Excimer intermediate in the unsymmetrical photodimerization of the anthracene ring system
Author:
Publisher
Elsevier BV
Subject
Physical and Theoretical Chemistry,General Physics and Astronomy
Reference11 articles.
1. Photocyclization of bis(9-anthryl) 1,1,3,3-tetramethyldisiloxane, unsymmetrical photodimerization of the anthracene ring.
2. Mechanism of photocycloaddition in α,ω-(bis-9-anthryl)-n-alkanes
3. Comment on “mechanism of photocycloadditon in in α,ω-bis-(9-anthryl)-n-alkanes”
4. A spectroscopic study of the photodimerization of anthracene sandwich dimers in dianthracene
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1. Excimer formation from particially overlapped anthracene dimer based on saddle-shaped cyclooctatetrathiophene as spacer;Journal of Photochemistry and Photobiology A: Chemistry;2018-03
2. Anthracene adamantylbisurea receptors: switching of anion binding by photocyclization;Tetrahedron;2015-12
3. Anthracene photodimerization in a bis-chromophoric hydrogen-bonding receptor;Photochem. Photobiol. Sci.;2014
4. Optical switches with biplanemers obtained by intramolecular photocycloaddition reactions of tethered arenes;Chem. Soc. Rev.;2013
5. Structural Effects on the Ground and Excited-state Properties of Photoswitchable Hydrogen-Bonding Receptors;The Journal of Organic Chemistry;2006-09-30
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