Показать сокращенную информацию
dc.contributor.author | Arbuzov B. | |
dc.contributor.author | Mareev Y. | |
dc.contributor.author | Shagidullin R. | |
dc.contributor.author | Vinogradova V. | |
dc.contributor.author | Shakirov I. | |
dc.date.accessioned | 2018-09-14T20:44:14Z | |
dc.date.available | 2018-09-14T20:44:14Z | |
dc.date.issued | 1984 | |
dc.identifier.issn | 0568-5230 | |
dc.identifier.uri | https://dspace.kpfu.ru/xmlui/handle/net/132651 | |
dc.description.abstract | 1. 2-Chloro-, 2-methoxy-, and 2-tert-butoxy-4,6,6-trimethyl-1,3,2-dioxastibinanes and 2-tert-butoxy-5,5-dimethyl-and 2-tert-butoxy-4-methyl-1,3,2-dioxastibinanes were synthesized by the transetherification of chlorodiethoxy-, trimethoxy-, and tri-tert-butoxyantimony with the respective glycols. 2. According to the data on the vibration spectra, the 2-chloro and 2-alkoxy derivatives of 1,3,2-dioxastibinane are associated at the Sb-O bonds in the crystalline phase. The degree of association is determined by steric factors. 2-tert-Butoxy-4,6,6-trimethyl-1,3,2-dioxastibinane exists in the monomeric form. © 1985 Plenum Publishing Corporation. | |
dc.relation.ispartofseries | Bulletin of the Academy of Sciences of the USSR Division of Chemical Science | |
dc.title | Production of some derivatives of 1,3,2-dioxastibinane and their vibrational spectra | |
dc.type | Article | |
dc.relation.ispartofseries-issue | 8 | |
dc.relation.ispartofseries-volume | 33 | |
dc.collection | Публикации сотрудников КФУ | |
dc.relation.startpage | 1686 | |
dc.source.id | SCOPUS05685230-1984-33-8-SID34250142423 |