The cation radicals of cis- and trans-stilbene have been generated in solution under conditions where they do not interconvert by means of pulsed-laser-induced electron transfer from biphenyl to singlet 9,10-dicyanoanthracene followed by secondary electron transfer from the stilbenes to the biphenyl cation radical. The cis-stilbene cation radical is found to be configurationally stable on the microsecond time scale. Cage escape quantum yields have been measured for the photogenerated ion pairs of 9,10-dicyanoanthracene with cis-stilbene (0.134) and trans-stilbene (0.254), and these values have been used to analyze the quantum yields for electron-transfer-induced isomerization and oxygenation of the stilbenes.
|Original language||English (US)|
|Number of pages||2|
|Journal||Journal of Physical Chemistry|
|Publication status||Published - 1988|
ASJC Scopus subject areas
- Physical and Theoretical Chemistry