The kinetics of the reactions of 2,2,6,6-tetramethylpiperidine-1-oxyl
and 2,2,6,6-tetramethyl-4-benzoyloxypiperidine-1-oxyl with phenol, p-c
hlorophenol, p-methylphenol, and p-nitrophenol is studied in a liquid
phase and in polypropylene by using EPR spectroscopy. The rate constan
ts and activation energies are measured. It is shown that these reacti
ons are bimolecular and proceed in the kinetic regime, both in benzene
and polypropylene. In a polymeric matrix, the reaction rates are lowe
r; in this case, the bigger the molecular volume of reactants, the hig
her the additional Gibbs energy typical of solid phase.