
Bulletin of the Chemical Society of Japan p. 2395 - 2400 (1987)
Update date:2022-08-11
Topics:
Oguchi, Takahisa
Arai, Tatsuo
Sakuragi, Hirochika
Tokumaru, Katsumi
The quantum yield of trans-cis isomerization of 3,3-dimethyl-1-(2-naphthyl)-1-butene was measured in the presence of various electron-accepting quenchers in benzene or in acetonitrile.In benzene the quantum yield was increased by addition of some of the quenchers; however, in acetonitrile it was decreased under similar conditions.This was attributed to more efficient formation of olefin triplets through an exciplex in benzene than through radical ion pairs in acetonitrile.
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