Five selected reactive dyes were used to perform theoretical calculations of photochemical reactivity indicators in electro-(SE) and nucleophilic reactions (SN). The study utilised reactive dyes in which the reactive group is cyanuric chloride, but which differ in their chromophore structure. They belong to the groups of monoazo, disazo and anthraquinone dyes. The influence of changes in these indicators after the formation of the dye-cellulose covalent bond on their light fastness was analyzed. Using the PM3 limit molecular orbital method (MO), the electron density distribution was calculated for dyes in the highest occupied orbital (HOMO) and the lowest unoccupied (LUMO) in the singlet state. These values reflect the tendency towards an electrophilic reaction with a singlet oxygen atom 1O2 or a nucleophilic reaction with the superoxide radical anion
on atoms in the dye molecule. Reactivity indicators as super delocalization (SE, SN) and electron density distribution in the ground and excited states were calculated. The values of the super delocalization coefficients indicate the activity of sites in the molecules in the oxidation reaction, the resistance of these dyes to photo-oxidation and their influence on the durability of chemical bonds with the cellulose. It was found that the formation of bonds with the cellulose slightly affects the resistance in the electrophilic oxidation reaction, but this effect is significant in the nucleophilic reaction.
References
[1]
Giles, C.H. (1957) The Light Fastness of Dyed Fibres—A Statistical Study. JournaloftheSocietyofDyersandColourists, 73, 127-160. https://doi.org/10.1111/j.1478-4408.1957.tb02185.x
[2]
Clark, M. (2011) Handbook of Textile and Industrial Dyeing. Woodhead Publishing Ltd, 211-223. https://doi.org/10.1533/9780857094919
[3]
Horton, F.J., Patterson, D. and Rizzo, F.J. (1976) Photoconductivity and Fading. I. The Dyes Used in the ISO Light-Fastness Test. JournaloftheSocietyofDyersandColourists, 92, 269-272. https://doi.org/10.1111/j.1478-4408.1976.tb03292.x
[4]
Baranova, G.S., Romanova, M.G. and Chekalin, M.A. (1972) Fading of Reactive Dyes. Textil’naa Promy?lennost, 32, 70-71.
[5]
Ingamells, W. (1963) The Enhanced Fading of Dyes Caused by Crease-Resist Resins: A Proposed Mechanism. Journal of the Society of Dyers and Colourists, 79, 651-660. https://doi.org/10.1111/j.1478-4408.1963.tb02525.x
[6]
Daruwalla, E.H. (1974) Physical Chemistry of Dyeing: State of Dye in Dyebath and in Substrate. In: The Chemistry of Synthetic Dyes, Elsevier, 69-113. https://doi.org/10.1016/b978-0-12-717007-7.50010-x
[7]
Zakharova T.D., Soloveva V.B. and Zaitseva V.N. (1971) Influence of Covalent Bonding between Reactive Dyes and Cellulose in Fibers on Light Fastness of the Dyes. Pleiades Publishing.
[8]
Krichevsk, G.E., Vachobov, B., Ershov, Y.A. and Dovb, E.B. (1975) Lightfastness of Reactive Dyes. TextileResearchJournal, 45, 608-619. https://doi.org/10.1177/004051757504500809
[9]
Stephen, W.E. (1965) The Early Work on Reactive Dyes for Cellulose. Chimia, 19, 261. https://doi.org/10.2533/chimia.1965.261
[10]
Rattee, I.D. (1984) Reactive Dyes for Cellulose 1953-1983. Review of Progress in Coloration and Related Topics, 14, 50-57. https://doi.org/10.1111/j.1478-4408.1984.tb00044.x
[11]
Stewart, J.J.P. (1989) Optimization of Parameters for Semiempirical Methods I. Method. JournalofComputationalChemistry, 10, 209-220. https://doi.org/10.1002/jcc.540100208
[12]
Morita, Z. and Hada, S. (1999) A Semiempirical Molecular Orbital Study on the Reaction of an Aminopyrazolinyl Azo Dye with Singlet Molecular Oxygen. DyesandPigments, 41, 1-10. https://doi.org/10.1016/s0143-7208(98)00038-2
[13]
