Siloxide tripodal ligands as a scaffold for stabilizing lanthanides in the +4 oxidation state.

Synthetic strategies to isolate molecular complexes of lanthanides, other than cerium, in the +4 oxidation state remain elusive, with only four complexes of Tb(iv) isolated so far. Herein, we present a new approach for the stabilization of Tb(iv) using a siloxide tripodal trianionic ligand, which allows the control of unwanted ligand rearrangements, while tuning the Ln(iii)/Ln(iv) redox-couple. The Ln(iii) complexes, [LnIII((OSiPh2Ar)3-arene)(THF)3] (1-LnPh) and [K(toluene){LnIII((OSiPh2Ar)3-arene)(OSiPh3)}] (2-LnPh) (Ln = Ce, Tb, Pr), of the (HOSiPh2Ar)3-arene ligand were prepared. The redox properties of these complexes were compared to those of the Ln(iii) analogue complexes, [LnIII((OSi(OtBu)2Ar)3-arene)(THF)] (1-LnOtBu) and [K(THF)6][LnIII((OSi(OtBu)2Ar)3-arene)(OSiPh3)] (2-LnOtBu) (Ln = Ce, Tb), of the less electron-donating siloxide trianionic ligand, (HOSi(OtBu)2Ar)3-arene. The cyclic voltammetry studies showed a cathodic shift in the oxidation potential for the cerium and terbium complexes of the more electron-donating phenyl substituted scaffold (1-LnPh) compared to those of the tert-butoxy (1-LnOtBu) ligand. Furthermore, the addition of the -OSiPh3 ligand further shifts the potential cathodically, making the Ln(iv) ion even more accessible. Notably, the Ce(iv) complexes, [CeIV((OSi(OtBu)2Ar)3-arene)(OSiPh3)] (3-CeOtBu) and [CeIV((OSiPh2Ar)3-arene)(OSiPh3)(THF)2] (3-CePh), were prepared by chemical oxidation of the Ce(iii) analogues. Chemical oxidation of the Tb(iii) and Pr(iii) complexes (2-LnPh) was also possible, in which the Tb(iv) complex, [TbIV((OSiPh2Ar)3-arene)(OSiPh3)(MeCN)2] (3-TbPh), was isolated and crystallographically characterized, yielding the first example of a Tb(iv) supported by a polydentate ligand. The versatility and robustness of these siloxide arene-anchored platforms will allow further development in the isolation of more oxidizing Ln(iv) ions, widening the breadth of high-valent Ln chemistry.

Multimetallic Uranium Nitride Cubane Clusters from Dinitrogen Cleavage.

Dinitrogen cleavage provides an attractive but poorly studied route to the assembly of multimetallic nitride clusters. Here, we show that the monoelectron reduction of the dinitrogen complex [{U(OC6H2-But3-2,4,6)3}2(µ-η2:η2-N2)], 1, allows us to generate, for the first time, a uranium complex presenting a rare triply reduced N2 moiety ((µ-η2:η2-N2)•3-). Importantly, the bound dinitrogen can be further reduced, affording the U4N4 cubane cluster, 3, and the U6N6 edge-shared cubane cluster, 4, thus showing that (N2)•3- can be an intermediate in nitride formation. The tetranitride cluster showed high reactivity with electrophiles, yielding ammonia quantitatively upon acid addition and promoting CO cleavage to yield quantitative conversion of nitride into cyanide. These results show that dinitrogen reduction provides a versatile route for the assembly of large highly reactive nitride clusters, with U6N6 providing the first example of a molecular nitride of any metal formed from a complete cleavage of three N2 molecules.

Multielectron Redox Chemistry of Uranium by Accessing the +II Oxidation State and Enabling Reduction to a U(I) Synthon.

