Journal of Sol-Gel Science and Technology

, Volume 32, Issue 1–3, pp 63–67 | Cite as

Lamellar Organo-Bridged Silicones

  • Joël J. E. Moreau
  • Luc Vellutini
  • Catherine Bied
  • Michel Wong Chi Man
Article

Abstract

The acid-hydrolysis of an organo-bridged bisdiethoxysilylated molecular precursor bearing urea groups, (EtO)2MeSi(CH2)3NHCONH(CH2)12NHCONH(CH2)3SiMe(OEt)2, has been performed in pure aqueous medium. Scanning electron microscopy (SEM) analysis of the resulting insoluble solid revealed plate-like forms with a lamellar structure as determined by powder X-ray diffraction (PXRD) studies with a sharp peak at 28.5 Å. The solid state 29Si MAS-NMR spectrum of this bridged siloxane hybrid is consistent with a moderately condensed material with complete preservation of the Si–C bonds throughout the hybrid network. In comparison, the classical sol–gel hydrolysis-condensation of the molecular precursor in ethanol with stoichiometric amount of water and fluoride anion as catalyst produced an amorphous featureless solid.

Keywords

lamellar silicones nano-structured materials organo-bridged hybrid sol–gel 

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. 1.
    K.J. Shea, D.A. Loy, and O.W. Webster, Chem. Mater. 1, 512 (1989).Google Scholar
  2. 1.
    K.J. Shea, D.A. Loy, and O.W. Webster, J. Amer. Chem. Soc. 114, 6700 (1992)Google Scholar
  3. 1.
    K.J. Shea, and D.A. Loy, Chem. Rev. 95, 1431 (1995)Google Scholar
  4. 1.
    K.J. Shea, and D.A. Loy, Chem. Mater. 19, 3306 (2001)Google Scholar
  5. 1.
    K.J. Shea, D.A. Loy, Acc. Chem. Res. 34, 707 (2001).Google Scholar
  6. 2.
    R.J.P. Corriu, J.J.E. Moreau, P. Thépot, and M. Wong Chi Man, Chem. Mater. 4, 1217 (1992)Google Scholar
  7. 2.
    R.J.P. Corriu, and D. Leclerc, Angew. Chem., Int. Ed. Engl. 35, 1420 (1996)Google Scholar
  8. 2.
    J.J.E. Moreau, and M. Wong Chi Man, Coord. Rev. 178–180, 1073 (1998)Google Scholar
  9. 2.
    R.J.P. Corriu, Angew. Chem., Int. Ed. Engl. 39, 1376 (2000).Google Scholar
  10. 3.
    U. Schubert, New J. Chem. 18, 1049 (1994)Google Scholar
  11. 3.
    U. Schubert, N. Hüsing, and A. Lorenz, Chem. Mater. 7, 2012 (1995)Google Scholar
  12. 3.
    A. Adima, J.J.E. Moreau, and M. Wong Chi Man, J. Mater. Chem. 7, 2331 (1997)Google Scholar
  13. 3.
    A. Adima, J.J.E. Moreau, and M. Wong Chi Man, Chirality 12, 411 (2000)Google Scholar
  14. 3.
    P. Hesemann, and J.J.E. Moreau, Tetrahedron: Asymmetry 11, 2183 (2000)Google Scholar
  15. 3.
    A. Adima, J.J.E. Moreau, and M. Wong Chi Man, Chirality 12, 411 (2000)Google Scholar
  16. 3.
    E. Lindner, T. Schneller, F. Auer, and H.A. Mayer, Angew. Chem., Int. Ed. Engl. 38, 2154 (1999).Google Scholar
  17. 4.
    J.-C. Broudic, O. Conocar, J.J.E. Moreau, D. Meyer, and M. Wong Chi Man, J. Mater. Chem. 9, 2283 (1999)Google Scholar
  18. 4.
    S. Bourg, J.-C. Broudic, O. Conocar, J.J.E. Moreau, D. Meyer, and M. Wong Chi Man, Mater. Res. Soc. Symp. Proc. 628, CC1.6.1 (2000).Google Scholar
  19. 5.
    B. Lebeau and S. Brasselet, J. Zyss, C. Sanchez, Chem. Mater. 9, 1012 (1997).Google Scholar
  20. 6.
    C.T. Kresge, M.E. Leonowicz, W.J. Roth, J.C. Vartulli, and J.S. Beck, Nature. 359, 710 (1992)Google Scholar
  21. 6.
    J.S. Beck, J.C. Vartulli, W.J. Roth, M.E. Leonowicz, C.T. Kresge, K.D. Schmitt, C.T.-W. Chu, D.H. Olson, E.W. Sheppard, S.B. McCullen, J.B. Higgins, and J.L. Schlenker, J. Am. Chem. Soc. 114, 10834 (1992).Google Scholar
  22. 7.
    S. Inagaki, S. Guan, Y. Fukushima, T. Ohsuna, and O. Terasaki, J. Am. Chem. Soc. 121, 9611 (1999)Google Scholar
  23. 7.
    S. Guan, S. Inagaki, T. Ohsuna, and O. Terasaki, J. Am. Chem. Soc. 122, 5660 (2000)Google Scholar
  24. 7.
    S. Guan, S. Inagaki, T. Ohsuna, and O. Terasaki, Nature 416, 304 (2002).Google Scholar
  25. 8.
    B.J. Melde, B.T. Holland, C.F. Blanford, and A. Stein, Chem. Mater. 11, 3302 (1999).Google Scholar
  26. 9.
    Asefa, M.J. MacLachlan, N. Coombs, and G.A. Ozin,. Nature 402, 867 (1999)Google Scholar
  27. 9.
    M.J. MacLachlan, T. Asefa, and G.A. Ozin, Chem. Eur. J. 2507 (2000).Google Scholar
  28. 10.
    Y. Lu, H. Fan, N. Doke, D.A. Loy, R.A. Assink, D.A. LaVan, and C.J. Brinker, J. Am. Chem. Soc. 122, 5258 (2000).Google Scholar
  29. 11.
    V. Goletto, A.-C. Bled, G. Trimmel, M. Wong Chi Man, H.-G. Woo, D. Durand, and F. Babonneau, Mater. Res. Soc. Symp. Proc. 726, 123 (2002).Google Scholar
  30. 12.
    J.J.E. Moreau, L. Vellutini, M. Wong Chi Man, and C. Bied, J. Amer. Chem. Soc. 123, 1509 (2001).Google Scholar
  31. 13.
    J.J.E. Moreau, L. Vellutini, M. Wong Chi Man, and C. Bied, Chem. Eur. J. 9, 1594 (2003).Google Scholar
  32. 14.
    J.J.E. Moreau, L. Vellutini, M. Wong Chi Man, C. Bied, J.-L. Bantignies, P. Dieudonné, and J.-L. Sauvajol, J. Amer. Chem. Soc. 123, 7957 (2001).Google Scholar
  33. 15.
    H. Tang, J. Sun, J. Jiang, X. Zhou, T. Hu, P. Xie, and R. Zhang, J. Amer. Chem. Soc. 124, 10482 (2002).Google Scholar

Copyright information

© Kluwer Academic Publishers 2004

Authors and Affiliations

  • Joël J. E. Moreau
    • 1
  • Luc Vellutini
    • 1
  • Catherine Bied
    • 1
  • Michel Wong Chi Man
    • 1
  1. 1.Hétérochimie Moléculaire et MacromoléculaireUMR CNRS 5076, (ENSCM) Ecole Nationale Supérieure de Chimie de Montpellier 8Montpellier Cédex 5France

Personalised recommendations