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dc.contributor.author | Vavilova A. | |
dc.contributor.author | Nosov R. | |
dc.contributor.author | Yakimova L. | |
dc.contributor.author | Antipin I. | |
dc.contributor.author | Stoikov I. | |
dc.date.accessioned | 2018-09-18T20:35:01Z | |
dc.date.available | 2018-09-18T20:35:01Z | |
dc.date.issued | 2013 | |
dc.identifier.issn | 1998-9539 | |
dc.identifier.uri | https://dspace.kpfu.ru/xmlui/handle/net/141379 | |
dc.description.abstract | New p-tert-butyl thiacalix[4]arene derivatives containing simultaneously the 4-amidoazobenzene and ethoxycarbonyl fragments at the lower rim in cone and 1,3-alternate conformation of tri and tetrasubstituted derivatives, correspondingly, were synthesized. It was shown that the replacement of the hydroxyl group by ethoxycarbonyl fragment in a 1,3-disubstituted macrocycle with 4-amidoazobenzene groups leads to the binding of fluoride and chloride-anions. The substitution of two hydroxyl groups by ethoxycarbonyl fragments dramatically changed the binding properties of tetrasubstituted p-tert-butyl thiacalix[4]arene derivative. © ISUCT Publishing. | |
dc.relation.ispartofseries | Macroheterocycles | |
dc.subject | Anions | |
dc.subject | Photoisomerization | |
dc.subject | Receptor | |
dc.subject | Synthesis | |
dc.subject | Thiacalix[4]arenes | |
dc.title | Synthesis of photo-switchable derivatives of p-tert-butyl thiacalix[4]arenes containing ethoxycarbonyl and 4-amidoazobenzene fragments in the lower rim substituents | |
dc.type | Article | |
dc.relation.ispartofseries-issue | 3 | |
dc.relation.ispartofseries-volume | 6 | |
dc.collection | Публикации сотрудников КФУ | |
dc.relation.startpage | 219 | |
dc.source.id | SCOPUS19989539-2013-6-3-SID84909984890 |