The spin-exchange mechanism of catalysis of radical reactions and the
singlet-triplet conversion of the radical pairs (R(1), R(2)) in isotro
pic four-spin triads are theoretically studied. The triad (R(1), R(2),
M) is formed from a pair and the spin catalyst M, the ground state of
which is triplet with the total spin S = 1 (biradical, triplet molecu
le, or paramagnetic ion). S-T conversion of radical pairs is found to
be caused by triplet-triplet evolution of the (R(1), R(2), M) triad. I
n the case of zero magnetic fields, the spin dynamics and chemical dyn
amics of the reactions catalyzed by stable radicals R(3) and triplet s
pin catalyst M are shown to be alike.