DC Field | Value | Language |
dc.contributor.author | Mishurov, Dmytro | - |
dc.date.accessioned | 2020-03-02T10:50:17Z | - |
dc.date.available | 2020-03-02T10:50:17Z | - |
dc.date.created | 2019-02-28 | - |
dc.date.issued | 2019-02-28 | - |
dc.identifier.citation | Mishurov D. The sulfonation of 3,5,7,3',4'-pentahydroxyflavone and non-linear-optical activity of its sulfonic derivatives / Dmytro Mishurov // Chemistry & Chemical Technology. — Lviv : Lviv Politechnic Publishing House, 2019. — Vol 13. — No 1. — P. 33–37. | - |
dc.identifier.uri | https://ena.lpnu.ua/handle/ntb/46428 | - |
dc.description.abstract | Проведено синтез сульфокверцетину та
вивчення його структури й нелінійно оптичних властивостей.
Із використанням квантово-хімічних розрахунків, 13С і HSQC
ЯМР спектроскопії, ІЧ спектроскопії було показано, що
сульфонова група в знаходиться у положенні C8 кверцетину.
Визначено молекулярну гіперполяризованість отриманого
сульфокверцетину. Показано що сульфокверцетин можливо
використовувати для створення на його основі нових полі-
мерних НЛО матеріалів. | - |
dc.description.abstract | Synthesis of sulfoquercetin and studies of its
structure and nonlinear properties have been carried out.
Using quantum-chemical simulations, 13С and HSQC
NMR spectrometry, FTIR spectroscopy it was shown that
a sulphonic group occurs in C8 location of quercetin.
Molecular first hyperpolarizability of the obtained
8-sulfoquercetin was studied. It was shown that
8-sulfoquercetin can be used for creation the new polymer
NLO materials on its basis. | - |
dc.format.extent | 33-37 | - |
dc.language.iso | en | - |
dc.publisher | Видавництво Львівської політехніки | - |
dc.publisher | Lviv Politechnic Publishing House | - |
dc.relation.ispartof | Chemistry & Chemical Technology, 1 (13), 2019 | - |
dc.relation.uri | https://doi.org/10.1039/C4RA13250E | - |
dc.relation.uri | https://doi.org/10.3390/polym3030975 | - |
dc.relation.uri | https://doi.org/10.1134/S0965545X12100045 | - |
dc.relation.uri | https://doi.org/10.1039/C5CC03063C | - |
dc.relation.uri | https://doi.org/10.1002/anie.198406901 | - |
dc.relation.uri | https://doi.org/10.1021/j100179a026 | - |
dc.relation.uri | https://doi.org/10.1021/ja00176a001 | - |
dc.relation.uri | https://doi.org/10.1063/1.104625 | - |
dc.relation.uri | https://doi.org/10.1063/1.350724 | - |
dc.relation.uri | https://doi.org/10.1021/ja00020a030 | - |
dc.relation.uri | https://dx.doi.org/10.1007/s00214-007-0401-8 | - |
dc.relation.uri | https://doi.org/10.1063/1.444267 | - |
dc.relation.uri | https://doi.org/10.1007/BF00533485 | - |
dc.relation.uri | https://doi.org/10.1021/cr00031a013 | - |
dc.relation.uri | https://doi.org/10.1063/1.474671 | - |
dc.relation.uri | https://doi.org/10.15407/fm | - |
dc.subject | кверцетин | - |
dc.subject | сульфування | - |
dc.subject | нелінійно-оптична активність | - |
dc.subject | поляризовність | - |
dc.subject | властивості | - |
dc.subject | quercetin | - |
dc.subject | sulfonation | - |
dc.subject | nonlinear activity | - |
dc.subject | polarizability | - |
dc.subject | property | - |
dc.title | The sulfonation of 3,5,7,3',4'-pentahydroxyflavone and non-linear-optical activity of its sulfonic derivatives | - |
dc.title.alternative | Сульфування 3,5,7,3',4'-пентагідроксифлавону та нелінійно оптичні властивості його сульфопохідних | - |
dc.type | Article | - |
dc.rights.holder | © Національний університет „Львівська політехніка“, 2019 | - |
dc.rights.holder | © Mishurov D., 2019 | - |
dc.contributor.affiliation | National Technical University "Kharkiv Polytechnic Institute" | - |
