Molecular design and synthesis of N-arylsulfonated coumarin fluorescent dyes and their application to textiles

Dyes and Pigments

Volumn 76, Issue 3, 2008, Pages 741-747

  Christie, Robert M ^a   Morgan, Keith M ^a   Islam, M Saiful ^a  

^a HERIOT WATT UNIVERSITY   (United Kingdom)

Author keywords

Arylsulfonamide; Coumarin; Fluorescent; Lightfastness; Molecular modeling; Quantum yield; UV visible absorption

Indexed keywords

FLUORESCENCE; MOLECULAR MODELING; MOLECULAR STRUCTURE; QUANTUM YIELD; ULTRAVIOLET VISIBLE SPECTROSCOPY;

ARYLSULFONAMIDE; COUMARIN; FLUORESCENT DYES; LIGHTFASTNESS;

DYES;

AZO DYE; CHEMICAL PROPERTY; DYE PROPERTY; FABRIC PROPERTY; FLUORESCENCE; LIGHTFASTNESS; MOLECULAR STRUCTURE; POLYESTER FABRIC; SYNTHESIS;

EID: 34548690121     PISSN: 01437208     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.dyepig.2007.01.018     Document Type: Article

References (23)

1. Mach W, Augurt D, Scheuermann H. German Patent 2,253,538; 1972.
2. Christie R.M. Fluorescent dyes. Review of Progress in Coloration 23 (1993) 1-18
3. Christie R.M., and Lui C.-H. Studies of fluorescent dyes: part 1. An investigation of the electronic spectral properties of substituted coumarins. Dyes and Pigments 42 (1999) 85-93
4. Christie R.M., and Lui C.-H. Studies of fluorescent dyes: part 2. An investigation of the synthesis and electronic spectral properties of substituted 3-(2′-benzimidazolyl)coumarins. Dyes and Pigments 47 (2000) 79-89
5. Bamfield P. Chromic phenomena, the technological applications of colour chemistry (2001), RSC, Cambridge
6. Parker C.A., and Rees W.T. Correlation of fluorescence spectra and measurement of fluorescence quantum efficiency. Analyst 85 (1960) 587-600
7. Demas J.N., and Crosby G.A. The measurement of photoluminescence quantum yields. The Journal of Physical Chemistry 75 (1971) 991-1024
8. Miller J.N. Standards for fluorescence spectrometry (1981), Chapman and Hall, London
9. Forgues S.F., and Lavabre D. Are fluorescence quantum yields so tricky to measure? A demonstration using familiar stationary products. Journal of Chemical Education 76 (1999) 1260-1264
10. British Standards BS EN 201 - C03:1993/ISO 105 - C03; 1989.
11. British Standards BS 1006; 1990.
12. British Standards BS EN ISO 105 - E04; 1996.
13. British Standards BS EN ISO 105 - B02; 1999.
14. Hausermann H, Voltz J. U.S. Patent 3,014,041; 1961.
15. Kendall JD, Waddington HRJ, Duffin GF. British Patent 867,592; 1961.
16. Harnisch H. U.S. Patent 3,985,763; 1976.
17. Luo XJ, Cheng LB. Chinese Patent CN00101751.9; 2000.
18. Luo X., Naiyun X., Cheng L., and Huang D. Synthesis of coumarin dyes containing N-alkylsulfonamide groups. Dyes and Pigments 51 (2001) 153-159
19. Luo XJ, Xiu NY, Li XB. Chinese Patent CN200410025212.1; 2005.
20. Hrdina R, Burert L, Lunak S, Nepras M, Wandrol P, Gomes JINR. Relationship between structure and lightfastness of reactive dyes for wool and nylon. Proceedings of ColorChem 2000, International conference, Spindleruv Mlyn, Czech Republic; May 2000.
21. Blus K. Synthesis and properties of acid dyes derived from 1-phenyl-3-methyl-5-pyrazolone. Dyes and Pigments 20 (1992) 53-65
22. Christie R.M., Hill J.M., and Rosair G. The crystal structure of CI Pigment Yellow 97, a superior performance Hansa yellow pigment. Dyes and Pigments 71 (2006) 194-198
23. Reynolds G.A., and Drexhage K.H. New coumarin dyes with rigidized structure for flashlamp-pumped dye lasers. Optics Communications 13 (1975) 222-225