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Tetraethyl orthosilicate 1
Tetraethyl orthosilicate
Tetraethyl orthosilicate
Identifiers
CAS number 78-10-4
[1]
 
PubChem 6517
[2]
ChemSpider 6270
[3]
 
Jmol-3D images Image 1
[4]
Properties
Molecular formula SiC8
H20
O4
Molar mass 208.33 g mol−1
Appearance colourless liquid
Density 0.933 g/mL at 20°C
Melting point −77 °C, 196 K, -107 °F
Boiling point 166-169 °C, 439-442 K, 331-336 °F
Solubility in water miscible, but readily decomposes
Hazards
Main hazards Flammable, Harmful by inhalation
Flash point 45 °C
  (verify)
[5]
 (what is:  / ?)
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(OC
2
H
5
)
4
. Often abbreviated TEOS, this
molecule consists of four ethyl groups attached to SiO
4
4−
ion, which is called orthosilicate. As an ion in solution,
Tetraethyl orthosilicate 2
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:
SiCl
4
+ 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 and as a precursor to silicon dioxide in the
semiconductor industry.
[6]
Other applications include coatings for carpets and other objects. TEOS is used in the
production of aerogel. These applications exploit the reactivity of the Si-OR bonds.
[7]
Other reactions
TEOS has the remarkable property of easily converting into silicon dioxide. This reaction occurs upon the addition
of water:
Si(OC
2
H
5
)
4
+ 2 H
2
O → SiO
2
+ 4 C
2
H
5
OH
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. The Stöber process allows the formation of monodisperse silica particles.
At elevated temperatures (>600 °C), TEOS converts to silicon dioxide:
Si(OC
2
H
5
)
4
→ SiO
2
+ 2 (C
2
H
5
)
2
O
The volatile coproduct is diethyl ether.
References
[1] http://www.commonchemistry.org/ChemicalDetail.aspx?ref=78-10-4
[2] http://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=6517
[3] http://www.chemspider.com/6270
[4] http://chemapps.stolaf.edu/jmol/jmol.php?model=CCO%5BSi%5D%28OCC%29%28OCC%29OCC
[5] http://en.wikipedia.org/w/index.php?title=Special:ComparePages&rev1=470603747&page2=Tetraethyl+orthosilicate
[6] D. Bulla, Deposition of thick TEOS PECVD silicon oxide layers for integrated optical waveguide applications. Thin Solid Films. 1998;
334(1-2):60-64. Available at: http://linkinghub.elsevier.com/retrieve/pii/S0040609098011171.
[7][7] Lutz Rösch, Peter John, Rudolf Reitmeier "Silicon Compounds, Organic" Ullmann's Encyclopedia of Industrial Chemistry, 2002,
Wiley-VCH, Weinheim. . Article Online Posting Date: June 15, 2000
External links
‱ NIST Standard Reference Database 69, June 2005 Release: NIST Chemistry WebBook (http://webbook.nist.
gov/cgi/cbook.cgi?ID=C78104)
‱ Details of TEOS deposition process (http://timedomaincvd.com/CVD_Fundamentals/films/
TEOS_O2_thermal.html)
‱ CDC - NIOSH Pocket Guide to Chemical Hazards (http://www.cdc.gov/niosh/npg/npgd0282.html)
Article Sources and Contributors 3
Article Sources and Contributors
Tetraethyl orthosilicate  Source: http://en.wikipedia.org/w/index.php?oldid=577710285  Contributors: 2001:620:40B:1090:1C00:B4E5:754C:3339, A876, Akiry, Ambix, Andi47, Beetstra,
Carlog3, Chem-awb, Chris the speller, DutchDevil, Fvasconcellos, Graeme Bartlett, JWBE, JZNIOSH, Jkr2255, Kaos-pheory, Keenan Pepper, Kupirijo, Lamro, Mshearn, Penguinoid, Plasmic
Physics, Rembecki, Smokefoot, Suchirera, TMaster, Tomaxer, V8rik, Whoop whoop pull up, 17 anonymous edits
Image Sources, Licenses and Contributors
Image:Tetraethyl orthosilicate.svg  Source: http://en.wikipedia.org/w/index.php?title=File:Tetraethyl_orthosilicate.svg  License: Public Domain  Contributors: Fvasconcellos 16:01, 7 May 2007
(UTC)
Image:Tetraethyl orthosilicate 3D.png  Source: http://en.wikipedia.org/w/index.php?title=File:Tetraethyl_orthosilicate_3D.png  License: Public Domain  Contributors: Fvasconcellos 16:03, 7
May 2007 (UTC)
File:Yes check.svg  Source: http://en.wikipedia.org/w/index.php?title=File:Yes_check.svg  License: Public Domain  Contributors: Anomie
File:X mark.svg  Source: http://en.wikipedia.org/w/index.php?title=File:X_mark.svg  License: Public Domain  Contributors: User:Gmaxwell
License
Creative Commons Attribution-Share Alike 3.0
//creativecommons.org/licenses/by-sa/3.0/

