In this paper, a comparative study of the dynamic scattering propertie
s of some linear and cyclic copolymers in solution is presented. This
investigation is prompted by the recent elastic and quasielastic light
scattering measurements reported by Amis and co-workers on polystyren
e-polydimethylsiloxane cyclic diblock copolymers and their linear trib
lock counterpart. A formalism is presented which could provide a theor
etical framework for the analysis of some aspects of these data. The m
odel predicts that two relaxation modes characterize the dynamics of b
oth the cyclic diblock and the linear triblock copolymers. The amplitu
des and decay rates of these relaxation modes are investigated as a fu
nction of the polymer architecture, the concentration, and the scatter
ing wavevector. Questions related with phase transitions via aggregati
on or micellar formation are not addressed here.