3D model (JSmol)
|Abbreviations||TEA, TEAL, TEAl|
|Molar mass||228.34 g·mol−1|
|Density||0.8324 g/mL at 25 °C|
|Melting point||−46 °C (−51 °F; 227 K)|
|Boiling point||128 to 130 °C (262 to 266 °F; 401 to 403 K) at 50 mmHg|
|R-phrases (outdated)||R14 R17 R34|
|S-phrases (outdated)||S16 S43 S45|
|Flash point||−18 °C (0 °F; 255 K)|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|what is ?)(|
Triethylaluminium is an organoaluminium compound. Despite its name, the formula for this compound is Al2(C2H5)6, shortened to Al2Et6 (Et = ethyl). This volatile, colorless liquid is highly pyrophoric, igniting immediately upon exposure to air. It is normally stored in stainless steel containers either as a pure liquid or as a solution in hydrocarbon solvents such as hexane, heptane, or toluene. Triethylaluminium is mainly used as a co-catalyst in the industrial production of polyethylene, polypropylene and for the production of medium chain alcohols.
Structure and bonding
The compound is a dimer of triethylaluminium. One pair of ethyl groups bridge the two Al centers, and the other four groups are terminal ligands. The two bridging carbon centres are five-coordinate. The bonding is reminiscent of that of diborane, involving 3-centred, 2-electron bonds. As in trimethylaluminium, triethylaluminium is structurally fluctional resulting in rapid interchange of the terminal and bridging ethyl groups. At higher temperatures, the dimer cracks into monomeric AlEt3.
Synthesis and reactions
Triethylaluminium can be formed via several routes. The discovery of an efficient route was significant technologically. The multistep process uses aluminium metal, hydrogen gas, and ethylene, summarized as follows:
- 2 Al + 3 H2 + 6 C2H4 → Al2Et6
Because of this efficient synthesis, triethylaluminium is one of the most available organoaluminium compounds.
Triethylaluminium can also be generated from ethylaluminium sesquichloride (Al2Cl3Et3), which arises by treating aluminium powder with chloroethane. Reduction of ethylaluminium sesquichloride with an alkali metal such as sodium gives triethylaluminium:
- 3 Al2Cl3Et3 + 9 Na → 2 Al2Et6 + 2 Al + 9 NaCl
- Al2Et6 + 6 HX → 2 AlX3 + 6 EtH
For this reaction, even weak acids can be employed such as terminal acetylenes and alcohols.
- Al2Et6 + 2 L → 2 LAlEt3
Triethylaluminium is used industrially as an intermediate in the production of fatty alcohols, which are converted to detergents. The first step involves the oligomerization of ethylene – the famed Aufbau reaction, which gives a mixture of trialkylaluminium compounds (simplified here as octyl groups):
- Al2(C2H5)6 + 18 C2H4 → Al2(C8H17)6
Subsequently, these trialkyl compounds are oxidized to aluminium alkoxides, which are then hydrolysed:
- Al2(C8H17)6 + 3 O2 → Al2(OC8H17)6
- Al2(OC8H17)6 + 6 H2O → 6 C8H17OH + 2 "Al(OH)3"
Reagent in organic and organometallic chemistry
Triethylaluminium ignites on contact with air and will ignite and/or decompose on contact with water, and with any other oxidizer—it is one of the few substances pyrophoric enough to ignite on contact with cryogenic liquid oxygen. Its easy ignition makes it particularly desirable as a rocket engine ignitor. The SpaceX Falcon 9 rocket uses a triethylaluminium-triethylborane mixture as a first-stage ignitor.
Triethylaluminium thickened with polyisobutylene is used as an incendiary weapon, as a pyrophoric alternative to napalm, e.g. in the M74 rockets for the M202A1 launchers. In this application it is known as TPA, for thickened pyrotechnic agent or thickened pyrophoric agent. The usual amount of the thickener is 6%. The amount of thickener can be decreased to 1% if other diluents are added. For example, n-hexane, can be used with increased safety by rendering the compound non-pyrophoric until the diluent evaporates, at which point a combined fireball results from both the triethylaluminium and the hexane vapors.
- Triethylborane, used as an ignitor in the Pratt & Whitney J58 turbojet/ramjet engines.
- Mission Status Center, June 2, 2010, 1905 GMT, SpaceflightNow, accessed 2010-06-02, Quotation: "The flanges will link the rocket with ground storage tanks containing liquid oxygen, kerosene fuel, helium, gaserous nitrogen and the first stage ignitor source called triethylaluminum-triethylborane, better known as TEA-TAB."
- Malpass, Dennis B.; Band, Elliot (2012). Introduction to Industrial Polypropylene: Properties, Catalysts Processes. John Wiley & Sons. ISBN 9781118463208.
- "Gulbrandsen Chemicals, Metal Alkyls: Triethylaluminum (TEAl)". Gulbrandsen. Retrieved December 12, 2017.
Triethylaluminum (TEAl) is a pyrophoric liquid...
- Gábor Vass, György Tarczay, Gábor Magyarfalvi, András Bödi, and László Szepes “HeI Photoelectron Spectroscopy of Trialkylaluminum and Dialkylaluminum Hydride Compounds and Their Oligomers” Organometallics, 2002, volume 21, pp. 2751–2757. doi:10.1021/om010994h
- Michael J. Krause, Frank Orlandi, Alfred T. Saurage, Joseph R. Zietz Jr. “Aluminum Compounds, Organic” in Ullmann's Encyclopedia of Industrial Chemistry 2002, Wiley-VCH, Weinheim. doi:10.1002/14356007.a01_543
- Krause, M. J; Orlandi, F; Saurage, A T.; Zietz, J R, "Organic Aluminum Compounds" Wiley-Science 2002.
- Elschenbroich, C. ”Organometallics” (2006) Wiley-VCH: Weinheim. ISBN 978-3-527-29390-2
- Wataru Nagata and Yoshioka Mitsuru (1988). "Diethylaluminum Cyanides". Organic Syntheses.; Collective Volume, 6, p. 436
- TEA Material Safety Data Sheet Archived 2006-11-14 at the Wayback Machine., accessed March 27, 2007
- M202A1 Flame Assault Shoulder Weapon (Flash), inetres.com
- Encyclopedia of Explosives and Related Items, Vol.8, US Army