Email this article Synthesis of New 3-Aminopropyl(ω-aminoalkoxy)trisiloxanes
- Authors: Vasiliev A.B.1, Lukin A.V.1, Ivanova K.Y.1, Kuzmin M.V.1, Kolyamshin O.A.1, Mitrasov Y.N.2
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Affiliations:
- Chuvash State University named after I.N. Ulyanov
- Chuvash State Pedagogical University named after I.Y. Yakovlev
- Issue: Vol 60, No 10 (2024)
- Pages: 1025-1029
- Section: Articles
- URL: https://journal-vniispk.ru/0514-7492/article/view/283137
- DOI: https://doi.org/10.31857/S0514749224100033
- EDN: https://elibrary.ru/QMZWUH
- ID: 283137
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Abstract
A one-pot, two-stage method for the synthesis of new aminotrisiloxanes has been developed, which consists of the sequential reaction of diphenylsilanediol with 3-aminopropyltriethoxysilane and amino alcohols.The synthesized di-, tetra-, and hexaaminotrisiloxanes have broad potential for use in both organic and macromolecular chemistry, in particular, as effective silicon-containing cross-linking agents and modifiers of epoxy resins.
About the authors
A. B. Vasiliev
Chuvash State University named after I.N. Ulyanov
Email: cool.karakyrt@ya.ru
ORCID iD: 0009-0004-0355-6335
Russian Federation, Moskovsky prosp., 15, Cheboksary, 428015
A. V. Lukin
Chuvash State University named after I.N. Ulyanov
Email: cool.karakyrt@ya.ru
ORCID iD: 0009-0001-5899-3813
Russian Federation, Moskovsky prosp., 15, Cheboksary, 428015
K. Y. Ivanova
Chuvash State University named after I.N. Ulyanov
Author for correspondence.
Email: cool.karakyrt@ya.ru
ORCID iD: 0000-0001-5982-0570
Russian Federation, Moskovsky prosp., 15, Cheboksary, 428015
M. V. Kuzmin
Chuvash State University named after I.N. Ulyanov
Email: cool.karakyrt@ya.ru
ORCID iD: 0000-0003-3880-9510
Russian Federation, Moskovsky prosp., 15, Cheboksary, 428015
O. A. Kolyamshin
Chuvash State University named after I.N. Ulyanov
Email: cool.karakyrt@ya.ru
ORCID iD: 0000-0002-3473-1827
Russian Federation, Moskovsky prosp., 15, Cheboksary, 428015
Yu. N. Mitrasov
Chuvash State Pedagogical University named after I.Y. Yakovlev
Email: cool.karakyrt@ya.ru
ORCID iD: 0000-0002-4083-7863
Russian Federation, Cheboksary, 38 K. Marx street, 428000
References
- Ivanova K.Yu., Kuzmin M.V., Rogozhina L.G., Patianova A. O., Semenov V.L., Alexandrov R.I. Chimica Techno Acta. 2021, 8, 1–5. doi: 10.15826/chimtech.2020.7.4.09
- Ефремов А.А., Загидуллин А.И., Колпакова М.В. [и др.]. Клеи. Герметики. Технологии. 2008, 4, 12–17.
- Ning X., Ishida H. J. Polym. Sci. Part A: Polym. Chem. 1994, 32, 1121–1129. doi: 10.1002/pola.1994.080320614
- Zhu L., Shi T., Zhang L., Qian Y., Yang L. J. Macromol. Sci. Part A, 2017, 54, 967–977. doi: 10.1080/10601325.2017.1387489
- Ivanova K.Yu., Kuzmin M.V., Kol′tsov N.I. Chimica Techno Acta. 2020, 7, 199–203. doi: 10.15826/chimtech.2021.8.3.05
- Иванова К.Ю., Кузьмин М.В., Колямшин О.А., Кольцов Н.И. Бутлеровские сообщ. 2020, 64, 28–32. doi: 10.37952/ROI-jbc-01/20-64-11-28
- Гарипов Р.М. Дисс. ... докт. хим. наук, Казань, 2004.
- Kovyazin V.A., Boev V.V., Kopylov V.M., Sokol′skaya I.B. Russ. J. Gen. Chem. 2008, 78, 216 –222. doi: 10.1134/S1070363208020114
- Брайнин Л.Б., Черкасов Р.А., Пудовик А.Н. ЖПХ, 1974, 47, 1807–1809.
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