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  2. Buckminsterfullerene - Wikipedia

    en.wikipedia.org/wiki/Buckminsterfullerene

    Solutions of C 60 can be oxygenated to the epoxide C 60 O. Ozonation of C 60 in 1,2-xylene at 257K gives an intermediate ozonide C 60 O 3, which can be decomposed into 2 forms of C 60 O. Decomposition of C 60 O 3 at 296 K gives the epoxide, but photolysis gives a product in which the O atom bridges a 5,6-edge.

  3. Fullerene - Wikipedia

    en.wikipedia.org/wiki/Fullerene

    The family is named after buckminsterfullerene (C 60), the most famous member, which in turn is named after Buckminster Fuller. The closed fullerenes, especially C 60, are also informally called buckyballs for their resemblance to the standard ball of association football ("soccer"). Nested closed fullerenes have been named bucky onions.

  4. 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.

  5. 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.

  6. 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. In this structure none of the pentagons make ...

  7. Transition metal fullerene complex - Wikipedia

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

    Complexes with more than one fullerene ligand are illustrated by Ir 4 (CO) 3 (μ 4-CH)(PMe 3) 2 (μ-PMe) 2 (CNCH 2 Ph)(μ-η 2:η 2 C 60)(μ 4-η 1:η 1:η 2:η 2 C 60). In this Ir 4 cluster two fullerene ligands with multiple types of mixed binding. Platinum, palladium, and nickel form complexes of the type C 60 ML 2 where L is a monodentate ...

  8. Pueblo D60 school board incumbent Anthony Perko running for ...

    www.aol.com/pueblo-d60-school-board-incumbent...

    Perko is a product of three Pueblo D60 schools — Sunset Park Elementary, Pitts Middle School and Central High School. After graduating from Central in 2005, he attended the University of ...

  9. Spherical aromaticity - Wikipedia

    en.wikipedia.org/wiki/Spherical_aromaticity

    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 ] In 2011, Jordi Poater and Miquel Solà expanded Hirsch's rule to open-shell spherical compounds, which have unfilled outer shells but are still aromatic.