The synthesis of molecular uranium complexes in oxidation states lower than +3 remains a challenge despite the interest for their multielectron transfer reactivity and electronic structures. Herein, we report the one- and two-electron reduction of a U(III) complex supported by an arene-tethered tris(siloxide) tripodal ligand leading to the mono-reduced complexes, [K(THF)U((OSi(OtBu)2Ar)3-arene)(THF)] (2) and [K(2.2.2-cryptand)][U((OSi(OtBu)2Ar)3-arene)(THF)] (2-crypt), and to the di-reduced U(I) synthons, [K2(THF)3U((OSi(OtBu)2Ar)3-arene)]∞ (3) and [(K(2.2.2-cryptand))]2[U((OSi(OtBu)2Ar)3-arene)] (3-crypt). EPR and UV/vis/NIR spectroscopies, magnetic, cyclic voltammetry, and computational studies provide strong evidence that complex 2-crypt is best described as a U(II), where the U(II) is stabilized by δ-bonding interactions between the arene anchor and the uranium frontier orbitals, whereas complexes 3 and 3-crypt are best described as having a U(III) ion supported by the di-reduced arene anchor. Three quasi-reversible redox waves at E1/2 = -3.27, -2.45, and -1.71 V were identified by cyclic voltammetry studies and were assigned to the U(IV)/U(III), U(III)/U(II), and U(II)/U(III)-(arene)2- redox couples. The ability of complexes 2 and 3 in transferring two- and three-electrons, respectively, to oxidizing substrates was confirmed by the reaction of 2 with azobenzene (PhNNPh), leading to the U(IV) complex, [K(Et2O)U((OSi(OtBu)2Ar)3-arene)(PhNNPh)(THF)] (4), and of complex 3 with cycloheptatriene, yielding the U(IV) complex, [(K(Et2O)2)U((OSi(OtBu)2Ar)3-arene)(η7-C7H7)]∞ (6). These results demonstrate that the arene-tethered tris(siloxide) tripodal ligand provides an excellent platform for accessing low-valent uranium chemistry while implementing multielectron transfer pathways as shown by the reactivity of complex 3, which provides the third example of a U(I) synthon.

A Route to Stabilize Uranium(II) and Uranium(I) Synthons in Multimetallic Complexes.

Herein, we report the redox reactivity of a multimetallic uranium complex supported by triphenylsiloxide (-OSiPh3 ) ligands, where we show that low valent synthons can be stabilized via an unprecedented mechanism involving intramolecular ligand migration. The two- and three-electron reduction of the oxo-bridged diuranium(IV) complex [{(Ph3 SiO)3 (DME)U}2 (µ-O)], 4, yields the formal "UII /UIV ", 5, and "UI /UIV ", 6, complexes via ligand migration and formation of uranium-arene δ-bond interactions. Remarkably, complex 5 effects the two-electron reductive coupling of pyridine affording complex 7, which demonstrates that the electron-transfer is accompanied by ligand migration, restoring the original ligand arrangement found in 4. This work provides a new method for controlling the redox reactivity in molecular complexes of unstable, low-valent metal centers, and can lead to the further development of f-elements redox reactivity.

Experimental and theoretical thermodynamic studies in Ba2MgReO6-the ground state in the context of Jahn-Teller effect.

We address the degeneracy of the ground state multiplet on the 5d1Re6+ion in double perovskite Ba2MgReO6using a combination of specific heat measurements and density functional calculations. For Ba2MgReO6, two different ground state multiplets have previously been proposed-a quartet (with degeneracyN= 4) (Hirai and Hiroi 2019J. Phys. Soc. Japan88064712) and a doublet (N= 2) (Marjerrisonet al2016Inorg. Chem.5510701). Here we employ two independent methods for the estimation of phonon contribution in heat capacity data to obtain the magnetic entropySmag, which reflects the degeneracy of the ground state multipletNthroughSmag=RlnN. In both cases, we obtain that in the temperature range covering 2 to 120 K the released entropy is better described bySmag=Rln2. The detailed nature of the ground state multiplet in Ba2MgReO6remains an open question.

Bonding and Reactivity in Terminal versus Bridging Arenide Complexes of Thorium Acting as ThII Synthons.

