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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 |