| 研究生: |
許惠晴 Hsu, Hui-Ching |
|---|---|
| 論文名稱: |
光聚合性膽固醇型液晶元件之製備及光學特性研究 Preparation and Optical Behavior of Photopolymerized Cholesteric Liquid Crystal Cells |
| 指導教授: |
劉瑞祥
Liu, Jui-Shiang |
| 學位類別: |
碩士 Master |
| 系所名稱: |
工學院 - 化學工程學系 Department of Chemical Engineering |
| 論文出版年: | 2004 |
| 畢業學年度: | 92 |
| 語文別: | 中文 |
| 論文頁數: | 112 |
| 中文關鍵詞: | 膽固醇液晶 、光聚合 |
| 外文關鍵詞: | cholesteric liquid crystal, photopolymerized |
| 相關次數: | 點閱:86 下載:4 |
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本實驗合成不同碳鏈長度的單官能性液晶單體4-butoxyphenyl- 4’-(6-acryloyloxyhexyloxy)benzoate、4-butoxyphenyl-4’-(3-acryloyloxy- propyloxy)benzoate、4-butoxyphenyl-4’-(11-acryloyloxyundecyloxy) benzoate、兩種雙官能性單體1,4-di-〔4-(6-acryloyloxyhexyloxy) benzoyloxy〕benzene與4,4’-bis(6-(acryloyloxy)hexyloxy)biphenyl,及含甲氧烷基之偶氮苯衍生物4-hexyloxy-4’-methoxy-azobenzene。所合成之化合物均使用FTIR、1H-NMR、EA、DSC等儀器來加以鑑定。實驗過程中,將液晶ZLI-2293與光學活性摻混物S811混和均勻,製作成膽固醇液晶薄膜,可調配出在可見光區域有選擇性光反射的光學薄膜;再分別添加入不同配方及比例的官能性單體,探討照光聚合後對膽固醇液晶主體選擇性光反射波段(△λ)移轉之影響。另外,亦於系統中添加不同的偶氮苯衍生物,其一具有旋光性,另一個則無;探討此二種偶氮苯衍生物在照光聚合前、後對系統選擇性光反射波段的影響。藉由照射紫外光與可見光之間的轉換,可得到不同的選擇性光反射波段。
A series of monofunctional liquid crystalline monomers of 4-butoxyphenyl-4’-(6-acryloyloxyhexyloxy)benzoate, 4-butoxyphenyl-4’ -(3-acryloyloxy-propyloxy)benzoate, 4-butoxyphenyl-4’-(11-acryloyloxy undecyloxy)benzoate with various spacer lengths, two kinds of difunctional monomers of 1,4-di-〔4-(6-acryloyloxyhexyloxy) benzoyloxy〕benzene and 4,4’-bis(6-(acryloyloxy)hexyloxy)biphenyl, and photoisomerizable 4-hexyloxy-4’-methoxy-azobenzene were synthesized. Compounds synthesized in this investigation were confirmed using FTIR, 1H-NMR, DSC, and EA. Cholesteric liquid crystal cells were fabricated using commercially available ZLI-2293/S811 cholesteric liquid crystals and synthesized functional monomers. Effects of chiral and achiral monomers on the reflected band, light transmittance, stability, and reliability of the cholesteric liquid crystal cells were investigated in detail. Azobenzene derivatives were found to affect the optical properties of the cholesteric liquid crystal cells. Optical textures of the prepared cholesteric liquid crystals and morphologies of polymer matrixes were all investigated.
1. 松本正一、角田市良合著,劉瑞祥譯,“液晶之基礎與應用”國立編譯館出版。
2. F. Reinitzer, Monatsh. Chem., Vol. 9, 421 (1888).
3. O. Z. Lehmann, Phys. Chem., 4, 4621 (1889).
4. 蔡宗岳,“含光學活性單體PSCT液晶顯示元件之光電特性研究”國立成功大學化工研究所碩士論文,(1999)。
5. 蔡月娥, “雙官能機單體間隙長度對PSCT液晶顯示器光電特性效應之研究” 國立成功大學化工研究所碩士論文,(2000)。
6. D. Demus, J. Goodby, G. W. Gray, H. W. Spiess, V. Vill, ”Handbook of Liquid crystals”, Vol. 2a, 2b, Wiley-VCH, (1998).
7. 黃啟炎, ”液晶-聚合物混合薄膜之光學二倍頻現象之研究” 國立成功大學物理研究所博士論文,(1997)。
8. 林志勤,“鐵電性液晶對聚合物穩定膽固醇液晶薄膜光電特性影響之研究”,國立成功大學物理研究所碩士論文,(1998)。
9. 湯宏東,“含環氧基鐵電性液晶體的合成及性質研究”國立成功大學化工研究所碩士論文,(1998)。
10. M. Irie, Chem. Rev., vol. 100, 1683 (2000).
11. H. Bouas-Laurent, H. Dürr, Pure Appl. Chem., Vol. 73, 639 (2001).
12. 邱顯堂,“化工技術”第八卷第六期,150.
