Difference between revisions of "Lithium aluminium hydride"
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| Coordination = tetrahedral (Al) | | Coordination = tetrahedral (Al) | ||
| CrystalStruct = [[monoclinic]] | | CrystalStruct = [[monoclinic]] | ||
− | | SpaceGroup = P2<sub>1</sub>/''c'' | + | | SpaceGroup = P2<sub>1</sub>/''c'' (No. 14) |
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| Section4 = {{Chembox Thermochemistry | | Section4 = {{Chembox Thermochemistry | ||
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==External links== | ==External links== | ||
{{wikipedia|Lithium aluminium hydride}} | {{wikipedia|Lithium aluminium hydride}} | ||
− | * | + | *{{OrgSynth preps|id=36257|name=Lithium aluminium hydride}} |
[[Category:Lithium compounds]] | [[Category:Lithium compounds]] |
Latest revision as of 11:21, 20 June 2010
Lithium aluminium hydride | |
---|---|
IUPAC name | Lithium tetrahydridoaluminate(1−) |
Identifiers | |
InChI | InChI=1/Al.Li.4H/q-1;+1;;;;/rAlH4.Li/h1H4;/q-1;+1 |
InChIKey | OCZDCIYGECBNKL-PDCCDREHAZ |
Standard InChI | InChI=1S/Al.Li.4H/q-1;+1;;;; |
Standard InChIKey | OCZDCIYGECBNKL-UHFFFAOYSA-N |
CAS number | [ ] |
EC number | |
RTECS | BD0100000 |
ChemSpider | |
Properties[1] | |
Chemical formula | LiAlH4 |
Molar mass | 37.954 g mol–1 |
Appearance | white or grey solid |
Density | 0.917 g cm–3 |
Melting point |
125 °C decomp. |
Solubility in water | reacts |
Solubility in diethyl ether | approx. 300 g dm–3 |
Structure[2] | |
Crystal structure | monoclinic |
Space group | P21/c (No. 14) |
Coordination geometry | tetrahedral (Al) |
Thermochemistry[3][4] | |
Std enthalpy of formation ΔfH |
–117.15 kJ mol–1 |
Standard molar entropy S |
87.90 J K–1 mol–1 |
Hazards[5] | |
EU index number | 001-002-00-4 |
GHS pictograms | |
GHS signal word | DANGER |
GHS hazard statements | H260 |
Related compounds | |
Other hydrides | aluminium hydride sodium borohydride sodium hydride |
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) |
Lithium aluminium hydride, LiAlH4, often abbreviated to LAH or "Lithal", is the lithium salt of the tetrahydridoaluminate(1−) anion. A moderately air-stable white or grey solid, it is widely used as a strong reducing agent in organic synthesis.
It was first prepared from the reaction between lithium hydride (LiH) and aluminium chloride:[6]
- 4 LiH + AlCl3 → LiAlH4 + 3 LiCl
The modern industrial synthesis involves the initial preparation of sodium aluminium hydride from the elements under high pressure and temperature:[7]
- Na + Al + 2 H2 → NaAlH4
LAH is then prepared by metathesis reaction according to:
- NaAlH4 + LiCl → LiAlH4 + NaCl
which proceeds in a high yield of LAH. Lithium chloride is removed by filtration from an ethereal solution of LAH, with subsequent precipitation of LAH to yield a product containing around 1% LiCl by mass.[7]
References
- ↑ CRC Handbook of Chemistry and Physics, 62nd ed.; Weast, Robert C., Ed.; CRC Press: Boca Raton, FL, 1981; p B-113. ISBN 0-8493-0462-8.
- ↑ Løvvik, O. M.; Opalka, Susanne M.; Brinks, Hendrik W.; Hauback, Bjørn C. Crystal structure and thermodynamic stability of the lithium alanates LiAlH4 and Li3AlH6. Phys. Rev. B 2004, 69 (13), 134117. DOI: 10.1103/PhysRevB.69.134117.
- ↑ Lithium tetrahydroaluminate. In NIST Chemistry WebBook; National Institute for Standards and Technology, <http://webbook.nist.gov/cgi/inchi/InChI%3D1S/Al.Li.4H/q-1;+1;;;;>. (accessed 20 June 2010).
- ↑ Smith, Martin B.; Bass, George E., Jr. Heats and Free Energies of Formation of the Alkali Aluminum Hydrides and of Cesium Hydride. J. Chem. Eng. Data 1963, 8 (3), 342–46. DOI: 10.1021/je60018a020.
- ↑ Index no. 001-002-00-4 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 340.
- ↑ Finholt, A. E.; Bond, A. C.; Schlesinger, H. I. Lithium Aluminum Hydride, Aluminum Hydride and Lithium Gallium Hydride, and Some of their Applications in Organic and Inorganic Chemistry. J. Am. Chem. Soc. 1947, 69 (5), 1199–1203. DOI: 10.1021/ja01197a061.
- ↑ 7.0 7.1 Holleman, A. F.; Wiberg, E.; Wiberg, N. Lehrbuch der Anorganischen Chemie, 102nd ed.; de Gruyter, 2007. ISBN 978-3-11-017770-1.
External links
See also the corresponding article on Wikipedia. |