Rhenium(V) oxo complexes with N-heterocyclic carbenes

Air-stable rhenium(V) oxo complexes are formed when [ReOCl(3)(PPh(3))(2)] is treated with N-heterocyclic carbenes of the 1,3-dialkyl-4,5-dimethylimidazol-2-ylidene type, L(R) (R = Me, Et, i-Pr). Complexes of the compositions [ReO(2)(L(R))(4)](+), [ReOCl(L(R))(4)](2+), or [ReO(OMe)(L(R))(4)](2+) can be isolated depending on the alkyl substituents at the nitrogen atoms of the ligands and the reaction conditions applied. Despite the steric overcrowding of the equatorial coordination spheres of the metal atoms by each of the four carbene ligands, stable complexes with six-coordinate rhenium atoms are obtained. Steric demands of the alkyl groups allow control of the stability of the mono-oxo intermediates. Air-stable cationic complexes of the compositions [ReOCl(L(Me))(4)](2+), [ReOCl(L(Et))(4)](2+), and [ReO(OMe)(L(Me))(4)](2+) have been isolated, whereas reactions of [ReOCl(3)(PPh(3))(2)] or other rhenium(V) precursors with the more bulky 1,3-diisopropyl-4,5-dimethylimidazol-2-ylidene (L(i)(-)(Pr)) directly yield the dioxo complex [ReO(2)(L(i)(-)(Pr))(4)](+). X-ray structures of [ReO(2)(L(i)(-)(Pr))(4)][ReO(4)], [ReO(2)(L(i)(-)(Pr))(4)][PF(6)], [ReO(2)(L(Me))(4)][ReO(4)](0.45)[PF(6)](0.55), [ReO(MeOH)(L(Me))(4)][PF(6)](2), and [ReOCl(L(Et))(4)][PF(6)](2) show that the equatorial coordination spheres of the rhenium atoms are essentially planar irrespective of the steric demands of the individual carbene ligands.     

The structural and spectroscopic characterisation of three actinyl complexes with coordinated and uncoordinated perrhenate: [UO2(ReO4)2(TPPO)3], [[(UO2)(TPPO)3]2(mu2-O2)][ReO4]2 and [NpO2(TPPO)4][ReO4

The first structural characterization of an actinide complex with coordinated perrhenate is reported, [UO2(ReO4)2(TPPO)3] (1). In this [UO2]2+ complex two [ReO4]- anions and three TPPO (triphenylphosphine oxide) P=O donor ligands are coordinated in the equatorial plane in a cisoid arrangement. This bonding arrangement, and apparent strain observed in the equatorially bonded ligands, is attributed to the solid state packing in adjacent molecules in which hydrophobic TPPO ligands form an effective "shell" around a hydrophilic core of two UO2(ReO4)2 moieties. Solid state vibrational spectroscopy (infrared and Raman), 31P CP MAS NMR and elemental analysis are also consistent with the formula of 1. Solution state vibrational spectroscopy and 31P NMR measurements in EtOH indicate the lability of the TPPO and [ReO4]- groups. The photolytic generation of peroxide in EtOH solutions of 1 leads to the formation of trace quantities of [[(UO2)(TPPO)3]2(mu2-O2)][ReO4]2, 2, in which the coordinated [ReO4]- groups of 1 have been displaced by bridging O2(2-), derived from atmospheric O2. Finally, attempts to synthesise a [NpO2]+ analogue of have resulted only in the formation of [NpO2(TPPO)4][ReO4], 3, in which [ReO4]- acts solely as a counter anion. From these results it can be concluded that [ReO4]- will bond to [UO2]2+, but will be readily displaced by a more strongly coordinating ligand (e.g. peroxide) and will not coordinate to an actinyl cation with a lower charge, [NpO2]+, under the same reaction conditions.     

