Inverse Trans Influence Research Articles

Actinide inverse trans influence versus cooperative pushing from below and multi-center bonding

Actinide-ligand bonds with high multiplicities remain poorly understood. Decades ago, an effect known as 6p pushing from below (PFB) was proposed to enhance actinide covalency. A related effect—also poorly understood—is inverse trans influence (ITI). The present computational study of actinide-ligand covalent interactions with high bond multiplicities quantifies the energetic contributions from PFB and identifies a hitherto overlooked fourth bonding interaction for 2nd-row ligands in the studied organometallic systems. The latter are best described by a terminal O/N ligand exhibiting quadruple bonding interactions with the actinide. The 4th interaction may be characterized as a multi-center or charge-shift bond involving the trans ligand. It is shown in this work that the 4th bonding interaction is a manifestation of ITI, assisted by PFB, and provides a long-sought missing piece in the understanding of actinide chemistry.

Source Data: Actinide Inverse Trans Influence: Cooperative `Pushing from Below' and Multi-Center Bonding

Source Data: Actinide Inverse Trans Influence: Cooperative `Pushing from Below' and Multi-Center Bonding

Ligand Control of Oxidation and Crystallographic Disorder in the Isolation of Hexavalent Uranium Mono-Oxo Complexes

The development of high-valent transuranic chemistry requires robust methodologies to access and fully characterize reactive species. We have recently demonstrated that the reducing nature of imidophosphorane ligands supports the two-electron oxidation of U4+ to U6+ and established the use of this ligand to evaluate the inverse-trans-influence (ITI) in actinide metal-ligand multiple bond (MLMB) complexes. To extend this methodology and analysis to transuranic complexes, new small-scale synthetic strategies and lower-symmetry ligand derivatives are necessary to improve crystallinity and reduce crystallographic disorder. To this end, the synthesis of two new imidophosphorane ligands, [N═PtBu(pip)2]- (NPC1) and [N═PtBu(pyrr)2]- (NPC2) (pip = piperidinyl; pyrr = pyrrolidinyl), is presented, which break pseudo-C3 axes in the tetravalent complexes, U[NPC1]4 and U[NPC2]4. The reaction of these complexes with two-electron oxygen-atom-transfer reagents (N2O, trimethylamine N-oxide (TMAO) and 2,3:5,6-dibenzo-7-azabicyclo[2.2.1]hepta-2,5-diene (dbabhNO)) yields the U6+ mono-oxo complexes U(O)[NPC1]4 and U(O)[NPC2]4. This methodology is optimized for direct translation to transuranic elements. Of the two ligands, the NPC2 framework is most suitable for facilitating detailed bonding analysis and assessment of the ITI. Theoretical evaluation of the U-(NPC) bonding confirms a substantial difference between axially and equatorially bonded N atoms, revealing markedly more covalent U-Nax interactions. The U 6d + 5f combined contribution for U-Nax is nearly double that of U-Neq, accounting for ITI shortening and increased bond order of the axial bond. Two distinct N-atom hybridizations in the pyrrolidine/piperidine rings are noted across the complexes, with approximate sp2 and sp3 configurations describing the slightly shorter P-N"planar" and slightly longer P-N"pyramidal" bonds, respectively. In all complexes, the NPC2 ligands feature more planar N atoms than NPC1, in accordance with a higher electron-donating capacity of the former.

Insights into the Electronic Structure of a U(IV) Amido and U(V) Imido Complex.

Reaction of the N‐heterocylic carbene ligand iPrIm (L1) and lithium bis(trimethylsilyl)amide (TMSA) as a base with UCl4 resulted in U(IV) and U(V) complexes. Uranium's +V oxidation state in (HL1)2[U(V)(TMSI)Cl5] (TMSI=trimethylsilylimido) (2) was confirmed by HERFD‐XANES measurements. Solid state characterization by SC‐XRD and geometry optimisation of [U(IV)(L1)2(TMSA)Cl3] (1) indicated a silylamido ligand mediated inverse trans influence (ITI). The ITI was examined regarding different metal oxidation states and was compared to transition metal analogues by theoretical calculations.

Characterization of Uranyl Coordinated by Equatorial Oxygen: Oxo in UO3 versus Oxyl in UO3.

