Trimethylgallium

Trimethylgallium

Structural formula of trimethylgallium
Ball-and-stick model of trimethylgallium
Names
IUPAC name trimethylgallane, trimethanidogallium
Identifiers
CAS Number	1445-79-0^Y
3D model (JSmol)	Interactive image
ChemSpider	14323^Y
ECHA InfoCard	100.014.452
PubChem CID	15051
CompTox Dashboard (EPA)	DTXSID2061696
InChI InChI=1S/3CH3.Ga/h3*1H3;^Y Key: XCZXGTMEAKBVPV-UHFFFAOYSA-N^Y InChI=1/3CH3.Ga/h3*1H3;/rC3H9Ga/c1-4(2)3/h1-3H3 Key: XCZXGTMEAKBVPV-YHXBHQJBAF
SMILES [Ga](C)(C)C
Properties
Chemical formula	Ga(CH3)3
Molar mass	114.827 g/mol
Appearance	colourless liquid
Melting point	−15 °C (5 °F; 258 K)
Boiling point	55.7 °C (132.3 °F; 328.8 K)
Solubility in water	Reacts with water
Hazards
Occupational safety and health (OHS/OSH):
Main hazards	Pyrophoric (can ignite spontaneously in air), reacts with water to release methane
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Y verify (what is ^YN ?) Infobox references

Trimethylgallium, often abbreviated to TMG or TMGa, is the organogallium compound with the formula Ga(CH₃)₃. It is a colorless, pyrophoric liquid.[1] Unlike trimethylaluminium, TMG adopts a monomeric structure.[2] When examined in detail, the monomeric units are clearly linked by multiple weak Ga---C interactions, reminiscent of the situation for trimethylindium.[3]

Preparation

Two forms of TMG are typically investigated: Lewis base adducts or TMG itself. All are prepared by reactions of gallium trichloride with various methylating agents. When the methylation is conducted with methylmagnesium iodide in diethyl ether, the product is the poorly volatile diethyl ether adduct. As noted by TMG discoverers Kraus and Toonder in 1933, the ether ligand is not readily lost, although it may be displaced with liquid ammonia.[4] When the alkylation is conducted with methyl lithium in the presence of a tertiary phosphine the air-stable phosphine adduct is obtained:

GaCl₃ + 3 MeLi + PR₃ → R₃P−GaMe₃ + 3 LiCl

Heating the solid phosphine adduct under vacuum liberates the base-free TMG:[1]

R₃P−GaMe₃ → R₃P + GaMe₃

Other non-volatile bases have been described.[5] Other methylating agents for the synthesis of TMG include dimethylzinc and trimethylaluminium.

Applications

TMG is the preferred metalorganic source of gallium for metalorganic vapour phase epitaxy (MOVPE) of gallium-containing compound semiconductors, such as GaAs, GaN, GaP, GaSb, InGaAs, InGaN, AlGaInP, InGaP, AlInGaNP and Ga₂O₃.[6] These material are used in the production of LED lighting and semiconductors as a metalorganic chemical vapor deposition precursor.

References

1. Bradley, D. C.; Chudzynska, H. C.; Harding, I. S. (1997). "Trimethylindium and Trimethylgallium". Inorganic Syntheses. Vol. 31. pp. 67–74. doi:10.1002/9780470132623.ch8. ISBN 978-0-470-13262-3.
2. Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. ISBN 978-0-08-037941-8.
3. Mitzel, Norbert W.; Lustig, Christian; Berger, Raphael J. F.; Runeberg, Nino (2002). "Luminescence Phenomena and Solid-State Structures of Trimethyl- and Triethylgallium". Angewandte Chemie International Edition. 41 (14): 2519–2522. doi:10.1002/1521-3773(20020715)41:14<2519::AID-ANIE2519>3.0.CO;2-2. PMID 12203520.
4. Kraus, C. A.; Toonder, F. E. (1933). "Trimethyl Gallium, Trimethyl Gallium Etherate and Trimethyl Gallium Ammine". PNAS. 19 (3): 292–8. Bibcode:1933PNAS...19..292K. doi:10.1073/pnas.19.3.292. PMC 1085965. PMID 16577510.
5. Foster, Douglas F.; Cole-Hamilton, David J. (1997). "Electronic Grade Alkyls of Group 12 and 13 Elements". Inorganic Syntheses. Vol. 31. p. 29-66. doi:10.1002/9780470132623.ch7. ISBN 978-0-471-15288-0.
6. Shenai-Khatkhate, D. V.; Goyette, R. J.; Dicarlo, R. L. Jr; Dripps, G. (2004). "Environment, health and safety issues for sources used in MOVPE growth of compound semiconductors". Journal of Crystal Growth. 272 (1–4): 816–21. Bibcode:2004JCrGr.272..816S. doi:10.1016/j.jcrysgro.2004.09.007.