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  2. 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 ...

  3. Fullerene - Wikipedia

    en.wikipedia.org/wiki/Fullerene

    A fullerene is an allotrope of carbon whose molecules consist of carbon atoms connected by single and double bonds ... chiral & non-chiral nanotubes, and C60 ...

  4. Endohedral fullerene - Wikipedia

    en.wikipedia.org/wiki/Endohedral_fullerene

    Endohedral fullerenes, also called endofullerenes, are fullerenes that have additional atoms, ions, or clusters enclosed within their inner spheres. The first lanthanum C 60 complex called La@C 60 was synthesized in 1985. [ 2 ]

  5. 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]

  6. 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.

  7. 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.

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