Difference between revisions of "Aluminium chloride"

From WikiChem
Jump to: navigation, search
(Imported from http://en.wikipedia.org/w/index.php?title=Aluminium_chloride&oldid=300971436)
 
 
(14 intermediate revisions by the same user not shown)
Line 1: Line 1:
 +
{{about|the trichloride, AlCl<sub>3</sub>, and its hexahydrate|the unstable monochloride, AlCl|Aluminium monochloride}}
 +
{{FixBunching|beg}}
 
{{chembox
 
{{chembox
|   Name =
+
| Name = Aluminium trichloride (anhydrous)
|  ImageFile = Aluminium-trichloride-hexahydrate-white-and-yellow.jpg
+
| ImageFile = Aluminium-trichloride-dimer-3D-balls.png
<!-- | ImageSize = 150px -->
+
|   ImageSize = 150px
|  ImageName = Aluminium chloride
+
ImageName = Aluminium trichloride dimer
|  ImageFile1 = Aluminium-trichloride-dimer-3D-balls.png
+
| IUPACName = aluminium trichloride<br/>trichloroalumane<br/>trichloridoaluminium
<!-- | ImageSize1 = 150px -->
 
ImageName1 = Aluminium trichloride dimer
 
|   IUPACName = aluminium trichloride<br />trichloroalumane<br />trichloridoaluminium
 
 
|  OtherNames = aluminum trichloride
 
|  OtherNames = aluminum trichloride
 
| Section1 = {{Chembox Identifiers
 
| Section1 = {{Chembox Identifiers
 +
|  InChI = 1/Al.3ClH/h;3*1H/q+3;;;/p-3
 +
|  StdInChI = 1S/Al.3ClH/h;3*1H/q+3;;;/p-3
 +
|  InChIKey = VSCWAEJMTAWNJL-DFZHHIFOAR
 +
|  StdInChIKey = VSCWAEJMTAWNJL-UHFFFAOYSA-K
 
|  CASNo = 7446-70-0
 
|  CASNo = 7446-70-0
|   CASNo_Ref = {{cascite}}
+
|   CASNo_Ref = {{cascite}}
CASOther = <br/>10124-27-3 (hexahydrate)
+
EC-number = 231-208-1
 +
|  ChemSpiderID = 22445
 
|  PubChem = 24012
 
|  PubChem = 24012
 
|  RTECS = BD0530000
 
|  RTECS = BD0530000
 
   }}
 
   }}
 
| Section2 = {{Chembox Properties
 
| Section2 = {{Chembox Properties
 +
|  Reference = <ref name="RubberBible">{{RubberBible62nd|page=B-73}}.</ref>
 
|  Formula = AlCl<sub>3</sub>
 
|  Formula = AlCl<sub>3</sub>
|  MolarMass = 133.34 g/mol (anhydrous)<br />241.43 g/mol (hexahydrate)
+
|  MolarMass = 133.34 g/mol (anhydrous)
|  Appearance = white or pale yellow solid,<br />[[hygroscopic]]
+
|  Appearance = white or pale yellow solid, very hygroscopic
|  Density = 2.48 g/cm<sup>3</sup> (anhydrous) <br> 1.3 g/cm<sup>3</sup> (hexahydrate)
+
|  Density = 2.44 g/cm<sup>3</sup> (25 ºC), solid<br/>1.31 g/cm<sup>3</sup> (200 ºC), liquid
|  Solubility = 43.9 g/100 ml (0 °C)<br />44.9 g/100 ml (10 °C)<br />45.8 g/100 ml (20 °C)<br />46.6 g/100 ml (30 °C)<br />47.3 g/100 ml (40 °C)<br />48.1 g/100 ml (60 °C)<br />48.6 g/100 ml (80 °C)<br />49 g/100 ml (100 °C)
+
|  Solubility = reacts violently
SolubleOther = soluble in hydrogen chloride, ethanol, chloroform, carbon tetrachloride <br> slightly soluble in benzene
+
|  Solubility1 = 100 g/100 ml
|  MeltingPt = 192.4 °C *anhydrous) <br> 0 °C (hexahydrate)
+
|    Solvent1 = ethanol
|  BoilingPt = 120 °C (hexahydrate)
+
|  Solubility2 = 0.072 g/100 ml
|  pKa =
+
|    Solvent2 = chloroform
 +
|  Solubility3 = slightly soluble
 +
|    Solvent3 = benzene
 +
Solubility4 = soluble in [[carbon tetrachloride]], [[diethyl ether]]
 +
|  MeltingPt = 190 °C at 2.5 atm
 +
|  BoilingPt = 177.8 °C subl.
 
