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dc.contributor.author | Vereshchagina Y. | |
dc.contributor.author | Timosheva A. | |
dc.contributor.author | Chachkov D. | |
dc.date.accessioned | 2018-09-18T20:19:04Z | |
dc.date.available | 2018-09-18T20:19:04Z | |
dc.date.issued | 2013 | |
dc.identifier.issn | 1070-4280 | |
dc.identifier.uri | https://dspace.kpfu.ru/xmlui/handle/net/138650 | |
dc.description.abstract | Conformational analysis of N-arylmaleimides and bis-maleimides was performed by the dipole moment method and quantum chemical calculations. The aromatic ring and heterocycle in N-arylmaleimides are turned with respect to each other through an angle of 42-44, which excludes conjugation between these fragments. No conjugation exists between the dioxopyrrole rings in bridged bis-maleimides. The structure of the examined compounds is controlled by steric factors. Pronounced inductive effect of chlorine atoms in chloro-substituted bis-maleimides is responsible for their reduced dipole moments. © 2013 Pleiades Publishing, Ltd. | |
dc.relation.ispartofseries | Russian Journal of Organic Chemistry | |
dc.title | Theoretical study of the structure of N-arylmaleimides and bis-maleimides | |
dc.type | Article | |
dc.relation.ispartofseries-issue | 10 | |
dc.relation.ispartofseries-volume | 49 | |
dc.collection | Публикации сотрудников КФУ | |
dc.relation.startpage | 1482 | |
dc.source.id | SCOPUS10704280-2013-49-10-SID84889010287 |