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Tetraethyl orthosilicate

  • 1. Tetraethyl orthosilicate 1 Tetraethyl orthosilicate Tetraethyl orthosilicate Identifiers CAS number 78-10-4 [1]   PubChem 6517 [2] ChemSpider 6270 [3]   Jmol-3D images Image 1 [4] Properties Molecular formula SiC8 H20 O4 Molar mass 208.33 g mol−1 Appearance colourless liquid Density 0.933 g/mL at 20°C Melting point −77 °C, 196 K, -107 °F Boiling point 166-169 °C, 439-442 K, 331-336 °F Solubility in water miscible, but readily decomposes Hazards Main hazards Flammable, Harmful by inhalation Flash point 45 °C   (verify) [5]  (what is:  / ?) 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(OC 2 H 5 ) 4 . Often abbreviated TEOS, this molecule consists of four ethyl groups attached to SiO 4 4− ion, which is called orthosilicate. As an ion in solution,
  • 2. Tetraethyl orthosilicate 2 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: SiCl 4 + 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 and as a precursor to silicon dioxide in the semiconductor industry. [6] Other applications include coatings for carpets and other objects. TEOS is used in the production of aerogel. These applications exploit the reactivity of the Si-OR bonds. [7] Other reactions TEOS has the remarkable property of easily converting into silicon dioxide. This reaction occurs upon the addition of water: Si(OC 2 H 5 ) 4 + 2 H 2 O → SiO 2 + 4 C 2 H 5 OH 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. The Stöber process allows the formation of monodisperse silica particles. At elevated temperatures (>600 °C), TEOS converts to silicon dioxide: Si(OC 2 H 5 ) 4 → SiO 2 + 2 (C 2 H 5 ) 2 O The volatile coproduct is diethyl ether. References [1] http://www.commonchemistry.org/ChemicalDetail.aspx?ref=78-10-4 [2] http://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=6517 [3] http://www.chemspider.com/6270 [4] http://chemapps.stolaf.edu/jmol/jmol.php?model=CCO%5BSi%5D%28OCC%29%28OCC%29OCC [5] http://en.wikipedia.org/w/index.php?title=Special:ComparePages&rev1=470603747&page2=Tetraethyl+orthosilicate [6] D. Bulla, Deposition of thick TEOS PECVD silicon oxide layers for integrated optical waveguide applications. Thin Solid Films. 1998; 334(1-2):60-64. Available at: http://linkinghub.elsevier.com/retrieve/pii/S0040609098011171. [7][7] Lutz Rösch, Peter John, Rudolf Reitmeier "Silicon Compounds, Organic" Ullmann's Encyclopedia of Industrial Chemistry, 2002, Wiley-VCH, Weinheim. . Article Online Posting Date: June 15, 2000 External links ‱ NIST Standard Reference Database 69, June 2005 Release: NIST Chemistry WebBook (http://webbook.nist. gov/cgi/cbook.cgi?ID=C78104) ‱ Details of TEOS deposition process (http://timedomaincvd.com/CVD_Fundamentals/films/ TEOS_O2_thermal.html) ‱ CDC - NIOSH Pocket Guide to Chemical Hazards (http://www.cdc.gov/niosh/npg/npgd0282.html)
  • 3. Article Sources and Contributors 3 Article Sources and Contributors Tetraethyl orthosilicate  Source: http://en.wikipedia.org/w/index.php?oldid=577710285  Contributors: 2001:620:40B:1090:1C00:B4E5:754C:3339, A876, Akiry, Ambix, Andi47, Beetstra, Carlog3, Chem-awb, Chris the speller, DutchDevil, Fvasconcellos, Graeme Bartlett, JWBE, JZNIOSH, Jkr2255, Kaos-pheory, Keenan Pepper, Kupirijo, Lamro, Mshearn, Penguinoid, Plasmic Physics, Rembecki, Smokefoot, Suchirera, TMaster, Tomaxer, V8rik, Whoop whoop pull up, 17 anonymous edits Image Sources, Licenses and Contributors Image:Tetraethyl orthosilicate.svg  Source: http://en.wikipedia.org/w/index.php?title=File:Tetraethyl_orthosilicate.svg  License: Public Domain  Contributors: Fvasconcellos 16:01, 7 May 2007 (UTC) Image:Tetraethyl orthosilicate 3D.png  Source: http://en.wikipedia.org/w/index.php?title=File:Tetraethyl_orthosilicate_3D.png  License: Public Domain  Contributors: Fvasconcellos 16:03, 7 May 2007 (UTC) File:Yes check.svg  Source: http://en.wikipedia.org/w/index.php?title=File:Yes_check.svg  License: Public Domain  Contributors: Anomie File:X mark.svg  Source: http://en.wikipedia.org/w/index.php?title=File:X_mark.svg  License: Public Domain  Contributors: User:Gmaxwell License Creative Commons Attribution-Share Alike 3.0 //creativecommons.org/licenses/by-sa/3.0/