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 |
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Pages (from-to) | 873-874 |
Number of pages | 2 |
Journal | Chemistry Letters |
Issue number | 9 |
DOIs | |
Publication status | Published - Jan 1 1997 |
ASJC Scopus subject areas
- Chemistry(all)