The energy gap law established for aromatic hydrocarbons and rare earth ion
s relates the nonradiative decay rate to the energy gap of a transition thr
ough a multiphonon emission process. We show that this energy gap law can b
e applied to the phosphoresce of a series of conjugated polymers and monome
rs for which the radiative decay rate has been enhanced through incorporati
on of a heavy metal. We find that the nonradiative decay rate from the trip
let state T-1 increases exponentially with decreasing T-1-S-0 gap for the p
olymers and monomers at 300 and 20 K. Comparison of the nonradiative decay
of polymers with that of their corresponding monomers highlights the role o
f electron-lattice coupling.