dc.contributor.author |
Podoprygorina G. |
|
dc.contributor.author |
Zhang J. |
|
dc.contributor.author |
Brusko V. |
|
dc.contributor.author |
Bolte M. |
|
dc.contributor.author |
Janshoff A. |
|
dc.contributor.author |
Böhmer V. |
|
dc.date.accessioned |
2018-09-17T21:33:58Z |
|
dc.date.available |
2018-09-17T21:33:58Z |
|
dc.date.issued |
2003 |
|
dc.identifier.issn |
1523-7060 |
|
dc.identifier.uri |
https://dspace.kpfu.ru/xmlui/handle/net/135157 |
|
dc.description.abstract |
(Equation presented) Octamethoxy calix[8]arenes substituted in the para position by amide, urea, and imide functions were synthesized from the octamethyl ether of tert-butylcalix[8]arene by ipso nitration, reduction, and acylation. Scanning force microscopy of spin coated samples on graphite suggests that these derivatives self-organize into tubular nanorods via hydrogen bonds between p-amide functions. A single-crystal X-ray structure reveals a centrosymmetric conformation for the octanitro derivative. |
|
dc.relation.ispartofseries |
Organic Letters |
|
dc.title |
Supramolecular Structures Formed by Calix[8]arene Derivatives |
|
dc.type |
Article |
|
dc.relation.ispartofseries-issue |
26 |
|
dc.relation.ispartofseries-volume |
5 |
|
dc.collection |
Публикации сотрудников КФУ |
|
dc.relation.startpage |
5071 |
|
dc.source.id |
SCOPUS15237060-2003-5-26-SID0347916935 |
|