   }}
 
   }}
 
| Section3 = {{Chembox Structure
 
| Section3 = {{Chembox Structure
|  MolShape = Trigonal planar<br />([[monomer]]ic vapour)
+
|  Coordination = Octahedral (Al<sup>3+</sup>)
|  Coordination = Octahedral (solid)<br />Tetrahedral (liquid)
 
 
|  CrystalStruct = [[Monoclinic]], [[Pearson symbol|mS16]]
 
|  CrystalStruct = [[Monoclinic]], [[Pearson symbol|mS16]]
 
|  SpaceGroup = C12/m1, No. 12
 
|  SpaceGroup = C12/m1, No. 12
 
   }}
 
   }}
 
| Section7 = {{Chembox Hazards
 
| Section7 = {{Chembox Hazards
EUClass = Corrosive ('''C''')
+
Reference = <ref>{{CLP Regulation|index=013-003-00-7|page=366}}</ref>
RPhrases = {{R34}}
+
ExternalMSDS = {{ICSC-small|1125}}
SPhrases = {{S1/2}}, {{S7/8}}, {{S28}}, {{S45}}
+
EUIndex = 013-003-00-7
|  LD50 = ''anhydrous:'' <br> 380 mg/kg, rat (oral) <hr> ''hexahydrate:'' <br> 3311 mg/kg, rat (oral)
+
|  GHSPictograms = {{GHS05|Skin Corr. 1B}}
 +
|  GHSSignalWord = DANGER
 +
|  HPhrases = {{H-phrases|314}}
 
   }}
 
   }}
 
| Section8 = {{Chembox Related
 
| Section8 = {{Chembox Related
|  OtherAnions = [[Aluminium fluoride]]<br />[[Aluminium bromide]]<br />[[Aluminium iodide]]
+
|  OtherAnions = [[Aluminium fluoride]]<br/>[[Aluminium bromide]]<br/>[[Aluminium iodide]]
|  OtherCations = [[Boron trichloride]]<br />[[Gallium trichloride]]<br />[[Indium(III) chloride]]<br />[[Thallium(III) chloride]]<br />[[Magnesium chloride]]
+
|  OtherCations = [[Boron trichloride]]<br/>[[Gallium(III) chloride]]<br/>[[Indium(III) chloride]]<br/>[[Thallium(III) chloride]]
|  Function = [[Lewis acid]]s
+
|  OtherFunctn = [[Iron(III) chloride]]<br/>[[Boron trifluoride]]
|  OtherFunctn = [[Iron(III) chloride]]<br />[[Boron trifluoride]]
+
|    Function = [[Lewis acid]]s
 
   }}
 
   }}
 
}}
 
}}
 +
{{FixBunching|mid}}
 +
{{chembox
 +
| Name = Aluminium trichloride hexahydrate
 +
| ImageFile = Aluminium-trichloride-hexahydrate-white-and-yellow.jpg
 +
|  ImageSize = 150px
 +
|  ImageName = Aluminium trichloride hexahydrate
 +
| IUPACName = aluminium trichloride—water (1/6)
 +
| Section1 = {{Chembox Identifiers
 +
|  InChI = 1/Al.3ClH.6H2O/h;3*1H;6*1H2/q+3;;;;;;;;;/p-3
 +
|  StdInChI = 1S/Al.3ClH.6H2O/h;3*1H;6*1H2/q+3;;;;;;;;;/p-3
 +
|  InChIKey = JGDITNMASUZKPW-DFZHHIFOAF
 +
|  StdInChIKey = JGDITNMASUZKPW-UHFFFAOYSA-K
 +
|  CASNo = 7784-13-6 <!-- verified with ChemSpider and the NZ HSNO Chemical Classification Information Database -->
 +
|  EC-number = 231-208-1
 +
|  ATCCode_prefix = D10
 +
|  ATCCode_suffix = AX01
 +
|  ChemSpiderID = 22970
 +
|  PubChem = 24012
 +
|  RTECS = BD0530000
 +
  }}
 +
| Section2 = {{Chembox Properties
 +
|  Reference = <ref name="RubberBible"/>
 +
|  Formula = AlCl<sub>3</sub>·6H<sub>2</sub>O
 +
|  MolarMass = 241.43 g/mol
 +
|  Appearance = colourless or white solid, hygroscopic
 +
|  Density = 2.398 g/cm<sup>3</sup>
 +
|  Solubility = 45.8 g/100 ml (20 °C)<br/>48.6 g/100 ml (80 °C)
 +
|  Solubility1 = 50 g/100 ml
 +
|    Solvent1 = ethanol
 +
|  Solubility2 = soluble
 +
|    Solvent2 = diethyl ether
 +
|  Solubility3 = slightly soluble
 +
|    Solvent3 = hydrochloric acid
 +
|  MeltingPt = 100 °C decomp.
 +
|  RefractIndex = 1.6
 +
  }}
 +
| Section7 = {{Chembox Hazards
 +
|  Reference = <ref>{{GHS class NZ|id=8011|accessdate=2009-08-22}}.</ref>
 +
|  GHSPictograms = {{GHS corrosion|Corr. Met. 1, Skin Corr. 1C, Eye Dam. 1}}{{GHS exclamation mark|Acute Tox. (oral) 4}}
 +
|  GHSSignalWord = DANGER
 +
|  HPhrases = {{H-phrases|280|290|302|314}}
 +
|  PPhrases = {{P-phrases|234|260|264|270|280|301+312|301+330+331|303+361+353|304+340|305+351+338 |310|321|363|405|406|501}}
 +
|  FlashPt = non-flammable
 +
  }}
 +
}}
 +
{{FixBunching|end}}
 +
'''Aluminium chloride''' (AlCl<sub>3</sub>) is a [[chemical compound|compound]] of [[aluminium]] and [[chlorine]].  The solid has a low melting and boiling point, and is [[Covalent bond|covalently bonded]]. It [[sublimation (physics)|sublimes]] at 178&nbsp;°C.  Molten AlCl<sub>3</sub> [[conductance|conducts]] [[electricity]] poorly,<ref name="G&E">{{Greenwood&Earnshaw1st|pages=262–66}}.</ref> unlike more [[ionic bond|ionic]] [[halide]]s such as [[sodium chloride]].
  
