Browse > Article

Synthesis and Photoalignment of Soluble Polyimides Containing 4-Styrylpyridine Derivatives as Photoreactive Side Groups  

김민우 (경북대학교 고분자공학과)
안득균 (경북대학교 고분자공학)
이동호 (경북대학교 고분자공학)
박이순 (경북대학교 고분자공학)
서관호 (경북대학교 고분자공학)
하기룡 (계명대학교 화학공학)
김우식 (경북대학교 고분자공학과)
Publication Information
Polymer(Korea) / v.28, no.4, 2004 , pp. 314-320 More about this Journal
Abstract
Soluble aromatic polyimides bearing 4-(4-oxyalkyleneoxystyryl)- pyridines (ethylene and hexylene) as photoreactive side groups were synthesized and characterized. The photoreactive polymers were soluble in various polar organic solvents and their films were easily formed by solution casting. The photoreactivities of the polymers in the film state were approximately 64% at an exposure energy of 1.5 J/$\textrm{cm}^2$. Transmittances of the polymer films were about 85% after annealing at 20$0^{\circ}C$. Therefore, these polymers can be evaluated to be photoreactive polyimides with good transparency and solubility. The dichroic ratios of the polymers with ethylene and hexylene groups as the alkylene spacers were 0.023 and 0.026, respectively. The order parameters of 4'-pentyl-4-bipheny1carbonitrile as a liquid crystal (LC) in the film cells of the former and latter polymers were 0.50 and 0.52, respectively. These results indicate that the polymers show the effect of alkylene spacer on the photoalignments. The LC in the film cells of the polymers was perpendicularly oriented to the electric vector of the linear polarized UV light (LPUVL).
Keywords
soluble polyimide film; liquid crystal; photoalignment; photoreactivity; 4-styrylpyridine.;
Citations & Related Records

Times Cited By Web Of Science : 2  (Related Records In Web of Science)
Times Cited By SCOPUS : 2
연도 인용수 순위
1 /
[ N. Kawatsuki;K. Matsuyoshi;M. Hayashi;H. Takatsuka;T. Yamamoto ] / Chem. Mater.   DOI   ScienceOn
2 /
[ M. Schadt;K. Schmitt;V. Kozinkov;V. Chigrinov ] / JPn. J. Appl. Phys.
3 /
[ I. H. Kim;W. S. Kim;K. R. Ha ] / Polymer(Korea)
4 /
[ A. Zhang;X. Li;C. W. Nah;K. J. Hwang;M. H. Lee ] / J. Polym. Chem. Sci., Polym. Sci.   DOI   ScienceOn
5 /
[ S. W. Lee;T. Chang;M. Ree ] / Macromol. Rapid Comun   DOI   ScienceOn
6 /
[ K. Ichimura;Y. Akita;H. Akiyama;K. Kudo;Y. Hayashi ] / Macromolecules   DOI   ScienceOn
7 /
[ M. Schadt;H. Siberle;A. Shuster ] / Nature   DOI   ScienceOn
8 /
[ M. Irie;Y. Hirano;S. Hashimoto;K. Hayashi ] / Macromolecules   DOI
9 /
[ K. Ichimura ] / Chem. Rev.   DOI   ScienceOn
10 /
[ N. Kawatsuki;T. Kawakami;T. Yamamoto ] / Mol. Cryst. and Liq. Cryst.   DOI
11 /
[ T. Kimura;J.Y.Kim;T.Fukuda;H.Matsuda ] / Macromol. Chem. Phys.   DOI   ScienceOn
12 /
[ M. Obi;S. Marino;K. Ichimura ] / Macromol. Rapid Commun.   DOI   ScienceOn
13 /
[ S. Yamaki;M. Nakagawa;K. Ichimura ] / Macromol. Chem. Phys.   DOI   ScienceOn
14 /
[ Y. Wang;C. Xu;A. Kanazawa;T. Shino;T. Ikeda ] / J. Appl. Phys.   DOI   ScienceOn
15 /
[ M. Nishikawa;J. L. West ] / J. Appl. Phys.   DOI
16 /
[ M. Nishikawa;T. Kosa;J. L. West ] / Jpn. J. Appl. Phys.   DOI
17 /
[ I. H. Kim;W. S. Kim;K. R. Ha ] / Polymer(Korea)
18 /
[ T. A. Chen;A. K. Y. Jen;Y. Cai ] / Macromolecules   DOI   ScienceOn
19 /
[ W. S. Kim;D. K. Ahn;M. W. Kim ] / Macrcomol. Chem. Phys.
20 /
[ T. Matsuura;Y. Hasuda;S. Nishi;N. Yamada ] / Macromolecules   DOI
21 /
[ E. D. Bergmann;S. Pinchas ] / J. Org. Chem.   DOI
22 /
[ S. Y. Koo;D. H. Lee;H. J. Choi;K. Y. Choi ] / J. Appl. Polym. Sci.   DOI   ScienceOn
23 /
[ D. H. Lee;S. Y. Koo;D. Y. Kim;H. J. Choi ] / J. Appl. Polym. Sci.   DOI   ScienceOn
24 /
[ O. Mitsunobu ] / Synthesis
25 /
[ W. S. Kim;H. S. Jang;K. H. Hong;K. H. Seo ] / Macromal. Rapid Commun.   DOI   ScienceOn
26 /
[ W. S. Kim;J. W. Lee;Y. W. Kwak;J. K. Lee;Y. T. Park;S. D. Yoh ] / Polymer J.   DOI   ScienceOn
27 /
[ K. H. Kim;S. Jang;F. W. Harris ] / Macronomecules   DOI   ScienceOn