Cyclic phosphazene-based fluorescent probes with schiff base units for ultralow-level Hg2+ detection in real samples and paper-based devices
Source abstract
Abstract
The design and synthesis of new fluorescence sensors based on Schiff base derivatives are essential for environmental and biological applications. In this study, novel anthracene-appended cyclic phosphazenes (compounds 4-6) were developed as selective and effective sensors for Hg2+ ions. Standard spectroscopic techniques confirmed their structures. Photophysical and fluorescence behaviors were investigated using UV-vis absorption, steady-state and time-resolved fluorescence, and excitation-emission matrix (EEM) analyses. Compounds 4 and 5 exhibited excellent sensitivity and selectivity toward Hg2+, with detection limits (LOD) and quantification limits (LOQ) of 0.15-0.28 mu M and 0.45-0.84 mu M, respectively, along with broad linear ranges (0.90-10.0 mu M for 4 and 0.50-6.00 mu M for 5). Density functional theory (DFT) calculations supported the proposed sensing mechanisms. Real sample analyses using spike/recovery methods confirmed their practical applicability. Importantly, both compounds were successfully applied as paper-based test kits, enabling rapid and visible detection of Hg2+ ions in environmental diagnostics due to their clear colorimetric responses.
Source: openaire · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Molecular Sensors and Ion Detection · Luminescence and Fluorescent Materials · Advanced biosensing and bioanalysis techniques
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (51)
Show source-provided references
1. Goshisht · Mater. Adv. · 2022 · 3 · 261210.1039/D1MA01175H ↗
2. Karimi-Maleh · Chemosphere · 2023 · 33210.1016/j.chemosphere.2023.138815 ↗
3. Chua · Mater. Chem. Front. · 2021 · 5 · 65910.1039/D0QM00607F ↗
4. Ejidike · Bioinorgan. Chem. Appl. · 2016 · 9672451
5. Memon · Curr. Anal. Chem. · 2014 · 10 · 39310.2174/157341101003140521113731 ↗
6. Sahu · RSC Adv. · 2025 · 15 · 3046610.1039/D5RA03890A ↗
7. Berrones-Reyes · Mater. Chem. Phys. · 2019 · 233 · 8910.1016/j.matchemphys.2019.05.035 ↗
8. Pan · RSC Adv. · 2017 · 7 · 3600710.1039/C7RA05064J ↗
9. Harathi · Mater. Chem. Front. · 2020 · 4 · 147110.1039/C9QM00792J ↗
10. Chen · Inorgan. Chem. Commun. · 2013 · 38 · 7410.1016/j.inoche.2013.10.004 ↗
11. Okutan · J. Fluoresc. · 2016 · 26 · 233310.1007/s10895-016-1929-6 ↗
12. Tümay · J. Photochem. Photobiol. Chem. · 2021 · 40710.1016/j.jphotochem.2020.113093 ↗
13. B. Agrahari, S. Layek, Anuradha, R. Ganguly, D.D. Pathak, Inorgan. Chim. Acta 471 (2018) 345–354.10.1016/j.ica.2017.11.018 ↗
14. Mondal · New J. Chem. · 2018 · 42 · 958810.1039/C8NJ00418H ↗
15. Pandey · Spectrochim. Acta Part A Mol. Biomol. Spectroscopy · 2025 · 337
16. Sek · Spectrochim. Acta Part A Mol. Biomol. Spectroscopy · 2017 · 175 · 2410.1016/j.saa.2016.12.013 ↗
17. Xiong · Analyst · 2018 · 143 · 487010.1039/C8AN00940F ↗
18. Shyamal · Sens. Actuat. B Chem. · 2018 · 263 · 34710.1016/j.snb.2018.02.130 ↗
19. Sharma · J. Mol. Struct. · 2025 · 132910.1016/j.molstruc.2025.141398 ↗
20. Berhanu · TrAC Trends Anal. Chem. · 2019 · 116 · 7410.1016/j.trac.2019.04.025 ↗
21. Santhoshkumar · Inorgan. Chim. Acta · 2016 · 439 · 110.1016/j.ica.2015.09.030 ↗
