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Indexed by:Journal Papers

Date of Publication:2015-12-01

Journal:DYES AND PIGMENTS

Included Journals:SCIE、EI、Scopus

Volume:123

Page Number:44-54

ISSN No.:0143-7208

Key Words:Monoazo-anthraquinone structure; Reactive dye; Blue colour; Tautomerism; DFT calculation; Dyeing properties

Abstract:A new kind of reactive dyes containing both monoazo and anthraquinone chromophores was obtained by using 1,4-bis((4-aminophenyl)amino)anthrance ne-9,10-dione as diazo component and 1-amino-8-naphthol-3,6-disulfonicacid (H-add) derivatives as coupling components. The dyes were characterized by UV-Vis, IR, MS, H-1 NMR and C-13 NMR. The results showed that the maximum absorption wavelengths of the dyes were all about 590 nm, which indicated that they were a kind of blue dyes. H-1 NMR and C-13 NMR results revealed that there were two kinds of tautomerisms in dye structure and a new conjugated system formed between the anthraquinone ring and the phenyl azo linkage. Density functional theory (DFT) calculations also proved the formation of the new larger conjugated system from which the blue colour was generated. The fixations of the dyes on cotton were over 88% and the light fastness reached 5 grade. (C) 2015 Elsevier Ltd. All rights reserved.