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triethylaluminum

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triethylaluminum

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Also known as triethylalumane

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

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

~5 min read

Encyclopedic overview

10 sections
Contents
  • 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.