'''Aluminium chloride''' (AlCl<sub>3</sub>) is a [[chemical compound|compound]] of [[aluminium]] and [[chlorine]].  The solid has a low melting and boiling point, and is [[Covalent bond|covalently bonded]]. It [[sublimation (physics)|sublimes]] at 178 °[[Celsius|C]].  Molten AlCl<sub>3</sub> [[conductance|conducts]] [[electricity]] poorly,<ref name="Greenwood">N. N. Greenwood, A. Earnshaw, ''Chemistry of the Elements'', Pergamon Press, [[Oxford]], [[United Kingdom]], 1984.</ref> unlike more [[ionic bond|ionic]] [[halide]]s such as [[sodium chloride]].  It exists in the solid state as a six-coordinate layer lattice.
+
AlCl<sub>3</sub> adopts the [[Yttrium trichloride structure|YCl<sub>3</sub> structure]] in the solid, featuring  a cubic close packed array of chloride ions with Al<sup>3+</sup> ions occupying one-third of the octahedral holes, forming a layered structure.<ref name="Wells">{{Wells5th}}.</ref> Upon melting AlCl<sub>3</sub> gives the [[dimer]] Al<sub>2</sub>Cl<sub>6</sub>, which can [[vapour|vaporise]].  At higher [[temperature]]s this Al<sub>2</sub>Cl<sub>6</sub> dimer [[Dissociation|dissociates]] into trigonal planar AlCl<sub>3</sub>, which is structurally analogous to [[boron trifluoride|BF<sub>3</sub>]].
 
 
AlCl<sub>3</sub> adopts the "YCl<sub>3</sub>" structure, featuring  Al<sup>3+</sup> cubic close packed layered structure.<ref name="Wells">A. F. Wells,  ''Structural Inorganic Chemistry'', Oxford Press, [[Oxford]], [[United Kingdom]], 1984.</ref> In contrast, AlBr<sub>3</sub> has a more molecular structure, with the Al<sup>3+</sup> centers occupying adjacent tetrahedral holes of the close-packed framework of Br<sup>−</sup> ions.  Upon melting AlCl<sub>3</sub> gives the [[dimer]] Al<sub>2</sub>Cl<sub>6</sub>, which can [[vapour|vaporise]].  At higher [[temperature]]s this Al<sub>2</sub>Cl<sub>6</sub> dimer [[Dissociation (chemistry)|dissociates]] into trigonal planar AlCl<sub>3</sub>, which is structurally analogous to [[boron trifluoride|BF<sub>3</sub>]].
 
  
 
[[Image:Aluminium-trichloride-3D-structures.png|middle|480px|The three structures of aluminium trichloride]]
 
[[Image:Aluminium-trichloride-3D-structures.png|middle|480px|The three structures of aluminium trichloride]]
  
 
Aluminium chloride is highly [[deliquescent]], and can explode upon abrupt contact with [[water (molecule)|water]] because of the high heat of [[hydration]].  [[Aqueous]] [[solution]]s of AlCl<sub>3</sub> are ionic and thus [[conductance|conduct]] [[electricity]] well.  Such solutions are found to be [[acid]]ic, indicative of partial [[hydrolysis]] of the Al<sup>3+</sup> ion.  The reactions can be described (simplified) as:
 
Aluminium chloride is highly [[deliquescent]], and can explode upon abrupt contact with [[water (molecule)|water]] because of the high heat of [[hydration]].  [[Aqueous]] [[solution]]s of AlCl<sub>3</sub> are ionic and thus [[conductance|conduct]] [[electricity]] well.  Such solutions are found to be [[acid]]ic, indicative of partial [[hydrolysis]] of the Al<sup>3+</sup> ion.  The reactions can be described (simplified) as:
:[Al(H<sub>2</sub>O)<sub>6</sub>]<sup>3+</sup> + H<sub>2</sub>O {{unicode|⇌}} [Al(OH)(H<sub>2</sub>O)<sub>5</sub>]<sup>2+</sup> +  H<sub>3</sub>O<sup>+</sup>
+
:[Al(H<sub>2</sub>O)<sub>6</sub>]<sup>3+</sup> + H<sub>2</sub>O {{eqm}} [Al(OH)(H<sub>2</sub>O)<sub>5</sub>]<sup>2+</sup> +  H<sub>3</sub>O<sup>+</sup>
  
