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<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="research-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Russian Journal of General Chemistry</journal-id><journal-title-group><journal-title xml:lang="en">Russian Journal of General Chemistry</journal-title><trans-title-group xml:lang="ru"><trans-title>Журнал общей химии</trans-title></trans-title-group></journal-title-group><issn publication-format="print">0044-460X</issn><issn publication-format="electronic">3034-5596</issn><publisher><publisher-name xml:lang="en">The Russian Academy of Sciences</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">666955</article-id><article-id pub-id-type="doi">10.31857/S0044460X23060070</article-id><article-id pub-id-type="edn">FLDXQN</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>Articles</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>Статьи</subject></subj-group><subj-group subj-group-type="article-type"><subject>Research Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en">Synthesis and fluorescence properties of salts of cyclic amines with tetracyanobutadiene-containing pyridine</article-title><trans-title-group xml:lang="ru"><trans-title>Синтез и флуоресцентные свойства солей циклических аминов с пиридином, содержащим тетрацианобутадиеновый фрагмент</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Chunikhin</surname><given-names>S. S</given-names></name><name xml:lang="ru"><surname>Чунихин</surname><given-names>С. С</given-names></name></name-alternatives><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Ershov</surname><given-names>O. V</given-names></name><name xml:lang="ru"><surname>Ершов</surname><given-names>О. В</given-names></name></name-alternatives><email>oleg.ershov@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">I.N. Ulyanov Chuvash State University</institution></aff><aff><institution xml:lang="ru">Чувашский государственный университет имени И. Н. Ульянова</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2023-06-15" publication-format="electronic"><day>15</day><month>06</month><year>2023</year></pub-date><volume>93</volume><issue>6</issue><issue-title xml:lang="en">NO6 (2023)</issue-title><issue-title xml:lang="ru">№6 (2023)</issue-title><fpage>891</fpage><lpage>896</lpage><history><date date-type="received" iso-8601-date="2025-02-26"><day>26</day><month>02</month><year>2025</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2023, Russian Academy of Sciences</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2023, Российская академия наук</copyright-statement><copyright-year>2023</copyright-year><copyright-holder xml:lang="en">Russian Academy of Sciences</copyright-holder><copyright-holder xml:lang="ru">Российская академия наук</copyright-holder></permissions><self-uri xlink:href="https://transsyst.ru/0044-460X/article/view/666955">https://transsyst.ru/0044-460X/article/view/666955</self-uri><abstract xml:lang="en"><p>A method was developed for the preparation of six new salts based on cyclic amines and pyridine containing a tetracyanobutadiene fragment, 2-(dicyanomethylidene)-5-methyl-6-phenyl-1,2-dihydropyridine-3,4-dicarbonitrile, acting as an organic anion. Correlations between the parameters of solid-phase emission of the synthesized compounds and the structure of the cation included in the composition were characterized.</p></abstract><trans-abstract xml:lang="ru"><p>Разработан способ получения шести новых солей на основе циклических аминов и пиридином, содержащим тетрацианобутадиеновый фрагмент, - 2-(дицианометилиден)-5-метил-6-фенил-1,2-дигидропиридин-3,4-дикарбонитрилом, выступающим в качестве органического аниона. Были охарактеризованы корреляции между параметрами твердофазного испускания синтезированных соединений и строением входящего в состав катиона.