Uranium trioxide, UO3, has a T-shaped structure with bent uranyl, UO22+, coordinated by an equatorial oxo, O2-. The structure of cation UO3+ is similar but with an equatorial oxyl, O•-. Neutral and cationic uranium trioxide coordinated by nitrates were characterized by collision induced dissociation (CID), infrared multiple-photon dissociation (IRMPD) spectroscopy, and density functional theory. CID of uranyl nitrate, [UO2(NO3)3]- (complex A1), eliminates NO2 to produce nitrate-coordinated UO3+, [UO2(O•)(NO3)2]- (B1), which ejects NO3 to yield UO3 in [UO2(O)(NO3)]- (C1). Finally, C1 associates with H2O to afford uranyl hydroxide in [UO2(OH)2(NO3)]- (D1). IRMPD of B1, C1, and D1 confirms uranyl equatorially coordinated by nitrate(s) along with the following ligands: (B1) radical oxyl O•-; (C1) oxo O2-; and (D1) two hydroxyls, OH-. As the nitrates are bidentate, the equatorial coordination is six in A1, five in B1, four in D1, and three in C1. Ligand congestion in low-coordinate C1 suggests orbital-directed bonding. Hydrolysis of the equatorial oxo in C1 epitomizes the inverse trans influence in UO3, which is uranyl with inert axial oxos and a reactive equatorial oxo. The uranyl ν3 IR frequencies indicate the following donor ordering: O2-[best donor] ≫ O•-> OH-> NO3-.

Cis- and trans-Ligand Effects on the Inverse trans-Influence in [UVI(O)(L)Cl4]0/- (L = Unidentate Ligand) Complexes.

A comprehensive exploration of the inverse trans-influence (ITI) phenomenon in a series of cis-[UVI(O)(L)Cl4]0/- and trans-[UVI(O)(L)Cl4]0/- complexes involving a wide variety of neutral and anionic unidentate ligands L, using relativistic density functional theory, threw light on the still-intriguing physics of ITI, elucidated its origin, and deployed the ligands L in cis- and trans-ITI sequences (ladders). ITI is produced for the complete set of L in both series of [U(O)(L)Cl4]0/- complexes, but this is not reflected in the thermodynamic stability of the [U(O)(L)Cl4]0/- isomers. In effect the hard and strong σ-donor anionic ligands stabilize the trans isomers, but the opposite is true for the soft σ-donor/π-donor neutral and anionic ligands that stabilize the cis isomers. According to the ITI%(U-L) metrics the hard strong σ-donor anionic ligands exert stronger ITI than the soft σ-donor/π-donor neutral ones, while according to the ITI%(U-O) metrics ITI is produced only for the more stable trans-[U(O)(L)Cl4]0/- isomers involving the anionic ligands. In contrast the neutral ligands in the more stable cis-[U(O)(L)Cl4]0/- isomers produce the normal cis influence (CI). Furthermore, the more electronegative ligands produce stronger ITI. ITI%(U-O) cis- and trans-philicity ladders are also built for both series of complexes employing the isotropic σiso(SO) 17O NMR shielding constants as a sensitive metric of the ITI phenomenon. The NMR ITI%(U-O) metrics are consistent with the ITI%(U-O) ones illustrating that the isotropic 17O NMR shifts are sensitive metrics of the covalency of the multiple U-O bonding mode and, hence, of the ITI phenomenon. Interestingly the 2σ BD(U-O) natural bond orbitals play a key role in tuning the bond length and covalency of the U-O bond through the 2σ(U≡O) → 2σ*(U≡O) hyperconjugative interactions. The assessment of the magnitude of the ITI in the [UVI(O)(L)Cl4]0/- complexes and the recognition of the factors affecting ITI dispose a guide to experimentalists working in the area of uranium chemistry to develop strategies for stabilizing uranium-ligand linkages.

Two-Electron Oxidative Atom Transfer at a Homoleptic, Tetravalent Uranium Complex.

A tetrahomoleptic, pseudotetrahedral U4+ imidophosphorane complex, [U(NP(pip)3)4], 1-U(PN), is reported. This complex can be oxidized by two electrons with either mesityl azide or nitrous oxide. This two-electron atom/group transfer oxidation is the first example observed at a homoleptic, tetravalent uranium complex. The mesityl imido compound [U(NMes)(NP(pip)3)4], 2-U(PN)NMes, exhibits a unique square pyramidal geometry in contrast to the expected trigonal bipyramidal geometry of the oxo complex [U(O)(NP(pip)3)4], 2-U(PN)O. The bonding driving the structural dichotomy of these structures and the absence of a structurally observable inverse trans-influence in 2-U(PN)NMes were examined by DFT and natural bonding orbital analysis.

