Abstract
A new approach to the theory of the EPR of spin correlated radical pairs (SCRP) is formulated. It is based on spectral exchange methods as applied to the two-site model and takes into account explicitly both the motion of one quantum (transverse magnetization) and two quantum coherences (polarizations) of SCRPs. This innovation allows for the interpretation of anti phase structure (APS) spectral shape asymmetry and for the transformation of the initially created ST 0RPM polarization into the APS spectral pattern. The results of this method as applied to micellized spin correlated radical pairs have been compared with the exact numerical solution of the corresponding stochastic Liouville equation and is commented on.
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