Synthesis, characterization, and reactivity of a uranyl beta-diketiminate complex

Addition of 1 equiv of Li(Ar2nacnac) (Ar2nacnac = (2,6-(i)Pr2C6H3)NC(Me)CHC(Me)N(2,6-(i)Pr2C6H3)) to an Et2O suspension of UO2Cl2(THF)3 generates the uranyl dimer [UO2(Ar2nacnac)Cl]2 (1) in good yield. A second species can be isolated in low yield from the reaction mixtures of 1, namely [Li(OEt2)2][UO2(Ar2nacnac)Cl2] (2). The structures of both 1 and 2 have been confirmed by X-ray crystallography. Complex 1 reacts with Ph3PO to generate UO2(Ar2nacnac)Cl(Ph3PO) (3). In addition, 1 reacts with AgOTf and either 1 equiv of DPPMO2 or 2 equiv of Ph2MePO to provide [UO2(Ar2nacnac)(DPPMO2)][OTf] (4) and [UO2(Ar2nacnac)(Ph2MePO)2][OTf] (5), respectively. Both 4 and 5 have been fully characterized, including analysis by X-ray crystallography and cyclic voltammetry. Reduction of 4 with Cp2Co provides UO2(Ar2nacnac)(CH{Ph2PO}2) (6), a uranyl(VI) complex that is generated by the formal loss of H* from the DPPMO2 ligand. Labeling studies have been performed in an attempt to elucidate the mechanism of hydrogen loss. In contrast, reduction of 5 with Cp2Co provides UO2(Ar2nacnac)(Ph2MePO)2 (7), a rare example of a uranyl(V) complex. As expected, the solid-state molecular structure of 7 reveals slightly longer U-O(oxo) bond lengths relative to 5. Furthermore, complex 7 can be converted back into 5 by oxidation with AgOTf in toluene.     

The synthesis, structural, and spectroscopic characterization of uranium(IV) perrhenate complexes

We report the synthesis, structural, and spectroscopic characterization of a series of uranium(IV)-perrhenato complexes. Three isostructural complexes with general formula [U(ReO4)4(L)4] (where L = tri-n-butylphosphine oxide/TBPO (2), triethyl phosphate/TEP (3), or tri-iso-butyl phosphate/TiBP (4)), have been synthesized, both through the photoreduction of ethanolic {UO2}2+ solutions and also via a novel U(IV) starting material, U(ReO4)4.5H2O (1). Compound 1 has also been used in the preparation of [U(ReO4)4(TPPO)3(CH3CN)].2CH3CN (5) and [U(ReO4)(DPPMO2)3(OH)][ReO4]2.2CH3CN (6), where TPPO represents triphenylphosphine oxide and DPPMO2 represents bis(diphenylphosphino)methane dioxide. All six complexes have been spectroscopically characterized using NMR, UV-vis-NIR, and IR techniques, with 2, 3, 5, and 6 also fully structurally characterized. The U atoms in compounds 2-6 all exhibit eight-coordinate geometry with up to four perrhenate groups in addition to three (DPPMO2 and TPPO) or four (TEP, TiBP, TBPO) coordinated organic ligands. In the case of compounds 5 and 6, the coordination of eight ligands to the U(IV) center is completed by the binding of a solvent molecule (CH3CN) and OH-, respectively. Solid-state physical analysis (elemental and thermogravimetric) and infrared spectroscopy are in agreement with the structural studies. The crystallographic data suggest that the strength of the U(IV)-O-donor ligand bonds decreases across the series R3PO > [ReO4]- > (RO)3PO. Solution-state IR and 31P NMR spectroscopy appear to be in agreement with these solid-state results.     

Synthesis and reactivity of a uranyl-imidazolyl complex

Treatment of [UO(2)(Ar(2)nacnac)Cl](2) with 4 equiv. of Li(C(4)H(5)N(2)) results in the formation of a rare uranyl organometallic complex [Li(MeIm)][UO(μ-O)(Ar(2)nacnac)(μ-C,N-C(4)H(5)N(2))(2)] (2), in moderate yield. Reaction of 2 with 1 equiv. of MCl(2) (M = Fe, Co) yields the bimetallic complexes [MCl(MeIm)][UO(2)(Ar(2)nacnac)(μ-N,C-C(4)H(5)N(2))(2)] (M = Fe, 3; M = Co, 4).     

