Ярославль, Ярославская область, Россия
Ярославль, Ярославская область, Россия
Ярославль, Ярославская область, Россия
Иваново, Ивановская область, Россия
Иваново, Ивановская область, Россия
На основе реакции активированного ароматического нуклеофильного замещения, протекавшей между 4-хлорфталонитрилом, 4,5-дихлорфталонитрилом и моно- и бисфенолами, содержащими различные заместители, получены известные и не описанные в литературе моно- и бис(арилокси)фталонитрилы, а также 6-членные гетероциклические системы дибензо[1,4]диоксина
4-хлорфталонитрил, 4,5-дихлорфталонитрил, активированное ароматическое нуклеофильное замещение, замещённые арилоксифталонитрилы, арилендиоксидифталонитрилы, дибензо[1,4]диоксин
1. Smyslov R.Y., Tomilin F.N., Shchugoreva I.A., Nosova G.I., Zhukova, E.V., Litvinova L.S., Yakimansky AV., Kolesnikov I., Abramov l.G., Ovchinnikov S.G., Avramov P.V. Synthesis and photophysical properties of copolyfluorenes for light-emitting applications: Spectroscopic experimental study and theoretical DFT consideration // Polymer. 2019. Vol. 168. P. 185-198. DOI:https://doi.org/10.1016/j.polymer.2019.02.015.
2. Skvortsov I.Y., Kulichikhin V.G., Ponomarev I.I., Varfolomeeva L.A., Kuzin M. S., Razorenov D.Y., Skupov K.M. Some Specifics of Defect-Free Poly-(o-aminophenylene)naphthoylenimide Fibers Preparation by Wei Spinning // Materials. 2022. Vol. 15(3). P. 808. DOI: 10.3B90/mal5030808.
3. Kolesnikov T.I., Orlova A.M., Tsegelskaya A.Y., Cherkaev G.V., Buzin A.I., Kechekyan A.S., Dmitrya-kov P.V., Belousov S.I., Abramov I.G., Serushkina O.V., Kuznetsov A.A. Dualcuring propargyl-phthalonitrile imide-based thermoset: Synthesis, characterization and curing behavior // European Polymer Journal. 2021. 161 (5). 110865. DOI:https://doi.org/10.1016/j.eurpolymj.2021.110865. URL: https://doi.org/10.1016/j.eurpolymj.2021.110865
4. Caterino M., D'Aria F., Kustov A.V., Belykh D.V., Khudyaeva I.S., Starseva O.M., Berezin D.B., Pylina Y.I., Usacheva T. R., Amato J., Giancola C. Selective binding of a bioactive porphyrin-based photosensitizer to the G-quadruplex from the. Intern // J. Biol. Macromolecules. 2020. Vol. 145. P. 244–251. DOI:https://doi.org/10.1016/j.ijbiomac.2019.12.152.
5. Makarova E.S., Kabanova M.V., Filimonov S.I., Shetnev А.А., Suponitsky K.Yu. Synthesis of substituted hex-ahydro-2H-chromeno[4,3-d]pyrimidine-2,5-diones and their modification at the hydroxyl group // Russian Chemical Bulletin. Vol. 71, no. 5. P. 1034–1042. DOI:https://doi.org/10.1007/s11094-022-02596-0.
6. Terrier F. Nucleophilic aromatic displacement: the influence of the nitro group. New York: VSH Publishers, 1991.
7. Tsegelskaya A.Y., Soldatova A.E., Semenova G.I., Dutov M.D., Abramov I.G., Kuznetsov A.A. One-Stage High Temperature Catalytic Synthesis of Star-Shaped Oligoimides by (B4+AB) Scheme // Polymer Science. Se-ries В. 2019. Vol. 61, no. 2. P. 148–154. DOI:https://doi.org/10.1134/S1560090419010123.
