Trimethylaluminum; aluminium trimethyl; aluminum trimethyl
3D model (JSmol)
CompTox Dashboard (EPA)
|Molar mass||144.17 g/mol|
72.09 g/mol (C3H9Al)
|Melting point||15 °C (59 °F; 288 K)|
|Boiling point||125–130 °C (257–266 °F; 398–403 K) |
Heat capacity (C)
Std enthalpy of
Gibbs free energy (ΔfG˚)
|GHS Signal word||Danger|
|H250, H260, H314|
|P222, P223, P231+232, P280, P370+378, P422|
|NFPA 704 (fire diamond)|
|Flash point||−17.0 °C (1.4 °F; 256.1 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|what is ?)(|
Trimethylaluminium is one of the simplest examples of an organoaluminium compound. Despite its name it has the formula Al2(CH3)6 (abbreviated as Al2Me6 or TMA), as it exists as a dimer. This colorless liquid is an industrially important compound but must be handled with care due to its pyrophoricity; it evolves white smoke (aluminium oxides) when the vapor is released into the air.
Structure and bonding
Al2Me6 exists mostly as a dimer at room temperature and pressure, analogous in structure and bonding to diborane. As with diborane, the molecules are connected by 2 3-center-2-electron bonds: the shared methyl groups bridge between the two aluminium atoms. The Al-C(terminal) and Al-C(bridging) distances are 1.97 and 2.14 Å, respectively. The carbon atoms of the bridging methyl groups are each surrounded by five neighbors: three hydrogen atoms and two aluminium atoms. The methyl groups interchange readily intramolecularly and intermolecularly.
3-Centered-2-electron bonds are an example of "electron-deficient" molecules and tend to undergo reactions with Lewis bases that would give products consisting of 2-centered-2-electron bonds. For example, upon treatment with amines gives adducts R3N-AlMe3. Another reaction that gives products that follow the octet rule is the reaction of Al2Me6 with aluminium trichloride to give (AlMe2Cl)2.
The monomer species AlMe3, which has an aluminium atom bonded to three methyl groups, occurs at high temperature and low pressure. VSEPR Theory predicts and electron diffraction confirms that it has a trigonal planar (threefold) symmetry, as observed in BMe3.
Synthesis and applications
TMA is prepared via a two-step process that can be summarized as follows:
- 2 Al + 6 CH3Cl + 6 Na → Al2(CH3)6 + 6 NaCl
TMA is mainly used for the production of methylaluminoxane, an activator for Ziegler–Natta catalysts for olefin polymerisation. TMA is also employed as a methylation agent. Tebbe's reagent, which is used for the methylenation of esters and ketones, is prepared from TMA.
In combination with 20 to 100 mol % Cp2ZrCl2 (zirconocene dichloride), the (CH3)2Al-CH3 adds "across" alkynes to give vinyl aluminum species that are useful in organic synthesis in a reaction known as carboalumination.
Semiconductor grade TMA
TMA is the preferred metalorganic source for metalorganic vapour phase epitaxy (MOVPE) of aluminium-containing compound semiconductors, such as AlAs, AlN, AlP, AlSb, AlGaAs, AlInGaAs, AlInGaP, AlGaN, AlInGaN, AlInGaNP, etc. Criteria for TMA quality focus on (a) elemental impurities, (b) oxygenated and organic impurities.
- Sigma-Aldrich Co., Trimethylaluminum. Retrieved on 2014-05-05.
- Carlsson, J.; Gorbatkin, S.; Lubben, D.; Greene, J. E. (1991). "Thermodynamics of the homogeneous and heterogeneous decomposition of trimethylaluminum, monomethylaluminum, and dimethylaluminumhydride: Effects of scavengers and ultraviolet-laser photolysis". Journal of Vacuum Science and Technology B. 9 (6): 2759–2770. doi:10.1116/1.585642.
- Holleman, A. F.; Wiberg, E. (2001). Inorganic Chemistry. San Diego: Academic Press. ISBN 0-12-352651-5.
- Almennin, A.; Halvorse, S.; Haaland, A. (2005). "Gas Phase Electron Diffraction Investigation of Molecular Structures of Trimethylaluminum Monomer and Dimer". Acta Chemica Scandinavica. 44 (15): 2232–2234. doi:10.3891/acta.chem.scand.25-1937.
- Biswas, K.; Prieto, O.; Goldsmith, P. J.; Woodward, S. (2005). "Remarkably Stable (Me3Al)2 · DABCO and Stereoselective Nickel-Catalyzed AlR3 (R = Me, Et) Additions to Aldehydes". Angewandte Chemie International Edition. 44 (15): 2232–2234. doi:10.1002/anie.200462569. PMID 15768433.
- Negishi, E.; Matsushita, H. (1984). "Palladium-Catalyzed Synthesis of 1,4-Dienes by Allylation of Alkenyalane: α-Farnesene [1,3,6,10-Dodecatetraene, 3,7,11-trimethyl-]". Organic Syntheses. 62: 31.CS1 maint: multiple names: authors list (link); Collective Volume, 7, p. 245
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