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https://scidar.kg.ac.rs/handle/123456789/9809
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Поље DC-а | Вредност | Језик |
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dc.rights.license | openAccess | - |
dc.contributor.author | Đurđević Nikolić, Jelena | - |
dc.contributor.author | Gutman I. | - |
dc.date.accessioned | 2021-04-20T14:06:37Z | - |
dc.date.available | 2021-04-20T14:06:37Z | - |
dc.date.issued | 2012 | - |
dc.identifier.issn | 1857-5552 | - |
dc.identifier.uri | https://scidar.kg.ac.rs/handle/123456789/9809 | - |
dc.description.abstract | Within a systematic study of cyclic conjugation in the benzo-annelated derivatives of acenaphthylene and fluoranthene, a general regularity was discovered, named phenyl-cyclopentadienyl rule (PCP rule). According to this rule, six-membered rings connected to the five-membered ring by a single carbon-carbon bond increase the magnitude of cyclic conjugation in the five-membered ring. The greater the number of such six-membered rings is, the stronger the cyclic conjugation in the five-membered ring. The PCP rule was initially established by studying the energy effects of individual rings, and was eventually corroborated by a variety of other independent approaches (Wiberg bond orders, carbon-carbon bond lengths calculated by high-level ab initio DFT methods, multicenter delocalization indices, ring currents). | - |
dc.rights | info:eu-repo/semantics/openAccess | - |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/4.0/ | - |
dc.source | Macedonian Journal of Chemistry and Chemical Engineering | - |
dc.title | Phenyl-cyclopentadienyl rule | - |
dc.type | review | - |
dc.identifier.doi | 10.20450/mjcce.2012.52 | - |
dc.identifier.scopus | 2-s2.0-84864571632 | - |
Налази се у колекцијама: | Faculty of Science, Kragujevac |
Датотеке у овој ставци:
Датотека | Опис | Величина | Формат | |
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10.20450-mjcce.2012.52.pdf | 1.35 MB | Adobe PDF | ![]() Погледајте |
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