dc.contributor.author |
Stoikov I. |
|
dc.contributor.author |
Ibragimova D. |
|
dc.contributor.author |
Antipin I. |
|
dc.contributor.author |
Konovalov A. |
|
dc.contributor.author |
Gadiev T. |
|
dc.contributor.author |
Khairutdinov B. |
|
dc.contributor.author |
Karataeva F. |
|
dc.contributor.author |
Klochkov V. |
|
dc.date.accessioned |
2018-09-17T21:17:56Z |
|
dc.date.available |
2018-09-17T21:17:56Z |
|
dc.date.issued |
2004 |
|
dc.identifier.issn |
1066-5285 |
|
dc.identifier.uri |
https://dspace.kpfu.ru/xmlui/handle/net/134804 |
|
dc.description.abstract |
New derivatives of p-tert-butylthiacalix[4]arene were synthesized. The conformation of the macrocycles and interproton distances in the synthesized thiacalix[4]arenes in solutions were determined by NMR spectroscopy. p-tert-Butylthiacalix[4]arene distally disubstituted at the lower rim adopts the cone conformation, and the tetrasubstituted products are formed in the 1,3-alternate conformation. © 2004 Springer Science+Business Media, Inc. |
|
dc.relation.ispartofseries |
Russian Chemical Bulletin |
|
dc.subject |
Alkylation |
|
dc.subject |
Nanostructures |
|
dc.subject |
NOESY NMR spectroscopy |
|
dc.subject |
Stereoisomers |
|
dc.subject |
Thiacalix[4]arene |
|
dc.title |
New materials based on tubular nanodimensional structures 1. Synthesis, structural studies and determination of interproton distances in solutions of functionalized thiacalix[4]arenes according to NMR spectroscopic data (NOESY) |
|
dc.type |
Article |
|
dc.relation.ispartofseries-issue |
10 |
|
dc.relation.ispartofseries-volume |
53 |
|
dc.collection |
Публикации сотрудников КФУ |
|
dc.relation.startpage |
2269 |
|
dc.source.id |
SCOPUS10665285-2004-53-10-SID21644488314 |
|