Tetraethyl orthosilicate | |
---|---|
IUPAC name | tetraethoxysilane |
Other names | tetraethyl orthosilicate; ethyl silicate; silicic acid, tetraethyl ester; silicon ethoxide; TEOS |
Identifiers | |
CAS number | 78-10-4 |
PubChem | |
Properties | |
Molecular formula | SiC8H20O4 |
Molar mass | 208.32 |
Appearance | colourless liquid |
Density | 0.94 |
Melting point |
-77 °C |
Boiling point |
166-169 °C |
Solubility in water | decomp |
Hazards | |
Main hazards | Toxic |
Flash point | 45 °C |
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox references |
Tetraethyl orthosilicate is the chemical compound with the formula Si(OC2H5)4. Often abbreviated TEOS, this molecule consists of four ethyl groups attached to SiO44- ion, which is called orthosilicate. As an ion in solution, orthosilicate does not exist. Alternatively TEOS can be considered to be the ethyl ester of orthosilicic acid, Si(OH)4. It is a prototypical alkoxide.
TEOS is a tetrahedral molecule. Many analogues exist, and most are prepared by alcoholysis of silicon tetrachloride:
- SiCl4 + 4 ROH → Si(OR)4 + 4 HCl
where R = alkyl such as methyl, ethyl, propyl, etc.
Applications[]
TEOS is mainly used as a crosslinking agent in silicone polymers. Other applications include coatings for carpets and other objects. These applications exploit the reactivity of the Si-OR bonds.[1]
Other reactions[]
TEOS has the remarkable property of easily converting into silicon dioxide. This reaction occurs upon the addition of water:
- Si(OC2H5)4 + 2 H2O → SiO2 + 4 C2H5OH
This hydrolysis reaction is an example of a sol-gel process. The side product is ethanol. The reaction proceeds via a series of condensation reactions that convert the TEOS molecule into a mineral-like solid via the formation of Si-O-Si linkages. Rates of this conversion are sensitive to the presence of acids and bases, both of which serve as catalysts.
At elevated temperatures (>600 °C), TEOS converts to silicon dioxide:
- Si(OC2H5)4 → SiO2 + 2O(C2H5)2
The volatile coproduct is diethylether.
References[]
- ↑ Lutz Rösch, Peter John, Rudolf Reitmeier "Silicon Compounds, Organic" Ullmann's Encyclopedia of Industrial Chemistry, 2002, Wiley-VCH, Weinheim. doi:10.1002/14356007.a24_021. Article Online Posting Date: June 15, 2000
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