Aluminium chloride

Aluminium chloride
Aluminium(III) chloride
Aluminium trichloride hexahydrate, pure (top), and contaminated with iron(III) chloride (bottom)
Aluminium trichloride dimer
Aluminium trichloride dimer
Aluminium trichloride unit cell
Aluminium trichloride unit cell
Names
IUPAC name
Aluminium chloride
Other names
Aluminium(III) chloride
Aluminium trichloride
Trichloroaluminum
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.028.371
EC Number
  • 231-208-1
1876
RTECS number
  • BD0530000
UNII
  • InChI=1S/Al.3ClH/h;3*1H/q+3;;;/p-3 checkY
    Key: VSCWAEJMTAWNJL-UHFFFAOYSA-K checkY
  • InChI=1/Al.3ClH/h;3*1H/q+3;;;/p-3
    Key: VSCWAEJMTAWNJL-DFZHHIFOAR
  • monomer: Cl[Al](Cl)Cl
  • dimer: Cl[Al-]1(Cl)[Cl+] [Al-]([Cl+]1)(Cl)Cl
Properties
AlCl3
Molar mass
  • 133.341 g/mol (anhydrous)
  • 241.432 g/mol (hexahydrate)
[1]
Appearance Colourless crystals, hygroscopic
Density
  • 2.48 g/cm3 (anhydrous)
  • 2.398 g/cm3 (hexahydrate)
[1]
Melting point
  • 180 °C (356 °F; 453 K) (anhydrous, sublimes)[1]
  • 100 °C (212 °F; 373 K) (hexahydrate, decomposes)[1]
  • 439 g/L (0 °C)
  • 449 g/L (10 °C)
  • 458 g/L (20 °C)
  • 466 g/L (30 °C)
  • 473 g/L (40 °C)
  • 481 g/L (60 °C)
  • 486 g/L (80 °C)
  • 490 g/L (100 °C)
Solubility
  • Soluble in hydrogen chloride, ethanol, chloroform, carbon tetrachloride
  • Slightly soluble in benzene
Vapor pressure
  • 133.3 Pa (99 °C)
  • 13.3 kPa (151 °C)
[2]
Viscosity
  • 0.35 cP (197 °C)
  • 0.26 cP (237 °C)
[2]
Structure
Monoclinic, mS16
C12/m1, No. 12[3]
a = 0.591 nm, b = 0.591 nm, c = 1.752 nm[3]
0.52996 nm3
6
Octahedral (solid)
Tetrahedral (liquid)
Trigonal planar
(monomeric vapour)
Thermochemistry
91.1 J/(mol·K)[4]
109.3 J/(mol·K)[4]
−704.2 kJ/mol[4]
−628.8 kJ/mol[4]
Pharmacology
D10AX01 (WHO)
Hazards
GHS labelling:[5]
GHS05: Corrosive
Danger
H314
P260, P280, P301+P330+P331, P303+P361+P353, P305+P351+P338+P310, P310
NFPA 704 (fire diamond)
NFPA 704 four-colored diamond
3
0
2
Lethal dose or concentration (LD, LC):
380 mg/kg, rat (oral, anhydrous)
3311 mg/kg, rat (oral, hexahydrate)
NIOSH (US health exposure limits):
PEL (Permissible)
 None[6]
REL (Recommended)
 2 mg/m3[6]
IDLH (Immediate danger)
 N.D.[6]
Related compounds
Other anions
Other cations
Related Lewis acids
Supplementary data page
Aluminium chloride (data page)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)
Infobox references

Aluminium chloride, also known as aluminium trichloride, is an inorganic compound with the formula AlCl3. It forms a hexahydrate with the formula [Al(H2O)6]Cl3, containing six water molecules of hydration. Both the anhydrous form and the hexahydrate are colourless crystals, but samples are often contaminated with iron(III) chloride, giving them a yellow colour.

