Liquid crystal trimers. The synthesis and characterisation of the4,4′-bis[ω-(4-cyanobiphenyl-4′-yloxy)alkoxy]biphenyls

(Note: The full text of this document is currently only available in the PDF Version )

Corrie T. Imrie and Geoffrey R. Luckhurst


Abstract

The synthesis and characterisation of a homologous series of liquid crystal trimers, the 4,4′-bis[ω-(4-cyanobiphenyl-4′-yloxy)alkoxy]biphenyls, is reported in which the length of the flexible spacers is varied from 3 to 12 methylene units. All the members of the series exhibit enantiotropic nematic behaviour and, in addition, monotropic smectic A behaviour is observed for compounds with spacers containing from 4 to 11 methylene units. The formation of a smectic phase in these compounds is attributed to a specific interaction between the unlike mesogenic groups, namely, the central biphenyl and the terminal cyanobiphenyl units. The nematic–isotropic transition temperatures and the associated entropy changes exhibit a dramatic odd–even effect as the length and parity of the spacers is varied, in which the even members exhibit the higher values. This behaviour is interpreted in terms of the geometry as well as the flexibility of the spacers and how these control the average molecular shape. A comparison of the magnitudes of these odd–even effects with those for the analogous dimeric series suggests that in the nematic phase the mesogenic units in the trimers are correlated to the same extent as in the dimers but that their orientational ordering is significantly higher.


References

  1. H. Finkelmann, in Thermotropic Liquid Crystals, ed. G. W. Gray, Wiley, Chichester, 1987, ch. 6 Search PubMed.
  2. C. K. Ober, J.-I. Jin and R. W. Lenz, Adv. Polym. Sci., 1984, 59, 103 CAS.
  3. A. Blumstein and O. Thomas, Macromolecules, 1982, 15, 1264 CrossRef CAS.
  4. G. W. Gray, in The Molecular Physics of Liquid Crystals, ed. G. R. Luckhurst and G. W. Gray, Academic Press, London, 1979, ch. 1 Search PubMed.
  5. C. T. Imrie and G. R. Luckhurst, in Handbook of Liquid Crystals, vol. 2B, ed. D. Demus, J. Goodby, G. W. Gray, H.-W. Spiess and V. Vill, Wiley-VCH, Weinheim, 1998, ch. 10, pp. 801–834 Search PubMed.
  6. G. R. Luckhurst, Macromol. Symp., 1995, 96, 1 CAS.
  7. A. C. Griffin and T. R. Britt, J. Am. Chem. Soc., 1981, 103, 4957 CrossRef CAS.
  8. J. W. Emsley, G. R. Luckhurst, G. N. Shilstone and I. Sage, Mol. Cryst. Liq. Cryst. Lett., 1984, 102, 223 Search PubMed.
  9. H. Furuya, K. Asahi and A. Abe, Polym. J., 1986, 18, 779 Search PubMed.
  10. G. S. Attard and C. T. Imrie, Liq. Cryst., 1989, 6, 387 CAS.
  11. R. Centore, A. Roviello and A. Sirigu, Mol. Cryst. Liq. Cryst., 1990, 182B, 233 CAS.
  12. T. Ikeda, T. Miyamoto, S. Kurihara, M. Tsukada and S. Tazuke, Mol. Cryst. Liq. Cryst., 1990, 182B, 357 CAS.
  13. A. T. Marcelis, A. Koudijs and E. J. R. Sudhölterr, Liq. Cryst., 1996, 21, 87 CAS.
  14. A. T. Marcelis, A. Koudijs and E. J. R. Sudhölterr, Liq. Cryst., 1995, 18, 851 CAS.
  15. N. V. Tsvetkov, V. V. Zuev and V. N. Tsvetkov, Liq. Cryst., 1997, 22, 245 CrossRef CAS.
  16. A. C. Griffin, S. L. Sullivan and W. E. Hughes, Liq. Cryst., 1989, 4, 677 CAS.
  17. C. T. Imrie, D. Stewart, C. Remy, D. W. Christie, I. W. Hamley, R. Harding and J. Pople, unpublished work.
  18. D. Demus, Liq. Crys., 1989, 5, 75 Search PubMed.
  19. K. Zab, D. Joachimi, E. Novotna, S. Diele and C. Tschierske, Liq. Cryst., 1995, 18, 631 CAS.
  20. V. Percec and M. Kawasumi, J. Mater. Chem., 1993, 3, 725 RSC.
  21. J. W. Emsley, G. R. Luckhurst and G. N. Shilstone, Mol. Phys., 1984, 53, 1023 CAS.
  22. J. W. Emsley, G. R. Luckhurst and B. A. Timimi, Chem. Phys. Lett., 1985, 114, 19 CrossRef CAS.
  23. D. A. Dunmur and M. R. Wilson, J. Chem. Soc., Faraday Trans. 2, 1988, 84, 961 RSC.
  24. G. S. Attard, C. T. Imrie and F. E. Karasz, Chem. Mater., 1992, 4, 1246 CrossRef CAS.
  25. R. W. Date, C. T. Imrie, G. R. Luckhurst and J. M. Seddon, Liq. Cryst., 1992, 12, 203 CAS.
  26. J. L. Hogan, C. T. Imrie and G. R. Luckhurst, Liq. Cryst., 1988, 3, 645 CAS.
  27. G. S. Attard, S. Garnett, C. G. Hickman, C. T. Imrie and L. Taylor, Liq. Cryst., 1990, 7, 495 CAS.
  28. A. E. Blatch, I. D. Fletcher and G. R. Luckhurst, Liq. Cryst., 1995, 18, 801 CAS.
  29. C. T. Imrie, F. E. Karasz and G. S. Attard, Macromolecules, 1993, 26, 3803 CrossRef CAS.