AlCl<sub>3</sub> is probably the most commonly used [[Lewis acid]] and also one of the most powerful. It finds widespread application in the [[chemical industry]] as the classic [[catalyst]] for [[Friedel-Crafts]] reactions, both acylations and alkylations.  It also finds use in [[polymerization]] and [[isomerization]] reactions of [[hydrocarbon]]s.
+
AlCl<sub>3</sub> is probably the most commonly used [[Lewis acid]] and also one of the most powerful. It finds widespread application in the [[chemical industry]] as the classic [[catalyst]] for [[Friedel–Crafts reaction]]s, both acylations and alkylations.  It also finds use in [[polymerization]] and [[isomerization]] reactions of [[hydrocarbon]]s.
[[Aluminium]] also forms a lower [[chloride]], [[aluminium(I) chloride]] (AlCl), but this is very unstable and only known in the vapor phase.<ref name="Greenwood"/>
+
[[Aluminium]] also forms a lower [[chloride]], [[aluminium(I) chloride]] (AlCl), but this is very unstable and only known in the vapor phase.<ref name="G&E"/>
  
 
==Chemical properties==
 
==Chemical properties==
'''Aluminium chloride''' is a powerful [[Lewis acid]], capable of forming stable Lewis acid-base adducts with even weak [[Lewis base]]s such as [[benzophenone]] or [[mesitylene]].<ref name="Friedel">G. A. Olah (ed.), ''Friedel-Crafts and Related Reactions'', Vol. 1, [[John Wiley & Sons|Interscience]], [[New York]], 1963.</ref>  Not surprisingly it forms AlCl<sub>4</sub><sup>−</sup> in the presence of [[chloride]] ions.
+
Aluminium chloride is a powerful [[Lewis acid]], capable of forming stable Lewis acid-base adducts with even weak [[Lewis base]]s such as [[benzophenone]] or [[mesitylene]].<ref name="Olah">{{citation | editor1-first = G. A. | editor1-last = Olah | editorlink1 = George Andrew Olah | title = Friedel-Crafts and Related Reactions | volume = 1 | publisher = Wiley–Interscience | location = New York | year = 1963}}.</ref>  Not surprisingly it forms AlCl<sub>4</sub><sup>−</sup> in the presence of [[chloride]] ions.
  
In water, partial hydrolysis forms [[hydrogen chloride|HCl gas]] or H<sub>3</sub>O<sup>+</sup>, as described in the overview above.  [[Aqueous solution]]s behave similarly to other [[aluminium]] [[salt]]s containing hydrated Al<sup>3+</sup> [[ion]]s, giving a gelatinous [[precipitate]] of [[aluminium hydroxide]] upon reaction with the correct quantity of aqueous [[sodium hydroxide]]:
+
In water, partial hydrolysis forms [[hydrogen chloride]] or H<sub>3</sub>O<sup>+</sup>, as described in the overview above.  [[Aqueous solution]]s behave similarly to other [[aluminium]] [[salt]]s containing hydrated Al<sup>3+</sup> [[ion]]s, giving a gelatinous [[precipitate]] of [[aluminium hydroxide]] upon reaction with the correct quantity of aqueous [[sodium hydroxide]]:
 
+
:AlCl<sub>3</sub> + 3NaOH →  Al(OH)<sub>3</sub>  +  3NaCl
:AlCl<sub>3</sub>([[aqueous|aq]])  + 3 NaOH(aq)  →  Al(OH)<sub>3</sub>([[solid|s]]) 3[[sodium chloride|NaCl]](aq)
 
  
 
==Preparation==
 
==Preparation==
Aluminium chloride is manufactured on a large scale by the [[exothermic]] reaction of aluminium metal with chlorine or hydrogen chloride at temperatures between 650 to 750 °C.<ref name="Greenwood"/>
+
Aluminium chloride is manufactured on a large scale by the [[exothermic]] reaction of aluminium metal with chlorine or hydrogen chloride at 650–750&nbsp;°C.<ref name="G&E"/>
:2 Al 3 Cl<sub>2</sub>  →  2 AlCl<sub>3</sub>
+
:2Al 3Cl<sub>2</sub>  →  2AlCl<sub>3</sub>
:2 Al 6 HCl →  2 AlCl<sub>3</sub>  +  3 H<sub>2</sub>
+
:2Al 6HCl →  2AlCl<sub>3</sub>  +  3H<sub>2</sub>
Hydrated forms are prepared by dissolving aluminium oxides with dry [[hydrochloric acid]] at 150°C.
+
Hydrated forms are prepared by dissolving aluminium oxides with dry [[hydrochloric acid]] at 150&nbsp;°C.
  
 
==Uses==
 
==Uses==
The [[Friedel-Crafts reaction]]<ref name="Friedel"/> is the major use for aluminium chloride, for example in the preparation of [[anthraquinone]] (for the [[dye]]stuffs industry) from [[benzene]] and [[phosgene]].<ref name="Greenwood"/>  In the general [[Friedel-Crafts]] reaction, an [[acyl chloride]] or [[alkyl halide]] reacts with an [[aromatic]] system as shown:<ref name="Friedel"/>
+
The [[Friedel–Crafts reaction]] is the major use for aluminium chloride, for example in the preparation of [[anthraquinone]] (for the [[dye]]stuffs industry) from [[benzene]] and [[phosgene]].<ref name="G&E"/><ref name="Olah"/>  In the general Friedel–Crafts reaction, an [[acyl chloride]] or [[alkyl halide]] reacts with an [[aromatic]] system as shown:<ref name="Olah"/>
  
