The effect of the structural properties and the oxidation state of Mn on th
e O-18 isotope exchange behaviour of ternary manganites (La1-xSrxMnO3, La0.
5Sr1.5MnO4 and SrMnO3) has been studied. All types of (1)8O isotope exchang
e homomolecular, partially and completely heteromolecular) take place on th
e very active manganites with perovskite (LaMnO3 and La0.7Sr0.3MnO3) and pe
rovskite-like (SrMnO3) structure, but not on the less active K2NiF4-structu
re (La0.5Sr1.5MnO4). The highest O-18 exchange activity is observed for La0
.7Sr0.3MnO3, for which the completely heteromolecular O-18 exchange starts
to occur at 520 K, already, a T(o)n which is typical for excellent redox ca
talysts. The influence of the structural properties on the O-18 exchange an
d oxygen diffusion behaviour of the manganites is much more pronounced than
that of the Mn3+/Mn4+ ratio. The different reduction behaviour of the mang
anites with perovskite and K2NiF4-structure can be explained by means of th
e bond-valence model.