Wang, L., Wang, X. and Zhang, H. (2005) A Theoretical Study on Photobleaching Mechanisms of Hypocrellins. DyesandPigments, 67, 161-166. https://doi.org/10.1016/j.dyepig.2004.11.007
[14]
Guo, L., Meng, F.S., Gong, X.D., Xiao, H.M., Chen, K.C. and Tian, H. (2001) Synthesis and Spectral Properties of Soluble Trimethylsilyl Substituted Metal-Phthalocyanines. DyesandPigments, 49, 83-91. https://doi.org/10.1016/s0143-7208(01)00011-0
[15]
Fukui, K., Kato, H. and Yonezawa, T. (1961) “Frontier Electron Density” in Saturated Hydrocarbons. BulletinoftheChemicalSocietyofJapan, 34, 442-445. https://doi.org/10.1246/bcsj.34.442
[16]
Fukui, K., Nagata, C. and Yonezawa, T. (1958) Electronic Structure and Auxin Activity of Benzoic Acid Derivatives. JournaloftheAmericanChemicalSociety, 80, 2267-2270. https://doi.org/10.1021/ja01542a058
[17]
Wojciechowski, K. and Szuster, L. (2020) Prediction of Photofading of n-β-Hydroxyethylamino-o-Nitrophenyl Derivatives: A Theoretical Study. ColorationTechnology, 137, 134-144. https://doi.org/10.1111/cote.12517
[18]
Panchartek, J., Allan, Z.J. and Mu?ík, F. (1960) Aromatische Diazo-und Azoverbindungen XXXIX. Chromatographische Konstitutionsanalyse synthetischer Farbstoffe. CollectionofCzechoslovakChemicalCommunications, 25, 2783-2799. https://doi.org/10.1135/cccc19602783
[19]
Mihret, T., Gabbiye, N., Tegegne, B., Tibebe, D. and Alemu, A. (2025) Removal of Reactive Red 45 Dye from Aqueous Solution Using Activated Carbon Developed from Catha Edulis Stem as a Potential Biosorbent. Scientific Reports, 15, Article 28195. https://doi.org/10.1038/s41598-025-09956-2
[20]
Panchartek, J., Allan, Z.J. and Muzik, F. (1960) Aromatische Diazo-und Azoverbindungen XXXIX, Chromatographische Konstitutionsanalyse synthetischer Farbstoffe. Collection of Czechoslovak Chemical Communications, 25, 2783-2799. https://doi.org/10.1135/cccc19602783
[21]
Stamm, O.A., Zollinger, H., Z?hner, H. and G?umann, E. (1961) Die Bindung zwischen Reaktivfarbstoff und Cellulose. 7. Mitteilung über textilchemische Untersuchungen. HCA, 44, 1123-1125. https://doi.org/10.1002/hlca.19610440432
[22]
Wilkinson, F., Helman, W.P. and Ross, A.B. (1995) Rate Constants for the Decay and Reactions of the Lowest Electronically Excited Singlet State of Molecular Oxygen in Solution. an Expanded and Revised Compilation. JournalofPhysicalandChemicalReferenceData, 24, 663-677. https://doi.org/10.1063/1.555965
[23]
Griffiths, J. and Hawkins, C. (1977) Oxidation by Singlet Oxygen of Arylazonaphthols Exhibiting Azo-Hydrazone Tautomerism. Journal of the Chemical Society, Perkin Transactions 2, 6, 747-752. https://doi.org/10.1039/p29770000747
[24]
Jansen, L.M.G., Wilkes, I.P., Wilkinson, F. and Worrall, D.R. (1999) The Role of Singlet Molecular Oxygen in the Photodegradation of 1-Arylazo-2-Naphthols in Methanol and on Cotton. JournalofPhotochemistryandPhotobiologyA: Chemistry, 125, 99-106. https://doi.org/10.1016/s1010-6030(99)00095-7
[25]
Yamaguchi, S. and Sasaki, Y. (2001) Spectroscopic Determination of Very Low Quantum Yield of Singlet Oxygen Formation Photosensitized by Industrial Dyes. JournalofPhotochemistryandPhotobiologyA: Chemistry, 142, 47-50. https://doi.org/10.1016/s1010-6030(01)00470-1
[26]
Bandara, J. and Kiwi, J. (1999) Fast Kinetic Spectroscopy, Decoloration and Production of H2O2 Induced by Visible Light in Oxygenated Solutions of the Azo Dye Orange II. NewJournalofChemistry, 23, 717-724. https://doi.org/10.1039/a902425e
[27]
Batchelor, S.N., Carr, D., Coleman, C.E., Fairclough, L. and Jarvis, A. (2003) The Photofading Mechanism of Commercial Reactive Dyes on Cotton. DyesandPigments, 59, 269-275. https://doi.org/10.1016/s0143-7208(03)00118-9