Effect of Substitution of a 2-Anthryl Group at the N=N and N=C Unsaturated Bonds on Their Photoisomerization in the Triplet State
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/cl/23/5/23_5_825/_pdf
Reference11 articles.
1. “One-way” photoisomerization between cis- and trans-olefin. A novel adiabatic process in the excited state
2. New insight into “one-way” photoisomerization of anthrylethylenes: absorption spectra of the trans triplets as intermediates of the isomerization
3. Photochemical one-way adiabatic isomerization of aromatic olefins
4. Novel insights into photoisomerization of olefins
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1. E,Z- Isomerization and Accompanying Photoreactions of Oximes, Oxime Ethers, Nitrones, Hydrazones, Imines, Azo- and Azoxy Compounds, and Various Applications;CRC Handbookof Organic Photochemistry and Photobiology, Volumes 1 & 2, Second Edition;2003-09-29
2. Design of Conjugated Aromatic Unsaturated Molecules for Photonics to Control Trans to cis Isomerization Under Irradiation;Molecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals;1998-11
3. Investigation of the Surface Morphology and Photoisomerization of an Azobenzene-Containing Ultrathin Film;Langmuir;1996-01-01
4. PHOTOCHEMICAL E/Z ISOMERIZATION OF ARYL-SUBSTITUTED METHANIMINES - AM1-CI POTENTIAL-ENERGY CURVES ALONG THE CN DOUBLE-BOND TWISTING AND THE N-ATOM INPLANE INVERSION;J MOL STRUC-THEOCHEM;1995
5. Photochemical isomerization of aryl-substituted methanimines. AM1-CI potential energy curves along the CN double bond twisting and the N atom in-plane inversion;Journal of Molecular Structure: THEOCHEM;1995-11
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