Abstract
The strong temperature dependence of the phosphorescent decay rate of benzene is attributed to pseudorotational motion of benzene which has the lowered D2h symmetry in the triplet state. This model accounts for the unusual deuterium effect of the activation energy, the very large pre-exponential factor, the low onset temperature, and the solvent effects.
| Original language | English |
|---|---|
| Pages (from-to) | 397-400 |
| Number of pages | 4 |
| Journal | Chemical Physics Letters |
| Volume | 10 |
| Issue number | 4 |
| DOIs | |
| State | Published - 15 Aug 1971 |
| Externally published | Yes |
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