Abstract
The photophysical and photochemical properties of cis- and trans-1,2-bis(1-methyl-4-pyridinio)ethylene dication in acetonitrile are examined. These properties are significantly altered by the charge-transfer complexation in the ground state. The free olefins undergo cis-trans photoisomerization with a quantum yield of ca. 0.3. The cis isomer does not fluoresce unlike the trans isomer ({phi}{sub F} = 0.01, {tau}{sub F} = 5 {times} 10{sup {minus}11} s). The fluorescence of the trans isomer is quenched by complexation with iodide ions in the ground state. In addition, static quenching occurs within a 16-{angstrom} radius. The constants of the CT complexation with the iodide ion (in the ground state) are 1.6 M{sup {minus}1} for cis and 4.6 M{sup {minus}1} for trans. Upon excitation in the charge-transfer absorption band, the trans iodide complex gives the trans radical with a quantum yield of 0.06. The cis iodide complex leads not only to the formation of the cis radical isomer with a quantum yield of 0.02 but also to the trans isomer dication (quantum yield 0.05). The latter reaction can be interpreted either as a germinate pair catalyzed event or as isomerization in the excited charge-transfer state from the results of the nanosecond and picosecond laser flash photolysis experiments.
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