Aluminium iodide: Difference between revisions
Appearance
Content deleted Content added
Updating {{chembox}} (no changed fields - added verified revid - updated 'DrugBank_Ref', 'UNII_Ref', 'ChEMBL_Ref', 'ChEBI_Ref', 'KEGG_Ref', 'ChEBI_Ref') per Chem/Drugbox validation (report [[Wikipedia_talk:WikiProject_Chemicals|error |
Removed parameters. |
||
(72 intermediate revisions by 49 users not shown) | |||
Line 1: | Line 1: | ||
{{short description|Chemical compound}} |
|||
{{Chembox |
{{Chembox |
||
| Verifiedfields = changed |
|||
| verifiedrevid = 436539475 |
|||
| Watchedfields = changed |
|||
| ImageFile = Aluminium-iodide-3D-balls.png |
|||
| verifiedrevid = 449832810 |
|||
| ImageSize = 200px |
|||
| ImageFile = Aluminium-iodide-3D-balls.png |
|||
| ImageName = Ball and stick model of aluminium iodide dimer |
|||
| ImageSize = |
|||
| ImageFile2 = Jodid hlinitý.PNG |
|||
| ImageName = Ball and stick model of aluminium iodide dimer |
|||
| PIN = Aluminium iodide |
|||
| ImageFile2 = Jodid hlinitý.PNG |
|||
| OtherNames = Aluminium(III) iodide<br /> |
|||
| PIN = Aluminium iodide |
|||
| OtherNames = Aluminium(III) iodide<br /> |
|||
Aluminum iodide<br /> |
Aluminum iodide<br /> |
||
Aluminium triiodide<br /> |
Aluminium triiodide<br /> |
||
Aluminum triiodide |
Aluminum triiodide |
||
| |
|Section1={{Chembox Identifiers |
||
| |
| InChI = |
||
| InChIKey = |
| InChIKey =CECABOMBVQNBEC-DFZHHIFOAE |
||
| CASNo_Ref = {{cascite|correct|??}} |
|||
| CASNo = 7784-23-8 |
| CASNo = 7784-23-8 |
||
| |
| CASNo_Comment = (anhydrate) |
||
| CASNo1_Ref = {{cascite|correct|??}} |
|||
| CASNo1 = 10090-53-6 |
|||
| CASNo1_Comment = (hexahydrate) |
| CASNo1 = 10090-53-6 |
||
| CASNo1_Comment = (hexahydrate) |
|||
| UNII_Ref = {{fdacite|correct|FDA}} |
|||
| PubChem = 82222 |
|||
| UNII = L903Z8J9VR |
|||
| PubChem_Comment = (anhydrate) |
|||
| UNII_Comment = (anhydrate) |
|||
| PubChem_Ref = {{Pubchemcite}} |
|||
| UNII1_Ref = {{fdacite|correct|FDA}} |
|||
| ChemSpiderID = 74202 |
|||
| UNII1 = VWS43EUO9V |
|||
| ChemSpiderID_Comment = (anhydrate) |
|||
| UNII1_Comment = (hexahydrate) |
|||
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |
|||
| |
| PubChem = 82222 |
||
| PubChem_Comment = (anhydrate) |
|||
| UNNumber = UN 3260 |
|||
| ChemSpiderID = 74202 |
|||
| SMILES = I[Al](I)I |
|||
| ChemSpiderID_Comment = (anhydrate) |
|||
| StdInChI_Ref = {{stdinchicite|correct|chemspider}} |
|||
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |
|||
| StdInChI = 1S/Al.3HI/h;3*1H/q+3;;;/p-3 |
|||
| EINECS = 232-054-8 |
|||
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} |
|||
| UNNumber = UN 3260 |
|||
| SMILES = I[Al](I)I |
|||
| SMILES1 = I[Al-]1(I)[I+][Al-]([I+]1)(I)I |
|||
| SMILES1_Comment = [[dimer (chemistry)|dimer]] |
|||
| StdInChI_Ref = {{stdinchicite|changed|chemspider}} |
|||
| StdInChI = |
|||
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} |
|||
| StdInChIKey = CECABOMBVQNBEC-UHFFFAOYSA-K}} |
| StdInChIKey = CECABOMBVQNBEC-UHFFFAOYSA-K}} |
||
| |
|Section2={{Chembox Properties |
||
| |
| Formula = {{math|size=100%|AlI<sub>3</sub>}}, {{math|size=100%|AlI<sub>3</sub>·6H<sub>2</sub>O}} (hexahydrate) |
||
| |
| MolarMass = 407.695 g/mol (anhydrous) <br> 515.786 g/mol (hexahydrate)<ref name=b92/> |
||
| |
| Appearance = white (anhydrous) or yellow powder (hexahydrate)<ref name=b92/> |
||
| |
| Density = 3.98 g/cm<sup>3</sup> (anhydrous)<ref name=b92>{{RubberBible92nd|page=4.45}}</ref> 2.63 g/cm<sup>3</sup> (hexahydrate)<ref name="Perry2016">{{cite book|author=Perry, Dale L. |title=Handbook of Inorganic Compounds, Second Edition|url=https://books.google.com/books?id=SFD30BvPBhoC&pg=PA8|date=19 April 2016|publisher=CRC Press|isbn=978-1-4398-1462-8|page=8}}</ref> |
||
| MeltingPtC = 188.28 |
|||
