One-Step Synthesis of Monosilicon-Substituted Norbornenes with Siloxane and Aryl Fragments and Their Polymerization

Мұқаба

Дәйексөз келтіру

Толық мәтін

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

Аннотация

Three monosilicon-substituted norbornene monomers with phenyl and siloxane groups at the silicon atom are synthesized by the one-step hydrosilylation of 2,5-norbornadiene. The proposed method allows the synthesis of monomers with a higher content of polymerization-reactive exo-isomer in products compared with similar adducts formed by the Diels‒Аlder reaction. The synthesized monomers show high reactivity in both metathesis polymerization and addition polymerization more sensitive to the substituent volume. Using these monomers two series of high molecular weight silicon-substituted polynorbornenes are prepared which are found to be glassy and thermally stable polymers.

Авторлар туралы

M. Guseva

Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences

Email: d.alentiev@ips.ac.ru
119991, Moscow, Russia

P. Lezhnin

Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences

Email: d.alentiev@ips.ac.ru
119991, Moscow, Russia

D. Alentiev

Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences

Email: d.alentiev@ips.ac.ru
119991, Moscow, Russia

K. Zaitsev

Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences

Email: d.alentiev@ips.ac.ru
119991, Moscow, Russia

M. Bermeshev

Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences

Хат алмасуға жауапты Автор.
Email: d.alentiev@ips.ac.ru
119991, Moscow, Russia

Әдебиет тізімі

  1. Abakumov G.A., Piskunov A.V., Cherkasov V.K., Fedushkin I.L., Ananikov V.P., Eremin D.B., Gordeev E.G., Beletskaya I.P., Averin A.D., Bochkarev M.N., Trifonov A.A., Dzhemilev U.M., D’yakonov V.A., Egorov M.P., Vereshchagin A.N., Syroeshkin M.A., Jouikov V.V., Muza-farov A.M., Anisimov A.A., Arzumanyan A.V., Konone-vich Yu.N., Temnikov M.N., Sinyashin O.G., Budnikova Yu.H., Burilov A.R., Karasik A.A., Mironov V.F., Storozhenko P.A., Shcherbakova G.I., Trofimov B.A., Amosova S.V., Gusarova N.K., Potapov V.A., Shur V.B., Burlakov V.V., Bogdanov V.S., Andreev M.V. // Russ. Chem. Rev. 2018. V. 87. № 5. P. 393.
  2. Blanco I. // Polymers. 2021. V. 13. P. 188.
  3. Grushevenko E.A., Borisov I.L., Volkov A.V. // Pet. Chem. 2021. V. 61. № 9. P. 959.
  4. Khotimskii V.S., Filippova V.G., Bryantseva I.S., Bondar V.I., Shantarovich V.P., Yampolskii Yu.P. // J. Appl. Polym. Sci. 2000. V. 78. № 9. P. 1612.
  5. Kalmykov D., Balynin A., Yushkin A., Grushevenko E., Sokolov S., Malakhov A., Volkov A., Bazhenov S. // Membranes. 2022. V. 12. № 11. P. 1160.
  6. Wang X., Wilson T.J., Alentiev D., Gringolts M., Finkelshtein E., Bermeshev M., Long B.K. // Polym. Chem. 2021. V. 12. № 20. P. 2947.
  7. Alentiev D.A., Bermeshev M.V. // Polym. Rev. 2022. V. 62. № 2. P. 400.
  8. Zheng X.H., Zhao J.F., Zhao T.P., Yang T., Ren X.K., Liu C.Y., Yang S., Chen E.Q. // Macromolecules. 2018. V. 51. № 12. P. 4484.
  9. Sundell B.J., Lawrence J.A., Harrigan D.J., Vaughn J.T., Pilyugina T.S., Smith D.R. // RSC Adv. 2016. V. 6. № 57. P. 51619.
  10. Vaughn J.T., Harrigan D.J., Sundell B.J., Lawrence J.A., Yang J. // J. Membr. Sci. 2017. V. 522. P. 68.
  11. Maroon C.R., Townsend J., Gmernicki K.R., Harrigan D.J., Sundell B.J., Lawrence J.A., Mahurin S.M., Vogiatzis K.D., Long B.K. // Macromolecules. 2019. V. 52. № 4. P. 1589.
  12. Maroon C.R., Townsend J., Higgins M.A., Harrigan D.J., Sundell B.J., Lawrence J.A., O’Brien J.T., O’Neal D., Vogiatzis K.D., Long B.K. // J. Membr. Sci. 2020. V. 595. P. 117532.
  13. Hong T., Niu Z., Hu X., Gmernicki K., Cheng S., Fan F., Johnson J.C., Hong E., Mahurin S., Jiang D.E., Long B., Mays J., Sokolov A., Saito T. // Chem. Sus. Chem. 2015. V. 8. № 21. P. 3595.
  14. Gmernicki K.R., Hong E., Maroon C.R., Mahurin S.M., Sokolov A.P., Saito T., Long B.K. // ACS Macro Lett. 2016. V. 5. № 7. P. 879.
  15. Bermeshev M.V., Syromolotov A.V., Gringolts M.L., Lakhtin V.G., Finkelshtein E.Sh. // Tetrahedron Lett. 2011. V. 52. № 46. P. 6091.
  16. Guseva M.A., Alentiev D.A., Bermesheva E.V., Zamilatskov I.A., Bermeshev M.V. // RSC Adv. 2019. V. 9. № 57. P. 33029.
  17. García-Loma R., Albéniz A.C. // Asian J. Org. Chem. 2019. V. 8. № 3. P. 304.
  18. Suslov D.S., Bykov M.V., Kravchenko O.V. // Polymer Science C. 2019. V. 61. № 1. P. 145.
  19. Sundell B.J., Lawrence J.A., Harrigan D.J., Lin S., Headrick T.P., O’Brien J.T., Penniman W.F., Sandler N. // ACS Macro Lett. 2020. V. 9. № 9. P. 1363.
  20. Guseva M.A., Alentiev D.A., Bakhtin D.S., Borisov I.L., Borisov R.S., Volkov A.V., Finkelshtein E.Sh., Bermeshev M.V. // J. Membr. Sci. 2021. V. 638. P. 119656.
  21. Katsumata T., Shiotsuki M., Sanda F., Masuda T. // Polymer. 2009. V. 50. № 6. P. 1389.
  22. Gringol’ts M.L., Bermeshev M.V., Syromolotov A.V., Starannikova L.E., Filatova M.P., Makovetskii K.L., Finkel’shtein E.Sh. // Pet. Chem. 2010. V. 50. № 5. P. 352.

© М.А. Гусева, П.П. Лежнин, Д.А. Алентьев, К.В. Зайцев, М.В. Бермешев, 2023