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  2. Fullerene - Wikipedia

    en.wikipedia.org/wiki/Fullerene

    A fullerene is an allotrope of carbon whose ... There are two major families of fullerenes, with fairly distinct properties and ... 60 in extra virgin olive oil, ...

  3. Fullerene chemistry - Wikipedia

    en.wikipedia.org/wiki/Fullerene_chemistry

    Fullerene chemistry is a field of organic chemistry devoted to the chemical properties of fullerenes. [1] [2] [3] Research in this field is driven by the need to functionalize fullerenes and tune their properties. For example, fullerene is notoriously insoluble and adding a suitable group can enhance solubility. [1]

  4. 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 ...

  5. Solubility of fullerenes - Wikipedia

    en.wikipedia.org/wiki/Solubility_of_fullerenes

    C 60 in solution C 60 in extra virgin olive oil showing the characteristic purple color of pristine C 60 solutions. The solubility of fullerenes is generally low. Carbon disulfide dissolves 8g/L of C60, and the best solvent (1-chloronaphthalene) dissolves 53 g/L. up Still, fullerenes are the only known allotrope of carbon that can be dissolved in common solvents at room temperature.

  6. Endohedral fullerene - Wikipedia

    en.wikipedia.org/wiki/Endohedral_fullerene

    Besides unfilled fullerenes, endohedral metallofullerenes develop with different cage sizes like La@C 60 or La@C 82 and as different isomer cages. Aside from the dominant presence of mono-metal cages, numerous di-metal endohedral complexes and the tri-metal carbide fullerenes like Sc 3 C 2 @C 80 were also isolated. In 1999 a discovery drew ...

  7. Spherical aromaticity - Wikipedia

    en.wikipedia.org/wiki/Spherical_aromaticity

    They found that those with 2(n+1) 2 π-electrons could display aromatic properties, as spherical molcular orbitals are filled when there are 2(n+1) 2 π-electrons for some positive integer n. For example, in buckminsterfullerene (C 60) this happens for the species C 60 10+, which has 50 π-electrons: 50/2 = 25, which is a perfect square. [1]

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  9. Polyfullerene - Wikipedia

    en.wikipedia.org/wiki/Polyfullerene

    Polyfullerene is a basic polymer of the C 60 monomer group, in which fullerene segments are connected via covalent bonds into a polymeric chain without side or bridging groups. 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.