| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 9590523 | Journal of Molecular Structure: THEOCHEM | 2005 | 8 Pages |
Abstract
Ab initio studies show the possibility of involvement of cyclic, planar, singlet and/or triplet 2-X-2,4,6,8-cyclononatetraenylidenes, carbenic transition states (1X-S* and/or 1X-T*), in the conversion of cyclic conjugated non-planar allenes, 1-X-1,2,4,6,8-cyclonona-pentaenes (1X), to their corresponding mirror images, 1Xâ² (where X=H, F, Cl and Br).
Related Topics
Physical Sciences and Engineering
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Physical and Theoretical Chemistry
Authors
M.Z. Kassaee, M. Koohi,