A colorimetric chemosensor for distinct color change with (E)-2-(1-(3-aminophenyl)ethylideneamino)benzenethiol to detect Cu2+ in real water samplesopen access
- Authors
- Patil, Nilima; Dhake, R. B.; Phalak, Raju; Fegade, Umesh; Inamuddin; Naushad, Mu.; Bathula, Chinna; Kanchi, Suvardhan; Govender, Krishna
- Issue Date
- Aug-2023
- Publisher
- SPRINGER NATURE
- Keywords
- Colorimetry; Chemosensor; Schiff base; Water samples; DFT studies
- Citation
- Analytical Sciences, v.39, no.8, pp 1413 - 1423
- Pages
- 11
- Indexed
- SCIE
SCOPUS
- Journal Title
- Analytical Sciences
- Volume
- 39
- Number
- 8
- Start Page
- 1413
- End Page
- 1423
- URI
- https://scholarworks.dongguk.edu/handle/sw.dongguk/21170
- DOI
- 10.1007/s44211-023-00355-z
- ISSN
- 0910-6340
1348-2246
- Abstract
- The study reports the synthesis of chemosensor (E)-2-(1-(3-aminophenyl)ethylideneamino)benzenethiol (C1), a highly sensitive, colorimetric metal probe that shows distinct selectivity for the detection of Cu2+ ion in various real water samples. Upon complexation with Cu2+ in CH3OH/H2O (60:40 v/v) (aqueous methanol), the C1 demonstrate significant enhancement in the absorption at 250 nm and 300 nm with a color change from light yellow to brown which was visualized using naked-eye. Therefore, these properties make C1 as an effective candidate for on-site Cu2+ ions detection. The emission spectrum of C1 illustrated "TURN-ON" recognition of Cu2+ with a limit of detection (LOD) of 46 nM. Furthermore, Density Functional Theory (DFT) calculations were performed to better understand the interactions between C1 and Cu2+. The obtained results suggested that the electron clouds present around the -NH2 in nitrogen and sulfur in -SH play a pivotal role in the formation of a stable complex. The computational results were in good agreement with the experimental UV-visible spectrometry results.
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Collections - College of Engineering > Department of Electronics and Electrical Engineering > 1. Journal Articles

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