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- W4310857083 endingPage "114465" @default.
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- W4310857083 abstract "In this manuscript, the aggregation-induced emission (AIE) behaviour of a Schiff base salicylaldehyde hydrazone (SH) was investigated in DMSO-HEPES mixed solvents. The non-fluorescent SH in pure DMSO becomes a highly yellow-luminescent SH upon increasing the HEPES fraction ≥ 70 % in DMSO. The results of UV–vis, DLS, and SEM investigations supported the formation of SH self-aggregates, which inhibited the intramolecular rotation of SH and activated the excited state intramolecular proton transfer (ESIPT) mechanism to emit a bright yellow fluorescence at 535 nm. The AIEgen SH was applied for the sensing of cations, aldehydes, and nitroaromatics in HEPES buffer (5 % DMSO, 10 mM, pH 7.4) medium. The fluorescence of AIEgen SH was quenched by Cu2+, 2-hydroxy-5-nitrobenzaldehyde, and para-nitrophenol with a limit of detection of 3.74, 0.76, and 1.52 µM, respectively, among the other tested metal ions, aldehydes, and nitroaromatics. The cotton buds coated with the AIEgen SH were designed for the qualitative visual detection of Cu2+. The AIEgen SH was also employed for the detection of Cu2+ in mung bean sprouts. Moreover, the AIEgen SH was used to quantify the selective analytes in a real environmental water sample. Additionally, the AIEgen SH was employed to make yellow fluorescent gel and to visualize latent fingerprints (LFPs) on a non-porous glass slide." @default.
- W4310857083 created "2022-12-19" @default.
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- W4310857083 date "2023-03-01" @default.
- W4310857083 modified "2023-10-18" @default.
- W4310857083 title "Aggregation-induced emission active salicylaldehyde hydrazone with multipurpose sensing applications" @default.
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- W4310857083 doi "https://doi.org/10.1016/j.jphotochem.2022.114465" @default.
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