Iminodiacetic derivatives of p-tert-butylthiacalix[4]arene: Synthesis and influence of conformation on the aggregation with bismarck brown Y

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,1H 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. © ISUCT Publishing.

Authors
Mostovaya O.A.1 , Padnya P.L.1 , Shurpik D.N. 1, 2 , Vavilova A.A.1 , Evtugyn V.G.3 , Osin Y.N.3 , Stoikov I.I.1
Number of issue
2
Language
English
Pages
154-163
Status
Published
Volume
10
Year
2017
Organizations
  • 1 Kazan Federal University, A.M. Butlerov Chemical Institute, Kazan, 420008, Russian Federation
  • 2 RUDN University, Faculty of Science, Organic Chemistry Department, Moscow, 117198, Russian Federation
  • 3 Kazan Federal University, Interdisciplinary Centre for Analytical Microscopy, Kazan, 420008, Russian Federation
Keywords
Bismarck brown Y; Macrocyclic receptors; Self-assembly; Thiacalix[4]arene
Date of creation
19.10.2018
Date of change
19.10.2018
Short link
https://repository.rudn.ru/en/records/article/record/5824/
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