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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 |