Inverse Trans Influence in Low-Valence Actinide-Group 10 Metal Complexes of Phosphinoaryl Oxides: A Theoretical Study via Tuning Metals and Donor Ligands.

The recognition and in-depth understanding of inverse trans influence (ITI) have successfully guided the synthesis of novel actinide complexes and enriched actinide chemistry. Those complexes, however, are mainly limited to the involvement of high-valence actinide and/or metal-ligand multiple bonds. Examples containing both low oxidation state actinide and metal-metal single bond remain rare. Herein, more than 20 actinide-transition metal (An-TM) complexes of phosphinoaryl oxide ligands have been designed in accordance with several experimentally known analogs, by changing the metal atoms (An = Th, Pa, U, Np, and Pu; and TM = Ni, Pd, and Pt), actinide oxidation states (IV and III) and metal-metal axial donor ligands (X = Me3SiO, F, Cl, Br, and I). The relativistic density functional theory study of structural (trans-An-X and cis-An-O toward An-TM), bonding (topological electron/energy density), and electronic properties reveals the order of the ITI stabilizing actinide-metal bond. Computed electron affinity (EA) values, related to the electrochemical reduction, linearly correlate with experimentally measured reduction potentials. Although the same ITI order for the ligand donors was shown as in a previous study, the correlation between electrochemical reduction and the ITI was found to be weak when the actinide atoms were changed. For most complexes, the reduction is primarily of an actinide-based mechanism with minor participation of transition metal and phosphinoaryl oxide, whereas that of thorium-nickel complexes is different.

Emergence of the structure-directing role of f-orbital overlap-driven covalency

FEUDAL (f’s essentially unaffected, d’s accommodate ligands) is a longstanding bonding model in actinide chemistry, in which metal-ligand binding uses 6d-orbitals, with the 5f remaining non-bonding. The inverse-trans-influence (ITI) is a case where the model may break down, and it has been suggested that ionic and covalent effects work synergistically in the ITI. Here, we report an experimentally grounded computational study that quantitatively explores the ITI, and in particular the structure-directing role of f-orbital covalency. Strong donor ligands generate a cis-ligand-directing electrostatic potential (ESP) at the metal centre. When f-orbital participation, via overlap-driven covalency, becomes dominant via short actinide-element distances, this ionic ESP effect is overcome, favouring a trans-ligand-directed geometry. This study contradicts the accepted ITI paradigm in that here ionic and covalent effects work against each other, and suggests a clearly non-FEUDAL, structure-directing role for the f-orbitals.

Understanding the origins of Oyl-U-Oyl bending in the uranyl (UO22+) ion.

The structure of the uranyl ion (UO22+) has been the topic of investigation for almost a century. Since the first structural study of uranyl in 1935, over 4000 uranyl complexes have been characterized by X-ray crystallography. The vast majority of these complexes feature a linear uranyl group (e.g., Oyl-U-Oyl = 180°); however, there are a handful of complexes that feature much more acute Oyl-U-Oyl angles. In fact, the smallest experimentally observed Oyl-U-Oyl angles are ca. 161°. This Frontier Article catalogs every reported uranyl complex that features an Oyl-U-Oyl angle below 172°, and attempts to rationalize the origins of the observed Oyl-U-Oyl bending. In particular, I describe two distinct causes of Oyl-U-Oyl bending: (1) bending that occurs as a result of unfavourable steric interactions between the equatorial co-ligands and the uranyl oxo groups; and (2) bending that appears to have an electronic origin. In addition, I describe several possible avenues for future investigation. Understanding the effect that Oyl-U-Oyl bending has on uranyl electronic structure could ultimately provide insight into several unique aspects of the uranyl ion, such as the inverse trans influence and the involvement of the "pseudo-core" U6p orbitals in U-Oyl bonding.

Elucidation of the inverse trans influence in uranyl and its imido and carbene analogues via quantum chemical simulation.

The inverse trans influence (ITI) is investigated in uranyl, UO22+, and its isoelectronic imido (U(NH)22+) and carbene (U(CH2)22+) analogues at the density functional and complete active space self consistent field levels of theory. The quantum theory of atoms in molecules is employed to quantify, for the first time, the effect of the ITI on covalent bond character and its relationship to bond lengths and complex stability.

