Issue

Vol. 36 No. 7 (2024): Vol 36 Issue 7, 2024

Copyright (c) 2024 Dr. Supriya Dutta, Dr. Animesh Sahana

Creative Commons License

This work is licensed under a Creative Commons Attribution 4.0 International License.

Synthetic Fluorometric and Colorimetric Sensors for Identification of Fluoride Anion: A Short Review

https://doi.org/10.14233/ajchem.2024.31507
Supriya Dutta
Department of Chemistry, Nistarini College, Purulia-723101, India
https://orcid.org/0009-0004-3069-9059
Animesh Sahana
Department of Chemistry, Nistarini College, Purulia-723101, India
https://orcid.org/0009-0009-9509-8197

Corresponding Author(s) : Animesh Sahana

sahana.animesh@gmail.com

Asian Journal of Chemistry, Vol. 36 No. 7 (2024): Vol 36 Issue 7, 2024

Abstract

Over two decades of research in fluoride ion detection has been an intriguing field and many papers have been published enriching the possibilities of fluoride ion detection in even nano molar concentration levels. However, few reviews have been published, critically analyzing the design strategies, especially to detect fluoride ions in aqueous and real samples. About 21 colorimetric sensors and fluorescent probes, published during 1999 to 2014 have been covered to analyze their design strategies, speed of detection, limit of detection and their applicability in real samples and in aqueous medium. The fundamental principles can be broadly classified into 5 categories namely Si-O bond cleavage, B-F monomer formation, deprotonation of amide hydrogen, Si-F bond formation and Sb-F bond formations which enable fluoride ion detection. Variations in the organic substituents attached to the Si-O bond, B-F monomer and amide groups is the key to the efficacy of the sensor. Optimization of applicability of the sensors in aqueous solvents vis-a-vis maintaining the sensitivity, range of detection, speed of detection, both quantitatively and qualitatively are a challenge. This review aims to present a comprehensive and critically analyzed discussion of the published probes, which will encourage further research in this field.

