Phenylalanine-embedded carbazole-based fluorescent ‘turn-off’ chemosensor for the detection of metal ions

Fluorescent chemosensors are highly important for various applications including medical diagnostics, environmental monitoring, and industrial processing. Significant advancements have been made to produce sensors capable of detecting biologically and environmentally relevant ions. Specifically, carbazole-derived fluorophores are chemically stable agents with the ability to detect anions, cations, and small bioorganic molecules. However, most carbazole-based fluorescent probes for the detection of metal ions are Schiff bases and require stringent pH control to prevent hydrolysis. On the other hand, amide-based sensors that utilize stable amino acid scaffolds provide a robust sensing platform as well as a soft-chemical environment for detecting both soft and heavy metal ions. Herein, we explored an aromatic amino acid Phe-containing carbazole-based "turn-off" fluorescent chemosensor to improve the sensor specificity using π-conjugation and additional binding sites. The structure of the novel chemosensor was characterized by electrospray ionization mass spectrometry (ESI-MS) and nuclear magnetic resonance (NMR) spectroscopy. In addition, the sensing properties towards metal ions were studied using UV-vis and fluorescence spectroscopy. Among the various metal ions tested, the chemosensor showed high selectivity and sensitivity towards Co<sup>2+</sup>, Ni<sup>2+</sup>, and Cu<sup>2+</sup> ions. The detection limits for Co<sup>2+</sup>, Ni<sup>2+</sup>, and Cu<sup>2+</sup> ions were found to be 4.78 µM, 3.50 µM, and 5.17 µM respectively. Furthermore, the interaction of Phe-amino-carbazole with the various tested metal ions resulted in a flakes-like supramolecular structure, similar to the native Phe-amino-carbazole, whereas the interaction of the designed chemosensor with the Pb<sup>2+</sup> metal ion resulted in a uniform 3D-circular disc-like supramolecular structure, as confirmed by electron microscopy experiment. This highlights the potential of the Phe-containing carbazole-derived chemosensor for the detection of multiple cations with a decrease in the fluorescence response with a lower detection limit.

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Publication Details

Journal
Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy
Published
2024-10-11
DOI
https://doi.org/10.1016/j.saa.2024.125277
Citations
10
Primary Topic
Molecular Sensors and Ion Detection
Type
article
Field-Weighted Citation Impact
2.41

Funders

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article

Phenylalanine-embedded carbazole-based fluorescent ‘turn-off’ chemosensor for the detection of metal ions

Sigal Rencus‐Lazar, Om Shanker Tiwari, Varun Rawat, Ehud Gazit
10 citations
Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy
Molecular Sensors and Ion Detection
2.41
article

Phenylalanine-embedded carbazole-based fluorescent ‘turn-off’ chemosensor for the detection of metal ions

Sigal Rencus‐Lazar, Om Shanker Tiwari, Varun Rawat, Ehud Gazit
article en
10 citations

Abstract

Fluorescent chemosensors are highly important for various applications including medical diagnostics, environmental monitoring, and industrial processing. Significant advancements have been made to produce sensors capable of detecting biologically and environmentally relevant ions. Specifically, carbazole-derived fluorophores are chemically stable agents with the ability to detect anions, cations, and small bioorganic molecules. However, most carbazole-based fluorescent probes for the detection of metal ions are Schiff bases and require stringent pH control to prevent hydrolysis. On the other hand, amide-based sensors that utilize stable amino acid scaffolds provide a robust sensing platform as well as a soft-chemical environment for detecting both soft and heavy metal ions. Herein, we explored an aromatic amino acid Phe-containing carbazole-based "turn-off" fluorescent chemosensor to improve the sensor specificity using π-conjugation and additional binding sites. The structure of the novel chemosensor was characterized by electrospray ionization mass spectrometry (ESI-MS) and nuclear magnetic resonance (NMR) spectroscopy. In addition, the sensing properties towards metal ions were studied using UV-vis and fluorescence spectroscopy. Among the various metal ions tested, the chemosensor showed high selectivity and sensitivity towards Co<sup>2+</sup>, Ni<sup>2+</sup>, and Cu<sup>2+</sup> ions. The detection limits for Co<sup>2+</sup>, Ni<sup>2+</sup>, and Cu<sup>2+</sup> ions were found to be 4.78 µM, 3.50 µM, and 5.17 µM respectively. Furthermore, the interaction of Phe-amino-carbazole with the various tested metal ions resulted in a flakes-like supramolecular structure, similar to the native Phe-amino-carbazole, whereas the interaction of the designed chemosensor with the Pb<sup>2+</sup> metal ion resulted in a uniform 3D-circular disc-like supramolecular structure, as confirmed by electron microscopy experiment. This highlights the potential of the Phe-containing carbazole-derived chemosensor for the detection of multiple cations with a decrease in the fluorescence response with a lower detection limit.

Spectrochimica Acta Part A Molecular and Biomolecular SpectroscopyVol. 326
Tel Aviv University (IL), Exact Sciences (United States) (US)
Tel Aviv University, Air Force Office of Scientific Research, Air Force Research Laboratory
Openalex Percentile: Top 11%
Molecular Sensors and Ion Detection
2.41
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