Thorium redox chemistry is extremely scarce due to the high stability of ThIV . Here we report two unique examples of thorium arenide complexes prepared by reduction of a ThIV -siloxide complex in presence of naphthalene, the mononuclear arenide complex [K(OSi(Ot Bu)3 )3 Th(η6 -C10 H8 )] (1) and the inverse-sandwich complex [K(OSi(Ot Bu)3 )3 Th]2 (µ-η6 ,η6 -C10 H8 )] (2). The electrons stored in these complexes allow the reduction of a broad range of substrates (N2 O, AdN3 , CO2 , HBBN). Higher reactivity was found for the complex 1 which reacts with the diazoolefin IDipp=CN2 to yield the unexpected ThIV amidoalkynyl complex 5 via a terminal N-heterocyclic vinylidene intermediate. This work showed that arenides can act as convenient redox-active ligands for implementing thorium-ligand cooperative multielectron transfer and that the reactivity can be tuned by the arenide binding mode.

Assembling diuranium complexes in different states of charge with a bridging redox-active ligand.

Radical-bridged diuranium complexes are desirable for their potential high exchange coupling and single molecule magnet (SMM) behavior, but remain rare. Here we report for the first time radical-bridged diuranium(iv) and diuranium(iii) complexes. Reaction of [U{N(SiMe3)2}3] with 2,2'-bipyrimidine (bpym) resulted in the formation of the bpym-bridged diuranium(iv) complex [{((Me3Si)2N)3UIV}2(µ-bpym2-)], 1. Reduction with 1 equiv. KC8 reduces the complex, affording [K(2.2.2-cryptand)][{((Me3Si)2N)3U}2(µ-bpym)], 2, which is best described as a radical-bridged UIII-bpym˙--UIII complex. Further reduction of 1 with 2 equiv. KC8, affords [K(2.2.2-cryptand)]2[{((Me3Si)2N)3UIII}2(µ-bpym2-)], 3. Addition of AgBPh4 to complex 1 resulted in the oxidation of the ligand, yielding the radical-bridged complex [{((Me3Si)2N)3UIV}2(µ-bpym˙-)][BPh4], 4. X-ray crystallography, electrochemistry, susceptibility data, EPR and DFT/CASSCF calculations are in line with their assignments. In complexes 2 and 4 the presence of the radical-bridge leads to slow magnetic relaxation.

Nitrogen activation and cleavage by a multimetallic uranium complex.

Multimetallic-multielectron cooperativity plays a key role in the metal-mediated cleavage of N2 to nitrides (N3-). In particular, low-valent uranium complexes coupled with strong alkali metal reducing agents can lead to N2 cleavage, but often, it is ambiguous how many electrons are transferred from the uranium centers to cleave N2. Herein, we designed new dinuclear uranium nitride complexes presenting a combination of electronically diverse ancillary ligands to promote the multielectron transformation of N2. Two heteroleptic diuranium nitride complexes, [K{UIV(OSi(O t Bu)3)(N(SiMe3)2)2}2(µ-N)] (1) and [Cs{UIV(OSi(O t Bu)3)2(N(SiMe3)2)}2(µ-N)] (3-Cs), containing different combinations of OSi(O t Bu)3 and N(SiMe3)2 ancillary ligands, were synthesized. We found that both complexes could be reduced to their U(iii)/U(iv) analogues, and the complex, [K2{UIV/III(OSi(O t Bu)3)2(N(SiMe3)2)}2(µ-N)] (6-K), could be further reduced to a putative U(iii)/U(iii) species that is capable of promoting the 4e- reduction of N2, yielding the N2 4-complex [K3{UV(OSi(O t Bu)3)2(N(SiMe3)2)}2(µ-N)(µ-η2:η2-N2)], 7. Parallel N2 reduction pathways were also identified, leading to the isolation of N2 cleavage products, [K3{UVI(OSi(O t Bu)3)2(N(SiMe3)2)([triple bond, length as m-dash]N)}(µ-N)2{UV(OSi(O t Bu)3)2(N(SiMe3)2)}]2, 8, and [K4{(OSi(O t Bu)3)2UV)([triple bond, length as m-dash]N)}(µ-NH)(µ-κ2:C,N-CH2SiMe2NSiMe3)-{UV(OSi(O t Bu)3)2][K(N(SiMe3)2]2, 9. These complexes provide the first example of N2 cleavage to nitride by a uranium complex in the absence of reducing alkali metals.

