How to cite this paper
Udhayakumari, D. (2023). Pyrrole Based Schiff Base as a Highly Sensitive Fluorescent Sensor for Fe3+ and Sn2+ Ions.Current Chemistry Letters, 12(2), 369-374.
Refrences
1. Balamurugan G., & Velmathi S. (2018) Coplanarity driven fluorescence turn-on sensor for chromium (III) and its application for bio-imaging. Photochem. Photobio. Sci.17, 239-244.
2. Bejugam V., Wei X., & Roper DK. (2016) Reductive spectrophotometry of divalent tin sensitization on soda lime glass. Appl. Surf. Sci. 376, 43-51.
3. Hu Y., Zhao F., Hu S., Dong Y., Li D., & Su Z. (2017) A novel turn-on colorimetric and fluorescent sensor for Fe3+ and its application in living cells. J. Photochem. Photobiol. 332, 351-356.
4. Huang Y., Lin T., Hou L., Ye F., & Zhao S. (2019) Colorimetric detection of thioglycolic acid based on the enhanced Fe3+ ions Fenton reaction. J. Microc. 144, 190-194.
5. Lee S., Jang H., Lee J., Jeon S.H., Sohn Y., & Ra C.S. (2017) Selective and sensitive morpholine-type rhodamine B-based colorimetric and fluorescent chemosensor for Fe(III) and Fe(II). Sens. Actuators, B. 248, 646-656.
6. Priyadarshini E., & Pradhan N. (2017) Gold nanoparticles as efficient sensors in colorimetric detection of toxic metal ions: A review. Sens. Actuators, B. 238, 888-902.
7. Soufeena P.P., & Aravindakshan K.K. (2019) Antipyrine derived Schiff base: A colurimetric sensor for Fe(III) and “turn-on” fluorescent sensor for Al(III). J Lumin. 205, 400-405.
8. Udhayakumari D. (2018) Chromogenic and fluorogenic chemosensors for lethal cyanide ion. A comprehensive review of the year 2016. Sens. Actuators, B. 259, 1022-1057. Doi: 10.1016/j.snb.2017.12.006.
9. Udhayakumari D, Naha S, & Velmathi S (2017) Colorimetric and fluorescent chemosensors for Cu2+. A comprehensive review from the years 2013–15. Anal. Methods. 9, 552.
10. Zhang S., Sun T., Xiao D., Yuan F., Wang E., Liu H., & Niu Q. (2018) A dual-responsive colorimetric and fluorescent chemosensor based on diketopyrrolopyrrole derivative for naked-eye detection of Fe3+ and its practical application. Spectrochim. Acta A. 189, 594-600.
11. Zhang Y., Zhou L., Liu Y., Liu D., Liu F., Liu F., Yan X., Liang X., Gao Y., & Lu G. (2018) Gas sensor based on samarium oxide loaded mulberry-shaped tin oxide for highly selective and sub ppm-level acetone detection. J Colloid Interface Sci. 531, 74-82.
12. Baranowski, M., Dyksik, M., & Płochocka, P. (2022) 2D Metal Halide Perovskites: A New Fascinating Playground for Exciton Fine Structure Investigations. Sci Rad. 1, 3-25.
13. Alharbi, K.H. (2022) A review on organic colorimetric and fluorescent chemosensors for the detection of Zn(II) ions. Crit Rev Anal Chem. https://doi.org/10.1080/10408347.2022.2033611.
14. Bag, R., Sikdar, Y., Sahu, S., Mukhopadhyay, C.D., Drew, M.G.B., & Goswami, S. (2022) Benzimidazole based ESIPT active chemosensors enable nano–molar detection of Cu2+ in 90% aqueous solution, MCF–7 cells, and plants. J. Photochem. Photobiol. A 431,114006
15. Kumar, V., Singh, D., Kumar, P., Chaudhary, G., Singh, A. P., & Gupta, R. (2022). Turn-on fluorescent detection of nickel and zinc ions by two related chemosensors containing naphthalimide ring(s). J. Mol. Struc. 1261, 132901.
16. Udhayakumari, D., & Velmathi, S. (2014) Colorimetric chemosensor for multi-signaling detection of metal ions using pyrrole based Schiff bases. Spectrochim. Acta - A: Mol. Biomol. 122, 428-435.
17. Bao, X., Cao, Q., Wu., X. Shu., H., Zhou., B., Geng, Y., & Zhu, J. (2016) Design and synthesis of a new selective fluorescent chemical sensor for Cu2+ based on a Pyrrole moiety and a Fluorescein conjugate. Tetrahedron Lett. 57, 942-948.
18. Sasan, S., Chopra, T., Gupta, A., Tsering, D., Kapoor, K.K., & Parkesh, R. (2022) Fluorescence “Turn-Off” and Colorimetric Sensor for Fe2+, Fe3+, and Cu2+ Ions Based on a 2,5,7-Triarylimidazopyridine Scaffold. ACS Omega. 13, 11114–11125.
19. Wang, Y., Mao, P-D., Wu, W-N., Mao, X-J., Fan, Y-C., Zhao, X-L., Xu, Z-Q., & Xu, Z-H. (2018) A novel New pyrrole-based single-molecule multianalyte sensor for Cu2+, Zn2+, and Hg2+ and its AIE activity. Sens. Actuators B Chem. 255, 3085-3092.