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Synthesis and Physical Properties of π -Conjugated Polymers Containing Mesogenic Group

Published online by Cambridge University Press:  10 February 2011

Y. Watanabe
Affiliation:
Department of Chemistry, Faculty of Science, Science University of Tokyo, Kagurazaka 1-3, Shinjuku-ku, Tokyo, 162 JAPAN, [email protected]
N. Koide
Affiliation:
Department of Chemistry, Faculty of Science, Science University of Tokyo, Kagurazaka 1-3, Shinjuku-ku, Tokyo, 162 JAPAN, [email protected]
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Abstract

Novel side chain type liquid crystalline polymers, polythiophene and poly(aryleneethynylene) [PAE], containing a mesogenic group in the side chain were synthesized. Polythiophene derivatives were obtained by dehalogenative polycondensation with zero-valence nickel complex under mild condition. PAE type polymers were obtained by coupling dihalo aromatic compound with diethynyl aromatic compound. Their thermal properties were examined by differential scanning calorimetry, optical microscopy and X-ray diffractometry. All polymers exhibited a smectic or nematic mesophase depending upon the polymer backbone and pendant mesogenic group. Polythiophene derivatives exhibited electrochemical activity. Annealing polythiophene derivatives led to a lower oxidation potential and a higher conductivity. The degree of the orientation of the polymer backbone was supported by polarized UV-vis measurement. An effective conjugated length became longer by introducing thiophene rings into the polymer backbone. A high quantum yield of fluorescence was observed for PAE type polymers.

Type
Research Article
Copyright
Copyright © Materials Research Society 1996

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References

1. Marsella, M. J., Carroll, P. J. and Swager, T. M., J. Am. Chem. Soc., 117, 9832 (1995)Google Scholar
2. Zhou, Q. and Swager, T. M., J. Am. Chem. Soc., 117, 12593 (1995)Google Scholar
3. Kang, I., Hwang, D. and Shim, H., Macromolecules, 29, 165 (1996)Google Scholar
4. Yoshino, K., Nakayama, S. and Sugimori, R., Jpn. J. Appl. Phys., 26, L1038 (1987)Google Scholar
5. Sato, M. and Mori, M., Polym. Commun., 32, 42 (1991)Google Scholar
6. Tanaka, S., Sato, M. and Kaeriyama, K., Synth. Met., 25, 277 (1988)Google Scholar
7. Daust, G. and Leclerc, M., Macromolecules, 24, 277 (1988)Google Scholar
8. Ozaki, M. and Yoshino, K., J. Chem. Soc., Chem. Commun., 578 (1977)Google Scholar
9. Akagi, K. et al., ICSM'86, P1–04, Abstracts, p22 (1986)Google Scholar
10. Koide, N. and lida, H., Mol. Cryst. Liq. Cryst. 262, 427 (1995)Google Scholar
11. Koide, N. and Moriya, N., Rep. Prog. Polym. Phys. Jn., 38,199 (1995)Google Scholar
12. Yamamoto, T., Morita, A., Kanbara, T. et al, Macromolecules, 25, 1214 (1992)Google Scholar
13. Miyazaki, Y. and Yamamoto, T., Synth. Met., 64, 69(1994)Google Scholar
14. Wilke, G., Angew. Chem., 72, 581 (1960)Google Scholar
15. Trumbo, D. L. and Marvel, C.S., J. Polym. Sci., Part A, Polym. Chem., 24, 2311 (1986)Google Scholar
16. Sanechika, K., Yamamoto, T. and Yamamoto, A., Bull. Chem. Soc. Jpn., 57, 752 (1984)Google Scholar
17. Sugimoto, R., Tanaka, S., Gu, H. B. and Yoshino, K., Chem. Express 1, 635 (1986)Google Scholar
18. Tourillion, G. and Gamier, F., J. electroanal. Chem., 135, 173 (1982)Google Scholar
19. Koide, N. et al, The annual meeting of the Chem. Soc. of Jpn., 1996 spring.Google Scholar
20. Portugall, M., Ringsdorf, H. and Zentel, R., Makromol. Chem., 183, 2311 (1982)Google Scholar
21. Watanabe, Y. and Koide, N., Unpublished work.Google Scholar