Formation of smectic and columnar liquid crystalline phases by cyclotriveratrylene (CTV) and cyclotetraveratrylene (CTTV) derivatives incorporating calamitic structural units

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Ralph Lunkwitz, Carsten Tschierske and Siegmar Diele


Abstract

Novel liquid crystalline oligomesogens, which consist of five, six or eight calamitic 4-cyanobiphenyl, 2-alkyl-5-phenyl-1,3,4-thiadiazole or 5-octyl-2-phenylpyrimidine units covalently linked by spacers of different length with a cyclotribenzylene central core (CTV derivatives, 2,3,7,8,12,13-hexa-substituted 10,15-dihydro-5H-tribenzo[a,d,g]cyclononenes) or a cyclotetrabenzylene central core (CTTV derivatives, 2,3,6,7,10,11,14,15-octa-substituted 5,10,15,20-tetrahydrotetrabenzo[a,d,g,j]cyclododecenes) have been synthesized. These compounds were investigated by polarizing microscopy, differential scanning calorimetry and some of them were also studied by X-ray diffraction. Many of the CTV derivatives show liquid crystalline properties. The cyanobiphenyl derivatives incorporating long spacer units have enantiotropic SA phases which can easily be supercooled. The thiadiazole derivatives and the pyrimidine derivatives have liquid crystalline phases only if the spacer units are rather short. Thiadiazole derivatives with an odd number of connecting atoms between the CTV core and the calamitic mesogens form SA phases, whereas those with even-numbered spacers display columnar mesophases. We propose that the columnar mesophases observed for these oligomesogens do not result from their ability to adopt a nearly disc-like shape. Instead, they represent ribbon phases which result from a steric frustration caused by the different space filling of the central cone-like core and the rod-like mesogenic groups. A chevron-like (banana-like) average shape of the molecules with even-numbered spacers is assumed to be responsible for the formation of the ribbon phases.

Also a CTTV derivative with eight appended phenylthiadiazole mesogens displays a columnar mesophase. A nematic phase was found for the corresponding cyanobiphenyl derivative, whereas the pyrimidine derivative is not liquid crystalline.


