期刊
CHEMICAL PHYSICS LETTERS
卷 738, 期 -, 页码 -出版社
ELSEVIER
DOI: 10.1016/j.cplett.2019.136894
关键词
Sensor; Fluorescence; Excited state; TDDFT; TICT
资金
- National Natural Science Foundation of China [21807034, 21503226]
- Open Fund of the State Key Laboratory of Molecular Reaction Dynamics in DICP, CAS [SKLMRD-K201801]
The fluoride-sensing mechanism of a Schiff-base type sensor (Dyes Pigments, 2015, 123, 166) has been investigated by time-dependent density functional theory. The experimental ultraviolet and fluorescence spectra of the sensor before and after fluoride addition were well reproduced. The theoretical results showed that sensor molecules had distinctly different geometries in the ground state and first singlet excited state, which corresponded with the proposed twisted intramolecular charge transfer process and explained how the sensor fluorescence quenched. Thus, the sensor analysis of the fluoride anion by fluorescent spectroscopy was explained.
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