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The C 60 fullerene dimerizes in a formal [2+2] cycloaddition to a C 120 bucky dumbbell in the solid state by mechanochemistry (high-speed vibration milling) with potassium cyanide as a catalyst. [47] The trimer has also been reported using 4-aminopyridine as catalyst (4% yield) [48] and observed with scanning tunneling microscopy as a monolayer ...
Nested closed fullerenes have been named bucky onions. Cylindrical fullerenes are also called carbon nanotubes or buckytubes. [1] The bulk solid form of pure or mixed fullerenes is called fullerite. [2] Fullerenes had been predicted for some time, but only after their accidental synthesis in 1985 were they detected in nature [3] [4] and outer ...
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,
C 70 fullerene is the fullerene molecule consisting of 70 carbon atoms. It is a cage-like fused-ring structure which resembles a rugby ball, made of 25 hexagons and 12 pentagons, with a carbon atom at the vertices of each polygon and a bond along each polygon edge.
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 ...
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These properties recommend DBU for use as a catalyst, for example as a curing agent for epoxy resins and polyurethane. It is used in the separation of fullerenes in conjunction with trimethylbenzene. It reacts with C 70 and higher fullerenes, but not with C 60. It is useful for dehydrohalogenations. [7]
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