Without addition of any metal ions or other catalysts, 1-chloroanthraquinone reacts readily with 6-aminocaproic acid or hexamethylenediamine in dimethylsulphone as solvent to give 1-(6-aminocaproic acid)anthraquinone and 1-(6-aminohexyl)amino]anthraquinone, respectively. 1,5-Dichloroor 1,8-dichloroa
Synthesis of polycondensable anthraquinone dyes and coloured nylon fibres: III
β Scribed by Liu, Zhenguo; Cao, Weixiao; Sun, Yanhui; Su, Aaron C. L.; Liotta, Charles L.
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 181 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0959-8103
No coin nor oath required. For personal study only.
β¦ Synopsis
A series of 1,5-diaryl-and 1,8-diaryl-substituted anthraquinone dyes, which contain wCOOH or groups, were prepared. The aryl-substituted wNH 2 anthraquinone dyes possess excellent thermostability and will keep their original colour in polycondensation with caprolactam at 260Γ280Β‘C. With di β erent aryl substituents the anthraquinone dyes exhibit di β erent colours and can be used to prepare a series of coloured nylon-6 Γbres.
π SIMILAR VOLUMES
The reaction of dihydroxyanthraquinone (DHA) and amines in the presence of catalyst has been reported. We found that DHA reacted easily with hexamethylenediamine in chloroform or toluene without addition of any catalyst, and mono-or dihexamethylenediamine-substituted anthraquinone, a violet green co