A dual pyridinium-tetraarylimidazole fluorescent sensor for the detection of the herbicide quizalofop-p-ethyl

Abstract

Quizalofop-p-ethyl is a highly effective herbicide, but threatens both human health and environmental safety when improperly used. Therefore, a simple and in situ method for detecting quizalofop-p-ethyl is urgently required. In this work, we designed and synthesized a dual pyridinium-tetraarylimidazole (DPT) via a simple and straightforward synthetic route. Upon binding quizalofop-p-ethyl, DPT exhibits a turn-on blue-green fluorescence response. High selectivity was demonstrated across 28 different herbicides and ions. The probe shows good linearity over a quizalofop-p-ethyl concentration range of 0–0.1 equiv., with a limit of detection of 1.05 × 10−7 M. Mechanistic studies indicate that the turn-on fluorescence could be attributed to the strong molecular interaction based on hydrogen bonding, electrostatic interaction, π–π stacking and hydrophobic interaction between the host and guest. The sensing capability of DPT has been successfully validated in test-strip assays, soil detection, plastic films and simulated water samples, demonstrating that this sensor enables simple, rapid, and on-site detection of quizalofop-p-ethyl in complex environments.

Graphical abstract: A dual pyridinium-tetraarylimidazole fluorescent sensor for the detection of the herbicide quizalofop-p-ethyl

Supplementary files

Article information

Article type
Paper
Submitted
24 Feb 2026
Accepted
27 Apr 2026
First published
30 Apr 2026

New J. Chem., 2026, Advance Article

A dual pyridinium-tetraarylimidazole fluorescent sensor for the detection of the herbicide quizalofop-p-ethyl

H. Lin, S. Wu, X. Fang, L. Lin, H. Guo and F. Yang, New J. Chem., 2026, Advance Article , DOI: 10.1039/D6NJ00696E

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements