Poly(butylene terephthalate) (PET) was depolymerized in refluxing o-di
chlorobenzene using stannoxane catalysts to produce good yields of cyc
lic oligomers. We have studied how the ring size distribution varies a
s a function of the starting concentration of monomer units, Over a co
ncentration range of 0.05 to 0.2 M, there is little change in the ring
size distribution. This result suggests that the depolymerizations we
re performed above the critical monomer concentration. Application of
a recent model by Mandolini (an adaptation of the Jacobson-Stockmayer
model) for thermodynamically controlled cyclizations contradicts the e
xperimental results by suggesting that the experiments were run below
the critical monomer concentration. It appears that Mandolini's model
may not be appropriate, in its present form, for depolymerizations. We
further studied the experimental data using RIS modeling in which the
probability of zero end-to-end distance for linear oligomers was used
to calculate macrocyclization equilibrium constants. Reasonable agree
ment was observed between calculated and experimental data with greate
r deviation for smaller ring sizes, as might be expected. Incorporatio
n of the width of the distribution and skewness into the calculation d
epressed the macrocyclization values.