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设计并合成了一类新型的含1, 3, 2-二氧硼杂环的二苯乙炔类液晶, 其相变行为通过DSC及偏光显微镜进行了观察和测试. 整个系列化合物仅呈现一个向列相, 在所合成的化合物中, 随着碳链的增长, 相变温度变化不大.

参考文献

[1] Haramoto, Yuichiro Kamogawa Hiroyoshi. A new group of liquid crystal materials with sulfur atoms incorporated in the principal structure [J]. J. Chem. Soc. Chem. Commun., 1983 (2):75-76.
[2] Haramoto Y, Kamogawa H. 2-(p-cyanophenyl)-5-alkyl-1,3-oxathianes in liquid crystal mixture [J]. Mol. Cryst. Liq. Cryst., 1985,131(3-4):201-207.
[3] Haramoto Y, Yin M, Matukawa Y. A new ionic liquid crystal compound with viologen group in the principal structure [J]. Liq. Cryst., 1995, 19(3):319-320.
[4] Haramoto Yuichiro, Nanasawa Masato. New side chain liquid crystalline polysiloxanes containing 1,3-dithiane or 1,3-dioxane rings as mesogenic side groups [J]. Liq. Cryst., 1997, 23(2): 263-267.
[5] Bezborodov V S, Dabrowski R, Dziaduszek J. The synthesis and properties of some mesomorphic cyclohexene derivatives [J]. Liq. Cryst., 1997, 23(1):69-75.
[6] Dabrowski R, Bezborodov V S, Lapanik V J. Mesomorphic properties of phenyl 4-(5-alkyl-1,3,2-dioxaborin-2-yl)benzoates [J]. Liq. Cryst., 1995, 18(2):213-218.
[7] Reiffenrath Volker, Hittich Reinhard, Plach Herbert. Dioxaborinane derivatives, their use in liquid crystal media, the media, and electrooptical displays using the media [P]. Ger. Offen., DE 4014488 A1, 1991.
[8] Ooiwa Masaki, Inoe Kanji (Seimi Chem Kk, Japan). Preparation of 1,3,2-dioxaborinane derivatives, liquid-crystal compositions containing them, and liquid-crystal display devices [P]. Jpn. Kokai Tokkyo Koho JP 05148259 A2, 1993, 06, 15.
[9] Yang Yonggang, Chen Baoquan, Wen Jianxun. Synthesis and mesomorphic properties of semi-perfluorinated chain liquid crystals [J]. Liq. Cryst.,1999, 26(6):893-896.
[10] Demus D, Richter L. Textures of Liquid Crystals [M]. New York:Verlag Chemie, Weinheim, 1978.
[11] Gray G W, Goodby J W. Smectic Liquid Crystals: Textures and Structures [M]. Philadelphia: Heyden & Son Inc., 1984.
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