Email this article Ag-selective nanotubes based on bisthiacalix[4]arene with ethylene sulfide bridges
- Authors: Muravev A.A.1, Trushina E.A.2, Yakupov A.T.3, Solovieva S.E.1, Antipin I.S.3
-
Affiliations:
- Arbuzov Institute of Organic and Phusical Chemistry of the Kazan’ Scientific Center of the Russian Academy of Sciences
- Ural Federal University
- Kazan Federal University
- Issue: Vol 487, No 5 (2019)
- Pages: 515-518
- Section: Chemistry
- URL: https://journals.eco-vector.com/0869-5652/article/view/15892
- DOI: https://doi.org/10.31857/S0869-56524875515-518
- ID: 15892
Cite item
Full Text
Abstract
An approach to a new type of molecular nanotubes based on bisthiacalix[4]arene with ethylene sulfide bridges in cone stereoisomeric form has been suggested and implemented. This ligand has shown selective liquid-phase extraction of Ag+.
About the authors
A. A. Muravev
Arbuzov Institute of Organic and Phusical Chemistry of the Kazan’ Scientific Center of the Russian Academy of Sciences
Author for correspondence.
Email: antonm@iopc.ru
Russian Federation, 8, Acad. Arbuzov str., Kazan, Tatarstan, 420029
E. A. Trushina
Ural Federal University
Email: antonm@iopc.ru
Russian Federation, 51, Lenina ave., Ekaterinburg, 620000
A. T. Yakupov
Kazan Federal University
Email: antonm@iopc.ru
Russian Federation, 18, Kremliovskaya street, Kazan, 420008
S. E. Solovieva
Arbuzov Institute of Organic and Phusical Chemistry of the Kazan’ Scientific Center of the Russian Academy of Sciences
Email: antonm@iopc.ru
Russian Federation, 8, Acad. Arbuzov str., Kazan, Tatarstan, 420029
I. S. Antipin
Kazan Federal University
Email: antonm@iopc.ru
Corresponding Member of the Russian Academy of Sciences
Russian Federation, 18, Kremliovskaya street, Kazan, 420008References
- Calixarenes and Beyond / Eds. P. Neri, J. L. Sessler, M.-X. Wang. N.Y.: Springer, 2016. 1062 p.
- Kumar R., Lee Y. O., Bhalla V., et al. // Chem. Soc. Rev. 2014. V. 43. P. 4824-4870.
- Konovalov A. I., Antipin I. S., Burilov V. A., et al. // Russ. J. Org. Chem. 2018. V. 54. P. 157-371.
- Solovieva S. E., Burilov V. A., Antipin I. S. // Macrohe-terocycles. 2017. V. 10. P. 134-146.
- Rambo B. M., Kim S. K., Kim J. S., et al. // Chem. Sci. 2010. V. 1. P. 716-722.
- Solovieva S., Muravev A., Zakirzyanov R., et al. // Macroheterocycles. 2012. V. 5. P. 17-22.
- Kumar M., Bhalla V., Dhir A., Babu J. N. // Dalton Trans. 2010. V. 39. Р. 10 116-10 121.
- Schmitt P., Beer P. D., Drew M. G.B., Sheen P. D. // Angew. Chem. Int. Ed. Engl. 1997. V. 36. P. 1840-1842.
- Lee J. Y., Lee S. Y., Seo J., et al. // Inorg. Chem. 2007. V. 46. P. 6221-6223.
- Kim J.-Y., Park I.-H., Lee J. Y., et al. // Inorg. Chem. 2013. V. 52. P. 10 176-10 182.
- Park I.-H., Kim J.-Y., Kim K., Lee S. S. // Cryst. Growth Des. 2014. V. 14. P. 6012-6023.
- Muravev A., Galieva F., Bazanova O., et al. // Supramol. Chem. 2016. V. 28. P. 589-600.
- Demirel A., Dogan A., Akkus G., et al. // Electroanalysis. 2006. V. 18. P. 1019-1027.
- Smirnov I. V., Stepanova E. S., Tyupina M. Yu., et al. // Radiochemistry. 2016. V. 58. P. 381-388.
- Smirnov I. V., Stepanova E. S., Tyupina M. Yu., et al. // Macroheterocycles. 2017. V. 10. P. 196-202.
Supplementary files
