Chloroauric acid

From Wikipedia, the free encyclopedia
Jump to: navigation, search
Chloroauric acid
Identifiers
CAS number 16903-35-8 YesY
16961-25-4 (trihydrate)
PubChem 28133
ChemSpider 26171 YesY
Jmol-3D images Image 1
Properties
Molecular formula HAuCl4
Molar mass 339.785 g/mol (anhydrous)
393.833 g/mol (trihydrate)
411.85 g/mol (tetrahydrate)
Appearance orange-yellow needle-like crystals
hygroscopic
Density 3.9 g/cm3 (anhydrous)
2.89 g/cm3 (tetrahydrate)
Melting point

254 °C, 527 K, 489 °F (decomp)

Solubility in water 350 g HAuCl4 / 100 g H2O
Solubility soluble in alcohol, ester, ether, ketone
Related compounds
Other anions Tetrabromoauric acid
Hazards
MSDS JT Baker
EU classification not listed
NFPA 704
NFPA 704.svg
0
3
1
 YesY (verify) (what is: YesY/N?)
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
Infobox references

Chloroauric acid is the inorganic compound with the formula HAuCl4. It is an orange-yellow solid, a common precursor to other gold compounds and an intermediate in the purification of gold metal. Commercial samples have the composition HAuCl4n H2O with n = 3 or 4.

Contents

Preparation [edit]

It is produced by dissolving gold in aqua regia (a mixture of concentrated nitric and hydrochloric acids) followed by careful evaporation of the solution:[1]

Au + HNO3 + 4 HCl → HAuCl4 + NO + 2 H2O

Under some conditions, oxygen can be used as the oxidant.[2] For higher efficiency, these processes are conducted in autoclaves, which allows greater control of temperature and pressure. Alternatively, a solution of HAuCl4 can be produced by electrolysis of gold metal in hydrochloric acid:

2 Au + 8 HCl → 2 HAuCl4 + 3 H2

To prevent the deposition of gold on the cathode, the electrolysis is carried out in a cell equipped with a membrane. This method is used for refining gold. Some gold remains in solution in the form of [AuCl2]-.[3]

A solution of HAuCl4 can also be obtained by the action of chlorine or chlorine water on metallic gold in hydrochloric acid:

2 Au + 3 Cl2 + 2 HCl → 2 HAuCl4

This reaction is widely used for extracting gold from electronic and other "rich" materials.

In addition to the above routes, many other ways exist to dissolve gold, differing in the choice of the oxidant (hydrogen peroxide, hypochlorites) or variations of conditions. It is possible also to convert the trichloride (Au2Cl6) or the oxide (Au2O3x H2O).

Properties [edit]

The compound crystallizes as a yellow-orange hygroscopic needles. It is soluble not only in water, but also in many oxygen-containing solvents, such as alcohols, esters, ethers, and ketones. For example, in dry dibutyl ether of diethylene glycol, the solubility exceeds 1 mol/L. Saturated solutions in the organic solvents often are the liquid solvates of specific stoichiometry.

When heated in air of solid HAuCl4n H2O, it melts in the water of crystallization, quickly darkens and becomes dark brown. Heating of HAuCl4n H2O in a stream of chlorine gives gold(III) chloride (Au2Cl6)[4]

The AuCl4- anion has square planar molecular geometry. The Au-Cl distances are around 2.28 Å. Other d8 complexes adopt similar structrures, e.g. [PtCl4]2-.

Reactions [edit]

As a strong acid, HAuCl4 converts to the alkali metal salts MAuCl4 (M = Li, Na, K, etc.), which are soluble. The related thallium salt is poorly soluble in all nonreacting solvents. Salts of quaternary ammonium cations are known.[5] Other complex salts include [Au(bipy)Cl2][AuCl4][6] and [Co(NH3)6][AuCl4]Cl2.

Chloroauric acid is reduced by many substances. This redox is used in many syntheses of gold(I) complexes, especially with organic ligands. Often the ligand serves as reducing agent as illustrated with thiourea ((H2N)2CS):

AuCl4- + 4 (H2N)2CS + H2O → Au((H2N)2CS)2+ + (NH2)2CO + S + 2 Cl- + 2 HCl

Chloroauric acid is the precursor to gold nanoparticles by precipitation onto mineral supports.[7]

Applications [edit]

Chloroauric acid is the precursor used in the purification of gold by electrolysis.

Liquid-liquid extraction of chloroauric acid is used for the recovery, concentrating, purification, and analytical determinations of gold. Of great importance is the extraction of HAuCl4 from hydrochloric medium by oxygen-containing extractants, such as alcohols, ketones, ethers and esters. The concentration of gold(III) in the extracts may exceed 1 mol/L.[8][9][10] The most frequently used extractants for this purpose are dibuthyl glycol, methyl isobuthyl ketone, tributhyl phosphate, dichlorodiethyl ether (chlorex).

References [edit]

  1. ^ Handbook of Preparative Inorganic Chemistry, 2nd Ed. Edited by G. Brauer, Academic Press, 1963, NY.
  2. ^ Novoselov, R. I.; Makotchenko, E. V. "Application of oxygen as ecologically pure reagent for the oxidizing of non-ferrous and precious metals, sulphide minerals" Chemistry for sustainable development, 1999, vol. 7, p. 321—330.
  3. ^ Belevantsev V. I., Peschevitskii, B. I.; Zemskov, S. V. "New data on chemistry of gold compounds in solutions" Izvestiya Sibirskogo Otdeleniya AN SSSR, ser. khim. nauk. 1976. N4. Issue 2. P. 24-45.
  4. ^ Mellor J. W. A comprehensive treatise on inorganic and theoretical chemistry. Vol. 3. 1946. p. 593.
  5. ^ Makotchenko, E. V.; Kokovkin, V. V. (2010). "Solid contact \AuCl4]−-selective electrode and its application for evaluation of gold(III) in solutions". Russian Journal of General Chemistry 80 (9): 1733. doi:10.1134/S1070363210090021.  edit
  6. ^ Mironov, I. V.; Tsvelodub, L. D. "Equilibria of the substitution of pyridine, 2,2 '-bipyridyl, and 1,10-phenanthroline for Cl- in AuCl4- in aqueous solution" Russian Journal of Inorganic Chemistry. 2001, vol. 46, p. 143-148.
  7. ^ Gunanathan, C.; Ben-David, Y.; Milstein, D. (2007). "Direct Synthesis of Amides from Alcohols and Amines with Liberation of H2". Science 317 (5839): 790–792. doi:10.1126/science.1145295. PMID 17690291.  edit
  8. ^ Mironov, I. V.; Natorkhina, K. I. (2012). "On the selection of extractant for the preparation of high-purity gold". Russian Journal of Inorganic Chemistry 57 (4): 610. doi:10.1134/S0036023612040195.  edit
  9. ^ Feather, A; KC Sole, Lj Bryson (July 1997). "Gold refining by solvent extraction-the minataur tm process" (PDF). Journal of the Southern African Institute of Mining and Metallurgy: 169—173. Retrieved 2013-03-17. 
  10. ^ Morris D. F. C., Khan M. A. Application of solvent extraction to the refining of precious metals, Part 3: purification of gold" Talanta, 1968. vol. 15, pp. 1301—1305.