 
[[Image:AlCl3 FriedelCrafts.gif|300px]]
 
[[Image:AlCl3 FriedelCrafts.gif|300px]]
  
With [[benzene]] [[derivative]]s, the major product is the [[para]] [[isomer]].  The alkylation reaction has many associated problems, such as in [[Friedel-Crafts]], so it is less widely used than the acylation reaction. For both reactions, the aluminium chloride, as well as other materials and the equipment, must be moderately dry, although a trace of moisture is necessary for the reaction to proceed. A general problem with the Friedel-Crafts reaction is that the aluminium chloride "[[catalyst]]" needs to be present in full [[stoichiometry|stoichiometric]] quantities in order for the reaction to go to completion, because it [[Complex (chemistry)|complex]]es strongly with the products (see chemical properties above).  This makes it very difficult to recycle, so it must be destroyed after use, generating a large amount of corrosive waste. For this reason chemists are examining the use of more [[green chemistry|environmentally benign]] catalysts such as [[ytterbium]](III) [[triflate]] or [[dysprosium]](III)
+
With [[benzene]] [[derivative]]s, the major product is the ''[[para]]''-isomer.  The alkylation reaction has many associated problems, so it is less widely used than the acylation reaction. For both reactions, the aluminium chloride, as well as other materials and the equipment, must be moderately dry, although a trace of moisture is necessary for the reaction to proceed. A general problem with the Friedel–Crafts reaction is that the aluminium chloride "[[catalyst]]" needs to be present in full [[stoichiometry|stoichiometric]] quantities in order for the reaction to go to completion, because it [[complex]]es strongly with the products (see chemical properties above).  This makes it very difficult to recycle, so it must be destroyed after use, generating a large amount of corrosive waste. For this reason chemists are examining the use of more [[green chemistry|environmentally benign]] catalysts such as [[ytterbium(III) triflate]] or [[dysprosium(III) triflate]], which can be [[recycling|recycled]].
triflate, which can be
 
[[recycling|recycled]].
 
  
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]]):<ref>L. G. Wade, ''Organic Chemistry'', 5th edition, [[Prentice Hall]], [[Upper Saddle River, New Jersey|Upper Saddle River]], [[New Jersey]], United States, 2003.</ref>
+
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]]:<ref>{{citation | first = L. G. | last = Wade | title = Organic Chemistry | edition = 5th | publisher = Prentice Hall | location = New York | year = 2003}}.</ref>
  
 
[[Image:AlCl3 formylation.gif|300px]]
 
[[Image:AlCl3 formylation.gif|300px]]
  
Aluminium chloride finds a wide variety of other applications in [[organic chemistry]].<ref>P. Galatsis, in: ''Handbook of Reagents for Organic Synthesis: Acidic and Basic Reagents'', (H. J. Reich, J. H. Rigby, eds.), pp. 12–15, [[John Wiley & Sons|Wiley]], [[New York]], 1999.</ref> For example, it can catalyse the "[[ene reaction]]", such as the addition of [[3-buten-2-one]] (methyl vinyl ketone) to [[carvone]]:<ref>{{cite journal | author = B. B. Snider | title = Lewis-acid catalyzed ene reactions | journal = [[Acc. Chem. Res.]] | volume = 13 | pages = 426 | year = 1980 | doi = 10.1021/ar50155a007}}</ref>
+
Aluminium chloride finds a wide variety of other applications in [[organic chemistry]].<ref>{{citation | first = P. | last = Galatsis | title = Handbook of Reagents for Organic Synthesis: Acidic and Basic Reagents | editor1-first = Hans J. | editor1-last = Reich | editor2-first = James H. | editor2-last = Rigby | pages = 12–15 | publisher = Wiley | location = New York | year = 1999 | isbn = 0471979252}}.</ref> For example, it can catalyse the "[[ene reaction]]", such as the addition of [[3-buten-2-one]] (methyl vinyl ketone) to [[carvone]]:<ref>{{citation | first = B. B. | last = Snider | title = Lewis-acid catalyzed ene reactions | journal = Acc. Chem. Res. | volume = 13 | issue = 11 | pages = 426–32 | year = 1980 | doi = 10.1021/ar50155a007}}.</ref>
  
 
[[Image:AlCl3 ene rxn.gif|400px]]
 
[[Image:AlCl3 ene rxn.gif|400px]]
  
AlCl<sub>3</sub> is also widely used for [[polymerization]] and [[isomerization]] reactions of [[hydrocarbon]]s.  Important examples<ref name="Greenwood"/> include the manufacture of [[ethylbenzene]], which used to make [[styrene]] and thus [[polystyrene]], and also production of [[dodecylbenzene]], which is used for making [[detergent]]s.
+
AlCl<sub>3</sub> is also widely used for [[polymerization]] and [[isomerization]] reactions of [[hydrocarbon]]s.  Important examples include the manufacture of [[ethylbenzene]], which used to make [[styrene]] and thus [[polystyrene]], and also production of [[dodecylbenzene]], which is used for making [[detergent]]s.<ref name="G&E"/>
  
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 so-called [[Ernst Otto Fischer|Fischer]]-Hafner synthesis.
+
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 so-called [[Fischer–Hafner synthesis]].
  
 
Aluminium chloride, often in the form of derivatives such as [[aluminium chlorohydrate]], is a common component in [[antiperspirant]]s at low concentrations.  [[Hyperhidrosis]] sufferers need a much higher concentration (15% or higher), sold under such brand names as Drysol, Maxim, Odaban, CertainDri, B+Drier, Anhydrol Forte and Driclor.
 
Aluminium chloride, often in the form of derivatives such as [[aluminium chlorohydrate]], is a common component in [[antiperspirant]]s at low concentrations.  [[Hyperhidrosis]] sufferers need a much higher concentration (15% or higher), sold under such brand names as Drysol, Maxim, Odaban, CertainDri, B+Drier, Anhydrol Forte and Driclor.
  
==Chemical Reactions==
+
==Chemical reactions==
Aluminium chloride reacts with calcium and magnesium hydrides in [[tetrahydrofuran]] forming tetrahydro aluminates:
+
Aluminium chloride reacts with calcium and magnesium hydrides in [[tetrahydrofuran]] forming tetrahydroaluminates:
: AlCl<sub>3</sub> + 3 LiH → AlH<sub>3</sub> + 3 LiCl
+
: AlCl<sub>3</sub> + 3LiH → AlH<sub>3</sub> + 3LiCl
  
The hexahydrate decomposes to [[aluminum oxide]] when heated at 300 °C: <ref>Pradyot Patnaik. ''Handbook of Inorganic Chemicals''. McGraw-Hill, 2002, ISBN 0070494398</ref>
+
The hexahydrate decomposes to [[aluminum oxide]] when heated at 300&nbsp;°C:<ref>{{citation | first = Pradyot | last = Patnaik | title = Handbook of Inorganic Chemicals | publisher = McGraw-Hill | location = New York | year = 2002 | isbn = 0070494398}}.</ref>
: 2 AlCl<sub>3</sub>·6H<sub>2</sub>O → 2 Al<sub>2</sub>O<sub>3</sub> + 6 HCl + 9 H<sub>2</sub>O
+
:2AlCl<sub>3</sub>·6H<sub>2</sub>O → Al<sub>2</sub>O<sub>3</sub> + 6HCl + 3H<sub>2</sub>O
  
 
==Precautions==
 
==Precautions==
Anhydrous AlCl<sub>3</sub> reacts vigorously with [[water (molecule)|water]] and [[base (chemistry)|base]]s, so suitable precautions are required. Hydrated salts are less problematic.
+
Anhydrous AlCl<sub>3</sub> reacts vigorously with [[water (molecule)|water]] and [[base]]s, so suitable precautions are required. Hydrated salts are less problematic.
  
 
==References==
 
==References==
<!--This article uses the Cite.php citation mechanism. If you would like more information on how to add references to this article, please see http://meta.wikimedia.org/wiki/Cite/Cite.php -->
+
{{reflist}}
<references/>
 
  
 
==External links==
 
==External links==
* [http://loradchemical.com/aluminum-chloride-2.html Aluminum Chloride Information]
+
*{{ICSC|1125}}
* [http://www.ilo.org/public/english/protection/safework/cis/products/icsc/dtasht/_icsc11/icsc1125.htm International Chemical Safety Card 1125]
+
*{{PGCH|0024}}
* [http://www.orgsyn.org/orgsyn/chemname.asp?nameID=33169 Index of Organic Synthesis procedures that utilize AlCl<sub>3</sub>]
+
*{{EHC|194|name=Aluminium}}
 +
*{{HSDB|name=Aluminum chloride}}
 +
*{{OrgSynth preps|id=33169|name=aluminium chloride}}
 +
* [http://loradchemical.com/aluminum-chloride-2.html Aluminum chloride Information]
 
* [http://www.chemguide.co.uk/inorganic/period3/chlorides.html The period 3 chlorides]
 
* [http://www.chemguide.co.uk/inorganic/period3/chlorides.html The period 3 chlorides]
* [http://www.solvaychemicals.us/static/wma/pdf/5/1/1/8/ALCL.pdf MSDS]
 
 
{{Aluminium compounds}}
 
  
 +
[[Category:Aluminium compounds]]
 
[[Category:Chlorides]]
 
[[Category:Chlorides]]
 
[[Category:Metal halides]]
 
[[Category:Metal halides]]
[[Category:Aluminium compounds]]
 
 
[[Category:Reagents for organic chemistry]]
 
[[Category:Reagents for organic chemistry]]
 +
[[Category:Anti-acne preparations]]
  
 
{{Imported from Wikipedia|name=Aluminium chloride|id=300971436}}
 
{{Imported from Wikipedia|name=Aluminium chloride|id=300971436}}

Latest revision as of 07:02, 13 December 2009

Aluminium trichloride (anhydrous)
Aluminium trichloride dimer
IUPAC name aluminium trichloride
trichloroalumane
trichloridoaluminium
Other names aluminum trichloride
Identifiers
InChI InChI=1/Al.3ClH/h;3*1H/q+3;;;/p-3
InChIKey VSCWAEJMTAWNJL-DFZHHIFOAR
Standard InChI InChI=1S/Al.3ClH/h;3*1H/q+3;;;/p-3
Standard InChIKey VSCWAEJMTAWNJL-UHFFFAOYSA-K
CAS number [7446-70-0]
EC number 231-208-1
RTECS BD0530000
ChemSpider 22445
PubChem 24012
Properties[1]
Chemical formula AlCl3
Molar mass 133.34 g/mol (anhydrous)
Appearance white or pale yellow solid, very hygroscopic
Density 2.44 g/cm3 (25 ºC), solid
1.31 g/cm3 (200 ºC), liquid
Melting point

190 °C at 2.5 atm

Boiling point

177.8 °C subl.

