dc.contributor.author |
Zhang J. |
|
dc.contributor.author |
Podoprygorina G. |
|
dc.contributor.author |
Brusko V. |
|
dc.contributor.author |
Böhmer V. |
|
dc.contributor.author |
Janshoff A. |
|
dc.date.accessioned |
2018-09-17T20:49:39Z |
|
dc.date.available |
2018-09-17T20:49:39Z |
|
dc.date.issued |
2005 |
|
dc.identifier.issn |
0897-4756 |
|
dc.identifier.uri |
https://dspace.kpfu.ru/xmlui/handle/net/134117 |
|
dc.description.abstract |
With the intention of building hollow tubular structures by self-assembly, we have designed and successfully synthesized a series of calix[8]arene derivatives. Their phenolic units were functionalized in p-position by various groups which are able to interact via hydrogen bonding or π-π stacking. Ethynyl, amide, urea, or imide links were chosen for the covalent attachment of these functional groups, to ensure the adjustment of an optimal distance for their interaction. Two different kinds of nanostructures selfassembled on a highly oriented pyrolytic graphite (HOPG) surface were found by scanning force microscopy: parallel aligned nanorods in which the calixarene molecules are adsorbed edge-on on the graphite, providing evidence that these calix[8]arene derivatives stack in a tubular fashion, and micrometer long fiber bundles most probably composed of many nanorods. © 2005 American Chemical Society. |
|
dc.relation.ispartofseries |
Chemistry of Materials |
|
dc.title |
Functionalized calix[8]arenes, synthesis and self-assembly on graphite |
|
dc.type |
Article |
|
dc.relation.ispartofseries-issue |
9 |
|
dc.relation.ispartofseries-volume |
17 |
|
dc.collection |
Публикации сотрудников КФУ |
|
dc.relation.startpage |
2290 |
|
dc.source.id |
SCOPUS08974756-2005-17-9-SID18744363924 |
|