High-throughput DoE synthesis of chalcones and pyrazolines for fluorescent sensing

Pyrazolines are attractive scaffolds for fluorescent sensors due to their unique photophysical properties and the ease of their synthesis from chalcone precursors. While both chalcones and pyrazolines have been widely explored, a systematic optimization of their synthesis using design of experiments (DoE) has yet to be reported. Here, we apply a data-driven DoE strategy, evaluating multiple variables across more than 105 datapoints, to establish highly optimized conditions for the Claisen-Schmidt condensation of chalcones and their subsequent conversion to pyrazolines. High-throughput screening of the resulting library revealed pyrazoline P10 with unusual "turn on" fluorescence at 590 nm in the presence of Zn<sup>2+</sup> only. This integrated DoE-HTS workflow demonstrates a powerful approach for accelerating sensor discovery.

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Publication Details

Journal
Organic & Biomolecular Chemistry
Published
2025-12-23
DOI
https://doi.org/10.1039/d5ob01684c
Primary Topic
Molecular Sensors and Ion Detection
Type
article
Field-Weighted Citation Impact
0.00

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article

High-throughput DoE synthesis of chalcones and pyrazolines for fluorescent sensing

Alexander Ciupa
Organic & Biomolecular Chemistry
Molecular Sensors and Ion Detection
article

High-throughput DoE synthesis of chalcones and pyrazolines for fluorescent sensing

Alexander Ciupa
article en

Abstract

Pyrazolines are attractive scaffolds for fluorescent sensors due to their unique photophysical properties and the ease of their synthesis from chalcone precursors. While both chalcones and pyrazolines have been widely explored, a systematic optimization of their synthesis using design of experiments (DoE) has yet to be reported. Here, we apply a data-driven DoE strategy, evaluating multiple variables across more than 105 datapoints, to establish highly optimized conditions for the Claisen-Schmidt condensation of chalcones and their subsequent conversion to pyrazolines. High-throughput screening of the resulting library revealed pyrazoline P10 with unusual "turn on" fluorescence at 590 nm in the presence of Zn<sup>2+</sup> only. This integrated DoE-HTS workflow demonstrates a powerful approach for accelerating sensor discovery.

Organic & Biomolecular ChemistryVol. 24(4)
University of Liverpool (GB)
Research England
Openalex Percentile: Top 40%
Molecular Sensors and Ion Detection
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