Solubility in water reacts violently
Solubility in ethanol 100 g/100 ml
Solubility in chloroform 0.072 g/100 ml
Solubility in benzene slightly soluble
Solubility soluble in carbon tetrachloride, diethyl ether
Structure
Crystal structure Monoclinic, mS16
Space group C12/m1, No. 12
Coordination geometry Octahedral (Al3+)
Hazards[2]
Material safety data sheet (MSDS) ICSC 1125
EU index number 013-003-00-7
GHS pictograms Skin Corr. 1B
GHS signal word DANGER
GHS hazard statements H314
Related compounds
Other anions Aluminium fluoride
Aluminium bromide
Aluminium iodide
Other cations Boron trichloride
Gallium(III) chloride
Indium(III) chloride
Thallium(III) chloride
Other Lewis acids Iron(III) chloride
Boron trifluoride
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
Aluminium trichloride hexahydrate
Aluminium trichloride hexahydrate
IUPAC name aluminium trichloride—water (1/6)
Identifiers
InChI InChI=1/Al.3ClH.6H2O/h;3*1H;6*1H2/q+3;;;;;;;;;/p-3
InChIKey JGDITNMASUZKPW-DFZHHIFOAF
Standard InChI InChI=1S/Al.3ClH.6H2O/h;3*1H;6*1H2/q+3;;;;;;;;;/p-3
Standard InChIKey JGDITNMASUZKPW-UHFFFAOYSA-K
CAS number [7784-13-6]
EC number 231-208-1
RTECS BD0530000
ATC code D10AX01
ChemSpider 22970
PubChem 24012
Properties[1]
Chemical formula AlCl3·6H2O
Molar mass 241.43 g/mol
Appearance colourless or white solid, hygroscopic
Density 2.398 g/cm3
Melting point

100 °C decomp.

Solubility in water 45.8 g/100 ml (20 °C)
48.6 g/100 ml (80 °C)
Solubility in ethanol 50 g/100 ml
Solubility in diethyl ether soluble
Solubility in hydrochloric acid slightly soluble
Refractive index (nD) 1.6
Hazards[3]
GHS pictograms Corr. Met. 1, Skin Corr. 1C, Eye Dam. 1Acute Tox. (oral) 4
GHS signal word DANGER
GHS hazard statements H280, H290, H302, H314
GHS precautionary statements P234, P260, P264, P270, P280, P301+312, P301+330+331, P303+361+353, P304+340, P305+351+338, P310, P321, P363, P405
Flash point non-flammable
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)

Aluminium chloride (AlCl3) is a compound of aluminium and chlorine. The solid has a low melting and boiling point, and is covalently bonded. It sublimes at 178 °C. Molten AlCl3 conducts electricity poorly,[4] unlike more ionic halides such as sodium chloride.

AlCl3 adopts the YCl3 structure in the solid, featuring a cubic close packed array of chloride ions with Al3+ ions occupying one-third of the octahedral holes, forming a layered structure.[5] Upon melting AlCl3 gives the dimer Al2Cl6, which can vaporise. At higher temperatures this Al2Cl6 dimer dissociates into trigonal planar AlCl3, which is structurally analogous to BF3.

The three structures of aluminium trichloride

Aluminium chloride is highly deliquescent, and can explode upon abrupt contact with water because of the high heat of hydration. Aqueous solutions of AlCl3 are ionic and thus conduct electricity well. Such solutions are found to be acidic, indicative of partial hydrolysis of the Al3+ ion. The reactions can be described (simplified) as:

[Al(H2O)6]3+ + H2O [Al(OH)(H2O)5]2+ + H3O+

AlCl3 is probably the most commonly used Lewis acid and also one of the most powerful. It finds widespread application in the chemical industry as the classic catalyst for Friedel–Crafts reactions, both acylations and alkylations. It also finds use in polymerization and isomerization reactions of hydrocarbons. Aluminium also forms a lower chloride, aluminium(I) chloride (AlCl), but this is very unstable and only known in the vapor phase.[4]

Chemical properties

Aluminium chloride is a powerful Lewis acid, capable of forming stable Lewis acid-base adducts with even weak Lewis bases such as benzophenone or mesitylene.[6] Not surprisingly it forms AlCl4 in the presence of chloride ions.

