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

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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.

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Sobre autores

E. Kudryashova

Lobachevsky Nizhny Novgorod State University

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

V. Otvagin

Lobachevsky Nizhny Novgorod State University

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

K. Romanov

Lobachevsky Nizhny Novgorod State University

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

E. Afanasyeva

Lomonosov Moscow State University

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

O. Morozov

Lomonosov Moscow State University

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

A. Babkin

Lomonosov Moscow State University

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

A. Kepman

Lomonosov Moscow State University

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

A. Fedorov

Lobachevsky Nizhny Novgorod State University

Autor responsável pela correspondência
Email: afedorovNN@yandex.ru
Rússia, 23, Gagarin Ave., Nizhny Novgorod, 603950

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

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3. Scheme 2. Literature methods for the preparation of bismaleimides 7

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4. Table 1. Dehydration of bismaleamic acid 9

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

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

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7. Scheme 4. Preparation of diallyl bisphenol A 15

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8. Table 4. Optimisation of conditions for the preparation of diallyl ether of bisphenol A

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9. Table 5. Optimisation of conditions for DABA production

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