| Автор | Koide, Naoyuki |
| Автор | Iida, Hirofumi |
| Дата выпуска | 1995 |
| dc.description | AbstractVarious kinds of polythiophene derivatives were synthesized and thermal properties were examined by DSC, polarized microscopic and X-ray diffraction observations. Fusibility and solubility of these polymers deeply depends upon the polymerization methods and polarity of the mesogenic group. Polymerization was carried out by oxidation and polycondensation methods. The polarity at the end of mesogenic group plays an important role for solubility and fusibility of the polymer in the case of oxidative polymerization. 3-Substituted polythiophene having polar group such as cyano or nitro at the end of mesogenic group was soluble in polar solvent and fusibility at higher temperature. The polymer having polar group at the end of mesogenic group prepared by mild polymerization condition such as polycondensation exhibited a clear smectic texture and also showed electrochemically active by cyclic voltamograms. |
| Формат | application.pdf |
| Издатель | Taylor & Francis Group |
| Копирайт | Copyright Taylor and Francis Group, LLC |
| Название | Synthesis and Properties of Polythiophene Containing Mesogenic Group at 3-Position of Thiophene Ring |
| Тип | research-article |
| DOI | 10.1080/10587259508033487 |
| Print ISSN | 1058-725X |
| Журнал | Molecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals |
| Том | 261 |
| Первая страница | 427 |
| Последняя страница | 436 |
| Аффилиация | Koide, Naoyuki; Department of Chemistry, Faculty of Science, Science University of Tokyo |
| Аффилиация | Iida, Hirofumi; Department of Chemistry, Faculty of Science, Science University of Tokyo |
| Выпуск | 1 |
| Библиографическая ссылка | Percec, V. P. and Pugh, C. 1989. Side Chain Liquid Crystal Polymers, Edited by: McArdle, C. B. 30Glasgow: Blackie and Son Ltd.. Chap. 3 |
| Библиографическая ссылка | Yoshino, K., Nakayama, S. and Sugimori, R. 1987. Jpn. J. Appl. Phys., 26: L1038 |
| Библиографическая ссылка | Sato, M. and Mori, M. 1991. Polym. Commun., 32: 42 |
| Библиографическая ссылка | Tanaka, S., Sato, M. and Kaeriyama, K. 1988. Synth. Met., 25: 277 |
| Библиографическая ссылка | Daust, G. and Leclerc, M. 1988. Macromolecules, 24: 277 |
| Библиографическая ссылка | Ikenoue, Y., Chiang, J., Partel, A. O., Wudl, F. and Heeger, A. J. 1989. Synth. Met., 30: 305 |
| Библиографическая ссылка | Sato, M., Tanaka, S. and Kaeriyama, K. 1989. J. Chem. Soc., Chem. Comnun., : 1725 |
| Библиографическая ссылка | Ozaki, M. and Yoshino, K. 1977. J. Chem. Soc., Chem. Comnun., 578 |
| Библиографическая ссылка | Akagi, K. 1986. ICSM 1986 1–04. 22 Abstracts |
| Библиографическая ссылка | Shirakawa, H. |
| Библиографическая ссылка | Se-Oh, Y., Akagi, K., Shirakawa, H. and Araya, K. 1993. Makromolecules, 26: 6203 |
| Библиографическая ссылка | Iida, H. and Koide, N. 1993. Rep. Prog. Polym. Phys. Jpn., 36: 255 |
| Библиографическая ссылка | Colon, I. and Kelsey, D. R. 1986. J. Org. Chem., 51: 2627 |
| Библиографическая ссылка | Miyazaki, Y. and Yamamoto, T. 1994. Synth. Met., 64: 69 |
