Factors distinguishing one-way and two-way photoisomerization of aromatic olefins. Effects of substituents on triplet energy surfaces of 8-fluoranthenylethylenes
Author:
Publisher
Elsevier BV
Subject
Physical and Theoretical Chemistry,General Physics and Astronomy
Reference24 articles.
1. Novel insights into photoisomerization of olefins
2. “One-way” photoisomerization between cis- and trans-olefin. A novel adiabatic process in the excited state
3. New insight into “one-way” photoisomerization of anthrylethylenes: absorption spectra of the trans triplets as intermediates of the isomerization
4. Transient Raman evidence of the one-way cis to trans isomerization in the lowest excited triplet state of 2-styrylanthracene
5. EFFECT OF OXYGEN ON THE PHOTOSTATIONARY STATE COMPOSITION IN TRIPLET SENSITIZED ISOMERIZATION OF 3,3-DIMETHYL-1-(2-NAPHTHYL)-1-BUTENE
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1. Present Status of the Photoisomerization About Ethylenic Bonds;Advances in Photochemistry;2007-01-05
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3. Mechanism for Photocleavage ofN-(Anthroyloxy)-9-fluorenylideneamines and Dynamic Behavior of Anthroyloxyl Radicals;Bulletin of the Chemical Society of Japan;2002-09
4. On the Z−E Photoisomerization of Chiral 2-Pentenoate Esters: Stationary Irradiations, Laser-Flash Photolysis Studies, and Theoretical Calculations;The Journal of Organic Chemistry;2000-09-21
5. Effects of a sulfur substituent on the behavior and generation mode of aroyloxyl radicals in the photolysis of diaroyl peroxides;Chemical Physics Letters;1999-12
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