Addition of 6 equiv of (LiOBu)-Bu-t to a THF/Et2O Solution Of UCl4 at -25 degrees C generates [Li(THF)](2)[U((OBu)-Bu-t)(6)] (1) in 61% yield. 1 is soluble in polar organic solvents and is stable for several days in THF. However, 1. slowly decomposes in benzene or hexanes, forming the dinuclear uranium(IV) species [Li(THF)][U-2((OBu)-Bu-t)(9)] (2) as one of the decomposition products. Alternatively, 2 can be directly prepared in moderate yield by the addition of 4.5 equiv (LiOBu)-Bu-t to UCl4 in hexanes/THF at room temperature. The decomposition of 1 has been studied by H-1 and Li-7{H-1} NMR spectroscopies to elucidate the nature of this transformation. Oxidation of 1 occurs readily in the presence of 0.5 or 1 equiv Of I-2 to give [Li(Et2O)][U((OBu)-Bu-t)(6)] (3) and U((OBu)-Bu-t)(6) (4), respectively, in good yields. Alternately, 3 can be generated by comproportionation of 1 and 4. 1-4 have been fully characterized, including analysis by X-ray crystallography. In the solid-state these complexes possess large U-O-C-q bond angles, suggestive of a significant U-O pi interaction, In addition, we have studied the redox properties of 4 by cyclic voltammetry.