Wikidata
EC Number
  • 231-842-9
13676
RTECS number
  • GL6990000
UNII
  • InChI=1S/ClH.Cu/h1H;/q;+1/p-1 checkY
    Key: OXBLHERUFWYNTN-UHFFFAOYSA-M checkY
  • InChI=1/ClH.Cu/h1H;/q;+1/p-1
    Key: OXBLHERUFWYNTN-REWHXWOFAC
  • Cl[Cu]
Properties
Chemical formula
 CuCl
Molar mass 98.999 g/mol[1]
Appearance white powder, slightly green from oxidized impurities
Density 4.14 g/cm3[1]
Melting point 423 °C (793 °F; 696 K) [1]
Boiling point 1,490 °C (2,710 °F; 1,760 K) (decomposes)[1]
0.047 g/L (20 °C)[1]
1.72×10−7
Solubility insoluble in ethanol,
acetone;[1] soluble in concentrated HCl, NH4OH
Band gap 3.25 eV (300 K, direct)[2]
Magnetic susceptibility (χ)
 -40.0·10−6 cm3/mol[3]
Refractive index (nD)
 1.930[4]
Structure
Zincblende, cF20
Space group
 F43m, No. 216[5]
a = 0.54202 nm
Lattice volume (V)
 0.1592 nm3
4
Hazards
Safety data sheet JT Baker
GHS labelling:
GHS07: Exclamation markGHS09: Environmental hazard
Signal word
 Warning
H302, H410
P264, P270, P273, P301+P312, P330, P391, P501
NFPA 704 (fire diamond)
3
0
0
Flash point Non-flammable
Lethal dose or concentration (LD, LC):
LD50 (median dose)
 140 mg/kg
NIOSH (US health exposure limits):
PEL (Permissible)
 TWA 1 mg/m3 (as Cu)[6]
REL (Recommended)
 TWA 1 mg/m3 (as Cu)[6]
IDLH (Immediate danger)
 TWA 100 mg/m3 (as Cu)[6]
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).
checkY  (what is checkY☒N ?)
Infobox references
A white precipitate of Copper(I) Chloride suspended in a solution of Ascorbic Acid in a 2 dram vial.
IR absorption spectrum of copper(I) chloride

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 (CuCl2).[7]

  • Copper(I)chloride crystal 01.jpg
  • Copper(I) chloride.jpg

History[]

Copper(I) chloride was first prepared by Robert Boyle in the mid-seventeenth century[8] from mercury(II) chloride ("Venetian sublimate") and copper metal:

HgCl2 + 2 Cu → 2 CuCl + Hg

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.[9]

An acidic solution of CuCl was formerly used for analysis of carbon monoxide content in gases, for example in Hempel's gas apparatus[clarification needed].[10] This application was significant[11] during the nineteenth and early twentieth centuries when coal gas was widely used for heating and lighting.

Synthesis[]

Copper(I) chloride is produced industrially by the direct combination of copper metal and chlorine at 450–900 °C:[12][13]

Copper(I) chloride can also be prepared by reducing copper(II) chloride with sulfur dioxide, or with ascorbic acid (vitamin C) that acts as a reducing sugar:

Many other reducing agents can be used.[14]

Properties[]

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).[5]

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

CuCl + 1 P(C6H5)3 → 1/4 {CuCl[P(C6H5)3]}4
CuCl + 2 P(C6H5)3 → CuCl[P(C6H5)3)]2
CuCl + 3 P(C6H5)3 → CuCl[P(C6H5)3)]3

Although CuCl is insoluble in water, it dissolves in aqueous solutions containing suitable donor molecules. It forms complexes with halide ions, for example forming H3O+ CuCl2− in concentrated hydrochloric acid. Chloride is displaced by CN− and S2O32−.

Solutions of CuCl in HCl or NH3 absorb carbon monoxide to form colourless complexes such as the chloride-bridged dimer [CuCl(CO)]2. The same hydrochloric acid solutions also react with acetylene gas to form [CuCl(C2H2)]. Ammoniacal solutions of CuCl react with acetylenes to form the explosive copper(I) acetylide, Cu2C2. Alkene complexes o can be prepared by reduction of CuCl2 by sulfur dioxide in the presence of the alkene in alcohol solution. Complexes with dienes such as 1,5-cyclooctadiene are particularly stable:[15]

Structure of COD complex of CuCl

In absence of other ligands, its aqueous solutions are unstable with respect to disproportionation:[16]

2 CuCl → Cu + CuCl2

In part for this reason samples in air assume a green coloration.

Uses[]

The main use of copper(I) chloride is as a precursor to the fungicide copper oxychloride. For this purpose aqueous copper(I) chloride is generated by comproportionation and then air-oxidized:

Cu + CuCl2 → 2 CuCl
4 CuCl + O2 + 2 H2O → Cu3Cl2(OH)4 + CuCl2

Copper(I) chloride catalyzes a variety of organic reactions, as discussed above. Its affinity for carbon monoxide in the presence of aluminium chloride is exploited in the COPureSM process.

In organic synthesis[]

CuCl is used with carbon monoxide, aluminium chloride, and hydrogen chloride in the Gatterman-Koch reaction to form benzaldehydes.

In the Sandmeyer reaction.[17][18] Treatment of an arenediazonium salt with CuCl leads to an aryl chloride, for example:

(Example Sandmeyer reaction using CuCl)

The reaction has wide scope and usually gives good yields.

