Development of Methods for the Synthesis of Bis-(N-Maleimide)aryl and Bis-Diallyl Bisphenol Monomers for Thermosetting Polymers

Мұқаба

Дәйексөз келтіру

Толық мәтін

Ашық рұқсат Ашық рұқсат
Рұқсат жабық Рұқсат берілді
Рұқсат жабық Тек жазылушылар үшін

Аннотация

The method of obtaining bismaleimide monomers from aromatic diamines is optimized; the synthesis was tested on gram quantities with the possibility of further adaptation to kilogram quantities. Also, in order to obtain copolymers of bismaleimides with bisphenols, the conditions for obtaining diallyl bisphenol A were optimized.

Толық мәтін

Рұқсат жабық

Авторлар туралы

E. Kudryashova

Lobachevsky Nizhny Novgorod State University

Email: afedorovNN@yandex.ru
Ресей, 23, Gagarin Ave., Nizhny Novgorod, 603950

V. Otvagin

Lobachevsky Nizhny Novgorod State University

Email: afedorovNN@yandex.ru
Ресей, 23, Gagarin Ave., Nizhny Novgorod, 603950

K. Romanov

Lobachevsky Nizhny Novgorod State University

Email: afedorovNN@yandex.ru
Ресей, 23, Gagarin Ave., Nizhny Novgorod, 603950

E. Afanasyeva

Lomonosov Moscow State University

Email: afedorovNN@yandex.ru
Ресей, 1, Leninskie Gory, Moscow, 119991

O. Morozov

Lomonosov Moscow State University

Email: afedorovNN@yandex.ru
Ресей, 1, Leninskie Gory, Moscow, 119991

A. Babkin

Lomonosov Moscow State University

Email: afedorovNN@yandex.ru
Ресей, 1, Leninskie Gory, Moscow, 119991

A. Kepman

Lomonosov Moscow State University

Email: afedorovNN@yandex.ru
Ресей, 1, Leninskie Gory, Moscow, 119991

A. Fedorov

Lobachevsky Nizhny Novgorod State University

Хат алмасуға жауапты Автор.
Email: afedorovNN@yandex.ru
Ресей, 23, Gagarin Ave., Nizhny Novgorod, 603950