Elucidating bonding preferences in tetrakis(imido)uranate(VI) dianions.

Actinyl species, [AnO2]2+, are well-known derivatives of the f-block because of their natural occurrence and essential roles in the nuclear fuel cycle. Along with their nitrogen analogues, [An(NR)2]2+, actinyls are characterized by their two strong trans-An-element multiple bonds, a consequence of the inverse trans influence. We report that these robust bonds can be weakened significantly by increasing the number of multiple bonds to uranium, as demonstrated by a family of uranium(VI) dianions bearing four U-N multiple bonds, [M]2[U(NR)4] (M = Li, Na, K, Rb, Cs). Their geometry is dictated by cation coordination and sterics rather than by electronic factors. Multiple bond weakening by the addition of strong π donors has the potential for applications in the processing of high-valent actinyls, commonly found in environmental pollutants and spent nuclear fuels.

Charge control of the inverse trans-influence.

The synthesis and characterization of uranium(VI) mono(imido) complexes, by the oxidation of corresponding uranium(V) species, are presented. These experimental results, paired with DFT analyses, allow for the comparison of the electronic structure of uranium(VI) mono(oxo) and mono(imido) ligands within a conserved ligand framework and demonstrate that the magnitude of the ground state stabilization derived from the inverse trans-influence (ITI) is governed by the relative charge localization on the multiply bonded atom or group.

The inverse trans influence in a family of pentavalent uranium complexes.

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.

Reductive silylation of a uranyl dibenzoylmethanate complex: an example of controlled uranyl oxo ligand cleavage

Reaction of UO2(dbm)2(THF) (dbm = OC(Ph)CHC(Ph)O) with 1 equiv. of R3SiH (R = Ph, Et), in the presence of B(C6F5)3, results in the formation of U(OB{C6F5}3)(OSiR3)(dbm)2(THF) (R = Ph, 1; Et, 2), which were isolated as red-orange crystalline solids in good yields. Interestingly, the addition of 1 equiv. of H(dbm) to 2 results in protonation of the –OSiEt3 ligand and formation of U(OB{C6F5}3)(dbm)3 (4) in 33% yield, along with formation of HOSiEt3. Furthermore, addition of HOSiEt3 and 1 equiv. of THF to 4, results in the formation 2, revealing that this process is reversible. The two-step conversion of UO2(dbm)2(THF) to 4 represents a rare example of controlled uranyl oxo ligand cleavage at ambient temperature and pressure. Comparison of diffraction and density functional theory data for 4 suggests the presence of the inverse trans influence, with a very shallow potential energy well for distortion along the trans U–O bond.

Stable Uranium(VI) Methyl and Acetylide Complexes and the Elucidation of an Inverse Trans Influence Ligand Series

Thermally stable uranium(VI)-methyl and -acetylide complexes: U(VI)OR[N(SiMe3)2]3 R = -CH3, -C≡CPh were prepared in which coordination of the hydrocarbyl group is directed trans to the uranium-oxo multiple bond. The stability of the uranium-carbon bond is attributed to an inverse trans influence. The hydrocarbyl complexes show greater ITI stabilization than that of structurally related U(VI)OX[N(SiMe3)2]3 (X = F(-), Cl(-), Br(-)) complexes, demonstrated both experimentally and computationally. An inverse trans influence ligand series is presented, developed from a union of theoretical and experimental results and based on correlations between the extent of cis-destabilization, the complexes stabilities toward electrochemical reduction, the thermodynamic driving forces for U═O bond formation, and the calculated destabilization of axial σ* and π* antibonding interactions.

Uranium–Ligand Multiple Bonding in Uranyl Analogues, [L═U═L]n+, and the Inverse Trans Influence

