Adiabatic photocycloreversion of bridged benzene-anthracene biplanemers: Controlling of the efficiency of the excited product formation by auxiliary substituents on the side-chains

Hideki Okamoto; Kyosuke Satake; Masaru Kimura

doi:10.1246/cl.1997.873

Adiabatic photocycloreversion of bridged benzene-anthracene biplanemers: Controlling of the efficiency of the excited product formation by auxiliary substituents on the side-chains

Hideki Okamoto, Kyosuke Satake, Masaru Kimura

Research output: Contribution to journal › Article

7 Citations (Scopus)

Abstract

The efficiency for excited product formation in the adiabatic photocycloreversion of bridged biplanemer 1 was controlled by the size of its side-chain substituents which changed the interchromophore distance in the photoproduct 2.

Original language	English
Pages (from-to)	873-874
Number of pages	2
Journal	Chemistry Letters
Issue number	9
DOIs	https://doi.org/10.1246/cl.1997.873
Publication status	Published - Jan 1 1997

ASJC Scopus subject areas

Chemistry(all)

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10.1246/cl.1997.873

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Okamoto, H., Satake, K., & Kimura, M. (1997). Adiabatic photocycloreversion of bridged benzene-anthracene biplanemers: Controlling of the efficiency of the excited product formation by auxiliary substituents on the side-chains. Chemistry Letters, (9), 873-874. https://doi.org/10.1246/cl.1997.873

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abstract = "The efficiency for excited product formation in the adiabatic photocycloreversion of bridged biplanemer 1 was controlled by the size of its side-chain substituents which changed the interchromophore distance in the photoproduct 2.",

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