Liquid azo dyes

被引:12
|
作者
Biradar, Siddanagouda [1 ]
Kasugai, Ryohei [1 ]
Kanoh, Hisayoshi [1 ]
Nagao, Hitoshi [1 ]
Kubota, Yasuhiro [1 ]
Funabiki, Kazumasa [1 ]
Shiro, Motoo [2 ]
Matsui, Masaki [1 ]
机构
[1] Gifu Univ, Fac Engn, Dept Chem & Biomol Sci, Gifu 5011193, Japan
[2] Rigaku Corp, Xray Res Lab, Tokyo 1968666, Japan
关键词
Azo dyes; Melting point; Single X-ray crystallography; pi-pi-Stacking; Hydrogen bond; Glass transition temperature; SUBSTITUTED AZOBENZENES; FLUORESCENCE PROPERTIES;
D O I
10.1016/j.dyepig.2015.10.024
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Any liquid azo dyes, in which auxochrome such as dialkylamino, alkoxy, and amino group is attached in a molecule, were produced. In a series of 2-alkyl-4'-(dimethylamino)azobenzenes, the butyl, hexyl, octyl, and dodecyl derivatives were liquid at room temperature, whereas the propyl, 1-methylethyl, 1-methylpropyl, 1,1-dimethylethyl, and octadecyl derivatives were solid. Thus, it is essential for liquid azo dyes to have a medium n-alkyl group at the 2-position. In a series of 2-butyl-4'-(dialkylamino) azobenzenes, the dimethylamino, diethylamino, dibutylamino, dioctylamino, and didodecylamino derivatives were liquid. 2-Butyl-4'-methoxyazobenzene and 4-amino-3,5-dimethy1-2'-butylazobenenzne were also liquid, whereas 2-butyl-4'-hydroxyazobenznene, 4-amino-2'-butylazobenzene, and 2-butyl-4'-(methylamino)azobenzene were solid. The prevention of pi-pi stacking, alkyl alkyl interactions, and intermolecular hydrogen bond could produce liquid azo dyes. (c) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:249 / 258
页数:10
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