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  2. Fullerene chemistry - Wikipedia

    en.wikipedia.org/wiki/Fullerene_chemistry

    Fullerene or C 60 is soccer-ball-shaped or I h with 12 pentagons and 20 hexagons. According to Euler's theorem these 12 pentagons are required for closure of the carbon network consisting of n hexagons and C 60 is the first stable fullerene because it is the smallest possible to obey this rule.

  3. Fullerene - Wikipedia

    en.wikipedia.org/wiki/Fullerene

    The older, "bottom-up" theory proposes that they are built atom-by-atom. The alternative "top-down" approach claims that fullerenes form when much larger structures break into constituent parts. [74] In 2013 researchers discovered that asymmetrical fullerenes formed from larger structures settle into stable fullerenes.

  4. 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 ...

  5. Transition metal fullerene complex - Wikipedia

    en.wikipedia.org/wiki/Transition_metal_fullerene...

    Fullerenes are typically spheroidal carbon compounds, the most prevalent being buckminsterfullerene, C 60. [2] One year after it was prepared in milligram quantities in 1990, [3] C 60 was shown to function as a ligand in the complex [Ph 3 P] 2 Pt(η 2-C 60). [4] Since this report, a variety of transition metals and binding modes were demonstrated.

  6. 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,

  7. Spherical aromaticity - Wikipedia

    en.wikipedia.org/wiki/Spherical_aromaticity

    In organic chemistry, spherical aromaticity is formally used to describe an unusually stable nature of some spherical compounds such as fullerenes and polyhedral boranes.. In 2000, Andreas Hirsch and coworkers in Erlangen, Germany, formulated a rule to determine when a spherical compound would be aromatic.

  8. Diffuse interstellar bands - Wikipedia

    en.wikipedia.org/wiki/Diffuse_interstellar_bands

    Polycyclic aromatic hydrocarbons, long carbon-chain molecules such as polyynes, and fullerenes are all potentially important. [6] [13] These types of molecule experience rapid and efficient deactivation when excited by a photon, which both broadens the spectral lines and makes them stable enough to exist in the interstellar medium. [14] [15]

  9. Allotropes of carbon - Wikipedia

    en.wikipedia.org/wiki/Allotropes_of_carbon

    These electrons are free to move, so are able to conduct electricity. However, the electricity is only conducted along the plane of the layers. In diamond, all four outer electrons of each carbon atom are 'localized' between the atoms in covalent bonding. The movement of electrons is restricted and diamond does not conduct an electric current.