Answers are grounded in this paper and cite their sources.
Chemical biology study demonstrates polarity-adaptive Fe3+ detection and cellular imaging via dual resonance energy transfer, highlighting a strategy for robust biosensors.
Traditional fluorescent probes often exhibit compromised response and specificity due to poor adaptability to varying polar environments. Herein, we present the development of a robust Fe3+-specific small-molecule sensor by linking a tetraphenylsilole derivative and rhodamine 6G hydrazide via a Schiff-base π bridge to form a fluorescent donor–acceptor system. The dispersed silole moiety serves as dark donor, while the aggregated state of silole converts into emissive donor. Upon selective binding with Fe3+, the molecules are found to undergo fluorescence resonance energy transfer (FRET) and dark resonance energy transfer (DRET) to rhodamine moiety in a polarity-dependent manner. Hence, fluorescence quantitation of Fe3+ in both high-organic (>70%) and water-rich solutions (>70%) is successfully achieved with detection limits of 0.083 μM and 0.28 μM, respectively. Further, ratiometric intracellular imaging of Fe3+ is demonstrated using the probe. This sensing strategy can offer a promising avenue for the development of polarity-adaptive fluorescent probes targeting other metal ions in complex biological and environmental matrices.
No takes yet. Share an insight, caveat, or question.
Zhong et al. (2026) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: