2011
DOI: 10.1038/ncomms1431
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Carbon arc production of heptagon-containing fullerene[68]

Abstract: A carbon heptagon ring is a key unit responsible for structural defects in sp2-hybrized carbon allotropes including fullerenes, carbon nanotubes and graphenes, with consequential influences on their mechanical, electronic and magnetic properties. Previous evidence concerning the existence of heptagons in fullerenes has been obtained only in off-line halogenation experiments through top-down detachment of a C2 unit from a stable fullerene. Here we report a heptagon-incorporating fullerene C68, tentatively named… Show more

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Cited by 76 publications
(80 citation statements)
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“…S6). Interestingly, a heptagon-containing C 68 fullerene, although exohedrally stabilized by chlorine, has recently been found to form in carbon vapour 35 . C 64 and all larger clusters possess isotopic distributions that conform to growth by sequential carbon addition steps originating with the C 60 precursor.…”
Section: Resultsmentioning
confidence: 99%
“…S6). Interestingly, a heptagon-containing C 68 fullerene, although exohedrally stabilized by chlorine, has recently been found to form in carbon vapour 35 . C 64 and all larger clusters possess isotopic distributions that conform to growth by sequential carbon addition steps originating with the C 60 precursor.…”
Section: Resultsmentioning
confidence: 99%
“…The focus of studies of classical fullerenes is now moving on to applications [6,7]. However, an increasing number of experimental and theoretical observations indicate that non-classical isomers play an important role in the formation of metallofullerenes and fullerene derivatives [8][9][10]. Even for the fullerenes themselves, formation mechanisms are still unclear in terms of the roles of heptagons and/or squares [11].…”
Section: Introductionmentioning
confidence: 99%
“…a Krätschmer-Huffman graphite-arc-discharge process involving chlorine, [17] our 13 C-labeling experiments established the growth of pristine fullerenes in the arc zone at 2000-2500 K and their subsequent capture/stabilization by chlorination beyond the arc zone. [18] Therefore, the capture of #4348 C 66 as a chlorofullerene is reasonable in the present synthesis in a carbon arc in the presence of carbon tetrachloride.…”
mentioning
confidence: 98%