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Cited 45 time in webofscience Cited 47 time in scopus
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Multiple ion (Al3+, Cr3+, Fe3+, and Cu2+) sensing using a cell-compatible rhodamine-phenolphthalein-derived Schiff-base probeopen access

Authors
Das, BhriguramGhosh, AvijitDorairaj, Dorothy PriyankaDolai, MalayKarvembu, RamasamyMabhai, SubhabrataIm, HyunsikDey, SatyajitJana, AtanuMisra, Ajay
Issue Date
May-2022
Publisher
Elsevier BV
Keywords
Phenolphthalein; Rhodamine-B; CHEF on; PET off; Onsite detection; Cell imaging
Citation
Journal of Molecular Liquids, v.354, pp 1 - 14
Pages
14
Indexed
SCIE
SCOPUS
Journal Title
Journal of Molecular Liquids
Volume
354
Start Page
1
End Page
14
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/3157
DOI
10.1016/j.molliq.2022.118824
ISSN
0167-7322
1873-3166
Abstract
In this study, a novel rhodamine-phenolphthalein derivative (RBPF) was designed, synthesized, and char-acterized. RBPF exhibited the selective and sensitive colorimetric detection of Cu2+ and Fe3+ and fluoro-metric detection of Al3+ and Cr3+, thus functioning as a multiple-channel probe in MeOH-H2O (v/v = 9/1, 5 1.1M HEPES, pH 7.2) in the presence of other cations. A strong enhancement of the absorbance at around 555 nm was observed for the four mentioned cations. In contrast, in the presence of Al3+ and Cr3+, emis-sions were intensified within the red region of the spectra (583 and 586 nm, respectively). The RBPF sen-sor was found to bind to the metal ions at a 1:2 stoichiometric ratio. The proposed mechanism for the observed sensing behavior is the opening of the spirolactam ring of the rhodamine core in the presence of the four mentioned metal ions. The detection limits for Cu2+, Fe3+, Al3+, and Cr3+ were calculated to be 1.21 1.1M, 1.75 1.1M, 2.27 1.1M, and 1.29 1.1M, respectively. To test the practical use of the probe, TLC-based paper strips were fabricated. In addition, cell-imaging analysis of Al3+ and Cr3+ ions in the A549 cancer cell line produced promising concentration and time-dependent detection results. (C) 2022 Elsevier B.V. All rights reserved.
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