The anhydrous form is important commercially. It has a low melting and boiling point. It is mainly produced and consumed in the production of aluminium metal, but large amounts are also used in other areas of the chemical industry.[7] The compound is often cited as a Lewis acid. It is an example of an inorganic compound that reversibly changes from a polymer to a monomer at mild temperature.

Structure

Anhydrous

AlCl3 adopts three structures, depending on the temperature and the state (solid, liquid, gas). Solid AlCl3 has a sheet-like layered structure with cubic close-packed chloride ions. In this framework, the Al centres exhibit octahedral coordination geometry.[8] Yttrium(III) chloride adopts the same structure, as do a range of other compounds. When aluminium trichloride is in its melted state, it exists as the dimer Al2Cl6, with tetracoordinate aluminium. This change in structure is related to the lower density of the liquid phase (1.78 g/cm3) versus solid aluminium trichloride (2.48 g/cm3). Al2Cl6 dimers are also found in the vapour phase. At higher temperatures, the Al2Cl6 dimers dissociate into trigonal planar AlCl3 monomer, which is structurally analogous to BF3. The melt conducts electricity poorly,[9] unlike more ionic halides such as sodium chloride.

Aluminium chloride monomer belongs to the point group D3h in its monomeric form and D2h in its dimeric form.

Hexahydrate

The hexahydrate consists of octahedral [Al(H2O)6]3+ cation centers and chloride anions (Cl−) as counterions. Hydrogen bonds link the cation and anions.[10] The hydrated form of aluminium chloride has an octahedral molecular geometry, with the central aluminium ion surrounded by six water ligand molecules. Being coordinatively saturated, the hydrate is of little value as a catalyst in Friedel-Crafts alkylation and related reactions.

Uses

Alkylation and acylation of arenes

AlCl3 is a common Lewis-acid catalyst for Friedel-Crafts reactions, both acylations and alkylations.[11] Important products are detergents and ethylbenzene. These types of reactions are the major use for aluminium chloride, for example, in the preparation of anthraquinone (used in the dyestuffs industry) from benzene and phosgene.[9] In the general Friedel-Crafts reaction, an acyl chloride or alkyl halide reacts with an aromatic system as shown:[11]

The alkylation reaction is more widely used than the acylation reaction, although its practice is more technically demanding. For both reactions, the aluminium chloride, as well as other materials and the equipment, should be dry, although a trace of moisture is necessary for the reaction to proceed.[12] Detailed procedures are available for alkylation[13] and acylation[14][15] of arenes.

A general problem with the Friedel-Crafts reaction is that the aluminium chloride catalyst sometimes is required in full stoichiometric quantities, because it complexes strongly with the products. This complication sometimes generates a large amount of corrosive waste. For these and similar reasons, the use of aluminium chloride has often been displaced by zeolites.[7]

Aluminium chloride can also be used to introduce aldehyde groups onto aromatic rings, for example via the Gattermann-Koch reaction which uses carbon monoxide, hydrogen chloride and a copper(I) chloride co-catalyst.[16]

Other applications in organic and organometallic synthesis

Aluminium chloride finds a wide variety of other applications in organic chemistry.[17] For example, it can catalyse the ene reaction, such as the addition of 3-buten-2-one (methyl vinyl ketone) to carvone:[18]

It is used to induce a variety of hydrocarbon couplings and rearrangements.[19][20]

Aluminium chloride combined with aluminium in the presence of an arene can be used to synthesize bis(arene) metal complexes, e.g. bis(benzene)chromium, from certain metal halides via the Fischer–Hafner synthesis. Dichlorophenylphosphine is prepared by reaction of benzene and phosphorus trichloride catalyzed by aluminium chloride.[21]

Reactions

Anhydrous aluminium chloride is a powerful Lewis acid, capable of forming Lewis acid-base adducts with even weak Lewis bases such as benzophenone and mesitylene.[11] It forms tetrachloroaluminate ([AlCl4]−) in the presence of chloride ions.

Aluminium chloride reacts with calcium and magnesium hydrides in tetrahydrofuran forming tetrahydroaluminates.

