Two uranium(III) anilido complexes were synthesized, Tp* 2 U(NH-C 6 H 4 -p-terpyridine) (2-terpy) and Tp* 2 U(NH-C 6 H 4 -p-CH 3 ) (2-ptol), where Tp* = hydrotris(3,5-dimethylpyrazolyl)borate, by protonation of Tp* 2 UBn (1-Bn; Bn = benzyl) with 4-[2,6-di(pyridin-2-yl)pyridin-4-yl]benzenamine or p-toluidine, respectively. Conversion to the respective uranium(IV) imido species was possible by oxidation and deprotonation, forming Tp* 2 U(N-C 6 H 4 -p-terpyridine) (3-terpy) and Tp* 2 U(N-C 6 H 4 -p-CH 3 ) (3-ptol). These compounds were characterized by multinuclear NMR spectroscopy, IR spectroscopy, electronic absorption spectroscopy, and X-ray crystallography.

Using a redox-active dioxophenoxazine ligand, DOPO (DOPO = 2,4,6,8-tetra-tert-butyl-1-oxo-1H-phenoxazine-9-olate), a family of actinide (U, Th, Np, and Pu) and Hf tris­(ligand) coordination compounds was synthesized. The full characterization of these species using 1H NMR spectroscopy, electronic absorption spectroscopy, SQUID magnetometry, and X-ray crystallography showed that these compounds are analogous and exist in the form M­(DOPOq)2(DOPOsq), where two ligands are of the oxidized quinone form (DOPOq) and the third is of the reduced semiquinone (DOPOsq) form. The electronic structures of these complexes were further investigated using CASSCF calculations, which revealed electronic structures consistent with metals in the +4 formal oxidation state and one unpaired electron localized on one ligand in each complex. Furthermore, f orbitals of the early actinides show a sizable bonding overlap with the ligand 2p orbitals. Notably, this is the first example of a plutonium–ligand radical species and a rare example of magnetic data being recorded for a homogeneous plutonium coordination complex.

New uranyl derivatives featuring the amide ligand, -N(SiHMe) Bu, were synthesized and characterized by X-ray crystallography, multinuclear NMR spectroscopy, and absorption spectroscopies. Steric properties of these complexes were also quantified using the computational program Solid-G. The increased basicity of the free ligand -N(SiHMe) Bu was demonstrated by direct comparison to -N(SiMe), a popular supporting ligand for uranyl. Substitutional lability on a uranyl center was also demonstrated by exchange with the -N(SiMe) ligand. The increased basicity of this ligand and diverse characterization handles discussed here will make these compounds useful synthons for future reactivity.

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The activation of U–N multiple bonds in an imido analogue of the uranyl ion is accomplished by using a system that is very electron-rich with sterically encumbering ligands. Treating the uranium­(VI) trans-bis­(imido) UI2(NDIPP)2(THF)3 (DIPP = 2,6-diisopropylphenyl and THF = tetrahydrofuran) with tert-butyl­(dimethylsilyl)­amide (NTSA) results in a reduction and rearrangement to form the uranium­(IV) cis-bis­(imido) [U­(NDIPP)2(NTSA)2]­K2 (1). Compound 1 features long U–N bonds, pointing toward substantial activation of the NUN unit, as determined by X-ray crystallography and 1H NMR, IR, and electronic absorption spectroscopies. Computational analyses show that uranium­(IV)–imido bonds in 1 are significantly weakened multiple bonds due to polarization toward antibonding and nonbonding orbitals. Such geometric control has important effects on the electronic structures of these species, which could be useful in the recycling of spent nuclear fuels.