The mean-square displacement, <Delta r(2)>, of very high molecular weight d
iblock copolymers in solutions near the disorder-to-order transition is inv
estigated by pulsed-field-gradient NMR. The thermodynamic potential influen
cing the motion leads to a time-independent <Delta r(2)> at short times fol
lowed by free-diffusional behavior. The plateau is attributed to a trapping
of the copolymer chains at the "quasi-interfaces" formed by slow compositi
on fluctuations.