Journal article

STONE-WALES PYRACYLENE TRANSFORMATIONS OF THE ISOMERS OF C84

Abstract:: Under the Stone-Wales (pyracylene) transformation, the 24 isolated-pentagon isomers of C84 fall into two disjoint families, each containing one leapfrog closed shell, suggesting that the experimental product will consist of a mixture of two isomers.

Publication status:: Published

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APA Style

Fowler, P., Manolopoulos, D., & Ryan, R. (1992). STONE-WALES PYRACYLENE TRANSFORMATIONS OF THE ISOMERS OF C84. JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 5, 408–410.

MLA Style

Fowler, P, et al. “STONE-WALES PYRACYLENE TRANSFORMATIONS OF THE ISOMERS OF C84.” JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, no. 5, 1992, pp. 408–10.

Chicago Style

Fowler, P, D Manolopoulos, and R Ryan. 1992. “STONE-WALES PYRACYLENE TRANSFORMATIONS OF THE ISOMERS OF C84.” JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, no. 5: 408–10.
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Publisher copy:: 10.1039/c39920000408

Authors

+ Fowler, P More by this author

Role:: Author

+ Manolopoulos, D More by this author

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

+ Ryan, R More by this author

Role:: Author

Journal:: JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS More from this journal
Issue:: 5
Pages:: 408-410
Publication date:: 1992-03-01
DOI:: 10.1039/c39920000408
ISSN:: 0022-4936

Pubs id:: pubs:43826
UUID:: uuid:f2b95b2d-baa3-4509-b5b5-bc3bdfa352da
Local pid:: pubs:43826
Source identifiers:: 43826
Deposit date:: 2012-12-19
ARK identifier:: ark:/29072/ora_f2b95b2dbaa34509b5b5bc3bdfa352da

Terms of use

Copyright date:: 1992

Licence:: Terms and Conditions of Use for Oxford University Research Archive

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