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  2. Fullerene chemistry - Wikipedia

    en.wikipedia.org/wiki/Fullerene_chemistry

    The C 60 fullerene dimerizes in a formal [2+2] cycloaddition to a C 120 bucky dumbbell in the solid state by mechanochemistry (high-speed vibration milling) with potassium cyanide as a catalyst. [47] The trimer has also been reported using 4-aminopyridine as catalyst (4% yield) [48] and observed with scanning tunneling microscopy as a monolayer ...

  3. Fullerene - Wikipedia

    en.wikipedia.org/wiki/Fullerene

    Nested closed fullerenes have been named bucky onions. Cylindrical fullerenes are also called carbon nanotubes or buckytubes. [1] The bulk solid form of pure or mixed fullerenes is called fullerite. [2] Fullerenes had been predicted for some time, but only after their accidental synthesis in 1985 were they detected in nature [3] [4] and outer ...

  4. Polyfullerene - Wikipedia

    en.wikipedia.org/wiki/Polyfullerene

    They are called intrinsic polymeric fullerenes, or more often all C 60 polymers. Fullerene can be part of a polymer chain in many different ways. Fullerene-containing polymers are divided into following structural categories: Intrinsic polymeric fullerene (homopolymer), Main-chain polymers, Side-chain polymers, Star polymers, Crosslinked polymers,

  5. Prato reaction - Wikipedia

    en.wikipedia.org/wiki/Prato_reaction

    Just as in other fullerene reactions like the Bingel reaction or Diels-Alder reactions this reaction can be reversed. A thermal cycloelimination of a pyrrolidinofullerene with a strong dipolarophile such as maleic acid and a catalyst such as Wilkinson's catalyst or copper triflate in 1,2-dichlorobenzene at reflux 8 to 18 hours regenerates the pristine C 60 fullerene. [9]

  6. Buckminsterfullerene - Wikipedia

    en.wikipedia.org/wiki/Buckminsterfullerene

    These endohedral fullerenes are usually synthesized by doping in the metal atoms in an arc reactor or by laser evaporation. These methods gives low yields of endohedral fullerenes, and a better method involves the opening of the cage, packing in the atoms or molecules, and closing the opening using certain organic reactions. This method ...

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  9. Potential applications of carbon nanotubes - Wikipedia

    en.wikipedia.org/wiki/Potential_applications_of...

    This presented an important advance in the field as CNT was shown to potentially outperform Si. At the time, a major challenge was ohmic metal contact formation. In this regard, palladium, which is a high-work function metal was shown to exhibit Schottky barrier-free contacts to semiconducting nanotubes with diameters >1.7 nm. [94] [95]