Reactivity and polymerization ability of styrylquinoline containing methacrylic monomers

Simple item page
dc.citation.epage52
dc.citation.issue1
dc.citation.spage47
dc.citation.volume12
dc.contributor.affiliationKyiv Taras Shevchenko National University
dc.contributor.authorKharchenko, Oksana
dc.contributor.authorSmokal, Vitaliy
dc.contributor.authorKrupka, Oksana
dc.contributor.authorKolendo, Aleksey
dc.coverage.placenameLviv
dc.date.accessioned2019-01-29T12:53:45Z
dc.date.available2019-01-29T12:53:45Z
dc.date.created2018-01-20
dc.date.issued2018-01-20
dc.description.abstractСинтезовано 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.
dc.description.abstractNovel 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.
dc.format.extent47-52
dc.format.pages6
dc.identifier.citationReactivity 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.
dc.identifier.citationenReactivity 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.
dc.identifier.urihttps://ena.lpnu.ua/handle/ntb/43931
dc.language.isoen
dc.publisherLviv Politechnic Publishing House
dc.relation.ispartofChemistry & Chemical Technology, 1 (12), 2-18
dc.relation.references[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.
dc.relation.references[2] Nahata A.: Opt. Soc. Am. B., 1993, 10, 1553.https://doi.org/10.1364/JOSAB.10.001553
dc.relation.references[3] Derkowska-Zielinska B. et al.: Proceedings of SPIE – The International Society for Optical Engineering, 2015, 9652, 965216.
dc.relation.references[4] Czaplicki R. et al.: Opt. Express., 2007, 15, 15268.https://doi.org/10.1364/OE.15.015268
dc.relation.references[5] Derkowska-Zielinska B. et al.: Opt. Mat., 2015, 49, 325.https://doi.org/10.1016/j.optmat.2015.10.001
dc.relation.references[6] Ayaz N. et al.: ISRN Polym. Sci., 2012, 2012, 13.https://doi.org/10.5402/2012/352759
dc.relation.references[7] Tang C., VanSlyke S.: Appl. Phys. Lett., 1987, 51, 913.https://doi.org/10.1063/1.98799
dc.relation.references[8] BudykaM., Potashova N.: Nanotechnol. Russia, 2012, 7, 280.https://doi.org/10.1134/S1995078012030032
dc.relation.references[9] BudykaM., Potashova N.: High Energ. Chem., 2010, 44, 404.https://doi.org/10.1134/S0018143910050097
dc.relation.references[10]Mekouar K., Mouscadet J.-F.: J. Med. Chem., 1998, 41, 2846.https://doi.org/10.1021/jm980043e
dc.relation.references[11] Podeszwa B., Niedbala H., Polanski J.: Bioorg. Med. Chem. Lett., 2007, 17, 6138. https://doi.org/10.1016/j.bmcl.2007.09.040
dc.relation.references[12]Mao F., Yan J., Li J.: Org. Biomol. Chem., 2014, 12, 5936.https://doi.org/10.1039/C4OB00998C
dc.relation.references[13]Mrozek-Wilczkiewicz A., Kalinowski D., Musiol R.: Bioorg. Med. Chem., 2010, 18, 2664.https://doi.org/10.1016/j.bmc.2010.02.025
dc.relation.references[14] Alfrey T., Price C.: J. Polym. Sci., 1947, 2, 101.
dc.relation.references[15] Gordon A., Ford R.: The Chemist’s Companion: A Handbook of Practical Data, Techniques, and References,Wiley, New York 1972.
dc.relation.references[16] FinemanM., Ross S.: J. Polym. Sci., 1950, 5, 259.https://doi.org/10.1002/pol.1950.120050210
dc.relation.references[17] Brandrup J., Immergut E., Grulke E.: Polymer Handbook. Wiley & sons, New York 1999.
dc.relation.referencesen[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.
dc.relation.referencesen[2] Nahata A., Opt. Soc. Am. B., 1993, 10, 1553.https://doi.org/10.1364/JOSAB.10.001553
dc.relation.referencesen[3] Derkowska-Zielinska B. et al., Proceedings of SPIE – The International Society for Optical Engineering, 2015, 9652, 965216.
