Motion of symmetric diblock copolymer chains in the macroscopically or
iented lamellar phase is studied by molecular-dynamics simulation. For
diblocks of length N = 40 (1.1N(e)) and 100 (3N(e)), where N-e is the
entanglement length of the homopolymer melt, the diffusion constant p
arallel to the interface D-parallel to is nearly independent of chi, w
hile the perpendicular component D-perpendicular to is strongly suppre
ssed as chi, the Flory-Huggins parameter, is increased in agreement wi
th theoretical predictions based on the Rouse model. For even longer c
hains (N up to 400) a strong reduction of entanglement effects is obse
rved. We argue that due to the reduced chain overlap in the lamellar p
hase in this intermediate regime the chain motion is similar to an ell
ipsoidal molecule in a smectic phase.