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trimethylgallium

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trimethylgallium

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

Chemical data

Formula
C3H9Ga
Molecular weight
114.83 g/mol
IUPAC name
trimethylgallane
SMILES
C[Ga](C)C
InChIKey
XCZXGTMEAKBVPV-UHFFFAOYSA-N
Polar surface area
0 Ų
H-bond donors
0
H-bond acceptors
0
Formal charge
0

via PubChem

Wikidata facts

Has part
carbon
Mass
113.995999
Show 4 more facts
canonical SMILES
C[Ga](C)C
chemical formula
C₃H₉Ga
Commons category
Trimethylgallium
boiling point
55.7
Sources (3)

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Encyclopedic overview

3 sections
Contents
  • Preparation
  • Applications
  • References

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

==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. When the alkylation is conducted with methyl lithium in the presence of a tertiary phosphine the air-stable phosphine adduct is obtained:

Excerpted from Wikipedia’s “trimethylgallium” article, available under the CC BY-SA 4.0 licence.