1位あるいは4位にナフチル基を有するジアリールシクロヘプタ-1,3-ジエンの特異的光閉環反応

健一 中林, 博智 江並, 秀秋 束元, 大内 秋比古
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Abstract

The direct photocyclization of four 1,4-diarylcyclohepta-1,3-dienes(1a–d) with different aryl groups (phenyl, 1-naphthyl, and 2-naphthyl groups) by a XeCl excimer laser (308 nm) in hexane gave 1,5-diarylbicyclo[3.2.0]hept-6-enes (2a–c). The efficiency of the photochemical cyclization and fluorescence quantum yield strongly depended upon the aromatic substituents and this is interpreted by the conformation of the molecules.
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1位或4位具有萘基的双烯环庚子-1,3-二烯的特异性光闭环反应
用XeCl准分子激光(308 nm)在己烷中与不同芳基(苯基、1-萘基和2-萘基)直接光环化4个1,4-二烷基环庚-1,3-二烯(1a-d),得到1,5-二烷基双环[3.2.0]庚-6-烯(2a-c)。光化学环化效率和荧光量子产率强烈依赖于芳香族取代基,这可以通过分子的构象来解释。
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