Early investigators observed that copper(I) halides catalyse 1,4-addition of Grignard reagents to alpha,beta-unsaturated ketones[19] led to the development of organocuprate reagents that are widely used today in organic synthesis:[20]

(Addition of RMgX to C=C-C=O mediated by CuCl)

This finding led to the development of organocopper chemistry. For example, CuCl reacts with methyllithium (CH3Li) to form "Gilman reagents" such as (CH3)2CuLi, which find extensive use in organic synthesis. Grignard reagents form similar organocopper compounds. Although other copper(I) compounds such as copper(I) iodide are now more often used for these types of reactions, copper(I) chloride is still recommended in some cases:[21]

(Alkylation of sorbate ester at 4-position mediated by CuCl)

Here, Bu indicates an n-butyl group. Without CuCl, the Grignard reagent alone gives a mixture of 1,2- and 1,4-addition products (i.e., the butyl adds at the C closer to the C=O).

Copper(I) chloride is also an intermediate formed from copper(II) chloride in the Wacker process.

In polymer chemistry[]

CuCl is used as a catalyst in Atom Transfer Radical Polymerization (ATRP).

Niche uses[]

Copper(I) chloride is also used in pyrotechnics as a blue/green coloring agent. In a flame test, copper chlorides, like all copper compounds, emit green-blue.

Natural occurrence[]

Natural form of CuCl is the rare mineral .[22][23]

References[]

  1. ^ a b c d e f Haynes, William M., ed. (2011). CRC Handbook of Chemistry and Physics (92nd ed.). Boca Raton, FL: CRC Press. p. 4.61. ISBN 1-4398-5511-0.
  2. ^ Garro, Núria; Cantarero, Andrés; Cardona, Manuel; Ruf, Tobias; Göbel, Andreas; Lin, Chengtian; Reimann, Klaus; Rübenacke, Stefan; Steube, Markus (1996). "Electron-phonon interaction at the direct gap of the copper halides". Solid State Communications. 98 (1): 27–30. Bibcode:1996SSCom..98...27G. doi:10.1016/0038-1098(96)00020-8.
  3. ^ Haynes, William M., ed. (2011). CRC Handbook of Chemistry and Physics (92nd ed.). Boca Raton, FL: CRC Press. p. 4.132. ISBN 1-4398-5511-0.
  4. ^ Patnaik, Pradyot (2002) Handbook of Inorganic Chemicals. McGraw-Hill, ISBN 0-07-049439-8
  5. ^ a b Hull, S.; Keen, D. A. (1994). "High-pressure polymorphism of the copper(I) halides: A neutron-diffraction study to ∼10 GPa". Physical Review B. 50 (9): 5868–5885. Bibcode:1994PhRvB..50.5868H. doi:10.1103/PhysRevB.50.5868. PMID 9976955.
  6. ^ a b c NIOSH Pocket Guide to Chemical Hazards. "#0150". National Institute for Occupational Safety and Health (NIOSH).
  7. ^ Pastor, Antonio C. (1986) U.S. Patent 4,582,579 "Method of preparing cupric ion free cuprous chloride" Section 2, lines 4–41.
  8. ^ Boyle, Robert (1666). Considerations and experiments about the origin of forms and qualities. Oxford. As reported in Mellor[full citation needed].
  9. ^ Proust, J. L. (1799). "Recherches sur le Cuivre". Ann. Chim. Phys. 32: 26–54.
  10. ^ Martin, Geoffrey (1917). Industrial and Manufacturing Chemistry (Part 1, Organic ed.). London: Crosby Lockwood. pp. 330–31.
  11. ^ Lewes, Vivian H. (1891). "The Analysis of Illuminationg Gases". Journal of the Society of Chemical Industry. 10: 407–413.
  12. ^ Richardson, H. W. (2003). "Copper Compounds". Kirk-Othmer Encyclopedia of Chemical Technology. doi:10.1002/0471238961.0315161618090308.a01.pub2. ISBN 0471238961.
  13. ^ Zhang, J.; Richardson, H. W. (2016). "Copper Compounds". Ullmann's Encyclopedia of Industrial Chemistry. pp. 1–31. doi:10.1002/14356007.a07_567.pub2. ISBN 978-3-527-30673-2.
  14. ^ Glemser, O.; Sauer, H. (1963). "Copper(I) Chloride". In Brauer, G. (ed.). Handbook of Preparative Inorganic Chemistry. 1 (2nd ed.). New York: Academic Press. p. 1005.
  15. ^ Nicholls, D. (1973) Complexes and First-Row Transition Elements, Macmillan Press, London.
  16. ^ Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. p. 1185. ISBN 978-0-08-037941-8.
  17. ^ Wade, L. G. (2003) Organic Chemistry, 5th ed., Prentice Hall, Upper Saddle River, New Jersey, p. 871. ISBN 013033832X.
  18. ^ March, J. (1992) Advanced Organic Chemistry, 4th ed., Wiley, New York. p. 723. ISBN 978-0-470-46259-1
  19. ^ Kharasch, M. S.; Tawney, P. O. (1941). "Factors Determining the Course and Mechanisms of Grignard Reactions. II. The Effect of Metallic Compounds on the Reaction between Isophorone and Methylmagnesium Bromide". J. Am. Chem. Soc. 63 (9): 2308. doi:10.1021/ja01854a005.
  20. ^ Jasrzebski, J. T. B. H.; van Koten, G. (2002) Modern Organocopper Chemistry, N. Krause (ed.). Wiley-VCH, Weinheim, Germany. p. 1. doi:10.1002/3527600086.ch1 ISBN 9783527600083.
  21. ^ Bertz, S. H.; Fairchild, E. H. (1999) Handbook of Reagents for Organic Synthesis, Volume 1: Reagents, Auxiliaries and Catalysts for C-C Bond Formation, R. M. Coates, S. E. Denmark (eds.). Wiley, New York. pp. 220–3. ISBN 978-0-471-97924-1.
  22. ^ "Nantokite".
  23. ^ "List of Minerals". 21 March 2011.

External links[]

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