Trimethylarsine
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Names | |||
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Preferred IUPAC name
Trimethanidoarsenic
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Systematic IUPAC name
Trimethylarsane
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Other names
Gosio gas
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Identifiers | |||
593-88-4 | |||
1730780 | |||
ChEBI | CHEBI:27130 | ||
ChemSpider | 62200 | ||
EC Number | 209-815-8 | ||
141657 | |||
Jmol 3D model | Interactive image Interactive image |
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MeSH | Trimethylarsine | ||
PubChem | 68978 | ||
RTECS number | CH8800000 | ||
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Properties | |||
C3H9As | |||
Molar mass | 120.03 g·mol−1 | ||
Appearance | Colourless liquid | ||
Density | 1.124 g cm−3 | ||
Melting point | −87.3 °C (−125.1 °F; 185.8 K) | ||
Boiling point | 56 °C (133 °F; 329 K) | ||
Slightly soluble | |||
Solubility in other solvents | organic solvents | ||
Structure | |||
Trigonal pyramidal | |||
0.86 D | |||
Vapor pressure | {{{value}}} | ||
Related compounds | |||
Related compounds
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Cacodylic acid Triphenylarsine |
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Supplementary data page | |||
Refractive index (n), Dielectric constant (εr), etc. |
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Thermodynamic
data |
Phase behaviour solid–liquid–gas |
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UV, IR, NMR, MS | |||
verify (what is ?) | |||
Infobox references | |||
Trimethylarsine is the chemical compound with the formula (CH3)3As, commonly abbreviated AsMe3 or TMAs. This organic derivative of arsine has been used as a source of arsenic in microelectronics industry,[1] a building block to other organoarsenic compounds, and serves as a ligand in coordination chemistry. It has distinct "garlic"-like smell. Trimethylarsine had been discovered as early as 1854.
Contents
Structure and preparation
As predicted by VSEPR theory, AsMe3 is a pyramidal molecule. The As-C distances average 1.519 Å, and the C-As-C angles are 91.83°[2] This bond angle is a strong indication of a low, if any, hybridisation of the atomic orbitals, leaving the lone pair in the s-orbital buried in the inner regions of the arsenic atom, rather than pointing outward like the lone pair of the ammonia molecule.
Trimethylarsine can be prepared by treatment of arsenic oxide with trimethylaluminium:[3]
- As2O3 + 1.5 [AlMe3]2 → 2 AsMe3 + 3/n (MeAl-O)n
Properties and reactions
Trimethylarsine is pyrophoric due to the exothermic nature of the following reaction, which initiates combustion:
- AsMe3 + 1/2 O2 → OAsMe3 (TMAO)
History
Poisoning events due to a gas produced by certain microbes was assumed to be associated with the arsenic in paint. In 1893 the Italian physician Bartolomeo Gosio published his results on "Gosio gas" that was subsequently shown to contain trimethylarsine.[4] Under wet conditions, the mold Scopulariopsis brevicaulis produces significant amounts of methyl arsines via methylation[5] of arsenic-containing inorganic pigments, especially Paris green and Scheele's Green, which were once used in indoor wallpapers. Newer studies show that trimethylarsine has a low toxicity and could therefore not account for the death and the severe health problems observed in the 19th century.[6] [7]
Safety
Trimethylarsine is potentially hazardous,[8][9][10] although its toxicity is often overstated.[6]
Importance
Trimethylarsine is the volatile byproduct of microbial action on inorganic forms of arsenic which are naturally occurring in rocks and soils at the parts-per-million level.[11] Trimethylarsine has been reported only at trace levels (parts per billion) in landfill gas from Germany, Canada, and the U.S.A., and is the major arsenic-containing compound in the gas.[12][13][14]
References
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- ↑ V. V. Gavrilenko, L. A. Chekulaeva, and I. V. Pisareva, "Highly efficient synthesis of trimethylarsine" Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 8, pp. 2122–2123, 1996.
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