Adiabatic Photocycloreversion of Bridged Benzene-Anthracene Biplanemers : Controlling of the Efficiency of the Excited Product Formation by Auxiliary Substituents on the Side-Chains
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The efficiency for excited product formation in the adiabatic photocycloreversion of bridged biplanemer <B>1</B> was controlled by the size of its side-chain substituents which changed the interchromophore distance in the photoproduct <B>2</B>.
- Chemistry Letters
Chemistry Letters 1997(9), 873-874, 1997-09
The Chemical Society of Japan