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Synthesis of polycondensable anthraquinone dyes and coloured nylon fibres: III

✍ 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

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✦ 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 260È280Β‘C. With di †erent aryl substituents the anthraquinone dyes exhibit di †erent colours and can be used to prepare a series of coloured nylon-6 Ðbres.


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Synthesis of polycondensable anthraquino
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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

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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