</p></trans-abstract><kwd-group xml:lang="en"><kwd>nitriles</kwd><kwd>polycyano compounds</kwd><kwd>pyridine</kwd><kwd>fluorescence</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>нитрилы</kwd><kwd>полицианосоединения</kwd><kwd>пиридин</kwd><kwd>флуоресценция</kwd></kwd-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>MacFarlane D.R., Forsyth S.A., Golding J., Deacon G.B. // Green Chem. 2002. Vol. 4. N 5. P. 444. doi 10.1039/B205641K</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Letaief S., Detelleir C. // Clays Clay Miner. 2008. Vol. 56. N 1. P. 82. doi 10.1346/CCMN.2008.0560107</mixed-citation></ref><ref id="B3"><label>3.</label><mixed-citation>Triolo A., Russina O., Fazio B., Appetecchi G.B., Carewska M., Passerini S. // J. Chem. Phys. 2009. Vol. 130. N 16. P. 164521. doi 10.1063/1.3119977</mixed-citation></ref><ref id="B4"><label>4.</label><mixed-citation>Lava K., Binnemans K., Cardinaels T. // J. Phys. Chem. (B). 2009. Vol. 113. N 28. P. 9506. doi 10.1021/jp903667e</mixed-citation></ref><ref id="B5"><label>5.</label><mixed-citation>Lethesh K.C., Shah S.N., Ayodele O.B., Mutalib M.I.A., Uemura Y. // J. Mol. Liq. 2016. Vol. 221. P. 1140. doi 10.1016/j.molliq.2016.06.092</mixed-citation></ref><ref id="B6"><label>6.</label><mixed-citation>Iwai N., Nakayama K., Kitazume T. // Bioorg. Med. Chem. Lett. 2011. Vol. 21. N 6. P. 1728. doi 10.1016/j.bmcl.2011.01.081</mixed-citation></ref><ref id="B7"><label>7.</label><mixed-citation>Kleszczyńska H., Sarapuk J., Oświȩcimska M., Witek S. // Polish J. Environ. Stud. 2000. Vol. 9, N 6. P. 475.</mixed-citation></ref><ref id="B8"><label>8.</label><mixed-citation>Kleszczyńska H., Oświȩcimska M., Bonarska D., Sarapuk J. // Zeitschrift fur Naturforsch. (С). 2002. Vol. 57. N 3-4. P. 344. doi 10.1515/znc-2002-3-424</mixed-citation></ref><ref id="B9"><label>9.</label><mixed-citation>Lin Y.H., Sakai1 N., Da1 P., Wu J., Sansom H.C., Ramadan A.J., Mahesh S., Liu J., Oliver R.D.J., Lim J., Aspitarte L., Sharma K., Madhu P.K., MoralesVilches A.B., Nayak P.K., Bai S., Gao F., Grovenor C.R.M., Johnston M.B., Labram J.G., Durrant J.R., Ball J.M., Wenger B., Stannowski B., Snaith H.J. // Science. 2020. Vol. 369. N 6499. P. 96. doi 10.1126/science.aba1628</mixed-citation></ref><ref id="B10"><label>10.</label><mixed-citation>Salem N., Nicodemou L., Abu-Lebdeh Y., Davidson I.J. // J. Electrochem. Soc. 2011. Vol. 159. N 2. P. A172. doi 10.1149/2.102202jes</mixed-citation></ref><ref id="B11"><label>11.</label><mixed-citation>Pohlmann S., Olyschläger T., Goodrich P., Vicente J.A., Jacquemin J., Balducci A. // Electrochim. Acta. 2015. Vol. 153. P. 426. doi 10.1016/j.electacta.2014.11.189</mixed-citation></ref><ref id="B12"><label>12.</label><mixed-citation>Pohlmann S., Olyschläger T., Goodrich P., Alvarez Vicente J., Jacquemin J., Balducci A. // J. Power Sources. 2015. Vol. 273. P. 931. doi 10.1016/j.jpowsour.2014.09.167</mixed-citation></ref><ref id="B13"><label>13.</label><mixed-citation>Kim K.S., Park S.Y., Choi S., Lee H. // J. Power Sources. 2006. Vol. 155. N 2. P. 385. doi 10.1016/j.jpowsour.2005.05.018</mixed-citation></ref><ref id="B14"><label>14.</label><mixed-citation>Kim K.S., Choi S., Demberelnyamba D., Lee H., Oh J., Lee B.B., Mun S.J. // Chem. Commun. 2004. Vol. 4, N 7. P. 828. doi 10.1039/B400198B</mixed-citation></ref><ref id="B15"><label>15.</label><mixed-citation>Yeon S.H., Kim K.S., Choi S., Lee H., Kim H.S., Kim H. // Electrochim. Acta. 2005. Vol. 50. N 27. P. 5399. doi 10.1016/j.electacta.2005.03.020</mixed-citation></ref><ref id="B16"><label>16.</label><mixed-citation>Rajkumar R., Praveen Kumar P. // J. Mol. Struct. 