DOI QR코드

DOI QR Code

Photo-alignment of Low-molecular Mass Nematic Liquid Crystals on Photochemically Bifunctional Chalcone-epoxy Film by Irradiation of a Linearly Polarized UV Light


Abstract

Photocrosslinkable chalcone-epoxy compound comprising 1,3-bis-(4-hydroxy-phenyl)-propenone was synthe-sized for fabricating the photo-alignment layer of liquid crystals. Chalcone group was introduced into the main chain unit of the epoxy oligomer. We observed a photodimerization behavior and an optical anisotropy of this material by irradiation of a linearly polarized UV(LP-UV) light. With a trace amount of cationic photoinitiator (TRS-HFA), polymerization of epoxy groups was also conducted at the similar wavelength range used for photodimerization. Linearly polarized UV irradiation on the chalcone-epoxy films with cationic photoinitiator induced optical anisotropy of the film and the resultant film can be used for alignment layers for low molecular weight nematic liquid crystals.

Keywords

References

  1. Chen, J.; Cull, B.; Bos, P.; Johnson, D.; Schadt, M. SID 95 Digest1995, 528.
  2. Park, B.; Jung, Y.; Choi, H.-H.; Hwang, H.-K.; Kim, Y.; Lee, S.;Jang, S.-H.; Kakimoto, M.; Takezoe, H. Jpn. J. Appl. Phys. 1998,37, 5663. https://doi.org/10.1143/JJAP.37.5663
  3. Ichimura, K. Chemical Review 2000, 100(5), 1847. https://doi.org/10.1021/cr980079e
  4. O'Neill, M.; Kelly, S. M. J. Phys. D: Appl. Phys. 2000, 33, R67. https://doi.org/10.1088/0022-3727/33/10/201
  5. Sekkat, Z.; Morichere, D.; Dumont, M.; Loucif-Saibi, R.; Delaire,J. J. Appl. Phys. 1992, 71, 1543. https://doi.org/10.1063/1.351228
  6. Ichimura, K.; Suzuki, T.; Kawanishi, Y.; Tamaki, T.; Aoki, K.Makromol. Chem. Rapid Commun. 1989, 10, 5. https://doi.org/10.1002/marc.1989.030100102
  7. Natansohn, A.; Rochon, P.; Meng, X.; Barrett, C.; Buffeteau, T.;Bonenfant, S.; Pezolet, M. Macromolecules 1998, 31, 1155. https://doi.org/10.1021/ma9712716
  8. Jain, S. C.; Kitzerow, H. S. Appl. Phys. Lett. 1994, 64, 2946. https://doi.org/10.1063/1.111419
  9. Ichimura, K. Liquid Crystals 1996, 3, 67.
  10. Schadt, M.; Seiberle, H.; Schuster, A. Nature 1996, 381, 212. https://doi.org/10.1038/381212a0
  11. Lien, A.; John, R. A.; Angelopoulos, M.; Lee, K. W.; Takano, H.;Tajima, K.; Takenaka, A. Appl. Phys. Lett. 1995, 67(21), 20.
  12. Murata, M.; Awaji, H.; Isurugi, M.; Uekita, M.; Tawada, Y. Jpn. J.Appl. Phys. 1992, 31, L189. https://doi.org/10.1143/JJAP.31.L189
  13. Janning, J. Appl. Phys. Lett. 1992, 21, 173. https://doi.org/10.1063/1.1654331
  14. Iimura, Y.; Kobayashi, S.; Hashimoto, T.; Sugiyama, T.; Katoh, K.IEICE Transactions on Electronics 1996, V.E79-C N.8.
  15. Makita, Y.; Natsui, T.; Kimura, S.; Kimura, M.; Matsuki, Y.;Takeuchi, Y. J. Photopoly. Sci. Technol. 1998, 11, 187. https://doi.org/10.2494/photopolymer.11.187
  16. Ichimura, K.; Akita, Y.; Akiyama, H.; Kudo, K.; Hayashi, Y.Macromolecules 1997, 30, 903. https://doi.org/10.1021/ma961225q
  17. Kaur, S.; Crivello, J. V.; Pascuzzi, N. J. Polym. Sci. A, Polym.Chem. Ed. 1999, 37(2), 199. https://doi.org/10.1002/(SICI)1099-0518(19990115)37:2<199::AID-POLA10>3.0.CO;2-4
  18. Crivello, J. V.; Liu, S. S. J. Polym. Sci. A, Polym. Chem. Ed. 1999,37(8), 1199. https://doi.org/10.1002/(SICI)1099-0518(19990415)37:8<1199::AID-POLA16>3.0.CO;2-L
  19. Lazauskaite, R.; Buika, G.; Grazulevicius, R.; Kavaliunas, R. Eur.Polym. J. 1998, 34(8), 1171. https://doi.org/10.1016/S0014-3057(97)00232-2
  20. Akelah, A.; Selim, A.; El-Deen, S. N. Polym. International 1992,28, 307. https://doi.org/10.1002/pi.4990280412
  21. Akelah, A.; Selim, A.; El-Deen, S. N. Polym. International 1993,32, 423. https://doi.org/10.1002/pi.4990320415
  22. Watanabe, S.; Harashima, S.; Tsukada, N. J. Polym. Sci. A Polym.Chem. Ed. 1986, 24, 1227. https://doi.org/10.1002/pola.1986.080240611
  23. Choi, D. H.; Oh, S. J.; Cha, H. B.; Lee, J. Y. Eur. Polym. J. 2001,37, 1943. https://doi.org/10.1016/S0014-3057(01)00092-1
  24. Kawatsuki, N.; Takatsuka, H.; Kawakami, Y.; Yamamoto, T.Polym. Adv. Technol. 1999, 10, 429. https://doi.org/10.1002/(SICI)1099-1581(199907)10:7<429::AID-PAT888>3.0.CO;2-Y
  25. Hsieh, H.-K.; Lee, T.-H.; Wang, J.-P.; Wang, J.-J.; Lin, C.-N.Pharmaceutical Research 1998, 15(1), 39. https://doi.org/10.1023/A:1011940401754
  26. Obi, M.; Morino, S.; Ichimura, K. Chem. Mater. 1999, 11, 656. https://doi.org/10.1021/cm980533v
  27. Choi, D. H.; Oh, S. J.; Ban, S. Y.; Oh, K. Y. Bull. Korean Chem.2001, 22(11), 1207.

