Trimethylsilyl cyclopentadiene

Chemical compound From Wikipedia, the free encyclopedia

Trimethylsilyl cyclopentadiene is an organosilicon compound with the chemical formula C5H5Si(CH3)3. It exists as a colorless liquid. It is used in the synthesis of some metal cyclopentadienyl complexes and has attracted interest for its fluxional structure.

Quick facts Names, Identifiers ...
Trimethylsilyl cyclopentadiene
Names
IUPAC name
cyclopenta-2,4-dien-1-yl(trimethyl)silane
Identifiers
3D model (JSmol)
ChemSpider
  • InChI=1S/C8H14Si/c1-9(2,3)8-6-4-5-7-8/h4-8H,1-3H3
    Key: VMFHCJPMKUTMMQ-UHFFFAOYSA-N
  • C[Si](C)(C)C1C=CC=C1
Properties
C8H14Si
Molar mass 138.285 g·mol−1
Appearance Colorless liquid
Density 0.833 g/mL[1]
Boiling point 138 to 140 °C (280 to 284 °F; 411 to 413 K)[1]
Hazards
GHS labelling:
GHS02: FlammableGHS07: Exclamation mark
Warning
H226, H315, H319, H335
P210, P233, P240, P241, P242, P243, P261, P264, P271, P280, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P370+P378, P403+P233, P403+P235, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Trimethylsilyl cyclopentadiene is an example of a molecule that undergoes rapid sigmatropic rearrangement. Observations of trimethylsilyl cyclopentadiene using gas phase NMR spectroscopy show that the protons on the ring are chemically equivalent, indicated by a single peak. This phenomenon, an example of fluxionality, is explained by the migration of the silyl group from carbon-to-carbon, thereby giving the appearance of equivalent CH signals.[2]

It has a refractive index (n20/D) of 1.471.[3]

Synthesis

Trimethylsilyl cyclopentadiene is prepared by the reaction trimethylsilyl chloride (Me3SiCl) with sodium cyclopentadienide (NaC5H5):[4][5]

(CH3)3SiCl + NaC5H5 → C5H5Si(CH3)3 + NaCl

References

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