A Novel Triphenylamine-Based Flavonoid Fluorescent Probe with High Selectivity for Uranyl in Acid and High Water Systems

• Published in: Sensors (Basel, Switzerland) Vol. 22; no. 18; p. 6987
• Main Authors: Liu, Bing, Cui, Wenbin, Zhou, Jianliang, Wang, Hongqing
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 01.09.2022; MDPI
• Subjects: Bioflavonoids; Caustic soda; Cobalt; Coordination; Density functional theory; Dimethyl sulfoxide; Electron transfer; Ethanol; Flavones; flavonoid; Flavonoids; Fluorescence; fluorescent probe; Investigations; NMR; Nuclear energy; Nuclear magnetic resonance; Raman spectroscopy; Selectivity; Solvents; triphenylamine; turn off; UO22; Water utilities; China; United States > US; Japan
• ISSN: 1424-8220; 1424-8220
• DOI: 10.3390/s22186987

Developing a fluorescent probe for UO22+, which is resistant to interference from other ions such as Cu2+ and can be applied in acidic and high-water systems, has been a major challenge. In this study, a “turn-off” fluorescent probe for triamine-modified flavonoid derivatives, 2-triphenylamine-3-hydroxy-4H-chromen-4-one (abbreviated to HTPAF), was synthesized. In the solvent system of dimethyl sulfoxide:H2O (abbreviated to DMSO:H2O) (v/v = 5:95 pH = 4.5), the HTPAF solution was excited with 364 nm light and showed a strong fluorescence emission peak at 474 nm with a Stokes shift of 110 nm. After the addition of UO22+, the fluorescence at 474 nm was quenched. More importantly, there was no interference in the presence of metal ions (Pb2+, Cd2+, Cr3+, Fe3+, Co2+, Th4+, La3+, etc.), especially Cu2+ and Al3+. It is worth noting that the theoretical model for the binding of UO22+ to HTPAF was derived by more detailed density functional theory (DFT) calculations in this study, while the coordination mode was further verified using HRMS, FT-IR and 1HNMR, demonstrating a coordination ratio of 1:2. In addition, the corresponding photo-induced electron transfer (PET) fluorescence quenching mechanism was also proposed.