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A rhodamine-2-thioxoquinazolin-4-one derivative ( R1 ) has been synthesized by an addition-elimination reaction of rhodamine 6G ethylenediamine with methyl 2-isothiocyanatobenzoate, which exhibits high selectivity and sensitivity as a fluorescent sensor toward Fe 3+ under physiological conditions. Moreover, R1 could sense Fe 3+ by “naked eye” with a color change from colorless to yellow. To test the practical use of the probe, the determination of Fe 3+ in real water samples was evaluated. The application of the fluorescent sensor in monitoring intracellular Fe 3+ in glioma cell line U251 has also been demonstrated. In addition, single crystal structures of R1 ·1·5H 2 O·0·5CH 3 CN, as well as the possible intermediate of R1 with Ag + and Hg 2+ ions were reported. [ABSTRACT FROM AUTHOR]

Carboxylesterases (CEs) are widely distributed in the body and catalyze the hydrolysis of endogenous and exogenous substrates. They play important roles in drug metabolism, and abnormal levels often result in numerous diseases such as cancers. Therefore, it is important to establish a highly selective and sensitive probe for the real-time sensing of CEs activity. Herein, we synthesized a novel fluorescence-electrochemical multichannel probe 1 containing a ferrocene unit, which not only serves as part of the structure of probe 1 but also provides electrochemical signals. The probe exhibited high selectivity to CEs with a "Turn-On" fluorescence response and was applied for imaging in complicated biological samples including Staphylococcus aureus , living cells, and zebrafish. Furthermore, the hydrolysis of the acetoxy group of probe 1 by CEs decreased the electrochemical signal. All these results suggest that probe 1 can act as a multi-modal probe for real-time tracking of the activity CEs in complex biological environments. • A ferrocene-chalcone-based probe for detecting CEs by fluorescence and electrochemical signals was developed. • Probe 1 exhibited rapid response, good optical performance, high selectivity, and high sensitivity in solution. • The crystal structure of probe 1 and product 1a were determined. • Endogenous imaging-based CEs-detection in a range of S. aureus species, C6 cells, and zebrafish was achieved. [ABSTRACT FROM AUTHOR]