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Synthesis and Application of Spiropyrane-Based Photochromic Dyes for Wool

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Abstract

Suffered from poor substantivity and water solubility, the direct application of spiropyrane-based photochromic dyes to protein fibers is limited. Herein this paper reported the synthesis of water-soluble photochromic dyes for woolen fiber coloration with good water solubility, substantivity, and washing fastness. The spiropyrane-based photochromic dyes were synthesized by a three-step reaction with sulfonate group as water-soluble group. Moreover, N-alkyl or aryl groups of variable size were introduced into the dyes to tailor the substantivity towards wool fiber and the chemical structures were confirmed by 1H-NMR and mass spectrum. Under optimum dyeing condition, the dyes showed high affinity toward wool fiber in the order of BnSP > HdSP > MeSP. Upon UV irradiation, the CIE chromaticity coordinates of the photochromism wools shifted from white region (0.33, 0.35) to the red region for MeSP (0.39, 0.34) and HdSP (0.39, 0.38), and blue region for BnSP (0.30, 0.31). A more improved washing fastness for the wools dyed with BnSP and HdSP (grade 4–5) was observed than the one dyed with MeSP (grade 4). The revealed structure–property relationships in the spiropyrane-based photochromic dyes provide a general guideline to design new photochromic dyes for wool fiber coloration.

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Data availability statement

The datasets generated during and/or analysed during the current study are available from the corresponding author on reasonable request.

References

  1. M. Vikova, M. Pechova, Text. Res. J. 90, 2070 (2020)

    Article  CAS  Google Scholar 

  2. J. Fan, B. Bao, Z. Wang, H. Li, Y. Wang, Y. Chen, W. Wang, D. Yu, Chem. Eng. J. 404, 126448 (2021). https://doi.org/10.1177/0040517520910217

    Article  CAS  Google Scholar 

  3. S. Long, Z. Ye, Y. Jin, J. Huang, Y. Huang, Y. Liao, X. Li, Macromol. Rapid Commun. 42(7), 2000701 (2021). https://doi.org/10.1002/marc.202000701

    Article  CAS  Google Scholar 

  4. Y. Qi, J. Fan, Y. Chang, Y. Li, B. Bao, B. Yan, H. Li, P. Cong, Dyes Pigm. 193, 109507 (2021)

    Article  CAS  Google Scholar 

  5. T. Zhang, L. Fu, Z. Chen, Y. Cui, X. Liu, Prog. Org. Coat. 100, 100 (2016). https://doi.org/10.1016/j.porgcoat.2016.02.001

    Article  CAS  Google Scholar 

  6. S. Bretler, S. Margel, Polymer 61, 68 (2015). https://doi.org/10.1016/j.polymer.2015.01.068

    Article  CAS  Google Scholar 

  7. V. Dryza, T.A. Smith, E.J. Bieske, Phys. Chem. Chem. Phys. 18, 5095 (2016). https://doi.org/10.1039/C5CP07400B

    Article  CAS  PubMed  Google Scholar 

  8. J. Mokhtari, A. Akbarzadeh, Z. Shahrestani, P. Ferdowsi, Fibers Polym. 16, 2299 (2015). https://doi.org/10.1007/s12221-015-5265-2

    Article  CAS  Google Scholar 

  9. L. Peng, R. Guo, S. Jiang, J. Lan, Y. He, X. Huang, Fibers Polym. 16, 1312 (2015). https://doi.org/10.1007/s12221-015-1312-2

    Article  CAS  Google Scholar 

  10. M. Tomasulo, S. Sortino, F.M. Raymo, Org. Lett. 7, 1109 (2005). https://doi.org/10.1021/ol050045a

    Article  CAS  PubMed  Google Scholar 

  11. Y. Kishimoto, J. Abe, J. Am. Chem. Soc. 131, 4227 (2009). https://doi.org/10.1021/ja810032t

    Article  CAS  PubMed  Google Scholar 

  12. C.M. Sousa, J. Berthet, S. Delbaere, P.J. Coelho, Dyes Pigm. 169, 118 (2019). https://doi.org/10.1016/j.dyepig.2019.05.013

