Selective photoexcitation of rotamers of 1,2-diarylethylenes
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Spectroscopy,Analytical Chemistry
Reference14 articles.
1. Emissions of sterically hindered stilbene derivatives and related compounds. Part IV. Large conformational differences between ground and excited states of sterically hindered stilbenes: implications regarding stokes shifts and viscosity or temperature dependence of fluorescence yields
2. Conformational equilibriums in 1,2-diarylethylenes manifested in their emission spectra and lifetimes
3. Conformational equilibriums in trans-1,2-diarylethylenes manifested in their emission spectra. 2. Phenanthryl and benzophenanthryl derivatives
4. Conformational Equilibria in Trans 1,2-Diarylethylenes Manifested In Their Emission Spectra. Part III. (1a). Pyridyl and quinolyl derivatives
5. Conformational equilibriums in trans-1,2-diarylethylenes manifested in their emission spectra. 4. 3-Anthryl and 3-pyrenyl derivatives
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2. A cationic naphthyl derivative defies the non-equilibrated excited rotamers principle;Physical Chemistry Chemical Physics;2017
3. A theoretical study on three conformational structures of 2,6-distyrylpyridine;International Journal of Quantum Chemistry;2009-07-06
4. Temperature and solvent effects on rotamer-specific photobehaviour of the cis and trans isomers of 2-styrylanthracene;Physical Chemistry Chemical Physics;1999
5. Double Stereochemical Labeling in Stilbene Photochemistry: Tracing Phenyl Rotation Reveals Stereochemically Distinct Reaction Pathways for Formation of the E Photoproducts;Journal of the American Chemical Society;1997-04-01
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