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dc.contributor.author | Kadyrov R. | |
dc.contributor.author | Shakirov I. | |
dc.contributor.author | Arshinova R. | |
dc.contributor.author | Gnevashev S. | |
dc.contributor.author | Shagidullin R. | |
dc.contributor.author | Arbuzov B. | |
dc.date.accessioned | 2018-09-14T20:46:07Z | |
dc.date.available | 2018-09-14T20:46:07Z | |
dc.date.issued | 1989 | |
dc.identifier.issn | 0568-5230 | |
dc.identifier.uri | https://dspace.kpfu.ru/xmlui/handle/net/132694 | |
dc.description.abstract | 1. On the basis of IR and Raman vibrational spectra,1H NMR spectra, and measurements of dipole moments of 4,7-dihydro-2-aroxy-1,3,2-dioxaphosphepines, their 5,6-dichloro analogs are conformationally homogeneous and have a flexible T conformation with anti orientation of the phenoxyl radical. 5,6-Benzo-2-phenoxy-1,3,2-dioxaphosphepine is characterized by a three-component equilibrium in which both chair conformations and the twist conformation participate, with predominance of the first two. 2. In phenoxy-substituted 1,3,2-dioxaphosphepines, the plane of the benzene ring is nearly orthogonal to the plane of the {Mathematical expression}. © 1989 Plenum Publishing Corporation. | |
dc.relation.ispartofseries | Bulletin of the Academy of Sciences of the USSR Division of Chemical Science | |
dc.title | Spatial structure of phosphorus-containing heterocycles. 49. Vibrational spectra, dipole moments, and conformations of 2-aroxy-1,3,2-dioxaphosphepines and their benzo analogs | |
dc.type | Article | |
dc.relation.ispartofseries-issue | 5 | |
dc.relation.ispartofseries-volume | 38 | |
dc.collection | Публикации сотрудников КФУ | |
dc.relation.startpage | 964 | |
dc.source.id | SCOPUS05685230-1989-38-5-SID1942469078 |