Excited-state kinetics of complexes of a functionalized zinc tetraphenylporphyrin (ZnTPP) derivative, zinc mono(4-pridyl)triphenylporphyrin (ZnPyP) in toluene and polystrene/toluene mixtures have been investigated by time-resolved fluorescence spectroscopy. In addition to similar to2.0 ns monomer fluorescence lifetime, a approximate to 1.5 ns component was found by applying global analysis to the time-resolved fluorescence decay. The 1.5 ns component is assigned to a cyclic porphyrin tetramer [Part 1], with a approximate to 1 ns rotational correlation time at 10 degreesC. The initial fluorescence anisotropy of the monomer is found to be 0.1. In the tetramer an additional depolarization process occurs with a correlation time of similar to31 ps, resulting in a further decrease of the anisotropy from 0.1 to 0.025. This additional depolarization is ascribed to singlet energy transfer between the porphyrin units that constitute the tetramer. The intramolecular energy transfer processes have been simulated using the Monte Carlo method, yielding rate constants of (26 +/- 4 ps)(-1) and less than or equal to (180 ps)(-1) for energy transfer between nearest neighbor and next nearest neighbor porphyrins in the tetramer.