Cited by

  1. Fabrication of pseudo-pi vertical alignment mode liquid crystal devices with ultra-violet polymerisation and investigations of their electro-optical characteristics vol.37, pp.8, 2010, https://doi.org/10.1080/02678291003746247
  2. Dynamic DSC curing kinetic study of epoxy resin of 1,3-bis(4-hydroxyphenyl) prop-2-en-1-one using aromatic diamines and phthalic anhydride vol.130, pp.1, 2013, https://doi.org/10.1002/app.39195
  3. Synthesis and characterisation of some new chalcone liquid crystals vol.44, pp.10, 2017, https://doi.org/10.1080/02678292.2017.1290283
  4. Synthesis and characterization of rigid rode shape homologous series: Effect of tail iodo group vol.652, pp.1, 2017, https://doi.org/10.1080/15421406.2017.1370958
  5. Synthesis and mesomorphic properties of calamitic shaped molecules with chalconyl-ester and lateral fluoro substituents vol.658, pp.1, 2017, https://doi.org/10.1080/15421406.2017.1412580
  6. ) tail groups vol.658, pp.1, 2017, https://doi.org/10.1080/15421406.2017.1412581
  7. Liquid crystalline photoactive hyperbranched and linear benzylidene polyester with terminal epoxy and pendant hydroxyl groups vol.45, pp.14, 2007, https://doi.org/10.1002/pola.22066
  8. Plasma-Beam-Processed Polyimide Films for the Alignment of Liquid Crystal Molecules vol.13, pp.12, 2002, https://doi.org/10.1149/1.3486449