    Article  CAS  Google Scholar 

  13. H.-H. Liu, Y. Chen, Dyes Pigm. 89, 212 (2011)

    Article  CAS  Google Scholar 

  14. G.H. Timmermans, B.W.H. Saes, M.G. Debije, Appl. Opt. 58, 9823 (2019). https://doi.org/10.1016/j.dyepig.2010.03.001

    Article  CAS  PubMed  Google Scholar 

  15. F. Struebe, S. Rath, J. Mattay, Eur. J. Org. Chem. 2011, 4645 (2011). https://doi.org/10.1002/ejoc.201100228

    Article  CAS  Google Scholar 

  16. N.A. Davidenko, I.I. Davidenko, E.V. Mokrinskaya, S.L. Studzinskiy, V.V. Kravchenko, J. Appl. Spectrosc. 88, 382 (2021). https://doi.org/10.1007/s10812-021-01186-

    Article  CAS  Google Scholar 

  17. M.A.M. Rashid, D. Hayati, K. Kwak, J. Hong, Nanomaterials 9(1), 119 (2019). https://doi.org/10.3390/nano9010119

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  18. Z. Ling, K. Liu, Q. Zou, Q. Li, K.-Q. Zhang, Z. Cui, W. Yuan, Y. Liu, RSC Adv. 8, 28581 (2018). https://doi.org/10.1039/C8RA05170D

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  19. T.A. Khattab, M. Rehan, T. Hamouda, Carbohydr. Polym. 195, 143 (2018). https://doi.org/10.1016/j.carbpol.2018.04.084

    Article  CAS  PubMed  Google Scholar 

  20. A.F. Little, R.M. Christie, Color. Technol. 127, 275 (2011). https://doi.org/10.1111/j.1478-4408.2011.00307.x

    Article  CAS  Google Scholar 

  21. S.M.R. Billah, R.M. Christie, K.M. Morgan, Fibers Polym. 12, 701 (2011). https://doi.org/10.1007/s12221-011-0701-4

    Article  CAS  Google Scholar 

  22. M. Aldib, R.M. Christie, Color. Technol. 127, 282 (2011)

    Article  CAS  Google Scholar 

  23. S.J. Lee, Y.A. Son, H.J. Suh, D.N. Lee, S.H. Kim, Dyes Pigm. 69, 18 (2006). https://doi.org/10.1016/j.dyepig.2005.02.019

    Article  CAS  Google Scholar 

  24. T. Cheng, T. Lin, R. Brady, X. Wang, Fibers Polym. 9, 521 (2008). https://doi.org/10.1007/s12221-008-0083-4

    Article  CAS  Google Scholar 

  25. B. Bao, J. Fan, W. Wang, D. Yu, Fibers Polym. 21, 733 (2020). https://doi.org/10.1007/s12221-020-9749-3

    Article  CAS  Google Scholar 

  26. A.F. Little, R.M. Christie, Color. Technol. 132, 304 (2016)

    Article  CAS  Google Scholar 

  27. T.V. Pinto, D.M. Fernandes, A. Guedes, N. Cardoso, N.F. Duraes, C. Silva, C. Pereira, C. Freire, Chem. Eng. J. 350, 856 (2018). https://doi.org/10.1016/j.cej.2018.05.155

    Article  CAS  Google Scholar 

  28. A. Sugahara, N. Tanaka, A. Okazawa, N. Matsushita, N. Kojima, Chem. Lett. 43, 281 (2014). https://doi.org/10.1246/cl.130904

    Article  CAS  Google Scholar 

Download references

Acknowledgements

The Project was supported by the Foundation (No. 2021KF10) of Guangxi Key Laboratory of Clean Pulp & Papermaking and Pollution Control, College of Light Industry and Food Engineering, Guangxi University.

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Correspondence to Sun Chang.

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Yunwen, L., Simeng, Y. & Chang, S. Synthesis and Application of Spiropyrane-Based Photochromic Dyes for Wool. Fibers Polym 24, 641–652 (2023). https://doi.org/10.1007/s12221-023-00069-z

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