Using slow diffusion methods at room temperature, five uranium coordination polymers were obtained, which either employ glutarate (Glut), terephthalate (TP), or 2-aminoterephthalate (TPNH 2 ) as bridging systems. Four of these networks are based on the uranyl(VI)-unit, UO 2 2+ , and one formed through the integration of tetravalent uranium as the coordinating metal center. 1) arranges as intermeshed one-dimensional (1D) infinite linear chains, locked into a three-dimensional (3D) network through hydrogen bonds with a uninodal 4-coordinated uom topology. 2) assembles as intermeshed two-dimensional (2D) layers, also stabilized as a 3D network through hydrogen bonding with a 2-nodal 4coordinated pts network topology. Na 2 [[UO 2 ] 2 (TP) 3 ]•9H 2 O (3) forms parallel layers that are stacked in an AB pattern. Layers possess the uninodal 3-coordinate honeycomb (hcb 4) assembles as a 3D-coordination network with a uninodal 3-c srs (SrSi 2 ) topology. The fifth compound contains uranium(IV) and the glutarate entity; U 6 (NO 3 ) 4 (Glut) 4 (O) 4 (OH) 4 (H 2 O) 6 •12H 2 O (5). The long-range structure of 5 adopts a 3D open framework, as it includes the flexible glutarate linker, in which U 6 O 8 secondary building units assemble as U 6 O 38 superclusters. These clusters are interlinked by the glutarate spacers resulting in a body centered cubic (bcu) topology.