The hexachlorocerate(III) anion, [CeCl], was found to be a potent photoreductant in acetonitrile solution with an estimated excited-state reduction potential of -3.45 V versus CpFe. Despite a short lifetime of 22.1(1) ns, the anion exhibited a photoluminescence quantum yield of 0.61(4) and fast quenching kinetics toward organohalogens allowing for its application in the photocatalytic reduction of aryl chloride substrates.
Systematic ligand variation in a structurally conserved framework of pentavalent uranium complexes of the formulas U(V)X2[N(SiMe3)2]3 (X = F, Cl, Br, N3, NCS, 2-naphthoxide) and U(V)OX[N(SiMe3)2]3(-) (X = -CCPh, -CN) allowed an investigation into the role of the inverse trans influence in pentavalent uranium complexes. The -CCPh and -CN derivatives were only stable in the presence of the trans-U═O multiple bond, implicating the inverse trans influence in stabilizing these complexes. Spectroscopic, structural, and density functional theory calculated electronic structural data are explored. Near-IR data of all complexes is presented, displaying vibronic coupling of 5f(1) electronic transitions along the primary axis. Electrochemical characterization allowed assessment of the relative donating ability of the various axial ligands in this framework. Electron paramagnetic resonance data presented display axial spectra, with hyperfine coupling along the primary axis.
Novel reaction pathways are illustrated in the synthesis of uranium(IV), uranium(V), and uranium(VI) monoimido complexes. In contrast to the straightforward preparation of U(V)(═NSiMe3)[N(SiMe3)2]3 (1), the synthesis of a uranium(V) tritylimido complex, U(V)(═NCPh3)[N(SiMe3)2]3 (4), from U(III)[N(SiMe3)2]3 and Ph3CN3 was found to proceed through multiple one-electron steps. Whereas the oxidation of 1 with copper(II) salts produced the uranium(VI) monoimido complexes U(VI)(═NSiMe3)X[N(SiMe3)2]3 (X = Cl, Br), the reaction of 4 with CuBr2 undergoes sterically induced reduction to form the uranium(VI) monoimido complex U(VI)(═NCPh3)Br2[N(SiMe3)2]2, demonstrating a striking difference in reactivity based on imido substituent. The facile reduction of compounds 1 and 4 with KC8 allowed for the synthesis of the uranium(IV) monoimido derivatives, K[U(IV)(═NSiMe3)[N(SiMe3)2]3] (1-K) and K[U(IV)(═NCPh3)[N(SiMe3)2]3] (4-K), respectively. In contrast, an analogous uranium(IV) monoimido complex, K[U(IV)(═NPh(F))[N(SiMe3)Ph(F)]], Ph(F) = -pentafluorophenyl (6), was prepared through a loss of N(SiMe3)2Ph(F) concomitant with one-electron oxidation of a uranium(III) center. The uranium(IV) monoimido complexes were found to be reactive toward electrophiles, demonstrating N-C and N-Si single bond formation. One-electron reduction of nitrite provided a route to the uranium(VI) oxo/imido complex, [Ph4P][U(VI)O(═NSiMe3)[N(SiMe3)2]3]. The energetics and electrochemical processes involved in the various oxidation reactions are discussed. Finally, comparison of the U(VI)(═NSiMe3)X[N(SiMe3)2]3, X = Cl, Br, complexes with the previously reported U(VI)OX[N(SiMe3)2]3, X = Cl, Br, complexes suggested that the donor strength of the trimethylsilylimido ligand is comparable to the oxo ligand.
A series of uranium(VI)-acetylide complexes of the general formula, U VI (O)(C≡C-C6H4-R)[N(SiMe3)2]3, with variation of the para substituent (R = NMe2, OMe, Me, Ph, H, Cl) on the aryl(acetylide) ring, were prepared. These compounds were analyzed by 13 C NMR spectroscopy, which showed that the acetylide carbon bound to the uranium(VI) center, U-C≡C-Ar, was shifted strongly downfield, with δ(13 C) values ranging from 392.1 to 409.7 ppm for Cl and NMe2 substituted complexes, respectively. These extreme high-frequency 13 C resonances are attributed to large negative paramagnetic (σ para) and relativistic spin-orbit (σ SO) shielding contributions, associated with extensive U(5f) and C(2s) orbital contributions to the U−C bonding in title complexes. The trend in the 13 C chemical shift of the terminal acetylide carbon is opposite of that observed in the series of parent (aryl)acetylenes, due to shielding effects of the para substituent. The 13 C chemical shifts of the acetylide carbon instead correlate with DFT computed U-C bond lengths and corresponding QTAIM delocalization indices or Wiberg bond orders. SQUID magnetic susceptibility measurements were indicative of the Van Vleck temperature independent paramagnetism (TIP) of the uranium(VI) complexes, suggesting a magnetic fieldinduced mixing of the singlet ground-state (f 0) of the U(VI) ion with low-lying (thermally inaccessible) paramagnetic excited states (involved also in the perturbation-theoretical treatment of the unusually large paramagnetic and SO contributions to the 13 C shifts). Thus, together with reported data, we demonstrate the sensitive 13 C NMR shifts serve as a direct, simple and accessible measure of uranium(VI)-carbon bond covalency.
Uranium complexes in the +3 and +4 oxidation states were prepared using the anionic PN (PN = ( N-(2-(diisopropylphosphino)-4-methylphenyl)-2,4,6-trimethylanilide) ligand framework. New complexes include the halide starting materials, (PN)UI (1) and (PN)UCl (2), which both yield (PN)U(N) (3) by reaction with NaN. Compound 3 was reduced with potassium graphite to produce a putative, transient uranium-nitrido moiety that underwent an intramolecular C-H activation to form a rare example of a parent imido complex, [K(THF)][(PN)U(═NH)[ PrP(CHMe)N(CHMeCH)]] (4). Calculated reaction energy profiles strongly suggest that a C-H insertion becomes unfavorable when a reductant is present, offering a distinctively different reaction pathway than previously observed for other uranium nitride complexes.
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