https://oldena.lpnu.ua/handle/ntb/43931| Title: | Reactivity and polymerization ability of styrylquinoline containing methacrylic monomers |
| Other Titles: | Реакційна та полімеризаційна здатність стирилхінолінвмісних метакрилових мономерів |
| Authors: | Kharchenko, Oksana Smokal, Vitaliy Krupka, Oksana Kolendo, Aleksey |
| Affiliation: | Kyiv Taras Shevchenko National University |
| Bibliographic description (Ukraine): | Reactivity and polymerization ability of styrylquinoline containing methacrylic monomers / Oksana Kharchenko, Vitaliy Smokal, Oksana Krupka, Aleksey Kolendo // Chemistry & Chemical Technology. — Lviv : Lviv Politechnic Publishing House, 2-18. — Vol 12. — No 1. — P. 47–52. |
| Bibliographic description (International): | Reactivity and polymerization ability of styrylquinoline containing methacrylic monomers / Oksana Kharchenko, Vitaliy Smokal, Oksana Krupka, Aleksey Kolendo // Chemistry & Chemical Technology. — Lviv : Lviv Politechnic Publishing House, 2-18. — Vol 12. — No 1. — P. 47–52. |
| Is part of: | Chemistry & Chemical Technology, 1 (12), 2-18 |
| Issue: | 1 |
| Volume: | 12 |
| Issue Date: | 20-Jan-2018 |
| Publisher: | Lviv Politechnic Publishing House |
| Place of the edition/event: | Lviv |
| Keywords: | 8-метакрилокси стирилхінолін метод Файнмана-Росса реакційна здатність мономеру вільно- радикальна полімеризація 8-methacryloyloxy styrylquinoline Fineman- Ross method monomer reactivity ratio free radical polymerization |
| Number of pages: | 6 |
| Page range: | 47-52 |
| Start page: | 47 |
| End page: | 52 |
| Abstract: | Синтезовано нові стирилхінолінвмісні
метакрилові мономери та їх кополімери з метилметак-
рилатом (ММА). Полімеризацію проводили в ДМФ, як ініці-
атор використовували AІБН. Продукти полімеризації охарак-
теризовано за допомогою 1H ЯМР. Реакційну здатність нових
метакрилових мономерів на основі стирилхіноліну для гомо-
генної вільно-радикальної кополімеризації з ММА визначено за
даними 1H ЯМР спектроскопії та проведено її оцінювання за
методом Файнмана-Росса і розрахунковим методом. Novel styrylquinoline methacrylic monomers and their copolymers with methylmethacrylate (MMA) are presented. The polymerization was carried out in DMF with AIBN as initiator. The products of polymerization were characterized by 1H NMR. The monomer reactivity ratios for the homogeneous free-radical copolymerization of styrylquinoline monomers and MMA were determined from 1H NMR spectroscopy data and estimated with the Fineman-Ross (FR) and calculation methods. |
| URI: | https://ena.lpnu.ua/handle/ntb/43931 |
| Copyright owner: | © Національний університет „Львівська політехніка“, 2018 © Kharchenko O., Smokal V., Krupka O., Kolendo A., 2018 |
| URL for reference material: | https://doi.org/10.1364/JOSAB.10.001553 https://doi.org/10.1364/OE.15.015268 https://doi.org/10.1016/j.optmat.2015.10.001 https://doi.org/10.5402/2012/352759 https://doi.org/10.1063/1.98799 https://doi.org/10.1134/S1995078012030032 https://doi.org/10.1134/S0018143910050097 https://doi.org/10.1021/jm980043e https://doi.org/10.1016/j.bmcl.2007.09.040 https://doi.org/10.1039/C4OB00998C https://doi.org/10.1016/j.bmc.2010.02.025 https://doi.org/10.1002/pol.1950.120050210 |