| MeltingPt = 189.4 °C (anhydrous) <br> 185 °C, decomp. (hexahydrate) |
|||
| MeltingPt_notes = (anhydrous) <br> 185 °C, decomposes (hexahydrate)<ref name=b92/><ref name="Perry2016"/> |
|||
| BoilingPt = 360 °C, sublimes |
|||
| BoilingPtC = 382 |
|||
| Solubility = reacts violently (anhydrous) <br> soluble (hexahydrate) |
|||
| BoilingPt_notes = anhydrous, sublimes<ref name=b92/> |
|||
| Solvent = [[alcohol]], [[ether]] |
|||
| |
| Solubility = very soluble, partial hydrolysis |
||
| Solvent = [[ethanol|alcohol]], [[diethyl ether|ether]] |
|||
| SolubleOther = soluble (hexahydrate) |
|||
}} |
|||
|Section3={{Chembox Structure |
|||
| Structure_ref =<ref name="TroyanovKrahl2004"/> |
|||
| CrystalStruct = [[Monoclinic]], [[Pearson symbol|''mP16'']] |
|||
| SpaceGroup = P2<sub>1</sub>/c, No. 14 |
|||
| Coordination = |
|||
| LattConst_a = 1.1958 nm |
|||
| UnitCellFormulas = 8 |
|||
| LattConst_b = 0.6128 nm |
|||
| LattConst_c = 1.8307 nm |
|||
| LattConst_alpha = 90 |
|||
| LattConst_beta = 90 |
|||
| LattConst_gamma = 90 |
|||
| MolShape = |
|||
| OrbitalHybridisation = |
|||
| Dipole = |
|||
}} |
|||
| Section4 = {{Chembox Thermochemistry |
|||
| Thermochemistry_ref =<ref name=b92/> |
|||
| HeatCapacity = 98.7 J/(mol·K) |
|||
| Entropy = 195.9 J/(mol·K) |
|||
| DeltaHf = -302.9 kJ/mol |
|||
| DeltaGf = |
|||
| DeltaHc = |
|||
}} |
}} |
||
}} |
}} |
||
'''Aluminium iodide''' is |
'''Aluminium iodide''' is a [[chemical compound]] containing [[aluminium]] and [[iodine]]. Invariably, the name refers to a compound of the composition {{chem|Al|I|3}}, formed by the reaction of aluminium and iodine<ref>{{cite book|doi=10.1002/9780470132357.ch39|chapter=Aluminum Iodide|title=Inorganic Syntheses|volume=4|pages=117–119|year=1953|last1=Watt|first1=George W|last2=Hall|first2=James L|last3=Taylor|first3=William Lloyd|last4=Kleinberg|first4=Jacob|isbn=9780470132357}}</ref> or the action of [[Hydrogen iodide|{{chem|H|I}}]] on {{chem|Al}} metal. The hexahydrate is obtained from a reaction between metallic aluminum or [[aluminum hydroxide]] with [[hydrogen iodide]] or [[hydroiodic acid]]. Like the related chloride and bromide, {{chem|Al|I|3}} is a strong [[Lewis acids and bases|Lewis acid]] and will absorb water from the atmosphere. It is employed as a [[reagent]] for the scission of certain kinds of C-O and N-O bonds. It cleaves aryl [[diethyl ether|ether]]s and deoxygenates [[epoxide]]s.<ref>{{cite book| author = Gugelchuk, M. | chapter=Aluminum Iodide|title =Encyclopedia of Reagents for Organic Synthesis |editor=L. Paquette| year = 2004| publisher =J. Wiley & Sons| place = New York| doi = 10.1002/047084289X.ra083| isbn=0471936235}}</ref> |
||
==Structure== |
|||
==Applications in organic synthesis== |
|||
Solid {{chem|Al|I|3}} is dimeric, consisting of {{chem|Al|2|I|6}}, similar to that of [[aluminium tribromide|{{chem|Al|Br|3|}}]].<ref name="TroyanovKrahl2004">{{cite journal|last1=Troyanov|first1=Sergey I.|last2=Krahl|first2=Thoralf|last3=Kemnitz|first3=Erhard|title=Crystal structures of {{math|size=100%|1=GaX<sub>3</sub>(X= Cl, Br, I)}} and {{math|size=100%|AlI<sub>3</sub>}}|journal=Zeitschrift für Kristallographie|volume=219|issue=2–2004|year=2004|pages=88–92|doi=10.1524/zkri.219.2.88.26320|s2cid=101603507}}</ref> The structure of monomeric and dimeric forms have been characterized in the gas phase.<ref name="HargittaiRéffy2006">{{cite journal|last1=Hargittai|first1=Magdolna|last2=Réffy|first2=Balázs|last3=Kolonits|first3=Mária|title=An Intricate Molecule: Aluminum Triiodide. Molecular Structure of {{math|size=100%|AlI<sub>3</sub>}}and {{math|size=100%|Al<sub>2</sub>I<sub>6</sub>}} from Electron Diffraction and Computation|journal=The Journal of Physical Chemistry A|volume=110|issue=10|year=2006|pages=3770–3777|doi=10.1021/jp056498e|pmid=16526661}}</ref> The monomer, {{chem|Al|I|3}}, is trigonal planar with a bond length of 2.448(6) Å, and the bridged dimer, {{chem|Al|2|I|6}}, at 430 K is a similar to [[Aluminium chloride|{{chem|Al|2|Cl|6}}]] and [[Aluminium bromide|{{chem|Al|2|Br|6}}]] with {{chem2|Al\sI}} bond lengths of 2.456(6) Å (terminal) and 2.670(8) Å (bridging). The dimer is described as floppy with an equilibrium geometry of D<sub>2h</sub>. |
