Molecular diffusion in zeolites of unidimensional channel structure is
studied by pulsed field gradient NMR. In contrast to ordinary diffusi
on, the mean square displacement increases in proportion with the squa
re root of the observation time. This behavior is explained by assumin
g that the molecules are unable to pass each other (''single-file'' di
ffusion). The diffusivity of an isolated molecule estimated from the m
obility in the single-file system is 2 orders of magnitude larger than
the largest intracrystalline diffusivities in zeolites so far observe
d. The finding is supported by both the observed concentration depende
nce and molecular dynamics simulations.