Structure and Reactivity of Polynuclear Divalent Lanthanide Disiloxanediolate Complexes.

Trinuclear molecular complexes of europium (II) and ytterbium(II) [Ln3{(Ph2SiO)2O}3(THF)6], 1-Ln3L3 (Ln = Eu and Yb), supported by the dianionic tetraphenyl disiloxanediolate ligand, were synthesized via protonolysis of the [Ln{N(SiMe3)2}2(THF)2] complexes. In contrast, the reaction of [Sm{N(SiMe3)2}2(THF)2] with the (Ph2SiOH)2O ligand led to the isolation of the mixed-valent Sm(II)/Sm(III) complex [Sm3{(Ph2SiO)2O}3{N(SiMe3)2}(THF)4], 2-Sm3L3, which was crystallographically characterized. The Eu(II) complex 1-Eu3L3 displays weak ferromagnetic coupling between the Eu(II) metal centers (J = 0.1035 cm-1). The addition of 3 equiv of (Ph2SiOK)2O to 1-Eu3L3 resulted in the formation of the polynuclear Eu(II) dimer of dimers [K4Eu2{(Ph2SiO)2O}4(Et2O)2]2, 3-Eu2L4. Complexes 1-Ln3L3 (Ln = Eu and Yb) are stable in solution at room temperature, while 3-Eu2L4 shows higher reactivity and rapidly decomposes to give the mixed-valent Eu(II)/Eu(III) species [K3Eu2{(Ph2SiO)2O}4], 4-Eu2L4. Complex 1-Yb3L3 affects the slow reductive disproportionation of carbon dioxide, but 1-Eu3L3 does not display any reactivity toward CO2. However, the presence of one additional (Ph2SiO-)2O per Eu(II) metal center in 3-Eu2L4 increases dramatically the reductive ability of the Eu(II) metal centers, affording the first example of carbon dioxide activation by an isolated divalent europium complex. The reduction of CO2 by 3-Eu2L4 is immediate, and carbonate is formed selectively after the addition of a stoichiometric amount of CO2.

Magnetic Field Induced Quantum Spin Liquid in the Two Coupled Trillium Lattices of K_{2}Ni_{2}(SO_{4})_{3}.

Quantum spin liquids are exotic states of matter that form when strongly frustrated magnetic interactions induce a highly entangled quantum paramagnet far below the energy scale of the magnetic interactions. Three-dimensional cases are especially challenging due to the significant reduction of the influence of quantum fluctuations. Here, we report the magnetic characterization of K_{2}Ni_{2}(SO_{4})_{3} forming a three-dimensional network of Ni^{2+} spins. Using density functional theory calculations, we show that this network consists of two interconnected spin-1 trillium lattices. In the absence of a magnetic field, magnetization, specific heat, neutron scattering, and muon spin relaxation experiments demonstrate a highly correlated and dynamic state, coexisting with a peculiar, very small static component exhibiting a strongly renormalized moment. A magnetic field B≳4 T diminishes the ordered component and drives the system into a pure quantum spin liquid state. This shows that a system of interconnected S=1 trillium lattices exhibits a significantly elevated level of geometrical frustration.

Assembly of High-Spin [Fe3] Clusters by Ligand-Based Multielectron Reduction.

