dc.contributor.author |
Vereshchagina Y.A. |
|
dc.contributor.author |
Ismagilova R.R. |
|
dc.contributor.author |
Chachkov D.V. |
|
dc.contributor.author |
Chernysheva N.A. |
|
dc.date.accessioned |
2021-02-25T20:38:41Z |
|
dc.date.available |
2021-02-25T20:38:41Z |
|
dc.date.issued |
2020 |
|
dc.identifier.issn |
1070-4280 |
|
dc.identifier.uri |
https://dspace.kpfu.ru/xmlui/handle/net/162150 |
|
dc.description.abstract |
© 2020, Pleiades Publishing, Ltd. Abstract: DFT quantum chemical calculations at the B3PW91/6-31G(d) level of theory have shown that the addition of secondary phosphine sulfides and phosphine selenides with alkyl, phenyl, and phenylalkyl substituents to pentyl vinyl and hexyl vinyl selenides follows a molecular mechanism against the Markovnikov rule through energetically favorable eight-membered transition state, leading to the formation of tertiary phosphine chalcogenides. Secondary phosphine selenides are more reactive than the corresponding phosphine sulfides. |
|
dc.relation.ispartofseries |
Russian Journal of Organic Chemistry |
|
dc.subject |
DFT calculations |
|
dc.subject |
hydrophosphinylation |
|
dc.subject |
phosphine selenides |
|
dc.subject |
phosphine sulfides |
|
dc.subject |
reaction mechanisms |
|
dc.subject |
vinyl selenides |
|
dc.title |
Quantum Chemical Study of the Addition of Secondary Phosphine Chalcogenides to Vinyl Selenides |
|
dc.type |
Article |
|
dc.relation.ispartofseries-issue |
10 |
|
dc.relation.ispartofseries-volume |
56 |
|
dc.collection |
Публикации сотрудников КФУ |
|
dc.relation.startpage |
1696 |
|
dc.source.id |
SCOPUS10704280-2020-56-10-SID85096568144 |
|