Әдебиет тізімі

  1. D’Alelio G., Пат US3929713A (1975). США.
  2. Kablov E.N., Erofeev V.T., Rimshin V.I., Zotkina M.M., Dergunova A.V., Moiseev V.V. J. Phys.: Conf. Ser, 2020. 1687, 12031. doi: 10.1088/1742-6596/1687/1/012031
  3. Evsyukov S., Pohlmann T., ter Wiel M. Rev. Curr. Trends Polym. Sci. 2020. 20.
  4. Валуева М.И., Зеленина И.В., Жаринов М.А., Ахмадиева К.Р., Труды ВИАМ, 2019, 12, 67–79. D oi 10.18577/2307-6046-2019-0- 12-67-79
  5. Stenzenberger H. Struct. Adhes. Dev. resins Prim. Elsevier Applied Science Publishers, London; New York, 1986.
  6. Iredale R.J., Ward C., Hamerton I. Prog. Polym. Sci. Elsevier, 2017, 69. 1–21. doi: 10.1016/j.progpolymsci.2016.12.002
  7. Мухаметов Р.Р., Петрова А.П. Авиационные материалы и технологии. 2019, 3, 48–58. doi: 10.18577/2071-9140-2019-0-3-48-58
  8. Mangalgiri P.D. Def. Sci. J. Defence Scientific Information & Documentation Centre, 2005, 55, 175. doi: 10.14429/DSJ.55.1980
  9. Zahir A.-C., Renner A. Пат. US4100140A (1978). США.
  10. Crivello J. V. J. Polym. Sci. Polym. Chem. Ed., 1973, 11, 1185–1200. doi: 10.1002/pol.1973.170110607
  11. Bargain M., Combet A., Grosjean P. Пат. FR1555565 (1969). Франция.
  12. Михайлин Ю.А. Термоустойчивые полимеры и полимерные материалы. СПб.: Профессия, 2006.
  13. Tung C.M., Lung C.L., Liar T.T., Polym. Mat. Sci. Eng., 1985, 52, 139–143.
  14. Zahir S.A.-C., Renner A. Пат. US 4100140 (1978), США.
  15. Stenzenberger H.D. Bismaleimide Resins, ASM handbook, 2001.
  16. Бабкин А.В., Эрдни-Горяев Э.М., Солопченко А.В., Кепман А.В., Известия высших учебных заведений. Химия и химическая технология, 2015, 58, 54–57.
  17. Xiong X., Chen P., Zhang J., Yu Q., Wang B., Thermochim. Acta., 2011, 514, 44–50. doi: 10.1016/j.tca.2010.12.001
  18. Orphanides G.G. Пат. US4154737A (1979), США.
  19. Petride H., Beiu S., Florea C., Rosu I., Dragus C., Mihis I., Пат. RO116193B1 (1994), Румыния.
  20. Li K., Yuan Ch., Zheng S., Fang Q., Tetrahedron Lett., 2012, 53, 4245–4247. doi: 10.1016/j.tetlet.2012.06.025
  21. Groth T., Piejko K.-E., Joentgen W., Kasbauer J., Alig B., Striiver W. Пат. US5773630 A (1998), США.
  22. Liao D.C., Hsieh K.H. Journal of Polymer Science Part A: Polymer Chemistry, 1994, 32, 1665–1672. doi: 10.1002/pola.1994.080320908
  23. Hsieh K., Han J.L., Yu C.T., Fu S.C., Polymer, 2001, 42, 2491–2500. doi: 10.1016/S0032-3861(00)00641-8
  24. Armarego W.L.F., Chai C.L.L. Purification of organic chemicals, Butterworth‐Heinemann Oxford, 2012.
  25. Шошева А.Л., Труды ВИАМ, 2022, 10, 23–41. doi: 10.18577/2307-6046-2022-0-10-23-41
  26. Wang W., Gu J., Hua W., Jia X., Xi K., Chem. Commun., 2014, 50, 8889–8891. doi: 10.1039/C4CC03306J
  27. Choi H.Y., Chi D.Y. J. Am. Chem. Soc., 2001, 123, 9202–9203. doi: 10.1021/ja0164374
  28. Donovan B.R., Ballenas J.E., Patton D.L. Macromolecules, 2016, 49, 7667–7675. doi: 10.1021/acs.macromol.6b01822
  29. Maji S., Asrey R., Kumar S., Saxena C., Kumar N., Vyas K.D., Banerjee S., J. Appl. Polym. Sci., 2010. 116, 3708–3717. doi: 10.1002/app.31942

Қосымша файлдар

Қосымша файлдар
Әрекет
1. JATS XML
2. Scheme 1. Copolymerisation of 4,4-bismaleinimidodiphenylmethane with diallyl bisphenol A

Жүктеу (94KB)
3. Scheme 2. Literature methods for the preparation of bismaleimides 7

Жүктеу (74KB)
4. Table 1. Dehydration of bismaleamic acid 9

Жүктеу (29KB)
5. Table 2. Optimisation of the preparation of 4,4-bis-(N-maleimidophenyl)methane 1 from methylenediphenyldiphenyldiamine 8

Жүктеу (27KB)
6. Scheme 3. Scheme for the synthesis of 2,4-bis-(N-maleimido)toluene 12

Жүктеу (49KB)
7. Scheme 4. Preparation of diallyl bisphenol A 15

Жүктеу (26KB)
8. Table 4. Optimisation of conditions for the preparation of diallyl ether of bisphenol A

Жүктеу (23KB)
9. Table 5. Optimisation of conditions for DABA production

Жүктеу (12KB)

© Russian Academy of Sciences, 2025