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dc.contributor.author | Stoikov I. | |
dc.contributor.author | Yantemirova A. | |
dc.contributor.author | Nosov R. | |
dc.contributor.author | Rizvanov I. | |
dc.contributor.author | Julmetov A. | |
dc.contributor.author | Klochkov V. | |
dc.contributor.author | Antipin I. | |
dc.contributor.author | Konovalov A. | |
dc.contributor.author | Zharov I. | |
dc.date.accessioned | 2018-09-18T20:22:52Z | |
dc.date.available | 2018-09-18T20:22:52Z | |
dc.date.issued | 2011 | |
dc.identifier.issn | 1477-0520 | |
dc.identifier.uri | https://dspace.kpfu.ru/xmlui/handle/net/139284 | |
dc.description.abstract | New p-tert-butyl thiacalix[4]arenes differently substituted at the lower rim with amide, hydroxyl and ester groups were synthesized. Binding properties of the compounds toward some tetrabutylammonium salts n-Bu4NX (X = F-, Cl-, Br-, I-, CH 3CO2 -, H2PO4 -, NO3 -) were studied by UV spectroscopy. It was found that the stoichiometry of the complexes, generally, is 1:1, and the association constants are in the range of 103-105 M-1. The p-tert-butyl thiacalix[4]arenes containing secondary amide groups trisubstituted at the lower rim bind the studied anions most effectively. Selective receptors for fluoride and dihydrogen phosphate salts of tetrabutylammonium were found. © 2011 The Royal Society of Chemistry. | |
dc.relation.ispartofseries | Organic and Biomolecular Chemistry | |
dc.title | P-tert-Butyl thiacalix[4]arenes functionalized at the lower rim by amide, hydroxyl and ester groups as anion receptors | |
dc.type | Article | |
dc.relation.ispartofseries-issue | 9 | |
dc.relation.ispartofseries-volume | 9 | |
dc.collection | Публикации сотрудников КФУ | |
dc.relation.startpage | 3225 | |
dc.source.id | SCOPUS14770520-2011-9-9-SID79954451035 |