Methanesulfonates of high-valent metals: syntheses and structural features of MoO2(CH3SO3)2, UO2(CH3SO3)2, ReO3(CH3SO3), VO(CH3SO3)2, and V2O3(CH3SO3)4 and their thermal decomposition under N2 and O2 atmosphere

Oxide methanesulfonates of Mo, U, Re, and V have been prepared by reaction of MoO(3), UO(2)(CH(3)COO)(2)·2H(2)O, Re(2)O(7)(H(2)O)(2), and V(2)O(5) with CH(3)SO(3)H or mixtures thereof with its anhydride. These compounds are the first examples of solvent-free oxide methanesulfonates of these elements. MoO(2)(CH(3)SO(3))(2) (Pbca, a=1487.05(4), b=752.55(2), c=1549.61(5) pm, V=1.73414(9) nm(3), Z=8) contains [MoO(2)] moieties connected by [CH(3)SO(3)] ions to form layers parallel to (100). UO(2)(CH(3)SO(3))(2) (P2(1)/c, a=1320.4(1), b=1014.41(6), c=1533.7(1) pm, β=112.80(1)°, V=1.8937(3) nm(3), Z=8) consists of linear UO(2)(2+) ions coordinated by five [CH(3)SO(3)] ions, forming a layer structure. VO(CH(3)SO(3))(2) (P2(1)/c, a=1136.5(1), b=869.87(7), c=915.5(1) pm, β=113.66(1)°, V=0.8290(2) nm(3), Z=4) contains [VO] units connected by methanesulfonate anions to form corrugated layers parallel to (100). In ReO(3)(CH(3)SO(3)) (P1, a=574.0(1), b=1279.6(3), c=1641.9(3) pm, α=102.08(2), β=96.11(2), γ=99.04(2)°, V=1.1523(4) nm(3), Z=8) a chain structure exhibiting infinite O-[ReO(2)]-O-[ReO(2)]-O chains is formed. Each [ReO(2)]-O-[ReO(2)] unit is coordinated by two bidentate [CH(3)SO(3)] ions. V(2)O(3)(CH(3)SO(3))(4) (I2/a, a=1645.2(3), b=583.1(1), c=1670.2(3) pm, β=102.58(3), V=1.5637(5) pm(3), Z=4) adopts a chain structure, too, but contains discrete [VO]-O-[VO] moieties, each coordinated by two bidentate [CH(3)SO(3)] ligands. Additional methanesulfonate ions connect the [V(2)O(3)] groups along [001]. Thermal decomposition of the compounds was monitored under N(2) and O(2) atmosphere by thermogravimetric/differential thermal analysis and XRD measurements. Under N(2) the decomposition proceeds with reduction of the metal leading to the oxides MoO(2), U(3)O(7), V(4)O(7), and VO(2); for MoO(2)(CH(3)SO(3))(2), a small amount of MoS(2) is formed. If the thermal decomposition is carried out in a atmosphere of O(2) the oxides MoO(3) and V(2)O(5) are formed.     

Chemistry of re with N,N'-bis(2-pyridylmethyl)ethylenediamine (H2pmen): hydrolysis, dehydrogenation, and ternary complexes

A number of Re complexes with N,N'-bis(2-pyridylmethyl)ethylenediamine (H2pmen) have been made from [NH4][ReO4]. [ReOCl2(H2pmen)]Cl, [ReOCl(Hpmen)][ReO4], and [ReO2(H2pmen)][ReO4] are related by hydrolysis/HCl substitution. [ReOCl(Hpmen)][ReO4] was structurally characterized and found to contain a water-stable amido-Re bond. Dehydrogenation of the N-donor ligand from each amine to imine with concomitant two-electron reduction of the Re center occurs readily in these systems. With suitable 3-hydroxy-4-pyrones, ternary complexes such as [ReIIICl(ma)(C14H14N4)][ReO4].CH3OH, 5, were made from [NH4][ReO4], H2pmen.4HCl and pyrones in one-pot syntheses. 5, a seven-coordinate ReIII complex, was structurally characterized.     

