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A novel quinoline derivative as dual chemosensor for selective sensing of Al3+ by fluorescent and Fe2+ by colorimetric methods

•A novel quinoline derivative chemosensor (QN) as dual chemosensor was designed, synthesized and characterized.•The chemosensor QN exhibits highly selectivity fluorescence enhancement to Al3+ and colorimetric sensing for Fe2+.•The plausible binding modes of QN-Al3+ and QN-Fe2+ were supported by theo...

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Published in:Journal of molecular structure 2021-05, Vol.1231, p.129965, Article 129965
Main Authors: Ding, Yongjie, Zhao, Chunxiang, Zhang, Pengcheng, Chen, Yahong, Song, Weiwu, Liu, Guanglu, Liu, Zengchen, Yun, Lin, Han, Ruiqi
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Language:English
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cited_by cdi_FETCH-LOGICAL-c242t-2690cd5fc2a48bcf9ebd7b97fe27ad9d7f3ae64316d0aa11b09dd590120c22db3
cites cdi_FETCH-LOGICAL-c242t-2690cd5fc2a48bcf9ebd7b97fe27ad9d7f3ae64316d0aa11b09dd590120c22db3
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container_start_page 129965
container_title Journal of molecular structure
container_volume 1231
creator Ding, Yongjie
Zhao, Chunxiang
Zhang, Pengcheng
Chen, Yahong
Song, Weiwu
Liu, Guanglu
Liu, Zengchen
Yun, Lin
Han, Ruiqi
description •A novel quinoline derivative chemosensor (QN) as dual chemosensor was designed, synthesized and characterized.•The chemosensor QN exhibits highly selectivity fluorescence enhancement to Al3+ and colorimetric sensing for Fe2+.•The plausible binding modes of QN-Al3+ and QN-Fe2+ were supported by theoretical calculations. A simple and novel quinoline derivative (QN), based on quinoline-8-carboxaldehyde and 3‑hydroxy-2-naphthoic hydrazide was synthesized. The structure of chemosensor QN was confirmed by X-ray Crystallography. The chemosensor QN as dual chemosensor showed selective fluorescence recognition of Al3+ and colorimetric detection of Fe2+. In the presence of Al3+, the sensor QN generated a noticeable fluorescence enhancement accompanied with obvious color change from colorless to yellowish green. Moreover, QN was successfully used for colorimetric sensing for Fe2+, while the solution color changed from pale yellow to dark green. The detection limit was obtained to be 1.22 × 10−8 mol L−1 for Al3+ and 1.04 × 10−7 mol L−1 for Fe2+. The sensing mechanism of sensor QN toward Al3+ and Fe2+ were investigated by 1H NMR, ESI-MS and IR. Moreover, the coordination modes of QN-Al3+ and QN-Fe2+were confirmed by theoretical calculations. [Display omitted]
doi_str_mv 10.1016/j.molstruc.2021.129965
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A simple and novel quinoline derivative (QN), based on quinoline-8-carboxaldehyde and 3‑hydroxy-2-naphthoic hydrazide was synthesized. The structure of chemosensor QN was confirmed by X-ray Crystallography. The chemosensor QN as dual chemosensor showed selective fluorescence recognition of Al3+ and colorimetric detection of Fe2+. In the presence of Al3+, the sensor QN generated a noticeable fluorescence enhancement accompanied with obvious color change from colorless to yellowish green. Moreover, QN was successfully used for colorimetric sensing for Fe2+, while the solution color changed from pale yellow to dark green. The detection limit was obtained to be 1.22 × 10−8 mol L−1 for Al3+ and 1.04 × 10−7 mol L−1 for Fe2+. The sensing mechanism of sensor QN toward Al3+ and Fe2+ were investigated by 1H NMR, ESI-MS and IR. Moreover, the coordination modes of QN-Al3+ and QN-Fe2+were confirmed by theoretical calculations. 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A simple and novel quinoline derivative (QN), based on quinoline-8-carboxaldehyde and 3‑hydroxy-2-naphthoic hydrazide was synthesized. The structure of chemosensor QN was confirmed by X-ray Crystallography. The chemosensor QN as dual chemosensor showed selective fluorescence recognition of Al3+ and colorimetric detection of Fe2+. In the presence of Al3+, the sensor QN generated a noticeable fluorescence enhancement accompanied with obvious color change from colorless to yellowish green. Moreover, QN was successfully used for colorimetric sensing for Fe2+, while the solution color changed from pale yellow to dark green. The detection limit was obtained to be 1.22 × 10−8 mol L−1 for Al3+ and 1.04 × 10−7 mol L−1 for Fe2+. The sensing mechanism of sensor QN toward Al3+ and Fe2+ were investigated by 1H NMR, ESI-MS and IR. Moreover, the coordination modes of QN-Al3+ and QN-Fe2+were confirmed by theoretical calculations. 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A simple and novel quinoline derivative (QN), based on quinoline-8-carboxaldehyde and 3‑hydroxy-2-naphthoic hydrazide was synthesized. The structure of chemosensor QN was confirmed by X-ray Crystallography. The chemosensor QN as dual chemosensor showed selective fluorescence recognition of Al3+ and colorimetric detection of Fe2+. In the presence of Al3+, the sensor QN generated a noticeable fluorescence enhancement accompanied with obvious color change from colorless to yellowish green. Moreover, QN was successfully used for colorimetric sensing for Fe2+, while the solution color changed from pale yellow to dark green. The detection limit was obtained to be 1.22 × 10−8 mol L−1 for Al3+ and 1.04 × 10−7 mol L−1 for Fe2+. The sensing mechanism of sensor QN toward Al3+ and Fe2+ were investigated by 1H NMR, ESI-MS and IR. Moreover, the coordination modes of QN-Al3+ and QN-Fe2+were confirmed by theoretical calculations. 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subjects Aluminum ion
Colorimetric
Ferrous ion
Fluorescent
Quinoline
Theoretical calculation
title A novel quinoline derivative as dual chemosensor for selective sensing of Al3+ by fluorescent and Fe2+ by colorimetric methods
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