dc.format.pages | 5 | - |
dc.identifier.citationen | Mishurov D. The sulfonation of 3,5,7,3',4'-pentahydroxyflavone and non-linear-optical activity of its sulfonic derivatives / Dmytro Mishurov // Chemistry & Chemical Technology. — Lviv : Lviv Politechnic Publishing House, 2019. — Vol 13. — No 1. — P. 33–37. | - |
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dc.relation.references | 20. Heneczkowski M., KopaczM., Nowak D., Kuźniar A.: Acta Polonise Pharmacuttica-Drug Resarch, 2001, 58, 415. | - |
dc.relation.referencesen | 1. Liu J., Xu G., Liu F. et al., RSC Adv., 2015, 5, 15784. https://doi.org/10.1039/P.4RA13250E | - |
dc.relation.referencesen | 2. Mishurov D., Roshal A., Brovko O., Polym. Polym. Composites, 2015, 23, 121. | - |
dc.relation.referencesen | 3. OhM.-C., Kim K.-J., Chu W.-S. et al., Polymers, 2011, 3, 975. https://doi.org/10.3390/polym3030975 | - |
dc.relation.referencesen | 4. Shevchenko V., Sidorenko A., Bliznyuk V. et al., Polym. Sci. Ser. A, 2013, 55, 1. https://doi.org/10.1134/S0965545X12100045 | - |
dc.relation.referencesen | 5. Greulich T., Suzuki N., Daniliuc C., Chem. Commun., 2016, 11, 1. https://doi.org/10.1039/P.5CC03063C | - |
dc.relation.referencesen | 6. Williams D., Angew. Chem. Int. Ed. Engl., 1984, 23, 690. https://doi.org/10.1002/anie.198406901 | - |
dc.relation.referencesen | 7. Cheng L.-T., TamW., Stevenson S. et al., J. Phys. Chem., 1991, 95, 10631. https://doi.org/10.1021/j100179a026 | - |
dc.relation.referencesen | 8. Ulman A., Willand C., Kohler W. et al., J. Am. Chem. Soc., 1990, 112, 7083. https://doi.org/10.1021/ja00176a001 | - |
dc.relation.referencesen | 9. Rikken G., Seppen C., Nijhuis S., Meijer E., Appl. Phys. Lett., 1991, 58, 435. https://doi.org/10.1063/1.104625 | - |
dc.relation.referencesen | 10. Burland D., Miller R., Reiser O. et al., J. Appl. Phys., 1992, 71, 410. https://doi.org/10.1063/1.350724 | - |
dc.relation.referencesen | 11. Stiegman A., Graham E., Perry K. et al., J. Am. Chem. Soc., 1991, 113, 7658. https://doi.org/10.1021/ja00020a030 | - |
dc.relation.referencesen | 12. Labanowski J., Andzelm J. (Eds.): Density Functional Methods in Chemistry. Springer-Verlag, New York 1991. | - |
dc.relation.referencesen | 13. Zhao Y., Truhlar D., Theor. Chem. Account, 2008, 119, 525. https://dx.doi.org/10.1007/s00214-007-0401-8 | - |
dc.relation.referencesen | 14. Francl M., PietroW., Hehre W. et al., J. Chem. Phys., 1982, 77, 3654. https://doi.org/10.1063/1.444267 | - |
dc.relation.referencesen | 15. Hariharan P., Pople J., Theor. Chim. Acta, 1973, 28, 213. https://doi.org/10.1007/BF00533485 | - |
dc.relation.referencesen | 16. FrischM., Trucks G., Schlegel H. et al., Gaussian 09, revision P.02; Gaussian, Inc.:Wallingford, CT. 2004 | - |
dc.relation.referencesen | 17. Tomasi J., PersicoM., Chem. Rev., 1994, 94, 2027. https://doi.org/10.1021/cr00031a013 | - |
dc.relation.referencesen | 18. Barone V., Cossi M., Mennucci B., Tomasi J., J. Chem. Phys., 1997, 107, 3210. https://doi.org/10.1063/1.474671 | - |
dc.relation.referencesen | 19. Mishurov D., Roshal A., Brovko O., Funct. Mater., 2017, 24, 68. https://doi.org/10.15407/fm 24.01.068 | - |
dc.relation.referencesen | 20. Heneczkowski M., KopaczM., Nowak D., Kuźniar A., Acta Polonise Pharmacuttica-Drug Resarch, 2001, 58, 415. | - |
dc.citation.issue | 1 | - |
dc.citation.spage | 33 | - |
dc.citation.epage | 37 | - |
dc.coverage.placename | Львів | - |
dc.coverage.placename | Lviv | - |
Appears in Collections: | Chemistry & Chemical Technology. – 2019. – Vol. 13, No. 1
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