Abstract
We designed and synthesized new smectic liquid crystalline monomers containing photopolymerizable acrylate groups and a mesogenic core unit composed of two benzene rings, one pyrimidine-based heteroaromatic ring and an acetylene linking group. The structures of monomers were characterized by 1H nuclear magnetic resonance spectroscopy, and their mesomorphic behaviors were investigated by differential scanning calorimetry and polarized optical microscopy. Both of monomers showed an enantiotropic phase transition behavior with exhibiting both nematic phase and highly ordered smectic phase. Both of monomers showed smectic phases during the cooling process in the temperature range of 144.2–94.0 °C and 154.0–85.8 °C, respectively. Neither of these compounds showed a homogeneous alignment even at various temperatures, and therefore, their 50:50 mixture was chosen for the preparation of guest-host mixture because of its lowest crystallization point, wide smectic phase temperature range and superior aligning property. Polymerizable “host-guest” mixture formulated from the host liquid crystalline monomer mixture, dichroic dye and additives was injected into the sandwiched glass substrates having rubbed alignment layers at the isotropic temperature. Subsequent in-situ photopolymerization by UV irradiation at room temperature successfully resulted in a thin film polarizer with good polarizing properties. The fabricated guest-host polarizer showed a dichroic ratio (DR) of 13.1 and a degree of polarization (DOP) of 95.5% with the thickness of 5 µm.
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References
P. Yeh and C. Gu, Optics of Liquid Crystal Displays, John Wiley & Sons, New Jersey, 2010.
K. J. Gåsvik, in Optical Metrology, John Wiley & Sons, West Sussex, England, 2003, pp 219–221.
X.-L. Ma, X.-C. Chen, L. Xiao, H.-Y. Wang, J.-F. Tan, P. Song, G. Shi, Y.-F. Yang, J. Lv, and D.-W. Wang, SID Symp. Digest, 48, 1735 (2017).
E. H. Land, J. Opt. Soc. Am., 41, 957 (1951).
M. M. Zwick, J. Polym. Sci. Part A-1: Polym. Chem., 4, 1642 (1966).
J. G. Pritchard and D. A. Akintola, Talanta, 19, 877 (1972).
W. J. Gunning and J. Foschaar, Appl. Opt., 22, 3229 (1983).
K. Miyasaka, Adv. Polym. Sci., 108, 91 (1993).
T. Yokoyama, K. Kaneyuki, H. Sato, H. Hamamatsu, and T. Ohta, Bull. Chem. Soc. Jpn., 68, 469 (1995).
W. Lyoo, J. Yeum, H. Ghim, J. Park, S. Lee, J. Kim, D. Shin, and J. Lee, Colloid Polym. Sci., 281, 416 (2003).
E. J. Shin, Y. H. Lee, and S. C. Choi, J. Appl. Polym. Sci., 91, 2407 (2004).
H. Mori, IMID’05 Digest, 1071 (2005).
F. Chimera, Flat Panel Display Materials: Trends and Forecasts 2009, Interlingua Publishing, Redondo Beach, 2009.
S.-M. Lee, J. H. Kwon, S. Kwon, and K. C. Choi, IEEE Trans. Elect. Devices, 64, 1922 (2017).
E. Peeters, J. Lub, J. A. M. Steenbakkers, and D. J. Broer, Adv. Mater., 18, 2412 (2006).
T. Sergan, T. Schneider, J. Kelly, and O. D. Lavrentovich, Liq. Cryst., 27, 567 (2000).
R. Piñol, J. Lub, M. P. García, E. Peeters, J. L. Serrano, D. Broer, and T. Sierra, Chem. Mater., 20, 6076 (2008).
S.-K. Park, S.-E. Kim, D.-Y. Kim, S.-W. Kang, S. Shin, S.-W. Kuo, S.-H. Hwang, S. H. Lee, M.-H. Lee, and K.-U. Jeong, Adv. Funct. Mater., 21, 2129 (2011).
P. Im, D.-G. Kang, D.-Y. Kim, Y.-J. Choi, W.-J. Yoon, M.-H. Lee, I.-H. Lee, C.-R. Lee, and K.-U. Jeong, ACS Appl. Mater. Interfaces, 8, 762 (2016).
H. Lu, Q. Zhang, J. Sha, M. Xu, J. Zhu, G. Zhang, Y. Ding, and L. Qiu, Liq. Cryst., 46, 1574 (2019).
V. G. Rumyantsev, A. V. Ivashchenko, V. M. Muratov, V. T. Lazareva, E. K. Prudnikova, and L. M. Blinov, Mol. Cryst. Liq. Cryst., 94, 205 (1983).
P. J. Collings, M. Hird, in Introduction to Liquid Crystals: Chemistry and Physics, CRC Press, Philadelphia, 2017, pp 43–46.
R. He, E. Oh, Y. Ye, P. Wen, K.-U. Jeong, S. H. Lee, X.-D. Li, and M.-H. Lee, Polymer, 176, 51 (2019).
A. V. Ivashchenko, Dichroic Dyes for Liquid Crystal Displays, CRC Press, 2018, Ch. 1.
G. Höfle, W. Steglich, and H. Vorbrüggen, Angew. Chem. Int. Ed., 17, 569 (1978).
B. Neises and W. Steglich, Angew. Chem. Inter. Ed., 17, 522 (1978).
A. Hassner and V. Alexanian, Tetrahedron Lett., 19, 4475 (1978).
K. Sonogashira, Y. Tohda, and N. Hagihara, Tetrahedron Lett., 17, 4467 (1975).
K. Sonogashira, J. Organomet. Chem., 653, 46 (2002).
K. T. Wong, F. C. Fang, Y. M. Cheng, P. T. Chou, G. H. Lee, and Y. Wang, J. Org. Chem., 69, 8038 (2004).
H. Sackmann and D. Demus, Mol. Cryst., 2, 81 (1966).
I. Dierking, in Textures of Liquid Crystals, John Wiley & Sons, 2003, pp 91–122.
D. Demus, J. W.Goodby, and G. W. Gray, Handbook of Liquid Crystals, Volume 2A: Low Molecular Weight Liquid Crystals I: Calamitic Liquid Crystals, John Wiley & Sons, 2011.
C. J. Kleverlaan and A. J. Feilzer, Dent. Mater., 21, 1150 (2005).
C. J. Drury, C. M. J. Mutsaers, C. M. Hart, M. Matters, and D. M. de Leeuw, Appl. Phys. Lett, 73, 108 (1998).
N. B. Cramer, J. W. Stansbury, and C. N. Bowman, J. Dent Res., 90, 402 (2010).
E. Smela and L. J. Martínez-Miranda, J. Appl. Phys., 73, 3299 (1993).
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Acknowledgments: This work was supported by the Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education (2018R1D1A1B07044250) and by Korea Institute for Advancement of Technology (KIAT) grant funded by the Korea Government (MOTIE) (P0002007, The Competency Development Program for Industry Specialist). MHL thanks to the financial support from the Polymer Materials Fusion Research Center and the research funds of Chonbuk National University in 2018.
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Ye, Y., He, R., Oh, E. et al. Syntheses and Properties of New Smectic Reactive Mesogens and Their Application in Guest-Host Polarizer. Macromol. Res. 28, 910–918 (2020). https://doi.org/10.1007/s13233-020-8121-1
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DOI: https://doi.org/10.1007/s13233-020-8121-1