The hexanuclear [Na12Fe6(tris-cyclo-salophen)2(THF)14], 1-THF, and the trinuclear [Na6Fe3(tris-cyclo-salophen)(py)9], 1-py, Fe(II) clusters can be easily assembled in one step from the ligand-based reduction of the [FeII(salophen)(THF)] complex. These complexes consist of triangular cores where three Fe(II) ions are held together, within range of bonding interaction, by the hexa-amide, hexaphenolate macrocyclic ligand tris-cyclo-salophen12-. The tris-cyclo-salophen12- ligand is perfectly suited for binding three Fe(II) centers at short distances, allowing for strong magnetic coupling between the Fe(II) centers. The macrocyclic ligand is generated by the reductive coupling of the imino groups of three salophen ligands, resulting in three new C-C bonds. The six electrons stored in the ligand become available for the reduction of carbon dioxide with selective formation of carbonate.

Accessing the +IV Oxidation State in Molecular Complexes of Praseodymium.

Out of the 14 lanthanide (Ln) ions, molecular complexes of Ln(IV) were known only for cerium and more recently terbium. Here we demonstrate that the +IV oxidation state is also accessible for the large praseodymium (Pr) cation. The oxidation of the tetrakis(triphenysiloxide) Pr(III) ate complex, [KPr(OSiPh3)4(THF)3], 1-PrPh, with [N(C6H4Br)3][SbCl6], affords the Pr(IV) complex [Pr(OSiPh3)4(MeCN)2], 2-PrPh, which is stable once isolated. The solid state structure, UV-visible spectroscopy, magnetometry, and cyclic voltammetry data along with the DFT computations of the 2-PrPh complex unambiguously confirm the presence of Pr(IV).

C-H Bond Activation by an Isolated Dinuclear U(III)/U(IV) Nitride.

Synthetic studies of bimetallic uranium nitride complexes with the N(SiMe3)2 ligand have generated a new nitride complex of U(III), which is highly reactive toward C-H bonds and H2. Treatment of the previously reported U(IV)/U(IV) nitride complex [Na(DME)3][((Me3Si)2N)2U(µ-N)(µ-κ2:CN̵-CH2SiMe2NSiMe3)U(N(SiMe3)2)2] (DME = 1,2-dimethoxyethane), 1, with 2 equiv of HNEt3BPh3 yielded the cationic U(IV)/U(IV) nitride complex, [{((Me3Si)2N)2U(THF)}2(µ-N)][BPh4] (THF = tetrahydrofuran), 3, by successive protonolysis of one N(SiMe3)2 ligand and the uranium-methylene bond. Reduction of 3 with KC8 afforded a rare example of a U(III) nitride, namely, the U(III)/U(IV) complex, [{((Me3Si)2N)2U(THF)}2(µ-N)], 4. Complex 4 is highly reactive and undergoes 1,2-addition of the C-H bond of the N(SiMe3)2 ligand across the uranium-nitride moiety to give the U(III)/U(IV) imide cyclometalate complex, [((Me3Si)2N)2(THF)U(µ-NH)(µ-κ2:C,N̵-CH2SiMe2NSiMe3)U(N(SiMe3)2))(THF)], 5. Complex 4 also reacts with toluene at -80 °C to yield an inverse sandwich imide complex arising from C-H bond activation of toluene, [{((Me3Si)2N)2U(THF)}2(µ-N)][{((Me3Si)2N)3U(µ-NH)U(N(SiMe3)2)}2(C7H8)], 6. Complex 4 effects the heterolytic cleavage of the C-H of phenylacetylene to yield the imide acetylide [{((Me3Si)2N)2U(THF)}2(µ-N)][((Me3Si)2N)2U(η1-CCPh)(µ2-NH)(µ2-η2:η1-CCPh)U(N(SiMe3)2)2], 7. Complex 4 also reacts with H2 to produce an imide hydride U(III)/U(IV) complex, [{((Me3Si)2N)2U(THF)}2(µ-NH)(µ-H)], 9. These data demonstrate that nitride complexes of U(III) are accessible with amide ligands and show the high reactivity of molecular U(III) nitrides in C-H bond activation.

Stabilization of the Oxidation State +IV in Siloxide-Supported Terbium Compounds.

