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ISOMERIZATIONS OF THE FULLERENES

Abstract:
The Stone-Wales (pyracylene) rearrangement is a hypothetical mechanism for interconversion of fullerene isomers, accounting for mobility of the pentagons on the surfaces of these clusters. Two versions of the transformation, involving patches of 4 and 12 rings, respectively, can be defined. Energetic and group-theoretical aspects of the transformation are discussed, symmetry-based selection rules devised and complete isomerisation maps presented for small fullerenes (C20 to C40) and isolated-pentagon isomers (C78 to C88). Fullerenes that self-racemise under this transformation include D2 C28. Limitations on the usefulness of this mechanism as a means of rationalising experimental isomer distributions are briefly discussed. © 1992.
Publication status:
Published

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Publisher copy:
10.1016/0008-6223(92)90065-5

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Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Physical & Theoretical Chem
Role:
Author


Journal:
CARBON More from this journal
Volume:
30
Issue:
8
Pages:
1235-1250
Publication date:
1992-01-01
DOI:
ISSN:
0008-6223


Keywords:
Pubs id:
pubs:44068
UUID:
uuid:95397a30-2743-4da0-8258-8e2ebc825214
Local pid:
pubs:44068
Source identifiers:
44068
Deposit date:
2012-12-19
ARK identifier:

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