A case of breakdown of the Kekulé-structure model
dc.contributor.author | Gutman I. | |
dc.contributor.author | Markovic, Svetlana | |
dc.contributor.author | Jeremic B. | |
dc.date.accessioned | 2021-04-20T15:02:24Z | |
dc.date.available | 2021-04-20T15:02:24Z | |
dc.date.issued | 2010 | |
dc.description.abstract | For a long time, Kekulé structures have been used to predict and rationalize the stability, geometry, and π-electron properties of polycyclic conjugated molecules, especially hydrocarbons. We now point out an example, demonstrating that the Kekulé-structure model is not generally applicable. Namely, the molecule of dibenzo[cd,mn]indeno[123, gf ]pyrene is perfectly planar and strain-free. Yet, its geometry (determined by means of an unrestricted symmetry-broken UB3LYP/6-311G(d,p) DFT method) is in complete disagreement with what one would expect on the basis of its Kekulé structures. © Taylor & Francis Group, LLC. | |
dc.identifier.doi | 10.1080/10406638.2010.503162 | |
dc.identifier.issn | 1040-6638 | |
dc.identifier.scopus | 2-s2.0-77956622983 | |
dc.identifier.uri | https://scidar.kg.ac.rs/handle/123456789/10162 | |
dc.rights | restrictedAccess | |
dc.source | Polycyclic Aromatic Compounds | |
dc.title | A case of breakdown of the Kekulé-structure model | |
dc.type | article |
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