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triethylaluminum
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Triethylaluminium is one of the simplest examples of an organoaluminium compound. Despite its name, the compound has the formula Al2(C2H5)6 (abbreviated as Al2Et6 or TEA). This colorless liquid is pyrophoric. It is an industrially important compound, closely related to trimethylaluminium.
Chemical data
- Formula
- C6H15Al
- Molecular weight
- 114.16 g/mol
- IUPAC name
- triethylalumane
- SMILES
- CC[Al](CC)CC
- InChIKey
- VOITXYVAKOUIBA-UHFFFAOYSA-N
- Polar surface area
- 0 Ų
- H-bond donors
- 0
- H-bond acceptors
- 0
- Formal charge
- 0
via PubChem
Wikidata facts
- Subclass of
- chemical compound
- Has part
- hydrogen
- Mass
- 114.099
Show 3 more facts
- canonical SMILES
- CC[Al](CC)CC
- chemical formula
- C₆H₁₅Al
- Commons category
- Triethylaluminium
Sources (2)
via Wikidata · CC0
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Encyclopedic overview
10 sectionsContents
- Structure and bonding
- Synthesis and reactions
- Reactivity
- Applications
- Precursors to fatty alcohols
- Co-catalysts in olefin polymerization
- Reagent in organic and organometallic chemistry
- Pyrophoric agent
- See also
- References
Triethylaluminium is one of the simplest examples of an organoaluminium compound. Despite its name, the compound has the formula Al2(C2H5)6 (abbreviated as Al2Et6 or TEA). This colorless liquid is pyrophoric. It is an industrially important compound, closely related to trimethylaluminium.
== Structure and bonding == The structure and bonding in Al2R6 and diborane are analogous (R = alkyl). Referring to Al2Me6, the Al-C(terminal) and Al-C(bridging) distances are 1.97 and 2.14 Å, respectively. The Al center is tetrahedral. The carbon atoms of the bridging ethyl groups are each surrounded by five neighbors: carbon, two hydrogen atoms and two aluminium atoms. The ethyl groups interchange readily intramolecularly. At higher temperatures, the dimer cracks into monomeric AlEt3.
Excerpted from Wikipedia’s “triethylaluminum” article, available under the CC BY-SA 4.0 licence.