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  2. Fullerene - Wikipedia

    en.wikipedia.org/wiki/Fullerene

    Fullerenes are soluble in many organic solvents, such as toluene, chlorobenzene, and 1,2,3-trichloropropane. Solubilities are generally rather low, such as 8 g/L for C 60 in carbon disulfide. Still, fullerenes are the only known allotrope of carbon that can be dissolved in common solvents at room temperature.

  3. Iron oxide nanoparticle - Wikipedia

    en.wikipedia.org/wiki/Iron_oxide_nanoparticle

    Water-in-oil is more popular for synthesizing many kinds of nanoparticles. The water and oil are mixed with an amphiphillic surfactant. The surfactant lowers the surface tension between water and oil, making the solution transparent. The water nanodroplets act as nanoreactors for synthesizing nanoparticles. The shape of the water pool is spherical.

  4. 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.

  5. Nanomaterials - Wikipedia

    en.wikipedia.org/wiki/Nanomaterials

    They are synthesized in a water-based solution in the presence of a base catalyst and a pore forming agent known as a surfactant. Surfactants are molecules that present the particularity to have a hydrophobic tail (alkyl chain) and a hydrophilic head (charged group, such as a quaternary amine for example).

  6. 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 .

  7. Buckminsterfullerene - Wikipedia

    en.wikipedia.org/wiki/Buckminsterfullerene

    Fullerenes are sparingly soluble in aromatic solvents and carbon disulfide, but insoluble in water. Solutions of pure C 60 have a deep purple color which leaves a brown residue upon evaporation. The reason for this color change is the relatively narrow energy width of the band of molecular levels responsible for green light absorption by ...

  8. Azafullerene - Wikipedia

    en.wikipedia.org/wiki/Azafullerene

    Spherical fullerenes are also called buckyballs, and they resemble the balls used in football (soccer). Fullerenes are similar in structure to graphite, which is composed of stacked graphene sheets of linked hexagonal rings; but they may also contain pentagonal (or sometimes heptagonal) rings.

  9. Endohedral fullerene - Wikipedia

    en.wikipedia.org/wiki/Endohedral_fullerene

    In this method Merrifield resin is modified as a cyclopentadienyl resin and used as a solid phase against a mobile phase containing the complex mixture in a column chromatography operation. Only very stable fullerenes such as [Sc 3 N] +6 @[C 80] −6 pass through the column unreacted. In Ce 2 @C 80 the two metal atoms exhibit a non-bonded ...