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A highly selective and sensitive ratiometric fluorescent probe for quantitative detection of Al(III) in different natural matrices

A highly selective and sensitive ratiometric fluorescent probe for quantitative detection of... A highly selective and sensitive assay of Al(III) using ratiometric fluorescence enhancement is reported in an aqueous solution. The probe (named RS5) exhibits a red-shift of 54 nm upon binding with Al(III) ion. The significant enhancement response of RS5 at 481 nm is attributed to the formation of a 1:1 complex between the probe and Al(III), wherein RS5 acts as a tridentate NNN-donor ligand. The complexation process is ascertained by 1H, 13C, and 27Al NMR and HR-MS spectral techniques. The binding constant of the complex is determined to be 1.3 × 105 M−1. The ratiometric change in fluorescence upon complexation with Al(III) is ascribed to an increase in intramolecular charge transfer (ICT) transition along with chelation enhanced fluorescence (CHEF) processes. The probe can be applied for monitoring Al(III) in a pH range of 6–8. The limit of detection (LOD) of RS5 for the examination of Al(III) is found to be 0.3 μM. With an aim to understand the sensing behavior of RS5, the optical properties of the probe and its Al(III) complex are investigated using density functional theory (DFT) and time-dependent density functional theory (TD-DFT) methods. The probe is successfully employed for the determination of Al(III), with very high recovery percentages, in natural matrices like deep well water, tap water, drinking water, pond water, river water, bovine serum albumin (BSA) solution and blood serum. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Methods and Applications in Fluorescence IOP Publishing

A highly selective and sensitive ratiometric fluorescent probe for quantitative detection of Al(III) in different natural matrices

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Publisher
IOP Publishing
Copyright
© 2022 IOP Publishing Ltd
eISSN
2050-6120
DOI
10.1088/2050-6120/ac6eca
Publisher site
See Article on Publisher Site

Abstract

A highly selective and sensitive assay of Al(III) using ratiometric fluorescence enhancement is reported in an aqueous solution. The probe (named RS5) exhibits a red-shift of 54 nm upon binding with Al(III) ion. The significant enhancement response of RS5 at 481 nm is attributed to the formation of a 1:1 complex between the probe and Al(III), wherein RS5 acts as a tridentate NNN-donor ligand. The complexation process is ascertained by 1H, 13C, and 27Al NMR and HR-MS spectral techniques. The binding constant of the complex is determined to be 1.3 × 105 M−1. The ratiometric change in fluorescence upon complexation with Al(III) is ascribed to an increase in intramolecular charge transfer (ICT) transition along with chelation enhanced fluorescence (CHEF) processes. The probe can be applied for monitoring Al(III) in a pH range of 6–8. The limit of detection (LOD) of RS5 for the examination of Al(III) is found to be 0.3 μM. With an aim to understand the sensing behavior of RS5, the optical properties of the probe and its Al(III) complex are investigated using density functional theory (DFT) and time-dependent density functional theory (TD-DFT) methods. The probe is successfully employed for the determination of Al(III), with very high recovery percentages, in natural matrices like deep well water, tap water, drinking water, pond water, river water, bovine serum albumin (BSA) solution and blood serum.

Journal

Methods and Applications in FluorescenceIOP Publishing

Published: Jul 1, 2022

Keywords: aluminium; ratiometric; fluorescence; sensing; TDDFT

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