8. Erzunov D.A, Tikhomirova T.V, Botnar A.A, Znoyko S.A, Abramov I.G, Mayzlish V.E., Martin Y.S. Bulky-substituted phthalodinitriles and cobalt and copper phthalocyanines based on them: synthesis, thermal analysis and spectroscopic properties // Journal of Thermal Analysis and Calorimetry. 2020. Vol. 142(5). Р. 1807–1816. DOI:https://doi.org/10.1007/s10973-020-10025-1.
9. Абрамов И.Г., Баклагин В.Л., Макарова Е.С., Клейкова Д.Э. Использование азотсодержащих гетеро-циклических O-, и S-нуклеофилов в реакциях с 4-нитрофталонитрилом и 4-бром-5-нитрофталонитрилом // От химии к технологии шаг за шагом. 2021. Т. 2, вып. 4. С. 43-50. DOI:https://doi.org/10.52957/2782I900_2021_04_43. URL: http: //chemintech.ru/index.php/tor/2021tom2no4
10. Chirkova Z.V., Filimonov S.I., Abramov I.G. Synthesis of Functional Derivatives of Benzofuran-5,6-dicarboxylic Acids // Russian Journal of General Chemistry. 2019. Vol. 89, no. 6. P. 1307–1309. DOI:https://doi.org/10.1134/S1070363219060276/.
11. Filimonov S.I., Chirkova Zh.V., Abramov I.G., Firgang S.I., Stashina G.A., Suponitsky K.Yu. Synthesis of Novel Substituted 4-Hydroxy-3-oxo-3,4-dihydro-2H-1,4-benzoxazine-6,7-dicarbonitriles // Heterocycles. 2011. Vol. 83, no. 4. Р. 755–763. DOI:https://doi.org/10.3987/COM-10-12128.
12. Chirkova Zh. V., Filimonov S.I., Abramov I.G. Synthesis of Substituted [1,2,4]oxadiazino[2,3-a]indole-7,8-dicarbonitriles // Mendeleev Commun. 2018. Vol. 28, no. 1. P. 86–87. DOI:https://doi.org/10.1016/j.mencom.2017.09.023/.
13. Abramov I.G., Dorogov M.V., Smirnov A.V., Ivanovskii S.A., Abramova M.B., Plachtinsky V.V.. The differing reactivity of the bromo and nitro groups in 4-bromo-5-nitrophthalonitrile towards nucleophilic attack. // Mendeleev Commun. 2000. Vol. 2. P. 78–80. DOI:https://doi.org/10.1070/MC2000v010n02ABEH001147.
14. Negrimovsky V.M., Volkov K.A., Suponitsky K.Yu., Lukyancts E.K. C-Nucleophilic substitution in tetrachlorophthalonitrile - An approach to some new hexadecasubstituted phthalocyanines // Journal of Porphyrins and Phthalocyanines. 2013. Vol. 17, no. 8-9. P. 799–806 DOI: 10.U42/S1088424613500429.
15. Kimura M., Nomoto H., Masaki N., Mori S. Dye Molecules for Simple Co-Sensitization Process: Fabrication of Mixed-Dye-Sensitized Solar Cells // Angewandte Chemie International Edition. 2012. Vol. 51, no. 18. P. 4371–4374. DOI:https://doi.org/10.1002/anie.201108610.
16. Kustov A.V., Smirnova N.L., Privalov O.A., Moryganova T.M., Strelnikov A.I., Morshnev P.K., Koifman O.I., Lyubimtsev A.V. Kustova T.V., Berezin D.B. Transurethral resection of non-muscle invasive bladder tumors combined with fluorescence diagnosis and photodynamic therapy with chlorin е6-type photosensitizers // Journal of Clinical Medicine. 2022. Vol. 11, no. 1. P. 233. DOI:https://doi.org/10.3390/jcmll010233.
