Article ID Journal Published Year Pages File Type
5399322 Journal of Luminescence 2015 7 Pages PDF
Abstract
Dipole-dipole interactions are shown to stabilize the excited Sππ⁎ state in the systems studied in the same way as for others heteroaromatic luminophores. Specific interactions in protic solvents cause in addition significant geometry deformation to the non-planar structure of the chromophore. Large intramolecular spin-orbit coupling between the lowest singlet and triplet excited states in the latter case is revealed. It proves that intersystem crossing between these states should be the main channel of fluorescent quenching of 4-(N,N′-dimethylamino)-chalcone in protic solvents.
Related Topics
Physical Sciences and Engineering Chemistry Physical and Theoretical Chemistry
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