dc.relation.referencesen[4] Czaplicki R. et al., Opt. Express., 2007, 15, 15268.https://doi.org/10.1364/OE.15.015268
dc.relation.referencesen[5] Derkowska-Zielinska B. et al., Opt. Mat., 2015, 49, 325.https://doi.org/10.1016/j.optmat.2015.10.001
dc.relation.referencesen[6] Ayaz N. et al., ISRN Polym. Sci., 2012, 2012, 13.https://doi.org/10.5402/2012/352759
dc.relation.referencesen[7] Tang C., VanSlyke S., Appl. Phys. Lett., 1987, 51, 913.https://doi.org/10.1063/1.98799
dc.relation.referencesen[8] BudykaM., Potashova N., Nanotechnol. Russia, 2012, 7, 280.https://doi.org/10.1134/S1995078012030032
dc.relation.referencesen[9] BudykaM., Potashova N., High Energ. Chem., 2010, 44, 404.https://doi.org/10.1134/S0018143910050097
dc.relation.referencesen[10]Mekouar K., Mouscadet J.-F., J. Med. Chem., 1998, 41, 2846.https://doi.org/10.1021/jm980043e
dc.relation.referencesen[11] Podeszwa B., Niedbala H., Polanski J., Bioorg. Med. Chem. Lett., 2007, 17, 6138. https://doi.org/10.1016/j.bmcl.2007.09.040
dc.relation.referencesen[12]Mao F., Yan J., Li J., Org. Biomol. Chem., 2014, 12, 5936.https://doi.org/10.1039/P.4OB00998C
dc.relation.referencesen[13]Mrozek-Wilczkiewicz A., Kalinowski D., Musiol R., Bioorg. Med. Chem., 2010, 18, 2664.https://doi.org/10.1016/j.bmc.2010.02.025
dc.relation.referencesen[14] Alfrey T., Price C., J. Polym. Sci., 1947, 2, 101.
dc.relation.referencesen[15] Gordon A., Ford R., The Chemist’s Companion: A Handbook of Practical Data, Techniques, and References,Wiley, New York 1972.
dc.relation.referencesen[16] FinemanM., Ross S., J. Polym. Sci., 1950, 5, 259.https://doi.org/10.1002/pol.1950.120050210
dc.relation.referencesen[17] Brandrup J., Immergut E., Grulke E., Polymer Handbook. Wiley & sons, New York 1999.
dc.relation.urihttps://doi.org/10.1364/JOSAB.10.001553
dc.relation.urihttps://doi.org/10.1364/OE.15.015268
dc.relation.urihttps://doi.org/10.1016/j.optmat.2015.10.001
dc.relation.urihttps://doi.org/10.5402/2012/352759
dc.relation.urihttps://doi.org/10.1063/1.98799
dc.relation.urihttps://doi.org/10.1134/S1995078012030032
dc.relation.urihttps://doi.org/10.1134/S0018143910050097
dc.relation.urihttps://doi.org/10.1021/jm980043e
dc.relation.urihttps://doi.org/10.1016/j.bmcl.2007.09.040
dc.relation.urihttps://doi.org/10.1039/C4OB00998C
dc.relation.urihttps://doi.org/10.1016/j.bmc.2010.02.025
dc.relation.urihttps://doi.org/10.1002/pol.1950.120050210
dc.rights.holder© Національний університет „Львівська політехніка“, 2018
dc.rights.holder© Kharchenko O., Smokal V., Krupka O., Kolendo A., 2018
dc.subject8-метакрилокси стирилхінолін
dc.subjectметод Файнмана-Росса
dc.subjectреакційна здатність мономеру
dc.subjectвільно- радикальна полімеризація
dc.subject8-methacryloyloxy styrylquinoline
dc.subjectFineman- Ross method
dc.subjectmonomer reactivity ratio
dc.subjectfree radical polymerization
dc.titleReactivity and polymerization ability of styrylquinoline containing methacrylic monomers
dc.title.alternativeРеакційна та полімеризаційна здатність стирилхінолінвмісних метакрилових мономерів
dc.typeArticle

Files

Original bundle

Now showing 1 - 2 of 2
Thumbnail Image
Name:
2-18v12n1_Kharchenko_O-Reactivity_and_polymerization_47-52.pdf
Size:
256.54 KB
Format:
Adobe Portable Document Format
Download
Thumbnail Image
Name:
2-18v12n1_Kharchenko_O-Reactivity_and_polymerization_47-52__COVER.png
Size:
516.68 KB
Format:
Portable Network Graphics
Download

License bundle

Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
2.99 KB
Format:
Plain Text
Description:
Download

Collections

Chemistry & Chemical Technology. – 2018. – Vol. 12, No. 1