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Synthesis of a higher fullerene precursor-an "unrolled" C84 fullerene

Konstantin Amsharov1, Martin Jansen

  • 1Max Planck Institute for Solid State Research, Stuttgart, Germany.

Chemical Communications (Cambridge, England)
|June 18, 2009
PubMed

Abstract:

We report the synthesis of the C(84)(20)-fullerene related hydrocarbon C(84)H(42), which possesses more than 83% of the C(84)(20)-fullerene connectivity, and its selective transformation to C(84) by flash vacuum pyrolysis (FVP).

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The chair conformation is the most stable form of cyclohexane due to the absence of angle and torsional strain. The absence of angle strain is a result of cyclohexane’s bond angle being very close to the ideal tetrahedral bond angle of 109.5° in its chair conformer. Similarly, the torsional strain is also absent owing to the perfectly staggered arrangement of bonds.
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