13. I. Shimizu, H. Kokado, E. Inoue, Bull. Chem. Soc. Jpn., Vol. 42, 1730 (1969).
14. 楊博智, “含硝基偶氮苯衍生基光敏性液晶高分子之合成及特性探討” 國立成功大學化工研究所碩士論文,(2003)。
15. H. K. Lee, A. Kanazawa, T. Shiono, T. Ikeda, Chem. Mater., Vol. 10,
1402 (1998).
16. H. K. Lee, K. Doi, H. Harada, O. Tsutsumi, A. Kanazawa, T. Shiono, T. Ikeda, J. Phys. Chem.B, Vol. 104, 7023 (2000).
17. T. Ikeda, O. Tsutsumi, Science, Vol. 268, 1873 (1995).
18. P. Rechon, J. Gosselin, A. Natansohn, S. Xie, Appl Phys Lett , Vol. 60, 4 (1992).
19. Y. Wu, A. Kanazawa, T. Shiono, T. Ikeda, Q. Zhang, Polymer, Vol. 40, 4787 (1999).
20. K. Amundson, M. Srinivasarao, Liquid crystals for advanced techenologies, 269 (1996).
21. H. K. Lee, K. Doi, A. Kanazawa, T. Shiono, T. Ikeda, T. Fujisawa, M. Aizawa, B. Lee, Polymer, Vol. 41, 1757 (2000).
22. N. Tamaoki, A. V. Parfenov, A. Masaki, H. Matsuda, Adv. Mater., Vol. 9, 1102 (1997).
23. M. Brehmer, J. Lub, P. van de Witte, Adv. Mater., Vol. 10, 1438 (1998).
24. E. Sackmann, J. Am. Chem. Soc. Vol. 93, 7088 (1971).
25. H. K. Lee, K. Doi, Hisako, O. Tsutsumi, A. Kanazawa, T. Shiono, T. Ikeda, J. Phys. Chem. B, Vol. 104, 7023 (2000).
26. R. A. M. Hikmet, H. Kemperman, Liquid Crystals, Vol. 26, 1645 (1999).
27. H. Guillard, P. Sixou, L. Reboul, A. Perichaud, Polymer, Vol. 42, 9753 (2001).
28. V. Shibaev, A. Bobrovsky, N. Boiko, Journal of Photochemistry and Photobiology A: Chemistry. Vol. 155, 3 (2003).
29. J. H. Liu, H.U. Wang, Journal of Applied Polymer Science, Vol. 91, 789 (2004).
30. M. Portugall, H. Ringsdorf, R. Zentel, Makromol. Chem.,Vol. 183, 2311 (1982).
31. X. Meng, A. Natansohn, C.Barrett, P, Rochon, Macromolecules, Vol. 29, 946 (1996).
32. K. Kürschner, P. Strohriegl, Liquid Crystals, Vol. 27, 1595 (2000).
33. M. C. Artal, M. B. Ros, J. L. Serrano, Chem. Mater., Vol. 13, 2056 (2001).
34. I. Dierking, L. L. kosbar, A. Afzali-Ardakani, A.C. Lowe, J. Appl. Phys., Vol. 81, 3007 (1997).
35. C.B McARDLE, “Side chain liquid crystal polymers”, (1989).
36. F. Simoni, “Nonlinear optical properties of liquid crystals”, Vol. 2 (1997).
37. M. O’neill, S. M. Kelly, J. Phys. D: Appl. Phys., 33 R67 (2000).
38. K. Ichimura, Chem. Rev., 1847 (2000).
39. O. Tsutsumi, T. Kitsunai, A. Kanazawa, T. Shiono, T. Ikeda, Macromolecules, Vol. 31, 355 (1998).
40. Z. Liang, H. Ming, Q. Zhang, J. Appl. Phys. Vol. 90, 5866 (2001).
41. T. Yoshioka, T. Ogata, A. M. Zahangir, T. Nonaka, S. Kulihara, Liquid Crystals, Vol. 31, 15 (2004).
42. G. Wang, M. Li, M. Yu, C. Guo, X. Chen, Liquid Crystals, Vol. 27, 867 (2000).
43. D. J. Broer, G. N. Mol, J. A. M. M. van Haaren, J. Lub, Adv. Mater., Vol. 11, 573 (1999).
44. R. A. M. Hikmet, H. Kemperman, Nature, Vol. 392, 476 (1998).