2019. Vol. 1179. P. 108. doi 10.1016/j.molstruc.2018.10.085</mixed-citation></ref><ref id="B17"><label>17.</label><mixed-citation>Elmaleh D.R., Padmanabhan S., Hassan M.A., Correia J.A., Herman L.W., Hanson R.N., Strauss H.W. // Nucl. Med. Biol. 1993. Vol. 20. N 4. P. 427. doi 10.1016/0969-8051(93)90073-4</mixed-citation></ref><ref id="B18"><label>18.</label><mixed-citation>Sengee G.I., Badraa N., Young K.S. // Int. J. Mol. Sci. 2008. Vol. 9, N 8. P. 1407. doi 10.3390/ijms9081407</mixed-citation></ref><ref id="B19"><label>19.</label><mixed-citation>Дяченко В.Д., Чернега А.Н., Дяченко С.В. // ЖОХ. 2012. Т. 82. Вып. 4. С. 634</mixed-citation></ref><ref id="B20"><label>20.</label><mixed-citation>Dyachenko V.D., Dyachenko S.V., Chernega A.N. // Russ. J. Gen. Chem. 2012. Vol. 82. N 4. P. 634. doi 10.1134/S1070363212040184</mixed-citation></ref><ref id="B21"><label>21.</label><mixed-citation>Курскова А.О., Доценко В.В., Фролов К.А., Аксенов Н.А., Аксенова И.В., Щербаков С.В., Овчаров С.Н., Кривоколыско Д.С., Кривоколыско С.Г. // ЖОХ. 2021. Т. 91. Вып. 6. С. 847</mixed-citation></ref><ref id="B22"><label>22.</label><mixed-citation>Kurskova A.O., Frolov K.A., Krivokolysko S.G., Dotsenko V.V., Aksenov N.A., Aksenova I.V., Shcherbakov S.V., Ovcharov S.N., Krivokolysko D.S. // Rus. J. Gen. Chem. 2021. Vol. 91. N 6. P. 971. doi 10.1134/S1070363221060037</mixed-citation></ref><ref id="B23"><label>23.</label><mixed-citation>Носова Н.В., Лежнина Д.Д., Гейн О.Н., Новикова В.В., Гейн В.Л. // ЖОХ. 2020. Т. 90. Вып. 10. С. 1479</mixed-citation></ref><ref id="B24"><label>24.</label><mixed-citation>Nosova N.V., Lezhnina D.D., Gein O.N., Novikova V.V., Gein V.L. // Rus. J. Gen. Chem. 2020. Vol. 90. N 10. P. 1817. doi 10.1134/S1070363221060037</mixed-citation></ref><ref id="B25"><label>25.</label><mixed-citation>Khan R., Periyayya U., Kim G.C., Lee I.H. // Solid State Sci. 2019. Vol. 97. P. 105986. doi 10.1016/j.solidstatesciences.2019.105986</mixed-citation></ref><ref id="B26"><label>26.</label><mixed-citation>Ameen S., Akhtar M.S., Shin H.S. // Mater. Lett. 2015. Vol. 148. P. 188. doi 10.1016/j.matlet.2015.02.049</mixed-citation></ref><ref id="B27"><label>27.</label><mixed-citation>Kamel A.H., Galal H.R., Awwad N.S. // Anal. Methods. 2018. Vol. 10. N 45. P. 5406. doi 10.1039/c8ay01811a</mixed-citation></ref><ref id="B28"><label>28.</label><mixed-citation>Oliveira S.M., Santos Castro Assis K.L., Paiva V.M., Hashempour M., Bestetti M., Araújo J.R., D'Elia E. // Bull. Mater. Sci. 2022. Vol. 45. N 2. Art. 100. doi 10.1007/s12034-022-02669-6</mixed-citation></ref><ref id="B29"><label>29.</label><mixed-citation>Kolliopoulos A. V., Metters J.P., Banks C.E. // Environ. Sci. Water Res. Technol. 2015. Vol. 1. N 1. P. 40. doi 10.1039/C4EW00033A</mixed-citation></ref><ref id="B30"><label>30.</label><mixed-citation>Oliveira S.M., Siguemura A., Lima H.O., Souza F.C., Magalhães A.A.O., Toledo R.M., D'Elia E. // J. Braz. Chem. Soc. 2014. Vol. 25. N 8. P. 1399. doi 10.5935/0103-5053.20140122</mixed-citation></ref><ref id="B31"><label>31.</label><mixed-citation>Chunikhin S.S., Ershov O. V., Ievlev M.Y., Belikov M.Y., Tafeenko V.A. // Dye. Pigment. 2018. Vol. 156. P. 357. doi 10.1016/j.dyepig.2018.04.024</mixed-citation></ref><ref id="B32"><label>32.</label><mixed-citation>Ershov O. V., Chunikhin S.S., Ievlev M.Y., Belikov M.Y., Tafeenko V.A. // CrystEngComm. 2019. Vol. 21. N 36. P. 5500. doi 10.1039/c9ce01089k</mixed-citation></ref><ref id="B33"><label>33.</label><mixed-citation>Chunikhin S.S., Ershov O.V., Yatsenko A.V., Tafeenko V.A., Dmitrieva N.E., Ievlev M.Y. // CrystEngComm. 2021. Vol. 23. N 15. P. 2816. doi 10.1039/D1CE00028D</mixed-citation></ref></ref-list></back></article>