The societal importance of uranium complexes containing the uranyl moiety [O═U═O](2+) continues to grow with the ongoing international nuclear enterprise and associated accumulating legacy waste. Further studies of the electronic structure of uranyl and its analogues are imperative for the development of crucial technologies, including lanthanide/actinide extractants and chemical and environmental remediation methodologies. Actinide oxo halides are a subset of the growing class of actinyl (uranyl) analogues. The understanding of their electronic structures links the detailed spectroscopic studies of uranyl, indicating the role of the pseudocore 6p orbitals in U-O bonding, to hypotheses about the 6p orbitals' role in the chemical bonding of uranyl analogues. These actinide oxo halides are a very small class of actinide compounds that present the inverse trans influence (ITI). This class of complexes was, until recently, limited to two crystallographically characterized compounds, namely, [UCl(5)O][PPh(4)] and [PaCl(5)O][NEt(4)](2). These complexes are important because they give a readily and clearly defined experimental observable: the difference between the M-X(trans) and M-X(cis) (here X = Cl) bond lengths in the solid state. This bond metric is a sensitive probe for the role of 6p, 6d, and 5f orbitals, as well as electrostatic interactions, in determining their electronic structure. This Viewpoint Article reviews the theoretical, experimental, and synthetic work on the ITI in actinide complexes and contextualizes it within broader studies on the electronic structure of uranyl and its analogues. Furthermore, our recent work on the ITI in high-valent uranium(V/VI) oxo and imido complexes is described as a whole. This work builds on the extant synthetic literature on the ITI and provides design parameters for the synthesis and characterization of high-valent uranium-ligand multiple bonds.

Trans and cis influences and effects in cobalamins and in their simple models

The interligand interactions in coordination compounds have been principally interpreted in terms of cis and trans influences and effects, which can be defined as the ability of a ligand X to affect the bond of another ligand, cis or trans to X, to the metal. This review analyzes these effects/influences in cobalamins (XCbl) and their simple models cobaloximes, LCo(chel)X. Important properties of these complexes, such as geometry, stability, and reactivity, can be rationalized in terms of steric and electronic factors of the ligands. Experimental evidence of normal and inverse trans influence is described in alkylcobaloximes for the first time. The study of simple B12 models has complemented that on the more complex cobalamins, with particular emphasis on the properties of the axial L-Co-X moiety. Some of the conclusions reached for the axial fragment of simple models have also been qualitatively detected in cobalamins and have furnished new insight into the as yet unestablished mechanism for the homolytic cleavage of the CoC bond in the AdoCbl-based enzymes.

Oxidation State Delineation via U LIII-Edge XANES in a Series of Isostructural Uranium Coordination Complexes

We present an X-ray absorption near-edge structure (XANES) study of a series of uranium coordination complexes that possess nearly identical first coordination spheres and geometries in a range of oxidation states from U(III) to U(VI). These compounds were obtained through the activation of small molecules, such as ketones, azides, and carbon dioxide, and upon oxidation of a high-valent U(V)≡O to [U(VI)≡O](+). Most of the compounds have been reported previously. All of them are fully characterized and their oxidation states have been confirmed by various spectroscopic methods (SQUID, (1)H NMR, and UV/vis/near-IR). Each uranium complex consists of a triazacyclononane anchor bearing three aryloxide side arms with bulky tert-butyl (t-Bu) or adamantyl (Ad) ortho substituents. All complexes have approximate C(3) symmetry and possess an axial cavity that is either empty (U(III)) or occupied by a seventh ligand, namely, terminal oxygen (U(V) and U(VI)) or an oxygen-containing ligand (U(IV)). The only exception is [(((t-Bu)ArO)(3)tacnU(VI)(O)][SbF(6)], which is the rare case of a complex that shows a strong inverse trans influence. The determined correlation between the uranium oxidation state and the U L(III)-edge XANES absorption in this series includes a single terminal oxo ligand bonded uranium(V,VI), for which data are essentially nonexistent. The correct assignment of the uranium valence in a U(IV)-L(•-) compound (L(•-) = ketyl radical) is shown to be only possible by a comparison to structurally similar compounds.

Observation of the Inverse Trans Influence (ITI) in a Uranium(V) Imide Coordination Complex: An Experimental Study and Theoretical Evaluation

An inverse trans influence has been observed in a high-valent U(V) imide complex, [(((Ad)ArO)(3)N)U(NMes)]. A thorough theoretical evaluation has been employed in order to corroborate the ITI in this unusual complex. Computations on the target complex, [(((Ad)ArO)(3)N)U(NMes)], and the model complexes [(((Me)ArO)(3)N)U(NMes)] and [(NMe(3))(OMe(2))(OMe)(3)U(NPh)] are discussed along with synthetic details and supporting spectroscopic data. Additionally, the syntheses and full characterization data of the related U(V) trimethylsilylimide complex [(((Ad)ArO)(3)N)U(NTMS)] and U(IV) azide complex [(((Ad)ArO)(3)N)U(N(3))] are also presented for comparison.