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  2. Buckminsterfullerene - Wikipedia

    en.wikipedia.org/wiki/Buckminsterfullerene

    The method was simple and efficient to prepare the material in gram amounts per day (1990) which has boosted the fullerene research and is even today applied for the commercial production of fullerenes. The discovery of practical routes to C 60 led to the exploration of a new field of chemistry involving the study of fullerenes.

  3. Endohedral hydrogen fullerene - Wikipedia

    en.wikipedia.org/wiki/Endohedral_hydrogen_fullerene

    Scheme 1 presents an overview of the first step, the creation of a 13 membered ring orifice on the fullerene surface. A 1,2,4-triazine 2 is fitted with two phenyl groups and a pyridine group for reasons of solubility and reacted in 1,2-dichlorobenzene with pristine C 60 fullerene 2 in a Diels-Alder reaction at high temperature and for an extended reaction time.

  4. Endohedral fullerene - Wikipedia

    en.wikipedia.org/wiki/Endohedral_fullerene

    The calculated data allows using C 60 fullerene as a Faraday cage, [13] which isolates the encapsulated atom from the external electric field. The mentioned relations should be typical for the more complicated endohedral structures (e.g., C 60 @C 240 [14] and giant fullerene-containing "onions" [15]).

  5. Fullerene - Wikipedia

    en.wikipedia.org/wiki/Fullerene

    According to the IUPAC, to name a fullerene, one must cite the number of member atoms for the rings which comprise the fullerene, its symmetry point group in the Schoenflies notation, and the total number of atoms. For example, buckminsterfullerene C 60 is systematically named (C 60-I h)[5,6]fullerene. The name of the point group should be ...

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  7. Exohedral fullerene - Wikipedia

    en.wikipedia.org/wiki/Exohedral_fullerene

    This page was last edited on 18 October 2024, at 13:16 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.

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