Journal article
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
Authors
- 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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- Copyright date:
- 1992
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