References

  1. B. Bahadur, Liquid Crystals Application and Uses, World Scientific, Singapore, 1990, Vol. 1–3 Search PubMed.
  2. D. M. Walba, M. B. Ros, T. Sierra, J. A. Rego, N. A. Clark, R. Shao, M. D. Wand, R. T. Vohra, K. E. Arnett and S. P. Velsco, Ferroelectrics, 1991, 121, 147; K. Schmitt, R.-P. Herr, M. Schadt, J. Fünfschilling, R. Buchecker, X. H. Chen and C. Benecker, Liq. Cryst., 1993, 14, 1735 CAS.
  3. F. Closs, K. Siemensmeyer, Th. Frey and D. Funhof, Liq. Cryst., 1993, 14, 629 CrossRef CAS.
  4. S. Chandrasekhar, Liq. Cryst., 1993, 14, 3 CrossRef CAS.
  5. S. Chandrasekhar, Mol. Cryst. Liq. Cryst., 1994, 243, 1 Search PubMed.
  6. K. Borisch, S. Diele, P. Göring, H. Müller and C. Tschierske, Liq. Cryst., 1995, 18, 175 CrossRef CAS.
  7. H.-T. Nguyen, C. Destrade and J. Malthete, Adv. Mater., 1997, 9, 375 CrossRef CAS.
  8. I. D. Fletcher and G. R. Luckhurst, Liq. Cryst., 1995, 18, 175 CrossRef CAS.
  9. W. Kreuder, H. Ringsdorf, O. Herrmann-Schönherr and J. H. Wendorff, Angew. Chem., 1987, 99, 1300 CAS.
  10. H. Budig, S. Diele, P. Göring, R. Paschke, C. Sauer and C. Tschierske, J. Chem. Soc., Chem. Commun., 1994, 2359 RSC.
  11. H. Budig, S. Diele, P. Göring, R. Paschke, C. Sauer and C. Tschierske, J. Chem. Soc., Perkin Trans. 2, 1995, 767 RSC.
  12. J. Malthete and A. Collet, J. Am. Chem. Soc., 1987, 109, 7544 CrossRef CAS.
  13. H. Zimmermann, R. Poupko, Z. Luz and J. Billard, Z. Naturforsch. Teil A, 1985, 40, 149.
  14. L. Lei, Mol. Cryst. Liq. Cryst., 1987, 146, 41.
  15. H. Zimmermann, R. Poupko, Z. Luz and J. Billard, Z. Naturforsch. Teil A, 1986, 41, 1137.
  16. C. Tschierske and H. Zaschke, J. Prakt. Chem., 1989, 331, 365 CrossRef CAS.
  17. A. S. Lindsey, J. Chem. Soc., 1965, 1685 RSC.
  18. V. Percec, C. G. Cho and C. Pugh, J. Mater. Chem., 1991, 1, 217 RSC.
  19. G. W. Gray, K. J. Harrison and J. A. Nash, Pramana, 1975, 1, 381 Search PubMed.
  20. A. Collet, Tetrahedron, 1987, 43, 5725 CrossRef CAS; J. A. Hyatt, E. N. Duesler, D. Y. Curtin and I. C. Paul, J. Org. Chem., 1980, 45, 5074 CrossRef CAS; A. Collet, J. Gabard, J. Jacques, M. Cesario, J. Guilhem and C. Pscard, J. Chem. Soc., Perkin Trans., 1981, 1630 Search PubMed.
  21. P. Barois, J. Pommier and J. Prost, in Solitons in Liquid Crystals, ed. L. Lam and J. Prost, Springer, Heidelberg, 1991, p. 191 Search PubMed.
  22. B. J. Ostrovskii, Liq. Cryst., 1993, 14, 131.
  23. F. Hardouin, A. M. Levelut, M. F. Achard and Sigaud, J. Chim. Phys., 1983, 80, 53 CAS.
  24. F. Hardouin, A. M. Levelut and G. Sigaud, J. Phys. Fr., 1981, 42, 71 Search PubMed.
  25. W. Weissflog, A. Wiegeleben, S. Diele and D. Demus, Liq. Cryst., 1984, 19, 983.
  26. J. Watanabe, Y. Nakata and K. Simizu, J. Phys. II, 1994, 4, 581 Search PubMed.
  27. P. Davidson, P. Keller and A. M. Levelut, J. Phys., 1985, 46, 939 Search PubMed.
  28. B. W. Endres, M. Ebert, J. H. Wendorff, B. Reck and H. Ringsdorf, Liq. Cryst., 1990, 7, 217 CAS.
  29. T. A. Lobko and B. I. Ostrovskii, Mol. Mater., 1992, 1, 99 Search PubMed.
  30. H. T. Nguyen, G. Sigaud, M. F. Achard, F. Hardouin, R. J. Twieg and K. Betterton, Liq. Cryst., 1991, 10, 389.
  31. R. W. Date, G. R. Luckhurst, M. Shuman and J. M. Seddon, J. Phys., 1995, 42, 587 Search PubMed.
  32. F. Hardouin, M. F. Achard, J.-I. Jin and Y.-K. Yun, J. Phys. II, 1995, 5, 927 Search PubMed.
  33. V. Faye, F. Babeau, F. Placin, H. T. Nguyen, P. Barios, V. Laux and N. Isaert, Liq. Cryst., 1996, 21, 485 CrossRef.
  34. T. Niori, T. Sekine, J. Watanabe, T. Furukawa and H. Takazoe, J. Mater. Chem., 1996, 6, 1231 RSC.
  35. C. Tschierske, H. Zaschke, H. Kresse, A. Mädicke and D. Demus, Mol. Cryst. Liq. Cryst., 1990, 191, 223 CAS.
  36. H. Zaschke and R. Stolle, Z. Chem., 1975, 15, 441 CAS.
  37. Organicum, Deutscher Verlag der Wissenschaften, Berlin 1993, pp. 577 and 591 Search PubMed.
  38. A. M. Levelut and K. Moriya, Liq. Cryst., 1996, 20, 119 CAS.
  39. G. H. Mehl and J. W. Goodby, Chem. Ber., 1996, 129, 521 CrossRef CAS.
  40. P. Göring, G. Pelzl, S. Diele, P. Delavier, K. Siemensmeyer and K. H. Etzbach, Liq. Cryst., 1995, 19, 629.
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