Novel insight into the photochemical cis-trans isomerization of olefins.
Tatsuo Arai, Katsumi Tokumaru
Abstract
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Tatsuo Arai, Katsumi Tokumaru
Abstract
Open-access reader
Contrary to the hitherto accepted concept that every olefins undergo mutual isomerization between their cis-and trans-isomers, olefins substituted by anthracenyl and other aromatic polycyclic groups undergo only one-way isomerization from their cis-to trans-isomers, and the reverse isomerization from their trans-tocis-isomers never occurs. The mechanism for the one-way isomerization and the features to distinguish one-way or two-way isomerization is discussed to get whole view of the isomerization of olefins.
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Contrary to the hitherto accepted concept that every olefins undergo mutual isomerization between their cis-and trans-isomers, olefins substituted by anthracenyl and other aromatic polycyclic groups undergo only one-way isomerization from their cis-to trans-isomers, and the reverse isomerization from their trans-tocis-isomers never occurs. The mechanism for the one-way isomerization and the features to distinguish one-way or two-way isomerization is discussed to get whole view of the isomerization of olefins.
Key concepts: Isomerization, Chemistry, Photochemistry, Catalysis, Organic chemistry