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Buckminsterfullerene is a black solid that dissolves in hydrocarbon solvents to produce a violet solution. The substance was discovered in 1985 and has received intense study, although few real world applications have been found. Molecules of buckminsterfullerene (or of fullerenes in general) are commonly nicknamed buckyballs. [3] [4]
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 ...
A related fullerene molecule, named buckminsterfullerene (or C 60 fullerene) consists of 60 carbon atoms. ... The name is a homage to Buckminster Fuller, ...
The name, ZTC, derives from their origin inside the pores of zeolites, crystalline silicon dioxide minerals. A vapor of carbon-containing molecules is injected into the zeolite, where the carbon gathers on the pores' walls, creating the negative curve.
The first fullerene molecule to be discovered, and the family's namesake, buckminsterfullerene (C 60), was prepared in 1985 by Richard Smalley, Robert Curl, James Heath, Sean O'Brien, and Harold Kroto at Rice University. The name was a homage to Buckminster Fuller, whose geodesic domes it resembles.
The unusual middle name, Buckminster, was an ancestral family name. As a child, Richard Buckminster Fuller tried numerous variations of his name. He used to sign his name differently each year in the guest register of his family summer vacation home at Bear Island, Maine. He finally settled on R. Buckminster Fuller. [13]
Chemical nomenclature, replete as it is with compounds with very complex names, is a repository for some names that may be considered unusual. A browse through the Physical Constants of Organic Compounds in the CRC Handbook of Chemistry and Physics (a fundamental resource) will reveal not just the whimsical work of chemists, but the sometimes peculiar compound names that occur as the ...
Rendering of a buckminsterfullerene containing a noble gas atom (M@C 60). Electron microscopy images of M 3 N@C 80 peapods. Metal atoms (M = Ho or Sc) are seen as dark spots inside the fullerene molecules; they are doubly encapsulated in the C 80 molecules and in the nanotubes. [1]
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