The synthesis of lanthanides other than cerium in the oxidation state +IV has remained a desirable but unmet target until recently, when two examples of TbIV with saturated coordination spheres were isolated. Here we report the third example of an isolated molecular complex of terbium(IV), where the supporting siloxide ligands do not saturate the coordination sphere. The fully characterized six-coordinate complex [TbIV (OSiPh3 )4 (MeCN)2 ], 2-TbPh , shows high stability and the labile MeCN ligands can be replaced by phosphinoxide ligands. Computational studies suggest that the stability is due to a strong π(O-Tb) interaction which is stronger than in the previously reported TbIV complexes. Cyclic-voltammetry experiments demonstrate that non-binding counterions contribute to the stability of TbIV in solution by destabilizing the +III oxidation state, while alkali ions promote TbIV /TbIII electron transfer.

Tuning the structure, reactivity and magnetic communication of nitride-bridged uranium complexes with the ancillary ligands.

Molecular uranium nitride complexes were prepared to relate their small molecule reactivity to the nature of the U[double bond, length as m-dash]N[double bond, length as m-dash]U bonding imposed by the supporting ligand. The U4+-U4+ nitride complexes, [NBu4][{(( t BuO)3SiO)3U}2(µ-N)], [NBu4]-1, and [NBu4][((Me3Si)2N)3U}2(µ-N)], 2, were synthesised by reacting NBu4N3 with the U3+ complexes, [U(OSi(O t Bu)3)2(µ-OSi(O t Bu)3)]2 and [U(N(SiMe3)2)3], respectively. Oxidation of 2 with AgBPh4 gave the U4+-U5+ analogue, [((Me3Si)2N)3U}2(µ-N)], 4. The previously reported methylene-bridged U4+-U4+ nitride [Na(dme)3][((Me3Si)2)2U(µ-N)(µ-κ2-C,N-CH2SiMe2NSiMe3)U(N(SiMe3)2)2] (dme = 1,2-dimethoxyethane), [Na(dme)3]-3, provided a versatile precursor for the synthesis of the mixed-ligand U4+-U4+ nitride complex, [Na(dme)3][((Me3Si)2N)3U(µ-N)U(N(SiMe3)2)(OSi(O t Bu)3)], 5. The reactivity of the 1-5 complexes was assessed with CO2, CO, and H2. Complex [NBu4]-1 displays similar reactivity to the previously reported heterobimetallic complex, [Cs{(( t BuO)3SiO)3U}2(µ-N)], [Cs]-1, whereas the amide complexes 2 and 4 are unreactive with these substrates. The mixed-ligand complexes 3 and 5 react with CO and CO2 but not H2. The nitride complexes [NBu4]-1, 2, 4, and 5 along with their small molecule activation products were structurally characterized. Magnetic data measured for the all-siloxide complexes [NBu4]-1 and [Cs]-1 show uncoupled uranium centers, while strong antiferromagnetic coupling was found in complexes containing amide ligands, namely 2 and 5 (with maxima in the χ versus T plot of 90 K and 55 K). Computational analysis indicates that the U(µ-N) bond order decreases with the introduction of oxygen-based ligands effectively increasing the nucleophilicity of the bridging nitride.

Persistent antiferromagnetic order in heavily overdoped Ca1-x La x FeAs2.

In the Ca1-x La x FeAs2 (1 1 2) family of pnictide superconductors, we have investigated a highly overdoped composition (x = 0.56), prepared by a high-pressure, high-temperature synthesis. Magnetic measurements show an antiferromagnetic transition at T N = 120 K, well above the one at lower doping (0.15 < x < 0.27). Below the onset of long-range magnetic order at T N, the electrical resistivity is strongly reduced and is dominated by electron-electron interactions, as evident from its temperature dependence. The Seebeck coefficient shows a clear metallic behavior as in narrow band conductors. The temperature dependence of the Hall coefficient and the violation of Kohler's rule agree with the multiband character of the material. No superconductivity was observed down to 1.8 K. The success of the high-pressure synthesis encourages further investigations of the so far only partially explored phase diagram in this family of Iron-based high temperature superconductors.

