Herein, we report the synthesis of two phenylaza-[18]crown-6 lariat ethers with a coumarin fluorophore (1 and 2) and we reveal that compound 1 is an excellent probe for K(+) ions under simulated physiological conditions. The presence of a 2-methoxyethoxy lariat group at the ortho position of the anilino moiety is crucial to the substantially increased stability of compounds 1 and 2 over their lariat-free phenylaza-[18]crown-6 ether analogues. Probe 1 shows a high K(+)/Na(+) selectivity and a 2.5-fold fluorescence enhancement was observed in the presence of 100 mM K(+) ions. A fluorescent membrane sensor, which was prepared by incorporating probe 1 into a hydrogel, showed a fully reversible response, a response time of 150 s, and a signal change of 7.8% per 1 mM K(+) within the range 1-10 mM K(+). The membrane was easily fabricated (only a single sensing layer on a solid polyester support), yet no leaching was observed. Moreover, compound 1 rapidly permeated into cells, was cytocompatible, and was suitable for the fluorescent imaging of K(+) ions on both the extracellular and intracellular levels.
Abstract-A novel portable fluorometer combining the attributes of a smartphone with an easy-fit, simple and compact sample chamber fabricated using 3D printing has been developed for pH measurements of environmental water in the field. A colour filter attached over the camera white light LED selects an excitation band centred around λ ~ 450 nm with a 3 dB bandwidth, ∆λ ~ 21 nm. An application-specific, temperature stable chemosensor based on the 4-aminonaphthalimide fluorophore was synthesized to absorb at this wavelength whilst emitting in the green region of visible spectra. The green emission is readily detected using the smartphone camera and a simple RGB Android application. Suppression of the green emission increases with increasing pH enabling a straightforward pH sensor. The system was calibrated against a commercial spectrofluorometer and pH measurements were taken at various locations around Sydney. The results were then compared directly with those obtained using conventional electrode based measurements. The data can be stored in the phone's available memory or transmitted by phone back to base for further realtime analysis.
The fluorescence response of a set of cyclam‐triazole‐dye ligands is controlled by the appended dye, but simple reversal of the triazole topology affords a novel probe for Zn2+ with a longer fluorescence lifetime and higher fluorescence quantum yield upon Zn2+ binding (<τ> = 2.0 ns, Φf = 0.76).
The new π-conjugated 1,2,3-triazol-1,4-diyl fluoroionophore 1 generated via Cu(I) catalyzed [3 + 2] cycloaddition shows high fluorescence enhancement factors (FEF) in the presence of Na(+) (FEF=58) and K(+) (FEF=27) in MeCN and high selectivity towards K(+) under simulated physiological conditions (160 mM K(+) or Na(+), respectively) with a FEF of 2.5 for K(+).
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