Chemistry:Dodecamethylcyclohexasilane

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Dodecamethylcyclohexasilane
Me12Si6.svg
Dodecamethylcyclohexasilane-from-xtal-3D-bs-17-grey.png
Names
IUPAC name
1,1,2,2,3,3,4,4,5,5,6,6-dodecamethylhexasilinane
Identifiers
3D model (JSmol)
ChemSpider
EC Number
  • 223-860-0
Properties
Si
6
(CH
3
)
12
Molar mass 348.930 g·mol−1
Appearance colorless solid
Density 0.988 g/cm3
Melting point 254–257 °C (489–495 °F; 527–530 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Dodecamethylcyclohexasilane is the organosilicon compound with the formula Si
6
(CH
3
)
12
. It is one of the more readily prepared and easily handled polysilanes. Dodecamethylcyclohexasilane is produced by reduction of dimethyldichlorosilane with sodium-potassium alloy:[1]

6 (CH
3
)
2
SiCl
2
+ 12 M → Si
6
(CH
3
)
12
+ 12 MCl

where M is Na or K. The reaction also produces a polymer poly(dimethylsilylene) [–Si(CH
3
)
2
–]
n
and a cyclic compound decamethylcyclopentasilane Si
5
(CH
3
)
10
.

The chair conformer of dodecamethylcyclohexasilane was confirmed by X-ray crystallography.[2][3]

Reactions

Dodecamethylcyclohexasilane reacts with potassium tert-butoxide to give the potassium derivative:[4]

(CH
3
)
12
Si
6
+ KOC(CH
3
)
3
→ K(CH
3
)
11
Si
6
+ CH
3
OC(CH
3
)
3

References

  1. West, Robert; Brough, Lawrence; Wojnowski, Wieslaw (1979). "Dodecamethylcyclohexasilane". Inorganic Syntheses 19: 265–268. doi:10.1002/9780470132500.ch62. ISBN 9780470132500. 
  2. Carrell, H. L.; Donohue, J. (1972). "Crystal and molecular structure of dodecamethylcyclohexasilane". Acta Crystallogr. B 28: 1566–1571. doi:10.1107/S0567740872004595. 
  3. Omatsu, Yamato; Mizuhata, Yoshiyuki; Tokitoh, Norihiro (2018). "Synthesis of Dodecaallylhexasilacyclohexane and Its Convertibility". Zeitschrift für Anorganische und Allgemeine Chemie 644 (17): 930–934. doi:10.1002/zaac.201800171. 
  4. Palitzsch, Wolfram; Beyer, Christian; Böhme, Uwe; Rittmeister, Ben; Roewer, Gerhard (1999). "Preparation, Characterization, and Properties of Various Novel Ionic Derivatives of Pentacarbonyltungsten". European Journal of Inorganic Chemistry 1999 (10): 1813–1820. doi:10.1002/(SICI)1099-0682(199910)1999:10<1813::AID-EJIC1813>3.0.CO;2-D.