| References (Ukraine): | [1] Dalton L.: Nonlinear Optical PolymericMaterials: From Chromophore Design to Commercial Applications [in:] Lee K.-S. (Ed.), Polymers for Photonics Applications I, Springer /Heidelberg Publisher, Berlin 2002, 1-86. [2] Nahata A.: Opt. Soc. Am. B., 1993, 10, 1553.https://doi.org/10.1364/JOSAB.10.001553 [3] Derkowska-Zielinska B. et al.: Proceedings of SPIE – The International Society for Optical Engineering, 2015, 9652, 965216. [4] Czaplicki R. et al.: Opt. Express., 2007, 15, 15268.https://doi.org/10.1364/OE.15.015268 [5] Derkowska-Zielinska B. et al.: Opt. Mat., 2015, 49, 325.https://doi.org/10.1016/j.optmat.2015.10.001 [6] Ayaz N. et al.: ISRN Polym. Sci., 2012, 2012, 13.https://doi.org/10.5402/2012/352759 [7] Tang C., VanSlyke S.: Appl. Phys. Lett., 1987, 51, 913.https://doi.org/10.1063/1.98799 [8] BudykaM., Potashova N.: Nanotechnol. Russia, 2012, 7, 280.https://doi.org/10.1134/S1995078012030032 [9] BudykaM., Potashova N.: High Energ. Chem., 2010, 44, 404.https://doi.org/10.1134/S0018143910050097 [10]Mekouar K., Mouscadet J.-F.: J. Med. Chem., 1998, 41, 2846.https://doi.org/10.1021/jm980043e [11] Podeszwa B., Niedbala H., Polanski J.: Bioorg. Med. Chem. Lett., 2007, 17, 6138. https://doi.org/10.1016/j.bmcl.2007.09.040 [12]Mao F., Yan J., Li J.: Org. Biomol. Chem., 2014, 12, 5936.https://doi.org/10.1039/C4OB00998C [13]Mrozek-Wilczkiewicz A., Kalinowski D., Musiol R.: Bioorg. Med. Chem., 2010, 18, 2664.https://doi.org/10.1016/j.bmc.2010.02.025 [14] Alfrey T., Price C.: J. Polym. Sci., 1947, 2, 101. [15] Gordon A., Ford R.: The Chemist’s Companion: A Handbook of Practical Data, Techniques, and References,Wiley, New York 1972. [16] FinemanM., Ross S.: J. Polym. Sci., 1950, 5, 259.https://doi.org/10.1002/pol.1950.120050210 [17] Brandrup J., Immergut E., Grulke E.: Polymer Handbook. Wiley & sons, New York 1999. |
| References (International): | [1] Dalton L., Nonlinear Optical PolymericMaterials: From Chromophore Design to Commercial Applications [in:] Lee K.-S. (Ed.), Polymers for Photonics Applications I, Springer /Heidelberg Publisher, Berlin 2002, 1-86. [2] Nahata A., Opt. Soc. Am. B., 1993, 10, 1553.https://doi.org/10.1364/JOSAB.10.001553 [3] Derkowska-Zielinska B. et al., Proceedings of SPIE – The International Society for Optical Engineering, 2015, 9652, 965216. [4] Czaplicki R. et al., Opt. Express., 2007, 15, 15268.https://doi.org/10.1364/OE.15.015268 [5] Derkowska-Zielinska B. et al., Opt. Mat., 2015, 49, 325.https://doi.org/10.1016/j.optmat.2015.10.001 [6] Ayaz N. et al., ISRN Polym. Sci., 2012, 2012, 13.https://doi.org/10.5402/2012/352759 [7] Tang C., VanSlyke S., Appl. Phys. Lett., 1987, 51, 913.https://doi.org/10.1063/1.98799 [8] BudykaM., Potashova N., Nanotechnol. Russia, 2012, 7, 280.https://doi.org/10.1134/S1995078012030032 [9] BudykaM., Potashova N., High Energ. Chem., 2010, 44, 404.https://doi.org/10.1134/S0018143910050097 [10]Mekouar K., Mouscadet J.-F., J. Med. Chem., 1998, 41, 2846.https://doi.org/10.1021/jm980043e [11] Podeszwa B., Niedbala H., Polanski J., Bioorg. Med. Chem. Lett., 2007, 17, 6138. https://doi.org/10.1016/j.bmcl.2007.09.040 [12]Mao F., Yan J., Li J., Org. Biomol. Chem., 2014, 12, 5936.https://doi.org/10.1039/P.4OB00998C [13]Mrozek-Wilczkiewicz A., Kalinowski D., Musiol R., Bioorg. Med. Chem., 2010, 18, 2664.https://doi.org/10.1016/j.bmc.2010.02.025 [14] Alfrey T., Price C., J. Polym. Sci., 1947, 2, 101. [15] Gordon A., Ford R., The Chemist’s Companion: A Handbook of Practical Data, Techniques, and References,Wiley, New York 1972. [16] FinemanM., Ross S., J. Polym. Sci., 1950, 5, 259.https://doi.org/10.1002/pol.1950.120050210 [17] Brandrup J., Immergut E., Grulke E., Polymer Handbook. Wiley & sons, New York 1999. |
| Content type: | Article |
| Appears in Collections: | Chemistry & Chemical Technology. – 2018. – Vol. 12, No. 1 |
| File | Description | Size | Format | |
|---|---|---|---|---|
| 2-18v12n1_Kharchenko_O-Reactivity_and_polymerization_47-52.pdf | 256.54 kB | Adobe PDF | View/Open | |
| 2-18v12n1_Kharchenko_O-Reactivity_and_polymerization_47-52__COVER.png | 516.68 kB | image/png | View/Open |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.