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 |
| Publication status | Published - 1997 |
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ASJC Scopus subject areas
- Chemistry(all)
Cite this
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.