22. S. Erdemir, S.J.J.o.L. Malkondu, 158 (2015), pp. 86-90.10.1016/j.jlumin.2014.09.038 ↗
23. Azadbakht · Spectrochim. Acta Part A Mol. Biomol. Spectroscopy · 2014 · 127 · 32910.1016/j.saa.2014.02.101 ↗
24. He · J. Mol. Struct. · 2021 · 1227 · 12952210.1016/j.molstruc.2020.129522 ↗
25. İbişoğlu · J. Lumin. · 2020 · 22210.1016/j.jlumin.2020.117125 ↗
26. Alidağı · Inorg. Chim. Acta. · 2017 · 457 · 9510.1016/j.ica.2016.12.013 ↗
27. Uslu · J. Photochem. Photobiol. C Photochem. Rev. · 2022 · 5310.1016/j.jphotochemrev.2022.100553 ↗
28. Carriedo · Macromolecules · 1996 · 29 · 532010.1021/ma951830d ↗
29. Issa · Spectrochim. Acta Part A Mol. Biomol. Spectrosc. · 2009 · 74 · 90210.1016/j.saa.2009.08.042 ↗
30. Zang · Tetrahedron · 2012 · 68 · 63610.1016/j.tet.2011.10.105 ↗
31. Khanmohammadi Chenab · Sol. Energy · 2022 · 234 · 910.1016/j.solener.2022.01.062 ↗
32. Keerthana · J. Fluoresc. · 2021 · 31 · 125110.1007/s10895-021-02770-9 ↗
33. Azab · J. Photochem. Photobiol. A Chem. · 2019 · 374 · 110.1016/j.jphotochem.2019.01.002 ↗
34. Chakraborty · J. Luminesc. · 2018 · 199 · 30210.1016/j.jlumin.2018.03.042 ↗
35. Shen · Mater. Chem. Front. · 2022 · 6 · 249110.1039/D2QM00542E ↗
36. Tümay · J. Lumin. · 2021 · 23110.1016/j.jlumin.2020.117813 ↗
37. Sivaraman · RSC Adv. · 2012 · 2 · 1060510.1039/c2ra21202a ↗
38. Şahin · Tetrahedron · 2016 · 72 · 584310.1016/j.tet.2016.08.004 ↗
39. S.O. Tümay, 6 (2021), pp. 10561-10572.10.1002/slct.202102052 ↗
40. Gugula · J. Mater. Chem. C · 2016 · 4 · 526310.1039/C6TC00943C ↗
41. Das · New J. Chem. · 2018 · 42 · 942410.1039/C7NJ05095J ↗
42. Tümay · New J. Chem. · 2018 · 42 · 1421910.1039/C8NJ02482K ↗
43. Wei · Sensor. Actuator. B Chem. · 2014 · 199 · 14210.1016/j.snb.2014.03.084 ↗
44. Andrade-Eiroa · Appl. Spectrosc. Rev. · 2013 · 48 · 7710.1080/05704928.2012.692105 ↗
45. Singh · J. Photochem. Photobiol. Chem. · 2023 · 441
46. M.J. Frisch, G.W. Trucks, H.B. Schlegel, G.E. Scuseria, M.A. Robb, J.R. Cheeseman, G. Scalmani, V. Barone, G.A. Petersson, H. Nakatsuji, X. Li, M. Caricato, A.V. Marenich, J. Bloino, B.G. Janesko, R. Gomperts, B. Mennucci, H.P. Hratchian, J.V. Ortiz, A.F. Izmaylov, J.L. Sonnenberg, Williams, F. Ding, F. Lipparini, F. Egidi, J. Goings, B. Peng, A. Petrone, T. Henderson, D. Ranasinghe, V.G. Zakrzewski, J. Gao, N. Rega, G. Zheng, W. Liang, M. Hada, M. Ehara, K. Toyota, R. Fukuda, J. Hasegawa, M. Ishida, T. Nakajima, Y. Honda, O. Kitao, H. Nakai, T. Vreven, K. Throssell, J.A. Montgomery Jr., J.E. Peralta, F. Ogliaro, M.J. Bearpark, J.J. Heyd, E.N. Brothers, K.N. Kudin, V.N. Staroverov, T.A. Keith, R. Kobayashi, J. Normand, K. Raghavachari, A.P. Rendell, J.C. Burant, S.S. Iyengar, J. Tomasi, M. Cossi, J.M. Millam, M. Klene, C. Adamo, R. Cammi, J.W. Ochterski, R.L. Martin, K. Morokuma, O. Farkas, J.B. Foresman, D.J. Fox, Gaussian, Inc., Wallingford CT, (2016).
47. Dong · J. Coord. Chem. · 2017 · 70 · 195310.1080/00958972.2017.1333113 ↗
48. Afrin · Sensors Diagnostics · 2023 · 2 · 98810.1039/D3SD00110E ↗
49. Behura · Inorg. Chem. Commun. · 2023 · 15410.1016/j.inoche.2023.110959 ↗
50. Uslu · Dalton Trans. · 2021 · 50 · 232410.1039/D0DT04095A ↗
51. Varadaraju · J. Incl. Phenom. Macrocycl. Chem. · 2019 · 95 · 7910.1007/s10847-019-00919-5 ↗