Abstract:
Sulfobetaine derivatives of p-tert-butylthiacalix[4]arene in cone conformation have been synthesized for the first time. It has been shown by dynamic light scattering that the compounds form submicron-sized particles with silver cation in water, and the particle size depends on the length of a linker in the sulfobetaine moiety.
Citation:
L. S. Yakimova, P. L. Padnya, A. F. Kunafina, A. R. Nugmanova, I. I. Stoikov, “Sulfobetaine derivatives of thiacalix[4]arene: synthesis and supramolecular self-assembly of submicron aggregates with AgI cations”, Mendeleev Commun., 29:1 (2019), 86–88
Linking options:
https://www.mathnet.ru/eng/mendc1431
https://www.mathnet.ru/eng/mendc/v29/i1/p86
This publication is cited in the following 17 articles:
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L.S. Yakimova, V.R. Sultanaev, A.A. Vavilova, K.S. Shibaeva, I.I. Stoikov, “Self-assembly of interpolyelectrolyte complexes and mixed micelles from guanidinium and phosphonate derivatives of p–tert–butylthiacalix[4]arene and solubilization of paclitaxel”, Journal of Molecular Liquids, 395 (2024), 123836
Anastasia Nazarova, Pavel Padnya, Arthur Khannanov, Aleksandra Khabibrakhmanova, Pavel Zelenikhin, Ivan Stoikov, “Towards Protection of Nucleic Acids from Herbicide Attack: Self-Assembly of Betaines Based on Pillar[5]arene with Glyphosate and DNA”, IJMS, 24:9 (2023), 8357
O. A. Mostovaya, A. A. Vavilova, I. I. Stoikov, “Supramolecular Systems Based on Thiacalixarene Derivatives and Biopolymers”, Colloid J, 84:5 (2022), 546
Luidmila Yakimova, Aisylu Kunafina, Olga Mostovaya, Pavel Padnya, Timur Mukhametzyanov, Alexandra Voloshina, Konstantin Petrov, Artur Boldyrev, Ivan Stoikov, “Albumin/Thiacalix[4]arene Nanoparticles as Potential Therapeutic Systems: Role of the Macrocycle for Stabilization of Monomeric Protein and Self-Assembly with Ciprofloxacin”, IJMS, 23:17 (2022), 10040
L. S. Yakimova, A. F. Kunafina, P. L. Padnya, I. I. Stoikov, “Synthesis and Albumin Binding of Stereoisomers of Sulfobetaine p-tert-Butylthiacalix[4]arene Derivatives”, Russ J Org Chem, 58:8 (2022), 1154
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Charles N. Moorefield, George R. Newkome, Progress in Heterocyclic Chemistry, 32, 2021, 615
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I. S. Antipin, M. V. Alfimov, V. V. Arslanov, V. A. Burilov, S. Z. Vatsadze, Ya. Z. Voloshin, K. P. Volcho, V. V. Gorbatchuk, Yu. G. Gorbunova, S. P. Gromov, S. V. Dudkin, S. Yu. Zaitsev, L. Ya. Zakharova, M. A. Ziganshin, A. V. Zolotukhina, M. A. Kalinina, E. A. Karakhanov, R. R. Kashapov, O. I. Koifman, A. I. Konovalov, V. S. Korenev, A. L. Maksimov, N. Zh. Mamardashvili, G. M. Mamardashvili, A. G. Martynov, A. R. Mustafina, R. I. Nugmanov, A. S. Ovsyannikov, P. L. Padnya, A. S. Potapov, S. L. Selektor, M. N. Sokolov, S. E. Solovieva, I. I. Stoikov, P. A. Stuzhin, E. V. Suslov, E. N. Ushakov, V. P. Fedin, S. V. Fedorenko, O. A. Fedorova, Yu. V. Fedorov, S. N. Chvalun, A. Yu. Tsivadze, S. N. Shtykov, D. N. Shurpik, M. A. Shcherbina, L. S. Yakimova, “Functional supramolecular systems: design and applications”, Russian Chem. Reviews, 90:8 (2021), 895–1107
Pavel Padnya, Vladimir Gorbachuk, Ivan Stoikov, “The Role of Calix[n]arenes and Pillar[n]arenes in the Design of Silver Nanoparticles: Self-Assembly and Application”, IJMS, 21:4 (2020), 1425
Vladimir Burilov, Ramilya Garipova, Elsa Sultanova, Diana Mironova, Ilya Grigoryev, Svetlana Solovieva, Igor Antipin, “New Amphiphilic Imidazolium/Benzimidazolium Calix[4]arene Derivatives: Synthesis, Aggregation Behavior and Decoration of DPPC Vesicles for Suzuki Coupling in Aqueous Media”, Nanomaterials, 10:6 (2020), 1143
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Han-Wen Tian, Yan-Cen Liu, Dong-Sheng Guo, “Assembling features of calixarene-based amphiphiles and supra-amphiphiles”, Mater. Chem. Front., 4:1 (2020), 46
G. V. Zyryanov, D. S. Kopchuk, I. S. Kovalev, S. Santra, M. Rahman, A. F. Khasanov, A. P. Krinochkin, O. S. Taniya, O. N. Chupakhin, V. N. Charushin, “Rational synthetic methods in creating promising (hetero)aromatic molecules and materials”, Mendeleev Commun., 30:5 (2020), 537–554
O. A. Mostovaya, Yu. A. Valiullina, Ch. T. Chan, O. S. Potrekeeva, P. L. Padnya, Yu. F. Zuev, I. I. Stoikov, “Synthetic modulator of chymotrypsin activity based on p-tert-butylthiacalix[4]arene”, Mendeleev Commun., 29:5 (2019), 520–522
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