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 |
|