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Self-assembly of chiral fluorescent nanoparticles based on water-soluble L-tryptophan derivatives of p-tert-butylthiacalix[4]arene.
Padnya, Pavel L; Khripunova, Irina A; Mostovaya, Olga A; Mukhametzyanov, Timur A; Evtugyn, Vladimir G; Vorobev, Vyacheslav V; Osin, Yuri N; Stoikov, Ivan I.
Afiliación
  • Padnya PL; Kazan Federal University, 420008 Kremlevskaya, 18, Kazan, Russian Federation.
  • Khripunova IA; Peoples Friendship University of Russia (RUDN University), 117198 Miklukho-Maklaya St., 6, Moscow, Russian Federation.
  • Mostovaya OA; Kazan Federal University, 420008 Kremlevskaya, 18, Kazan, Russian Federation.
  • Mukhametzyanov TA; Kazan Federal University, 420008 Kremlevskaya, 18, Kazan, Russian Federation.
  • Evtugyn VG; Kazan Federal University, 420008 Kremlevskaya, 18, Kazan, Russian Federation.
  • Vorobev VV; Kazan Federal University, 420008 Kremlevskaya, 18, Kazan, Russian Federation.
  • Osin YN; Kazan Federal University, 420008 Kremlevskaya, 18, Kazan, Russian Federation.
  • Stoikov II; Kazan Federal University, 420008 Kremlevskaya, 18, Kazan, Russian Federation.
Beilstein J Nanotechnol ; 8: 1825-1835, 2017.
Article en En | MEDLINE | ID: mdl-29046831
ABSTRACT
New water-soluble tetra-substituted derivatives of p-tert-butylthiacalix[4]arene containing fragments of L-tryptophan in cone and 1,3-alternate conformations were obtained. It was shown that the resulting compounds form stable, positively charged aggregates of 86-134 nm in diameter in water at a concentration of 1 × 10-4 M as confirmed by dynamic light scattering, scanning electron microscopy and transmission electron microscopy. It was established that these aggregates are fluorescently active and chiral. A distinctive feature of the compounds is the pronounced dependence of their spectral (emission and chiroptical) properties on the polarity of the solvent and the length of the linker between the macrocyclic and fluorophore parts of the molecule.
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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Beilstein J Nanotechnol Año: 2017 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Beilstein J Nanotechnol Año: 2017 Tipo del documento: Article