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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 |