|||
Aluminium iodide is employed as a [[catalyst]] to break certain kinds of C-O and N-O bonds. It cleaves aryl [[ether]]s and deoxygenates [[epoxide]]s.<ref>{{cite book| author = M. Gugelchuk | title =Aluminum Iodide, in Encyclopedia of Reagents for Organic Synthesis (Ed: L. Paquette)| year = 2004| publisher =J. Wiley & Sons| location = New York| doi = 10.1002/047084289}}</ref> |
|||
==Aluminium(I) iodide== |
==Aluminium(I) iodide== |
||
{{main|Aluminium monoiodide}} |
|||
The name "aluminium iodide" is widely assumed to describe the triiodide or its dimer. In fact, a monoiodide also enjoys a role in the Al-I system, although composition AlI is unstable at room temperature with respect to the triiodide<ref>{{cite journal| title = Aluminum(I) and Gallium(I) Compounds: Syntheses, Structures, and Reactions| author = Dohmeier, C.; Loos, D.; Schnöckel, H.| journal = Angewandte Chemie International Edition | year =1996| volume =35| pages =129–149| doi =10.1002/anie.199601291}}</ref> |
|||
[[File:06. Директна синтеза на алуминиум јодид.webm|thumb|left|280px|Experiment showing a direct synthesis of aluminum iodide. Few drops of water are added to a homogenised mixture of aluminum powder and powdered iodine. After short time (an induction period) a vigorous reaction occurs followed by emission of intense colored vapors. The purple vapours are due to evaporation of iodine as a consequence of increased temperature of the system, and the brown ones are probably due to smoke of an adduct of the reaction product with excess of iodine. The exergonic reaction {{chem2|2Al(s) + 3I2(s) -> 2AlI3(s)}} is at the origin of the phenomenon observed.]] |
|||
:3 AlI → AlI<sub>3</sub> + 2 Al |
|||
The name "aluminium iodide" is widely assumed to describe the triiodide or its dimer. In fact, a monoiodide also enjoys a role in the Al–I system, although the compound AlI is unstable at room temperature relative to the triiodide:<ref>{{cite journal| title = Aluminum(I) and Gallium(I) Compounds: Syntheses, Structures, and Reactions|author1=Dohmeier, C. |author2=Loos, D. |author3=Schnöckel, H. | journal = Angewandte Chemie International Edition | year =1996| volume =35|issue=2 | pages =129–149| doi =10.1002/anie.199601291}}</ref> |
|||
An illustrative derivative of aluminium monoiodide is the cyclic [[adduct]] formed with [[triethylamine]], AI<sub>4</sub>I<sub>4</sub>(NEt<sub>3</sub>)<sub>4</sub>. |
|||
:<chem>3AlI -> AlI3 + 2Al</chem> |
|||
An illustrative derivative of aluminium monoiodide is the cyclic [[adduct]] formed with [[triethylamine]], {{chem|Al|4|I|4|(NEt|3|)|4}}. |
|||
==Safety== |
|||
Hydrolysis of aluminium triiodide will release some HI, which is corrosive. Lewis acids are skin irritants. |
|||
==References== |
==References== |
||
{{reflist}} |
{{reflist}} |
||
==External links== |
|||
*{{Commonscatinline}} |
|||
{{Aluminium compounds}} |
{{Aluminium compounds}} |
||
{{Iodides}} |
|||
{{Use dmy dates|date=March 2018}} |
|||
[[Category:Iodides]] |
[[Category:Iodides]] |
||
[[Category:Aluminium compounds]] |
[[Category:Aluminium compounds|iodide]] |
||
[[Category:Metal halides]] |
[[Category:Metal halides]] |
||
{{inorganic-compound-stub}} |
|||
[[ar:يوديد ألومنيوم]] |
|||
[[cs:Jodid hlinitý]] |
|||
[[es:Yoduro de aluminio]] |
|||
[[ja:ヨウ化アルミニウム]] |
|||
[[pt:Iodeto de alumínio]] |
|||
[[ru:Иодид алюминия]] |
|||
[[sv:Aluminiumjodid]] |
|||
[[zh:碘化铝]] |