Synthesis of New N-[(4-N1-Arylamino)phenyl]-1H-pyrrole-2,5-diones
- Autores: Kolyamshin O.A.1, Mitrasov Y.N.2, Danilov V.A.1, Pylchikova Y.Y.1
-
Afiliações:
- I.N. Ulyanov Chuvash State University
- I.Ya. Yakovlev Chuvash State Pedagogical University
- Edição: Volume 60, Nº 10 (2024)
- Páginas: 1043-1047
- Seção: Articles
- URL: https://journals.eco-vector.com/0514-7492/article/view/682486
- DOI: https://doi.org/10.31857/S0514749224100066
- EDN: https://elibrary.ru/QLWZUW
- ID: 682486
Citar
Resumo
The interaction of N1-phenyl- and N1-(4-methoxyphenyl)phenylene-1,4-diamines with maleic anhydride produced the corresponding monoamides of maleic acid, cyclization of which in the presence of p-toluene sulfonic acid synthesized N-[4-(N1-phenylamino)- or N1-(4-methoxyphenylamino)]phenyl-1H-pyrrole-2,5-diones.
Sobre autores
O. Kolyamshin
I.N. Ulyanov Chuvash State University
Autor responsável pela correspondência
Email: kolyamshin.oleg@yandex.ru
ORCID ID: 0000-0002-3473-1827
Rússia, Moskovskij prosp., 15, Cheboksary, 428015
Yu. Mitrasov
I.Ya. Yakovlev Chuvash State Pedagogical University
Email: mitrasov_un@mail.ru
ORCID ID: 0000-0002-4083-7863
Rússia, ul. K. Marksa, 38, Cheboksary, 428000
V. Danilov
I.N. Ulyanov Chuvash State University
Email: kolyamshin.oleg@yandex.ru
ORCID ID: 0000-0001-9140-1747
Rússia, Moskovskij prosp., 15, Cheboksary, 428015
Yu. Pylchikova
I.N. Ulyanov Chuvash State University
Email: kolyamshin.oleg@yandex.ru
ORCID ID: 0000-0002-7526-9288
Rússia, Moskovskij prosp., 15, Cheboksary, 428015
Bibliografia
- Михайлин Ю.А. Термоустойчивые полимеры и полимерные материалы. СПб.: Профессия, 2006.
- Митрасов Ю.Н., Колямшин О.А., Данилов В.А. Малеинимиды: синтез, свойства и полимеры на их основе. Чебоксары: Чуваш. гос. пед. у-т, 2017.
- Robert J.I., Carwyn W., Ian H. Progress Polymer Sci. 2017, 69, 1–21. doi: 10.1016/j.progpolymsci.2016.12.002
- Shiwen Y., Xiaosheng D., Sha D., Jinghong Q., Zongliang D., Xu C., Haibo W. Chem. Engineering J. 2020, 398, 125654. doi: 10.1016/j.cej.2020.125654
- Shiwen Y., Shuang W., Xiaosheng D., Zongliang D., Xu C., Haibo W. Chem. Engineering J. 2020, 391, 23544. doi: 10.1016/j.cej.2019.123544
- Aizpuruaa J., Martin L., Formoso E., González A., Irusta L. Progress in Organic Coatings. 2019, 130, 31–43. doi: 10.1016/j.porgcoat.2019.01.008
- Yufei L., Min H., Daohai Z., Qian Z., Yang L., Shuhao Q., Yu J. Materials. 2018, 11, 2330. doi: 10.3390/ma11112330
- Qian Z., Yi-Kai Z., Yu-Fei L., Min H., Yong-Ji G. Polymer Sci. Ser. В. 2020, 62 (4), 368–374. doi: 10.1134/S1560090420040119
- Jeemol P.A., Suresh M., Reghunadhan C.P. N. J. Polymer Res. 2020, 27, 300. doi: 10.1007/s10965-020-02197-z
- Park J.O., Yoon B.-J., Srinivasarao M. J. Non-Newtonian Fluid Mechanics. 2011, 166, 925–931. doi: 10.1016/j.jnnfm.2011.04.015
- Gaina V., Gaina C. Designed Monomers and Polymers, Taylor and Francis Ltd Publ. 2007, 10 (1), 91–104.
- Mitica S. Designed Monomers and Polymers. 2013, 16 (1), 14–24. doi: 10.1080/15685551.2012.705485
- Bernard F., Walid M., Quang T.P., Jean C.M. J. Adhesion Adhesives. 2013, 42, 51–59. doi: 10.1016/j.ijadhadh.2012.12.002
- Froidevaux V., Decostanzi M., Manseri A., Caillol S., Boutevin B., Auvergne R. Front. Chem. Sci. Eng. 2021, 15, 330–339. doi: 10.1007/s11705-020-1929-6
- Химические добавки к полимерам (справочник), М.: Химия, 1981.
- Цвайфель Х., Маер Р.Д., Шиллер М. Добавки к полимерам. Справочник, пер. c англ. СПб: Профессия, 2010, 28–137.
- Патент №2547727 (2015). Россия. Б.И. 2015, №3.
- Xueting L., Liang X., Cuihua, Xin J., Yu W. Tetrahedron. 2019, 75, 721–731. doi: 10.1016/j.tet.2018.12.035
Arquivos suplementares
