M IV molecular oxo-clusters (M = Zr,Hf, Ce,T h, U, Np,P u) are prolific in bottoms-up material design, catalysis, and elucidating reaction pathwaysi nn ature and in synthesis. Here we introduce Ce 70 ,awheel-shaped oxo-cluster,[ Ce IV 70-(OH) 36 (O) 64 (SO 4) 60 (H 2 O) 10 ] 4À .C e 70 crystallizes into intricate high pore volume frameworks with divalent transition metals and Ce-monomer linkers.Eight crystal-structures feature four framework types in which the Ce 70-rings are linked as propellers,i no ffset-stacks,i natartan pattern, and as isolated rings.S mall-angle X-ray scattering of Ce 70 dissolved in butylamine,w ith and without added cations (Ce IV ,a lkaline earths, Mn II), shows the metals differentiating roles in ring linking, leading to supramolecular assemblies.T he large acidic pores and abundant terminal sulfates provideion-exchange behavior, demonstrated with U IV and Nd III .Frameworks featuring Ce III/IVmonomer linkers demonstrate both oxidation and reduction. This study opens the door to mixed-metal, highly porous framework catalysts,a nd new clusters for metal-organic framework design topology of M IV-oxo clusters is the hexamer (M 6 , [M IV 6 (OH,O) 8 ]), [5] which structurally resembles the M IV O 2 fluorite-type lattice.T his molecular oxide fragment has been stabilized and isolated with carboxylate,n itrate,s ulfate,a nd polyoxometalate ligands. [6] Combining rigid bicarboxylate linkers with Zr IV 6 led to the discovery of the metal-organic framework (MOF) known as UiO-66. [5a] This compound and its derivatives comprise an extensive MOF family known for high stability and functionalizabilty,exploited in separations, storage and catalysis. [8] Not suprising,U iO-66 analogues of Hf IV , [7] Ce IV , [8] Th IV , [9] U IV , [10] Np IV , [5f] and Pu IV [11] have all been discovered. Beyond the hexamer,l arger M IV-oxo clusters are built symmetrically around the M 6 core,a nd by extension, are larger fragments of the fluorite lattice.T he largest is M 38 , synthesized from Ce IV , [12] Pu IV , [2c] U IV [13] and Np IV. [14] Ceriumoxo clusters and nanomaterials are of special relevance. [6e, 12] Owed to facile Ce III-Ce IV redox behavior and concomitant oxygen transport, ceria nanoparticles are used as automotive redox catalysts,i no xide fuel cells,a nd as photoactive solar cell materials. [15] Atomically precise cerium-oxo clusters are valuable to understand form-function relationships;and Ce 10 , Ce 20 ,C e 22 ,C e 24 ,C e 38 and Ce 40 have been isolated, some of which have distinct Ce III and Ce IV sites. [6e,12] Farha and coworkers recently demonstrated catalytic activity of Ce 38 ,owed to the high porosity and redox activity of the solid material. [16] We exploited Ln III and TM II countercations to create an ew family of giant U IV-oxo clusters including the U 84 "superatom" (with Ln III)a nd U 70 wheel (with TM II). [4b, 17] Following U 70 ,t he Zr 70 analogue was described in multiple frameworks with transition metals,Mg 2+ ,Na + and no countercations. [18] This large toroid, with external...