17. Berezin D.B., MabrovV.V., Znoyko S.A., Mayzlish V.E., Kustov A.V. Aggregation of water soluble octaanionic phthalocyanines and their photoinactivation antimicrobial effect in vitro // Mendeleev Communications. 2020. Vol. 30, no. 5. P. 621–623. DOI:https://doi.org/10.1016/j.mencom.2020.09.023.
18. Chirkova Z.V., Kabanova М.V., Filimonov S.I., Abramov I.G., Petzer A., Hitge R., Petzer J.P., Suponitsky K.Y. Optimization of pyrrolo[3,4-f]indole-5,7-dione and indole-5,6-dicarbonitrile derivatives as inhibitors of monoamine oxidase // Drug Development Research. 2019. Vol. 80, no. 7. P. 970–980. DOI:https://doi.org/10.1002/ddr.21576.
19. Chirkova Zh.V., Kabanova M.V., Filimonov S.I., Abramov I.G., Petzer A., Petzer J.P., Suponitsky K.Yu. An evaluation of synthetic indole derivatives as inhibitors of monoamine oxidase // Bioorganic and Medicinal Chemistry Letters. 2016. Vol. 26, no. 9. P. 2214–2219. DOI:https://doi.org/10.1016/j.bmcl.2016.03.060.
20. Tverdova N.V., Giricheva N.I., Maizllsh V.E., Galanin, N.E., Girichev G.V. Molecular Structure, Vibrational Spectrum and Conformational Properties of 4-(4-Tritylphenoxy)phthalonitrile-Precursor for Synthesis of Phthalocyanines with Bulky Substituent // International Journal of Molecular Science. 2022. Vol. 23, no. 22. P. 13922. DOI:https://doi.org/10.3390/ijms232213922.
21. Botnar A.A., Domareva N.P., Kazaryan K.Y., Tikhomirova T.V., Abramova M.B. Vashurln A.S. Synthesis and spectral properties of tctraphenoxysubstituted erbium phthalocyanines containing peripheral phenyl and cyclohexyl fragments // Russian Chemical Bull. 2022. Vol. 71, no. 5. P. 953–961. DOI:https://doi.org/10.1007/slll72-022-3496-0.
22. Знойко С.А., Елизарова А.П., Кустова Т.В., Наконечная А.Н. Комплексы эрбия и лютеция «сэндвичевого» типа, содержащие фрагменты тетраантрахинонопорфиразина и замещенных фталоцианинов // Изв. вузов. Химия и хим. технология. 2021. Т. 64, вып. 4. С. 42-51. DOI: https://doi.org/10.6060/ivkkt.20216404.6380
23. Orlova A.M., Alentiev A.Yu., Kolesnikov T.I., Tsegelskaya A.Yu., Monakhova K.Z., Chirkov S.V., Nikiforov R. Yu., Abramov I.G., Kuznetsov A.A. Novel organo-soluble poly(etherimide)s based on diethyltoluenedia-mine: Synthesis, characterization and gas transport properties // Polymer. 2022. Vol. 256. P. 125258 DOI:https://doi.org/10.1016/J.polymer.2022.125258.
24. Soldatova A.E., Tsegelskaya A.Yu., Semenova G.K., Bezsudnov I.V., Polinskaya M.S., Abramov I.G., Kuznetsov A.A. Synthesis of tetraarm stars with polyetherimide-polyether block copolymer arms // Russian Chemical Bull. 2022. Vol. 71, no. 4. P. 777–786. DOI:https://doi.org/10.1007/s11172-022-3478-2
25. Orlova A.M., Tsegelskaya A.Yu., Kolesnikov T.I., Abramov I.G., Kuznetsov A.A. Novel Polyetherimides Based on 5-Methyl-l,3-phenylene-bis-4-oxyphthalic Acid Dianhydride: Synthesis and Physicochemical Proper-ties // Polymer Science. Series B. 2022. Vol. 64, no. 1. P. 17-25. DOI:https://doi.org/10.1134/S1560090422010031.
