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
相关论文
共 18 条
[1]  
Abeta S., 1989, KAISETSU SENRYOU KAG
[2]   Effects of the alkyl group in (dialkylamino) perfluorophenazines on the melting point and fluorescence properties [J].
Biradar, Siddanagouda ;
Shigemitsu, Yasuhiro ;
Kubota, Yasuhiro ;
Funabiki, Kazumasa ;
Sato, Hiroyasu ;
Matsui, Masaki .
RSC ADVANCES, 2014, 4 (103) :59387-59396
[3]   AROMATIC AZOCOMPOUNDS .6. FURTHER EXPERIMENTS PERTAINING TO AROMATIC ARYLATION OF ORTHO-SUBSTITUTED AZOBENZENES BY GRIGNARD REAGENTS [J].
BOZZINI, S ;
RISALITI, A ;
STENER, A .
TETRAHEDRON, 1970, 26 (16) :3927-&
[4]   COPLANARITY IN 2,6-DIMETHYLAZOBENZENES - A C-13 NMR-STUDY [J].
BYRNE, CJ ;
HAPPER, DAR .
AUSTRALIAN JOURNAL OF CHEMISTRY, 1993, 46 (06) :887-894
[5]  
Gregory P., 1991, HIGH TECHNOLOGY APPL
[6]  
Horiguchi H., 1969, GOUSEI SENRYOU
[7]   OXIDATION OF N-ACYLSULFILIMINES, N-SULFONYLSULFILIMINES, AND N-ARYLSULFILIMINES TO SULFOXIMINES BY META-CHLOROPEROXYBENZOATE ANION [J].
HUANG, SL ;
SWERN, D .
JOURNAL OF ORGANIC CHEMISTRY, 1979, 44 (14) :2510-2513
[8]  
Lubs H.A., 1965, CHEM SYNTHETIC DYES
[9]   STABILITY OF DISODIUM 2-ARYLAZO-1-NAPHTHOL-3,6-DISULFONATES TO OZONE [J].
MATSUI, M ;
MIDZUI, N ;
SHIBATA, K ;
MURAMATSU, H .
DYES AND PIGMENTS, 1992, 20 (01) :67-70
[10]  
Matsuoka M., 1990, INFRARED ABSORBING D