When the α-UO3, La2O3 and NaCl structure types are idealized by a topological distortion involving only an extension or contraction of the hexagonal c axis (cubic [111]) it is clear that they are related to each other, and to the CaF2 type, by crystallographic shear. A number of lanthanide and actinide oxide structures are of these types, or derived superstructure types containing ordered anion `vacancies' or `interstitial' anions. The structural relations suggest possible reduction mechanisms.
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B. G. Hyde (1971) studied this question.
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