Optical switching of the redox activity of a hydroxychromene
- 1 January 1995
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Chemical Communications
- No. 16,p. 1695-1696
- https://doi.org/10.1039/c39950001695
Abstract
Simultaneous illumination and oxidation allows the transient photoisomer of a hydroxychromene to be held open or ‘trapped’, with subsequent liberation of the trapped quinone by dark cathodic reduction.Keywords
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