A series of U(IV) complexes, ((R)ap)(2)U(THF)(2) [R = tert-butyl (t-Bu) (1), adamantyl (Ad) (2), diisopropylphenyl (dipp) (3)], supported by the redox-active 4,6-di-tert-butyl-2-(R)amidophenolate ligand, have been synthesized by salt metathesis of 2 equiv of the alkali metal salt of the ligand, M-2[(R)ap] [M = K (1 and 2), Na (3)], with UCl4. Exposure of these uranium complexes to 1 equiv of PhICl2 results in oxidative addition to uranium, forming the bis-(4,6-di-tert-butyl-2-(R)iminosemiquinone) ([(R)isq](1-)) uranium(IV) dichloride dimer, [((R)isq)(2)UCl](2)(mu(2)-Cl)(2) [R = t-Bu (4), Ad (5), dipp (6)]. The addition of iodine to 1 forms ((tBu)isq)(2)UI2(THF) (7), while the reactivity of I-2 with 2 and 3 results in decomposition. Complexes 1-7 have been characterized by H-1 NMR and electronic absorption spectroscopies. X-ray crystallography was employed to elucidate structural parameters of 2, 3, 5, and 7.