New Membrane Materials Via Catalytic Polymerization of Bis(Trimethylsilyl)-Substituted Norbornene Type Monomers

  • Maxim V. Bermeshev
  • Maria L. Gringolts
  • Ludmila E. Starannikova
  • Alexei V. Volkov
  • Eugene Sh. Finkelstein
Part of the NATO Science for Peace and Security Series A: Chemistry and Biology book series (NAPSA)

Abstract

In this work we summarize our results of investigation on ring-opening metathesis (ROMP) and addition polymerization (AP) of a range of norbornene, norbornadiene and tricyclononene monomers containing two Me3Sisubstituents. The tested monomers exhibited different reactivity in ROMP and AP. The new polymers obtained demonstrated high gas permeability and allowed defining some correlations between features of their chemical structure and gas separation characteristics.

Keywords

Silyl norbornenes ROMP Addition polymerization Gas permeability 

Notes

Acknowledgment

The authors would like to thank Dr. V. Lakhtin for the preparation of bis(trichlorosilyl)ethyne and 1,2-trans-bis(trichlorosilyl)ethylene.

This work was supported by The Russian Foundation of Basic Research 09-03-00342-a and The Russian Science Support Foundation.

References

  1. [1]
    Mulder M. Basic Principles of Membrane Technology. Dordrecht, Kluwer, 1998.Google Scholar
  2. [2]
    Makovetskii KL. Polym. Sci. Ser. C. 2008; 50: 22l–38.CrossRefGoogle Scholar
  3. [3]
    Ivin KJ, Mol JC. Olefin Metathesis and Metathesis Polymerization. San Diego, CA: Academic Press, 1997.Google Scholar
  4. [4]
    Grubbs RH (Ed.). Handbook of Metathesis. Weinheim. Wiley-VCH, 2003.CrossRefGoogle Scholar
  5. [5]
    Gaylord NG, Deshpande AB, Mandal BM, Martan M. J. Macromol. Sci. Chem. A. 1977; 11/5: 1053l–1070.CrossRefGoogle Scholar
  6. [6]
    Peetz RM, Moustafa AF, Kennedy JP. J Polym Sci Part A Polym Chem. 2003; 41: 732l–739.CrossRefGoogle Scholar
  7. [7]
    Diels O, Alder K. Ann. 1928; 460: 98.Google Scholar
  8. [8]
    Stockmann G. J. Org. Chem. 1971; 26: 2025l–2029.CrossRefGoogle Scholar
  9. [9]
    Finkelshtein ESh, Bespalova NB, Portnykh EB, Makovetskii KL, Ostrovskaya IYa, Shishatskii SM, Yampolskii YuP, Plate NA, Kaliuzhnyi NE. Polym. Sci. A. 1993; 35: 589.Google Scholar
  10. [10]
    Bondar V, Kukharskii Yu, Yampolskii Yu, Finkelshtein E, Makovetskii K. J. Polym. Sci. Part B: Polym. Phys. 1993; 31: 1273l–1283.CrossRefGoogle Scholar
  11. [11]
    Finkelshtein ESh, Gringolts ML, Ushakov NV, Lakhtin VG, Soloviev SA, Yampol'skii YuP. Polymer 2003; 44: 2843l–2851.CrossRefGoogle Scholar
  12. [12]
    Bermeshev MV, Gringolts ML, Lakhtin VG, Finkel–shtein Esh. Petroleum Chem. 2008; 48: 302l–308.CrossRefGoogle Scholar
  13. [13]
    Gringolts ML, Bermeshev MV, Makovetsky KL, Finkelshtein ESh, Eur. Pol. J. 2009; 45: 2142l–2149.CrossRefGoogle Scholar
  14. [14]
    Finkelshtein ESh, Makovetskii KL, Gringolts ML, Rogan YV, Golenko TG, Lakhtin VG, Filatova MP. J. Mol. Cat. A Chem. 2006; 257: 9l–13.CrossRefGoogle Scholar
  15. [15]
    Gringolts ML, Bermeshev MV, Starannikova LE, Rogan YV, Yampolskii YuP, Finkelshtein ESh. Polym. Sci. Ser. C. 2009, 51, in press.Google Scholar
  16. [16]
    Finkelshtein ESh, Makovetskii KL, Gringolts ML, Rogan YV, Golenko TG, Starannikova LE et al. Macromolecules. 2006; 39(20): 7022l–7029.CrossRefGoogle Scholar

Copyright information

© Springer Science+Business Media B.V. 2009

Authors and Affiliations

  • Maxim V. Bermeshev
    • 1
  • Maria L. Gringolts
    • 1
  • Ludmila E. Starannikova
    • 1
  • Alexei V. Volkov
    • 1
  • Eugene Sh. Finkelstein
    • 1
  1. 1.Russian Academy of SciencesA.V Topchiev Institute of Petrochemical SynthesisMoscowRussia

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