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In this paper, the novel fluorescence probe XP based on Schiff-base was designed, synthesized and characterized, which could detect Y3+selectively and sensitively. The recognition mechanism of XP toward Y3+ was studied by Job's plot and HRMS. It was investigated that stoichiometric ratio of the probe XP conjugated with Y3+ was 1:2. And the detection limit was calculated as 0.30 μM. In addition, Y3+ was recognized by the test paper made from XP. And the probe XP could detect Y3+ selectively in Caenorhabditis elegans and the main organs of mice. Thus, XP was considered to have some potential for application in bioimaging. [ABSTRACT FROM AUTHOR]

It's important to pay great attention to the detection of CN− due to its high toxicity. Based on ESIPT characteristics, we design, synthesize and characterize the colorimetric and fluorescence "turn-on" probe AHAM to recognize CN−, which has the large Stokes shift (228 nm), exhibits high sensitivity and excellent selectivity. The limit detection of the probe AHAM for CN− was 1.94 × 10−8 M, which was much lower than the standard set by WHO and many previously reported probes. The recognition mechanism between AHAM and CN− was investigated by spectroscopic analysis, 1H NMR titration and mass spectrometry. To our surprise, AHAM could not only identify CN− reversibly, but also recognize CN− accurately in test paper and silica gel plate applications. Furthermore, AHAM was successfully used for fluorescence imaging in C. elegans and mice. It provides the new easy, fast and accurate method to detect CN−. [Display omitted] • The Stokes shift of AHAM toward CN− reached 228 nm. • AHAM recognized CN− with low LOD selectively, sensitively and reversibly. • AHAM achieved to visualize CN− in C. elegans and mice. [ABSTRACT FROM AUTHOR]