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Dual Luminescence of 1‐(9‐Anthryl)Butane‐1,3‐dione
Author(s) -
Mirochnik Anatolii G.,
Yu Anton,
Fedorenko Elena V.
Publication year - 2020
Publication title -
chemistryselect
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.437
H-Index - 34
ISSN - 2365-6549
DOI - 10.1002/slct.201904327
Subject(s) - luminescence , intramolecular force , photochemistry , enol , excited state , acetone , chemistry , butane , density functional theory , materials science , computational chemistry , optoelectronics , organic chemistry , atomic physics , physics , catalysis
The luminescent properties 1‐(9‐antryl)butane‐1,3‐dione ( 1 ) have been investigated by means of time resolved and steady state luminescence. The results have been analyzed via the method of time‐dependent density functional theory (TD DFT). It has been shown that for compound 1 there are two forms of enol, A and B, which differ in the position of the luminescence bands. For compound 1 in polar solvents, the dual luminescence has been detected: the structured band of 420 nm and the wide diffuse band at 530 nm. In nonpolar solvents, only a broad band at 530 nm was observed. A long‐wavelength band at 530 nm was attributed to the processes of Excited‐State Intramolecular Proton Transfer (ESIPT) and Twisted Intramolecular Charge Transfer (TICT). For compound 1 in acetone, the intensity of the short‐wavelength band of the enol B increased along with the temperature increase.