Reactions with water

Anhydrous aluminium chloride is hygroscopic, having a very pronounced affinity for water. It fumes in moist air and hisses when mixed with liquid water as the Cl− ligands are displaced with H2O molecules to form the hexahydrate [Al(H2O)6]Cl3. The anhydrous phase cannot be regained on heating the hexahydrate. Instead HCl is lost leaving aluminium hydroxide or alumina (aluminium oxide):

[Al(H2O)6]Cl3 → Al(OH)3 + 3 HCl + 3 H2O

Like metal aquo complexes, aqueous AlCl3 is acidic owing to the ionization of the aquo ligands:

[Al(H2O)6]3+ ⇌ [Al(OH)(H2O)5]2+ + H+

Aqueous solutions behave similarly to other aluminium salts containing hydrated Al3+ ions, giving a gelatinous precipitate of aluminium hydroxide upon reaction with dilute sodium hydroxide:

AlCl3 + 3 NaOH → Al(OH)3 + 3 NaCl

Synthesis

Aluminium chloride is manufactured on a large scale by the exothermic reaction of aluminium metal with chlorine or hydrogen chloride at temperatures between 650 and 750 °C (1,202 and 1,382 °F).[9]

2 Al + 3 Cl2 → 2 AlCl3
2 Al + 6 HCl → 2 AlCl3 + 3 H2

Aluminium chloride may be formed via a single displacement reaction between copper(II) chloride and aluminium metal.

2 Al + 3 CuCl2 → 2 AlCl3 + 3 Cu

In the US in 1993, approximately 21,000 tons were produced, not counting the amounts consumed in the production of aluminium.[7]

Hydrated aluminium trichloride is prepared by dissolving aluminium oxides in hydrochloric acid. Metallic aluminium also readily dissolves in hydrochloric acid ─ releasing hydrogen gas and generating considerable heat. Heating this solid does not produce anhydrous aluminium trichloride, the hexahydrate decomposes to aluminium hydroxide when heated:

[Al(H2O)6]Cl3 → Al(OH)3 + 3 HCl + 3 H2O

Aluminium also forms a lower chloride, aluminium(I) chloride (AlCl), but this is very unstable and only known in the vapour phase.[9]

Natural occurrence

Anhydrous aluminium chloride is not found as a mineral. The hexahydrate, however, is known as the rare mineral chloraluminite.[22] A more complex, basic and hydrated aluminium chloride mineral is cadwaladerite.[23][22]

Safety

Anhydrous AlCl3 reacts vigorously with bases, so suitable precautions are required. It can cause irritation to the eyes, skin, and the respiratory system if inhaled or on contact.[24]