Molecular Complex of Tb in the +4 Oxidation State.

Lanthanides (Ln) usually occur in the +3, or more recently the +2, oxidation states. The only example of an isolated molecular Ln4+ so far remains Ce4+. Here we show that the +4 oxidation state is also accessible in a molecular compound of terbium as demonstrated by oxidation of the tetrakis(siloxide)terbium(III) ate complex, [KTb(OSi(O tBu)3)4], 1-Tb, with the tris(4-bromophenyl)amminium oxidant, [N(C6H4Br)3][SbCl6], to afford the Tb4+ complex [Tb(OSi(O tBu)3)4], 2-Tb. The solid state structures of 1-Tb and 2-Tb were determined by X-ray crystallography, and the presence of Tb4+ was unambiguously confirmed by electron paramagnetic resonance and magnetometry. Complex 2-Tb displays a similar voltammogram to the Ce4+ analogue but with redox events that are about 1 V more positive.

Correction: Facile N-functionalization and strong magnetic communication in a diuranium(v) bis-nitride complex.

[This corrects the article DOI: 10.1039/C8SC05721D.].

Facile N-functionalization and strong magnetic communication in a diuranium(v) bis-nitride complex.

Uranium nitride complexes are of high interest because of their ability to effect dinitrogen reduction and functionalization and to promote magnetic communication, but studies of their properties and reactivity remain rare. Here we have prepared in 73% yield the diuranium(v) bis-nitride complex [K2{[U(OSi(O t Bu)3)3]2(µ-N)2}], 4, from the thermal decomposition of the nitride-, azide-bridged diuranium(iv) complex [K2{[U(OSi(O t Bu)3)3]2(µ-N)(µ-N3)}], 3. The bis-nitride 4 reacts in ambient conditions with 1 equiv. of CS2 and 1 equiv. of CO2 resulting in N-C bond formation to afford the diuranium(v) complexes [K2{[U(OSi(O t Bu)3)3]2(µ-N)(µ-S)(µ-NCS)}], 5 and [K2{[U(OSi(O t Bu)3)3]2(µ-N)(µ-O)(µ-NCO)}], 6, respectively. Both nitrides in 4 react with CO resulting in oxidative addition of CO to one nitride and CO cleavage by the second nitride to afford the diuranium(iv) complex [K2{[U(OSi(O t Bu)3)3]2(µ-CN)(µ-O)(µ-NCO)}], 7. Complex 4 also effects the remarkable oxidative cleavage of H2 in mild conditions to afford the bis-imido bridged diuranium(iv) complex [K2{[U(OSi(O t Bu)3)3]2(µ-NH)2}], 8 that can be further protonated to afford ammonia in 73% yield. Complex 8 provides a good model for hydrogen cleavage by metal nitrides in the Haber-Bosch process. The measured magnetic data show an unusually strong antiferromagnetic coupling between uranium(v) ions in the complexes 4 and 6 with Neel temperatures of 77 K and 60 K respectively, demonstrating that nitrides are attractives linkers for promoting magnetic communication in uranium complexes.

The role of bridging ligands in dinitrogen reduction and functionalization by uranium multimetallic complexes.

Cooperativity between metal centres is identified as a crucial step in dinitrogen reduction both for the industrial Haber-Bosch process and for the natural fixation of nitrogen by nitrogenase enzymes, but the mechanism of N2 reduction remains poorly understood. This is in large part because multimetallic complexes that reduce and functionalize dinitrogen in the absence of strong alkali reducing agents are crucial to establish a structure-activity relationship, but remain extremely rare. Recently, we reported a multimetallic nitride-bridged diuranium(III) complex capable of reducing and functionalizing dinitrogen. Here we show that an analogous complex assembled with an oxo instead of a nitride linker also effects the four-electron reduction of dinitrogen, but the reactivity of the resulting oxo-(N2) complex differs significantly from that of the nitride-(N2). Computational studies show a different bonding scheme for the dinitrogen where the bridging nitride does participate in the binding and consequent activation of N2, while the oxide does not.