Azo Dyes from Substituted 2‐Aminothiophens

Autor: William H. Moore, Edmund B Towne, Melvin S Bloom, Joseph B Dickey, D. G. Hedberg, B. H. Smith Jr.
Rok vydání: 1958
Předmět:
Zdroj: Journal of the Society of Dyers and Colourists. 74:123-132
ISSN: 0037-9859
DOI: 10.1111/j.1478-4408.1958.tb02242.x
Popis: This paper concerns the effects of the position and the nature of substituents on the colour of azo dyes derived from 2-arainothiophens. Of primary interest is the colour shift from the red of phenylazo dyes to the greenish blue of the analogous 5-substituted 3-nitro-2-thienylazo dyes. The greenish blue of 2-amino-3-nitro-5-aeyl(or aroyl)thiophen dyes is in striking contrast with the violet—red of 2-amino-5-acylthiophen dyes and the violet of dyes from 2-amino-3:5-bismethylsulphonylthiophen. Even simple aniline coupling components afford blues to blue-greens with the 5-substituted 2-amino-3-nitrothiophens. However, progressively increased bathoehromic shifts to bluish green are obtained with the following coupler types— tetrahydroquinoline, benzomorpholine, and 2-alkoxy-5-acetamidoaniline. Dyes from 2-amino-3-nitro-5-acylthiophens, particularly, have excellent affinity for secondary cellulose acetate and give good exhaustion and level dyeing. They colour cellulose acetate deep, bright blues to greens. Dyed fabrics have superior gas-fume fastness, moderate light fastness, and good dischargeability.
Databáze: OpenAIRE