We report the fluorescence lifetimes of terrylene in crystalline and amorph
ous matrices at room temperature and at 4.2 K. The measurements at 4.2 K sh
ould indicate the single molecule natural linewidth limit. We find that the
natural linewidth calculated from the bulk lifetime results for terrylene
in p-terphenyl, for terrylene in hexadecane, and for terrylene in polyethyl
ene systems agrees with low temperature single molecule linewidths. Most im
portant, we find that the excited state lifetime is larger than some previo
usly determined values, which means that the natural linewidth is narrower
for most systems than previously thought. (C) 1999 Elsevier Science B.V. Al
l rights reserved.