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 › peer-review

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

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.",

author = "Hideki Okamoto and Kyosuke Satake and Masaru Kimura",

year = "1997",

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doi = "10.1246/cl.1997.873",

language = "English",

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journal = "Chemistry Letters",

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publisher = "Chemical Society of Japan",

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T2 - Controlling of the efficiency of the excited product formation by auxiliary substituents on the side-chains

AU - Okamoto, Hideki

AU - Satake, Kyosuke

AU - Kimura, Masaru

PY - 1997/1/1

Y1 - 1997/1/1

N2 - 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.

AB - 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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JF - Chemistry Letters

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ER -

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

Abstract

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