The nature of the red emission of aromatic thioketones
Author:
Publisher
Elsevier BV
Subject
General Physics and Astronomy,General Chemical Engineering,General Chemistry
Reference14 articles.
1. Photocycloadditionen der Thione an 1.2‐ und 1.3‐Diene und an elektronenarme Olefine
2. Photochemical synthesis. 49. Thione photochemistry. 9. Mechanism of photocycloaddition of thiobenzophenone at 366 nm
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1. Photochemical reactions of some aromatic thiones with bis(methylthio)ethyne; (4 + 2)- versus (2 + 2)-cycloaddition products. Spectroscopic evidence for the equilibrium thiete ⇄ α,β-unsaturated dithioester;Recueil des Travaux Chimiques des Pays-Bas;2010-09-02
2. Photochemical reactions of some aromatic thiones with bis(methylthio)ethyne; (4 + 2)- versus (2 + 2)-cycloaddition products. Spectroscopic evidence for the equilibrium thiete ⇄ α,β-unsaturated dithioester;Recueil des Travaux Chimiques des Pays-Bas;2010-09-02
3. Closed Nanocontainer Enables Thioketones to Phosphoresce at Room Temperature in Aqueous Solution;The Journal of Physical Chemistry B;2010-03-31
4. Ferrocene and ferrocenyl derivatives in luminescent systems;Journal of Photochemistry and Photobiology A: Chemistry;2000-04
5. Vibrational activation in the radiationless decay of the S2, S1, T1, and T2 states of aromatic thiones in solution: red edge effects;The Journal of Physical Chemistry;1992-10
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