dc.contributor.author |
Mostovaya O. |
|
dc.contributor.author |
Padnya P. |
|
dc.contributor.author |
Shurpik D. |
|
dc.contributor.author |
Vavilova A. |
|
dc.contributor.author |
Evtugyn V. |
|
dc.contributor.author |
Osin Y. |
|
dc.contributor.author |
Stoikov I. |
|
dc.date.accessioned |
2018-04-05T07:10:13Z |
|
dc.date.available |
2018-04-05T07:10:13Z |
|
dc.date.issued |
2017 |
|
dc.identifier.issn |
1998-9539 |
|
dc.identifier.uri |
http://dspace.kpfu.ru/xmlui/handle/net/130293 |
|
dc.description.abstract |
© ISUCT Publishing. Three conformers (cone, partial cone and 1,3-alternate) of tetrasubstituted at the lower rim p-tert-butylthiacalix[4] arene derivatives with iminodiacetic fragments were synthesized and characterized. It was shown by spectral methods (UV-Vis, 1 H NMR and DOSY spectroscopy, DLS) and TEM that the monodisperse nano-sized particles are formed by self-assembly of synthetic octaacids in water with azo dye Bismarck brown Y in the case of the partial cone and 1,3-alternate conformations. It was found that the dye associates with the acid binding sites of the macrocycle. |
|
dc.relation.ispartofseries |
Macroheterocycles |
|
dc.subject |
Bismarck brown Y |
|
dc.subject |
Macrocyclic receptors |
|
dc.subject |
Self-assembly |
|
dc.subject |
Thiacalix[4]arene |
|
dc.title |
Iminodiacetic derivatives of p-tert-butylthiacalix[4]arene: Synthesis and influence of conformation on the aggregation with bismarck brown Y |
|
dc.type |
Article |
|
dc.relation.ispartofseries-issue |
2 |
|
dc.relation.ispartofseries-volume |
10 |
|
dc.collection |
Публикации сотрудников КФУ |
|
dc.relation.startpage |
154 |
|
dc.source.id |
SCOPUS19989539-2017-10-2-SID85021781236 |
|