Synthesis, properties and application of amphiphilic copolymers based on poly(fluoroalkylmethacrylate)s with terminal peroxide group
Електронний науковий архів Науково-технічної бібліотеки Національного університету "Львівська політехніка"
Переглянути архів ІнформаціяПоле | Співвідношення | |
Title |
Synthesis, properties and application of amphiphilic copolymers based on poly(fluoroalkylmethacrylate)s with terminal peroxide group
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Creator |
Paiuk, Olena
Volianiuk, Kateryna Sobko, Iryna Nadashkevych, Zoriana Mitina, Nataliya Zaichenko, Olexandr |
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Contributor |
Lviv Polytechnic National University
Ivan Franko National University of Lviv |
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Subject |
fluoroalkyle methacrylate
peroxide group radical polymerization controlled synthesis |
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Description |
Polymers with terminal peroxide fragment were synrhesized via radical polymerization of fluoroalkyl methacrylates. Amphiphilic block-copolymers with hydrophilic block of different structure were synthesized by usage of obtained polymers with terminal peroxide group as macroinitiators. Kinethic peculiarities of polymerization were studied on both stages. The strucrure of polymers were confirmed by IR- and NMR-spectroscopy. |
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Date |
2018-04-12T13:05:53Z
2018-04-12T13:05:53Z 2017-12-23 2017-12-23 |
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Type |
Conference Abstract
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Identifier |
Synthesis, properties and application of amphiphilic copolymers based on poly(fluoroalkylmethacrylate)s with terminal peroxide group / Olena Paiuk, Kateryna Volianiuk, Iryna Sobko, Zoriana Nadashkevych, Nataliya Mitina, Olexandr Zaichenko // Litteris et Artibus : proceedings, 23–25 November, 2017. — Lviv : Lviv Polytechnic Publishing House, 2017. — P. 50–51. — (6th International academic conference «Chemistry & chemical technology 2017» (CCT-2017)).
978-966-941-108-2 http://ena.lp.edu.ua:8080/handle/ntb/40445 Synthesis, properties and application of amphiphilic copolymers based on poly(fluoroalkylmethacrylate)s with terminal peroxide group / Olena Paiuk, Kateryna Volianiuk, Iryna Sobko, Zoriana Nadashkevych, Nataliya Mitina, Olexandr Zaichenko // Litteris et Artibus : proceedings, 23–25 November, 2017. — Lviv : Lviv Polytechnic Publishing House, 2017. — P. 50–51. — (6th International academic conference «Chemistry & chemical technology 2017» (CCT-2017)). |
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Language |
en
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Relation |
Litteris et Artibus : матеріали, 2017
Litteris et Artibus : proceedings, 2017 [1] P. C. Nicolson, J. Vogt, "Soft contact lens polymers:an evolution," Biomaterials., vol. 22, pp.3273-3283,2001. [2] I. J. Park, S.-B. Lee, C. K. Choi, "Surface Properties of the Fluorine-Containing Graft Copolymer of Poly((perfluoroalkyl)ethyl methacrylate)-gpoly( methyl methacrylate)," Macromolecules., vol.31, №21, pp. 7555-7558, 1998. [3] F. Babudri, G. M. Farinola, F. Naso and R. Ragnia, "Fluorinated organic materials for electronic and optoelectronic applications: the role of the fluorine atom," Chem. Commun., 0, vol. , pp.1003-1022, 2007. [4] J. С. Ravey, A. Gherbi and M.J. Stebe, "Comparative study of fluorinated and hydrogenated nonionic surfactants. I. Surface activity properties and critical concentrations," Progr Colloid Polym Sci, vol. 76, pp.234-241, 1988. [5] J. C. Knight, P. G. Edwards, S. J. Paisey, "Fluorinated contrast agents for magnetic resonance imaging; a review of recent developments," RSC Advances, vol. 1 , pp.1415-1325, 2011. [6] H. Lu, F. Su, S. Q. Mei, Ya. Tian, W. Tian, R. H. Johnsona, D. R. Meldrum, "Using fluorinecontaining amphiphilic random copolymers to manipulate the quantum yields of aggregationinduced emission fluorophores in aqueous solutions and the use of these polymers for fluorescent bioimaging", Journal of materials chemistry, vol. 22, pp. 9890-9900, 2012. [7] M. Wang, H. Liu, L. Li, Yi. Cheng, " A fluorinated dendrimer achieves excellent gene transfection efficacy at extremely low nitrogen to phosphorous ratios," Nature communications., vol. 5, p. 3053, 2014. [1] P. C. Nicolson, J. Vogt, "Soft contact lens polymers:an evolution," Biomaterials., vol. 22, pp.3273-3283,2001. [2] I. J. Park, S.-B. Lee, C. K. Choi, "Surface Properties of the Fluorine-Containing Graft Copolymer of Poly((perfluoroalkyl)ethyl methacrylate)-gpoly( methyl methacrylate)," Macromolecules., vol.31, No 21, pp. 7555-7558, 1998. [3] F. Babudri, G. M. Farinola, F. Naso and R. Ragnia, "Fluorinated organic materials for electronic and optoelectronic applications: the role of the fluorine atom," Chem. Commun., 0, vol. , pp.1003-1022, 2007. [4] J. S. Ravey, A. Gherbi and M.J. Stebe, "Comparative study of fluorinated and hydrogenated nonionic surfactants. I. Surface activity properties and critical concentrations," Progr Colloid Polym Sci, vol. 76, pp.234-241, 1988. [5] J. C. Knight, P. G. Edwards, S. J. Paisey, "Fluorinated contrast agents for magnetic resonance imaging; a review of recent developments," RSC Advances, vol. 1 , pp.1415-1325, 2011. [6] H. Lu, F. Su, S. Q. Mei, Ya. Tian, W. Tian, R. H. Johnsona, D. R. Meldrum, "Using fluorinecontaining amphiphilic random copolymers to manipulate the quantum yields of aggregationinduced emission fluorophores in aqueous solutions and the use of these polymers for fluorescent bioimaging", Journal of materials chemistry, vol. 22, pp. 9890-9900, 2012. [7] M. Wang, H. Liu, L. Li, Yi. Cheng, " A fluorinated dendrimer achieves excellent gene transfection efficacy at extremely low nitrogen to phosphorous ratios," Nature communications., vol. 5, p. 3053, 2014. |
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Rights |
© Національний університет “Львівська політехніка”, 2017
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Format |
50-51
2 application/pdf image/png |
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Coverage |
23–25 листопада 2017 року
23–25 November, 2017 Львів Lviv |
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Publisher |
Видавництво Львівської політехніки
Lviv Polytechnic Publishing House |
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