In water, partial hydrolysis forms hydrogen chloride or H3O+, as described in the overview above. Aqueous solutions behave similarly to other aluminium salts containing hydrated Al3+ ions, giving a gelatinous precipitate of aluminium hydroxide upon reaction with the correct quantity of aqueous sodium hydroxide:

AlCl3 + 3NaOH → Al(OH)3 + 3NaCl

Preparation

Aluminium chloride is manufactured on a large scale by the exothermic reaction of aluminium metal with chlorine or hydrogen chloride at 650–750 °C.[4]

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

Hydrated forms are prepared by dissolving aluminium oxides with dry hydrochloric acid at 150 °C.

Uses

The Friedel–Crafts reaction is the major use for aluminium chloride, for example in the preparation of anthraquinone (for the dyestuffs industry) from benzene and phosgene.[4][6] In the general Friedel–Crafts reaction, an acyl chloride or alkyl halide reacts with an aromatic system as shown:[6]

AlCl3 FriedelCrafts.gif

With benzene derivatives, the major product is the para-isomer. The alkylation reaction has many associated problems, so it is less widely used than the acylation reaction. For both reactions, the aluminium chloride, as well as other materials and the equipment, must be moderately dry, although a trace of moisture is necessary for the reaction to proceed. A general problem with the Friedel–Crafts reaction is that the aluminium chloride "catalyst" needs to be present in full stoichiometric quantities in order for the reaction to go to completion, because it complexes strongly with the products (see chemical properties above). This makes it very difficult to recycle, so it must be destroyed after use, generating a large amount of corrosive waste. For this reason chemists are examining the use of more environmentally benign catalysts such as ytterbium(III) triflate or dysprosium(III) triflate, which can be recycled.

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:[7]

AlCl3 formylation.gif

Aluminium chloride finds a wide variety of other applications in organic chemistry.[8] For example, it can catalyse the "ene reaction", such as the addition of 3-buten-2-one (methyl vinyl ketone) to carvone:[9]

AlCl3 ene rxn.gif

AlCl3 is also widely used for polymerization and isomerization reactions of hydrocarbons. Important examples include the manufacture of ethylbenzene, which used to make styrene and thus polystyrene, and also production of dodecylbenzene, which is used for making detergents.[4]

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 so-called Fischer–Hafner synthesis.

Aluminium chloride, often in the form of derivatives such as aluminium chlorohydrate, is a common component in antiperspirants at low concentrations. Hyperhidrosis sufferers need a much higher concentration (15% or higher), sold under such brand names as Drysol, Maxim, Odaban, CertainDri, B+Drier, Anhydrol Forte and Driclor.

Chemical reactions

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

AlCl3 + 3LiH → AlH3 + 3LiCl

The hexahydrate decomposes to aluminum oxide when heated at 300 °C:[10]

2AlCl3·6H2O → Al2O3 + 6HCl + 3H2O

Precautions

Anhydrous AlCl3 reacts vigorously with water and bases, so suitable precautions are required. Hydrated salts are less problematic.

References

  1. 1.0 1.1 CRC Handbook of Chemistry and Physics, 62nd ed.; Weast, Robert C., Ed.; CRC Press: Boca Raton, FL, 1981; p B-73. ISBN 0-8493-0462-8.
  2. Index no. 013-003-00-7 of Annex VI, Part 3, to Regulation (EC) No 1272/2008 of the European Parliament and of the Council of 16 December 2008 on classification, labelling and packaging of substances and mixtures, amending and repealing Directives 67/548/EEC and 1999/45/EC, and amending Regulation (EC) No 1907/2006. OJEU L353, 31.12.2008, pp 1–1355 at p 366.
  3. HSNO Chemical Classification Information Database, <http://www.ermanz.govt.nz/Chemicals/ChemicalDisplay.aspx?SubstanceID=8011> (accessed 22 August 2009), New Zealand Environmental Risk Management Authority.
  4. 4.0 4.1 4.2 4.3 4.4 Greenwood, Norman N.; Earnshaw, A. Chemistry of the Elements; Pergamon: Oxford, 1984; pp 262–66. ISBN 0-08-022057-6.
  5. Wells, A. F. Structural Inorganic Chemistry, 5th ed.; Clarendon Press: Oxford, 1984. ISBN 0-19-855370-6.
  6. 6.0 6.1 6.2 Friedel-Crafts and Related Reactions; Olah, G. A., Ed.; Wiley–Interscience: New York, 1963; Vol. 1.
  7. Wade, L. G. Organic Chemistry, 5th ed.; Prentice Hall: New York, 2003.
  8. Galatsis, P. In Handbook of Reagents for Organic Synthesis: Acidic and Basic Reagents; Reich, Hans J.; Rigby, James H., Eds.; Wiley: New York, 1999; pp 12–15. ISBN 0471979252.
  9. Snider, B. B. Lewis-acid catalyzed ene reactions. Acc. Chem. Res. 1980, 13 (11), 426–32. DOI: 10.1021/ar50155a007.
  10. Patnaik, Pradyot Handbook of Inorganic Chemicals; McGraw-Hill: New York, 2002. ISBN 0070494398.

External links

Error creating thumbnail: Unable to save thumbnail to destination
Wikipedia-logo.png This page was originally imported from Wikipedia, specifically this version of the article "Aluminium chloride". Please see the history page on Wikipedia for the original authors. This WikiChem article may have been modified since it was imported. It is licensed under the Creative Commons Attribution–Share Alike 3.0 Unported license.