Abstract
The rate of triplet decay k has been measured to 32 kbar for 20 aromatic hydrocarbons at room temperature. The measured lifetimes are generally shortened by high pressure. The slope of lnk‐vs‐P plots were all linear above 15 kbar. This slope is positive except for terphenyl, and can be related to “activation volumes” ΔV for this kinetic process. The values −1.0 < ΔV < 0.2 Å3 / molecule are found for this class of compounds. The perdeuterated compounds have a larger negative “activation volume” than the corresponding perprotonated aromatics. Hence, environmental perturbations are most effective for slow processes which arise from weak intramolecular perturbations in the solute.