Sequential Dynamic Fluorescence Switching Driven by Oxa-/Thiol-Michael Conjugate Addition-Elimination Reactions

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Abstract

A dynamic molecular system undergoing sequential reconfiguration and multi-state fluorescence switching via intramolecular oxa/thiol-Michael conjugate addition-elimination reactions is reported. Triggered sequentially by chemical, solvent, and most importantly pH stimuli, the controlled progression through distinct molecular states was monitored by ratiometric absorption/fluorescence and NMR spectroscopy. This stimulus-controlled fluorescence switching demonstrates utility for real-time monitoring of processes, like chemically induced polymer degradation.

Original languageEnglish
Pages (from-to)6630-6634
Number of pages5
JournalOrganic Letters
Volume27
Issue number25
DOIs
StatePublished - 27 Jun 2025

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