Keywords

Fluoride detection Colorimetric sensors Fluorometric sensors Si-O bond cleavage N-H deprotonation
Dutta, S., & Sahana, A. (2024). Synthetic Fluorometric and Colorimetric Sensors for Identification of Fluoride Anion: A Short Review. Asian Journal of Chemistry, 36(7), 1447–1460. https://doi.org/10.14233/ajchem.2024.31507
Download Citation
Endnote/Zotero/Mendeley (RIS)
BibTeX
References
  1. D. Wu, A.C. Sedgwick, T. Gunnlaugsson, E.U. Akkaya, J. Yoon and T.D. James, Chem. Soc. Rev., 46, 7105 (2017); https://doi.org/10.1039/C7CS00240H
  2. J. Chan, S.C. Dodani and C.J. Chang, Nat. Chem., 4, 973 (2012); https://doi.org/10.1038/nchem.1500
  3. Z. Guo, S. Park, J. Yoon and I. Shin, Chem. Soc. Rev., 43, 16 (2014); https://doi.org/10.1039/C3CS60271K
  4. L. You, D. Zha and E.V. Anslyn, Chem. Rev., 115, 7840 (2015); https://doi.org/10.1021/cr5005524
  5. H. Zhu, J. Fan, B. Wang and X. Peng, Chem. Soc. Rev., 44, 4337 (2015); https://doi.org/10.1039/C4CS00285G
  6. Z. Yang, A. Sharma, J. Qi, X. Peng, D.Y. Lee, R. Hu, D. Lin, J. Qu and J.S. Kim, Chem. Soc. Rev., 45, 4651 (2016); https://doi.org/10.1039/C5CS00875A
  7. J. Li, D. Yim, W.D. Jang and J. Yoon, Chem. Soc. Rev., 46, 2437 (2017); https://doi.org/10.1039/C6CS00619A
  8. S. Singha, D. Kim, H. Seo, S.W. Cho and K.H. Ahn, Chem. Soc. Rev., 44, 4367 (2015); https://doi.org/10.1039/C4CS00328D
  9. J. Yan, S. Lee, A. Zhang and J. Yoon, Chem. Soc. Rev., 47, 6900 (2018); https://doi.org/10.1039/C7CS00841D
  10. J.W. Steed and J.L. Atwood, Supramolecular Chemistry, Wiley: Hoboken, edn. 2 (2009).
  11. Z. Wang, H. Luecke, N. Yao and F.A. Quiocho, Nat. Struct. Biol., 4, 519 (1997); https://doi.org/10.1038/nsb0797-519
  12. J.W. Pflugrath and F.A. Quiocho, Nature, 314, 257 (1985); https://doi.org/10.1038/314257a0
  13. C. Caltagirone and P.A. Gale, Chem. Soc. Rev., 38, 520 (2009); https://doi.org/10.1039/B806422A
  14. A.F. Li, J.H. Wang, F. Wang and Y.B. Jiang, Chem. Soc. Rev., 39, 3729 (2010); https://doi.org/10.1039/b926160p
  15. P.A. Gale, Chem. Soc. Rev., 39, 3746 (2010); https://doi.org/10.1039/c001871f
  16. P.A. Gale, Chem. Commun., 4525, 4525 (2008); https://doi.org/10.1039/b809508f
  17. M.E. Moragues, R. Martinez-Manez and F. Sancenon, Chem. Soc. Rev., 40, 2593 (2011); https://doi.org/10.1039/c0cs00015a
  18. M. Li, Z. Liu, H. Wang, A.C. Sedgwick, J.E. Gardiner, S.D. Bull, H.N. Xiao and T.D. James, Dyes Pigments, 149, 669 (2018); https://doi.org/10.1016/j.dyepig.2017.11.033
  19. X. Wu, X.X. Chen, B.N. Song, Y.J. Huang, W.J. Ouyang, Z. Li, T.D. James and Y.B. Jiang, Chem. Commun., 50, 13987 (2014); https://doi.org/10.1039/C4CC04542D
  20. T. Nishimura, S.Y. Xu, Y.B. Jiang, J.S. Fossey, K. Sakurai, S.D. Bull and T.D. James, Chem. Commun., 49, 478 (2013); https://doi.org/10.1039/C2CC36107H
  21. S.J.M. Koskela, T.M. Fyles and T.D. James, Chem. Commun., 945 (2005); https://doi.org/10.1039/b415522j
  22. C.M. López-Alled, A. Sanchez-Fernandez, K.J. Edler, A.C. Sedgwick, S.D. Bull, C.L. McMullin, G. Kociok-Köhn, T.D. James, J. Wenk and S.E. Lewis, Chem. Commun., 53, 12580 (2017); https://doi.org/10.1039/C7CC07416F
  23. M. Li, G.E.M. Lewis, T.D. James, Y.T. Long, B. Kasprzyk-Hordern, J.M. Mitchels and F. Marken, ChemElectroChem, 1, 1640 (2014); https://doi.org/10.1002/celc.201402181
  24. V. Amendola, D. Esteban-Gómez, L. Fabbrizzi and M. Licchelli, Acc. Chem. Res., 39, 343 (2006); https://doi.org/10.1021/ar050195l
  25. B.L. Schottel, H.T. Chifotides and K.R. Dunbar, Chem. Soc. Rev., 37, 68 (2008); https://doi.org/10.1039/B614208G
  26. V. Thiagarajan, P. Ramamurthy, D. Thirumalai and V.T. Ramakrishnan, Org. Lett., 7, 657 (2005); https://doi.org/10.1021/ol047463k
  27. E.B. Veale and T. Gunnlaugsson, J. Org. Chem., 73, 8073 (2008); https://doi.org/10.1021/jo8012594
  28. Y. Wu, X. Peng, J. Fan, S. Gao, M. Tian, J. Zhao and S. Sun, J. Org. Chem., 72, 62 (2007); https://doi.org/10.1021/jo061634c
  29. S.K. Kim, J.H. Bok, R.A. Bartsch, J.Y. Lee and J.S. Kim, Org. Lett., 7, 4839 (2005); https://doi.org/10.1021/ol051609d
  30. R. Martínez-Máñez and F. Sancenón, Chem. Rev., 103, 4419 (2003); https://doi.org/10.1021/cr010421e
  31. T.H. Kim and T.M. Swager, Angew. Chem. Int. Ed., 42, 4803 (2003); https://doi.org/10.1002/anie.200352075
  32. T.H. Kim and T.M. Swager, Angew. Chem., 115, 4951 (2003); https://doi.org/10.1002/ange.200352075
  33. R.M. Duke, E.B. Veale, F.M. Pfeffer, P.E. Kruger and T. Gunnlaugsson, Chem. Soc. Rev., 39, 3936 (2010); https://doi.org/10.1039/b910560n
  34. K.M.K. Swamy, Y.J. Lee, H.N. Lee, J. Chun, Y. Kim, S.J. Kim and J. Yoon, J. Org. Chem., 71, 8626 (2006); https://doi.org/10.1021/jo061429x
  35. P. Hou, S. Chen, H. Wang, J. Wang, K. Voitchovsky and X. Song, Chem. Commun., 50, 320 (2014); https://doi.org/10.1039/C3CC46630B
  36. A. Roy, D. Kand, T. Saha and P. Talukdar, Chem. Commun., 50, 5510 (2014); https://doi.org/10.1039/c4cc01665c
  37. B. Zhu, F. Yuan, R. Li, Y. Li, Q. Wei, Z. Ma, B. Du and X. Zhang, Chem. Commun., 47, 7098 (2011); https://doi.org/10.1039/c1cc11308a
  38. D. Kim, S. Singha, T. Wang, E. Seo, J.H. Lee, S.J. Lee, K.H. Kim and K.H. Ahn, Chem. Commun., 48, 10243 (2012); https://doi.org/10.1039/c2cc35668f
  39. B. Ke, W. Chen, N. Ni, Y. Cheng, C. Dai, H. Dinh and B. Wang, Chem. Commun., 49, 2494 (2013); https://doi.org/10.1039/C2CC37270C
  40. T. Sheshashena Reddy, R. Maragani and R. Misra, Dalton Trans., 45, 2549 (2016); https://doi.org/10.1039/C5DT04039F
  41. A. Roy, A. Datar, D. Kand, T. Saha and P. Talukdar, Org. Biomol. Chem., 12, 2143 (2014); https://doi.org/10.1039/c3ob41886c
  42. R. Misra, T. Jadhav, B. Dhokale and S.M. Mobin, Dalton Trans., 44, 16052 (2015); https://doi.org/10.1039/C5DT02356D
  43. A. Roy, D. Kand, T. Saha and P. Talukdar, RSC Adv., 4, 33890 (2014); https://doi.org/10.1039/C4RA06933A
  44. S.Y. Kim, J. Park, M. Koh, S.B. Park and J.I. Hong, Chem. Commun., 4735–4737, 4735 (2009); https://doi.org/10.1039/b908745a
  45. T.W. Hudnall and F.P. Gabbai, Chem. Commun., 4596-4597, 4596 (2008); https://doi.org/10.1039/b808740g
  46. A.B. Descalzo, D. Jiménez, J.E. Haskouri, D. Beltrán, P. Amorós, M.D. Marcos, R. Martínez-Máñez and J. Soto, Chem. Commun., 562-563, 562 (2002); https://doi.org/10.1039/b111128k
  47. M. Vázquez, L. Fabbrizzi, A. Taglietti, R.M. Pedrido, A.M. González-Noya and M.R. Bermejo, Angew. Chem. Int. Ed., 43, 1962 (2004); https://doi.org/10.1002/anie.200353148
  48. C.B. Black, B. Andrioletti, A.C. Try, C. Ruiperez and J.L. Sessler, J. Am. Chem. Soc., 121, 10438 (1999); https://doi.org/10.1021/ja992579a
  49. S. Yamaguchi, S. Akiyama and K. Tamao, J. Am. Chem. Soc., 122, 6793 (2000); https://doi.org/10.1021/ja001042q
  50. I.S. Ke, M. Myahkostupov, F.N. Castellano and F.P. Gabbai, J. Am. Chem. Soc., 134, 15309 (2012); https://doi.org/10.1021/ja308194w
  51. O.A. Bozdemir, F. Sozmen, O. Buyukcakir, R. Guliyev, Y. Cakmak and E.U. Akkaya, Org. Lett., 12, 1400 (2010); https://doi.org/10.1021/ol100172w
  52. X. Jiang, M.C. Vieweger, J.C. Bollinger, B. Dragnea and D. Lee, Org. Lett., 9, 3579 (2007); https://doi.org/10.1021/ol7014187
  53. S.Y. Kim and J.I. Hong, Org. Lett., 9, 3109 (2007); https://doi.org/10.1021/ol0711873
  54. S. Dutta and A. Sahana, Anal. Methods, 16, 344 (2024); https://doi.org/10.1039/D3AY01840G
Read More
Author biographies is not available.
Statistic
Read Counter : 0 Download : 0