Tetrasilane
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Other names
n-Tetrasilane
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Identifiers | |
3D model (JSmol)
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ChemSpider | |
ECHA InfoCard | 100.132.456 |
EC Number |
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PubChem CID
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
H10Si4 | |
Molar mass | 122.420 g·mol−1 |
Appearance | colourless liquid that self ignite in air[1] |
Density | 0.792 g·cm−3[2] |
Melting point | −89.9 °C[2] |
Boiling point | 108.1 °C[2] |
reacts[1] | |
Hazards | |
GHS labelling: | |
Danger | |
H250 | |
Related compounds | |
Related compounds
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butane |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Tetrasilane is a silane with the structure formula SiH3–(SiH2)2–SiH3. It is the silane analog of butane.
Preparation
Tetrasilane can be prepared by reacting magnesium silicide (Mg2Si) with acids like 20% phosphoric acid in 50–60 °C.[3]
The reaction can produce silanes up to n=15. The reaction of magnesium silicide with 25% hydrochloric acid produces 40% monosilane, 30% disilane, 15% trisilane, 10% tetrasilane and 5% higher silanes.[4] The mixture can be separated by fractional distillation.
In addition, higher silanes can also be obtained by discharges monosilane:[3]
Properties
Tetrasilane is a colourless, pyrophoric liquid that has a disgusting odour. Even below 54 °C, it will still spontaneous combust.[1] It is even more unstable than trisilane, slowly decomposing at room temperature, releasing hydrogen and forming shorter chain silanes.[5]
Reactions
Photochemical disproportionation of tetrasilane will produce 3-silylpentasilane and disilane.[6]
With the presence of aluminium chloride, heating tetrasilane in xylene will allow isomerization to isotetrasilane.[7]
References
- ^ a b c Material Safety Data Sheet for Tetrasilane (Si4H10) (PDF-Datei)
- ^ a b c Lide, D. R., ed. (2005). CRC Handbook of Chemistry and Physics (86th ed.). Boca Raton (FL): CRC Press. p. 81. ISBN 0-8493-0486-5.
- ^ a b Ralf Steudel (2014), [[1], p. 294, at Google Books Chemie der Nichtmetalle: Synthesen - Strukturen - Bindung – Verwendung] (in German), De Gruyter, pp. 294–295, ISBN 978-3-11-030797-9
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value (help) - ^ Egon Wiberg (2011), [[2], p. 320, at Google Books Lehrbuch der Anorganischen Chemie: Mit einem Anhang: Chemiegeschichte] (in German), Walter de Gruyter, pp. 319–320, ISBN 978-3-11-023832-7
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value (help) - ^ Alfred Stock, Paul Stiebeler, Friedrich Zeidler (1923-07-04), "Siliciumwasserstoffe, XVI.: Die höheren Siliciumhydride", Berichte der deutschen chemischen Gesellschaft (in German), vol. 56, no. 7, pp. 1695–1705, doi:10.1002/cber.19230560735
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: CS1 maint: multiple names: authors list (link) - ^ F. Fehér, I. Fischer (March 1976), "Beiträge zur Chemie des Siliciums und Germaniums, XXVIII. Die photochemische Disproportionierung von n-Tetrasilan, Darstellung und Eigenschaften von 3-Silylpentasilan", Zeitschrift für anorganische und allgemeine Chemie (in German), vol. 421, no. 1, pp. 9–14, doi:10.1002/zaac.19764210103
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