journal article·2025

Guanidine-based dual-responsive ‘turn on’ fluorometric probes for the selective detection of Zn 2+ cations and F − anions: spectral and theoretical investigations, smartphone assisted colorimetric detection, and applications in bio-imaging of the Artemia salina animal model and molecular logic gate operation

Abbas Khaja Raees Ahmed, Ramalingam Gajendhiran, Anbazhagan Sathiyaseelan, Lina Zhang, Myeong-Hyeon Wang, Rajakkani Paulpandiyan, Aziz Kalilur Rahiman

Journal of Materials Chemistry C· Volume 13· Issue 28
Publisher page

Abstract

Two guanidine-based fluorometric probes showed ‘turn on’ responses to Zn 2+ and F − ions. The bio-imaging studies showed Zn 2+ accumulation in the head region of A. salina . The probes exhibited INHIBIT logic gate behaviour with Zn 2+ and EDTA.
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Research context

OpenAlex topics: Molecular Sensors and Ion Detection · Advanced biosensing and bioanalysis techniques · Luminescence and Fluorescent Materials

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Post-Graduate and Research Department of Chemistry, The New College, University of Madras, Chennai – 600 014, India

Department of Bio-Health Convergence, Kangwon National University, Chuncheon 24341, Republic of Korea

Research Department of Chemistry, VHNSN College, Virudhunagar – 626 001, India

Funding

National Research Foundation of Korea

References (44)

Show source-provided references
1. Zhu · J. Lumin. · 2015 · 158 · 3810.1016/j.jlumin.2014.09.020 ↗
2. Kim · Spectrochim. Acta, Part A · 2019 · 211 · 3410.1016/j.saa.2018.11.058 ↗
3. Rout · Inorg. Chim. Acta · 2019 · 486 · 73310.1016/j.ica.2018.11.021 ↗
4. Li · Chem. Pap. · 2021 · 75 · 469710.1007/s11696-021-01684-x ↗
5. Ullah · ACS Appl. Mater. Interfaces · 2025 · 17 · 1776710.1021/acsami.4c01187 ↗
6. Huang · Spectrochim. Acta, Part A · 2020 · 243 · 11875410.1016/j.saa.2020.118754 ↗
7. Kaur · Coord. Chem. Rev. · 2018 · 358 · 1310.1016/j.ccr.2017.12.002 ↗
8. Li · Analyst · 2011 · 136 · 112410.1039/c0an00682c ↗
9. Tang · Sens. Actuators, B · 2013 · 185 · 18810.1016/j.snb.2013.04.109 ↗
10. Alhamami · Microchem. J. · 2024 · 197 · 10981710.1016/j.microc.2023.109817 ↗
11. Tayade · Inorg. Chim. Acta · 2014 · 421 · 53810.1016/j.ica.2014.05.014 ↗
12. Das · J. Photochem. Photobiol., A · 2022 · 427 · 11381710.1016/j.jphotochem.2022.113817 ↗
13. Marenco · Tetrahedron Lett. · 2012 · 53 · 67010.1016/j.tetlet.2011.11.126 ↗
14. Sivaraman · J. Lumin. · 2014 · 145 · 48010.1016/j.jlumin.2013.08.018 ↗
15. Khatri · J. Water Process Eng. · 2017 · 19 · 29110.1016/j.jwpe.2017.08.015 ↗
16. Zhou · Chem. Rev. · 2014 · 114 · 551110.1021/cr400352m ↗
17. Wang · Z. Naturforsch. B · 2018 · 73 · 60110.1515/znb-2018-0102 ↗
18. Otón · Chem. – Eur. J. · 2007 · 13 · 574210.1002/chem.200601757 ↗
19. Coles · Dalton Trans. · 2006 · 98510.1039/b515490a ↗
20. Blondeau · Chem. Soc. Rev. · 2007 · 36 · 19810.1039/B603089K ↗
21. Upadhyay · Talanta · 2010 · 81 · 71410.1016/j.talanta.2010.01.005 ↗
22. Sola · Dalton Trans. · 2012 · 41 · 840110.1039/c2dt30632h ↗
23. Hoque · New J. Chem. · 2022 · 46 · 1602510.1039/D2NJ03144B ↗
24. Kumar · Sens. Actuators, B · 2018 · 260 · 88810.1016/j.snb.2018.01.098 ↗
25. Mondal · J. Indian Chem. Soc. · 2015 · 92 · 1
26. Yang · Anal. Methods · 2018 · 10 · 183310.1039/C8AY00037A ↗
27. Yang · Langmuir · 2018 · 34 · 776710.1021/acs.langmuir.8b00947 ↗
28. Ahmed · J. Mater. Chem. B · 2025 · 13 · 62210.1039/D4TB01356E ↗
29. Manna · Microchem. J. · 2020 · 157 · 10486010.1016/j.microc.2020.104860 ↗
30. Gajendhiran · ACS Omega · 2024 · 9 · 5095710.1021/acsomega.4c04001 ↗
31. Subbaiah · Appl. Organomet. Chem. · 2025 · 39 · e7009310.1002/aoc.70093 ↗
32. Sethupathi · J. Photochem. Photobiol., B · 2020 · 207 · 11185410.1016/j.jphotobiol.2020.111854 ↗
33. Kaplan · Inorg. Chem. · 2024 · 63 · 225710.1021/acs.inorgchem.3c04229 ↗
34. Ji · Russ. J. Org. Chem. · 2019 · 55 · 139910.1134/S1070428019090215 ↗
35. Das · Spectrochim. Acta, Part A · 2019 · 212 · 22210.1016/j.saa.2018.12.053 ↗
36. Ramki · Methods · 2024 · 221 · 110.1016/j.ymeth.2023.11.010 ↗
37. Lee · New J. Chem. · 2015 · 39 · 390010.1039/C5NJ00169B ↗
38. Amuthakala · J. Mol. Struct. · 2020 · 1219 · 12864010.1016/j.molstruc.2020.128640 ↗
39. Manikandamathavan · RSC Adv. · 2015 · 5 · 2487710.1039/C5RA00002E ↗
40. Suresh · J. Photochem. Photobiol., A · 2019 · 385 · 11209210.1016/j.jphotochem.2019.112092 ↗
41. Sathiyaseelan · Carbohydr. Polym. · 2022 · 280 · 11902110.1016/j.carbpol.2021.119021 ↗
42. Sethupathi · J. Photochem. Photobiol., B · 2020 · 203 · 11173910.1016/j.jphotobiol.2019.111739 ↗
43. Gohil · ACS Sustainable Chem. Eng. · 2021 · 38 · 1309610.1021/acssuschemeng.1c05129 ↗
44. Chatterjee · Small · 2019 · 15 · 180474910.1002/smll.201804749 ↗