See also

References
  1. Haynes, William M., ed. (2011). CRC Handbook of Chemistry and Physics (92nd ed.). Boca Raton, FL: CRC Press. p. 4.45. ISBN 1-4398-5511-0.
  2. Aluminium chloride Archived 2014-05-05 at the Wayback Machine. Chemister.ru (2007-03-19). Retrieved on 2017-03-17.
  3. Ketelaar, J. A. A. (1935). "Die Kristallstruktur der Aluminiumhalogenide II". Zeitschrift für Kristallographie – Crystalline Materials. 90 (1–6): 237–255. doi:10.1524/zkri.1935.90.1.237. S2CID 100796636.
  4. Haynes, William M., ed. (2011). CRC Handbook of Chemistry and Physics (92nd ed.). Boca Raton, FL: CRC Press. p. 5.5. ISBN 1-4398-5511-0.
  5. Sigma-Aldrich Co., Aluminium chloride.
  6. NIOSH Pocket Guide to Chemical Hazards. "#0024". National Institute for Occupational Safety and Health (NIOSH).
  7. Helmboldt, Otto; Keith Hudson, L.; Misra, Chanakya; Wefers, Karl; Heck, Wolfgang; Stark, Hans; Danner, Max; Rösch, Norbert (2007). "Aluminum Compounds, Inorganic". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a01_527.pub2.
  8. In contrast, AlBr3 has a more molecular structure, with the Al3+ centers occupying adjacent tetrahedral holes of the close-packed framework of Br− ions. Wells, A. F. (1984) Structural Inorganic Chemistry, Oxford Press, Oxford, United Kingdom. ISBN 0198553706.
  9. Greenwood, Norman N.; Earnshaw, Alan (1984). Chemistry of the Elements. Oxford: Pergamon Press. ISBN 978-0-08-022057-4.
  10. Andress, K.R.; Carpenter, C. (1934). "Kristallhydrate II. Die Struktur von Chromchlorid- und Aluminiumchloridhexahydrat". Zeitschrift für Kristallographie – Crystalline Materials. 87. doi:10.1524/zkri.1934.87.1.446.
  11. Olah, G. A., ed. (1963). Friedel-Crafts and Related Reactions. Vol. 1. New York City: Interscience.
  12. Nenitzescu, Costin D.; Cantuniari, Ion P. (1933). "Durch Aluminiumchlorid Katalysierte Reaktion, VI. Mitteil.: Die Umlagerung des Cyclohexans in Metyl-cyclopentan". Berichte der Deutschen Chemischen Gesellschaft (A and B Series). 66 (8): 1097–1100. doi:10.1002/cber.19330660817. ISSN 1099-0682.
  13. Jonathan T. Reeves; Zhulin Tan; Daniel R. Fandrick; Jinhua J. Song; Nathan K. Yee; Chris H. Senanayake (2012). "Synthesis of Trifluoromethyl Ketones from Carboxylic Acids: 4-(3,4-Dibromophenyl)-1,1,1-trifluoro-4-methylpentan-2-one". Organic Syntheses. 89: 210. doi:10.15227/orgsyn.089.0210.
  14. Kamil Paruch; Libor Vyklicky; Thomas J. Katz (2003). "Preparation of 9,10-Dimethoxyphenanthrene and 3,6-Diacetyl-9,10-Dimethoxyphenanthrene". Organic Syntheses. 80: 227. doi:10.15227/orgsyn.080.0227.
  15. Alexander J. Seed; Vaishali Sonpatki; Mark R. Herbert (2002). "3-(4-Bromobenzoyl)propanoic Acid". Organic Syntheses. 79: 204. doi:10.15227/orgsyn.079.0204.
  16. Wade, L. G. (2003) Organic Chemistry, 5th edition, Prentice Hall, Upper Saddle River, New Jersey, United States. ISBN 013033832X.
  17. Galatsis, P. (1999) Handbook of Reagents for Organic Synthesis: Acidic and Basic Reagents, H. J. Reich, J. H. Rigby (eds.) Wiley, New York City. pp. 12–15. ISBN 978-0-471-97925-8.
  18. Snider, B. B. (1980). "Lewis-acid catalyzed ene reactions". Acc. Chem. Res. 13 (11): 426. doi:10.1021/ar50155a007.
  19. Reuben D. Rieke; Stephen E. Bales; Phillip M. Hudnall; Timothy P. Burns; Graham S. Poindexter (1979). "Highly Reactive Magnesium for the Preparation of Grignard Reagents: 1-Norbornanecarboxylic Acid". Organic Syntheses. 59: 85. doi:10.15227/orgsyn.059.0085.
  20. Sami A. Shama; Carl C. Wamser (1983). "Hexamethyl Dewar Benzene". Organic Syntheses. 61: 62. doi:10.15227/orgsyn.061.0062.
  21. B. Buchner; L. B. Lockhart Jr. (1951). "Phenyldichlorophosphine". Organic Syntheses. 31: 88. doi:10.15227/orgsyn.031.0088.
  22. "List of Minerals". www.ima-mineralogy.org. International Mineralogical Association. March 21, 2011.
  23. "Cadwaladerite". www.mindat.org.
  24. Aluminium Chloride. solvaychemicals.us
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