Steric control of substituted phenoxide ligands on product structures of uranyl aryloxide complexes

A series of uranyl aryloxide complexes has been prepared via metathesis reactions between [UO(2)Cl(2)(THF)(2)](2) and di-ortho-substituted phenoxides. Reaction of 4 equiv of KO-2,6-(t)()Bu(2)C(6)H(3) with [UO(2)Cl(2)(THF)(2)](2) in THF produces the dark red uranyl compound, UO(2)(O-2,6-(t)()Bu(2)C(6)H(3))(2)(THF)(2).THF, 1. Single-crystal X-ray diffraction analysis of 1 reveals a monomer in which the uranium is coordinated in a pseudooctahedral fashion by two apical oxo groups, two cis-aryloxides, and two THF ligands. A similar product is prepared by reaction of KO-2,6-Ph(2)C(6)H(3) with [UO(2)Cl(2)(THF)(2)](2) in THF. Single-crystal X-ray diffraction analysis of this compound reveals it to be the trans-monomer UO(2)(O-2,6-Ph(2)C(6)H(3))(2)(THF)(2), 2. Dimeric structures result from the reactions of [UO(2)Cl(2)(THF)(2)](2) with less sterically imposing aryloxide salts, KO-2,6-Cl(2)C(6)H(3) or KO-2,6-Me(2)C(6)H(3). Single-crystal X-ray diffraction analyses of [UO(2)(O-2,6-Cl(2)C(6)H(3))(2)(THF)(2)](2), 3, and [UO(2)Cl(O-2,6-Me(2)C(6)H(3))(THF)(2)](2), 4, reveal similar structures in which each U atom is coordinated by seven ligands in a pseudopentagonal bipyramidal fashion. Coordinated to each uranium are two apical oxo groups and five equatorial ligands (3, one terminal phenoxide, two bridging phenoxides, and two nonadjacent terminal THF ligands; 4, one terminal chloride, two bridging phenoxides, and two nonadjacent terminal THF ligands). Apparently, the phenoxide ligand steric features exert a greater influence on the solid-state structures than the electronic properties of the substituents. Emission spectroscopy has been utilized to investigate the molecularity and electronic structure of these compounds. For example, luminescence spectra taken at liquid nitrogen temperature allow for a determination of the dependence of the molecular aggregation of 3 on the molecular concentration. Electronic and vibrational spectroscopic measurements have been analyzed to examine trends in emission energies and stretching frequencies. However, comparison of the data for compounds 1-4 reveals that the innate electron-donating capacity of phenoxide ligands is only subtly manifest in either the electronic or vibrational energy distributions within these molecules.     

Synthesis, crystal structure and optical properties of [Ag(UO2)3(OAc)9][Zn(H2O)4(CH3CH2OH)2]: a novel compound containing closed-shell 3d10, 4d10 and 5d10 metal ions

[Ag(UO(2))(3) (OAc)(9)][Zn(H(2)O)(4)(CH(3)CH(2)OH)(2)] (, OAc = CH(3)COO(-)) crystallized from an ethanol solution and its structure was determined by IR spectroscopy, elemental analysis, (1)H NMR, (13)C NMR and X-ray crystallography; it is composed of [Zn(H(2)O)(4)(CH(3)CH(2)OH)(2)](2+) cations and [Ag(UO(2))(3)(OAc)(9)](2-) anions in which triuranyl [(UO(2))(OAc)(3)](3) clusters are linked by the Ag ion.     

Phosphato, chromato, and perrhenato complexes of titanium(IV) and zirconium(IV) containing Kläui's tripodal ligand

Treatment of titanyl sulfate in dilute sulfuric acid with 1 equiv of NaL(OEt) (L(OEt)(-) = [(eta(5)-C(5)H(5))Co{P(O)(OEt)(2)](3)](-)) in the presence of Na(3)PO(4) and Na(4)P(2)O(7) led to isolation of [(L(OEt)Ti)(3)(mu-O)(3)(mu(3-)PO(4))] (1) and [(L(OEt)Ti)(2)(mu-O)(mu-P(2)O(7))] (2), respectively. The structure of 1 consists of a Ti(3)O(3) core capped by a mu(3)-phosphato group. In 2, the [P(2)O(7)](4-) ligands binds to the two Ti's in a mu:eta(2),eta(2) fashion. Treatment of titanyl sulfate in dilute sulfuric acid with NaL(OEt) and 1.5 equiv of Na(2)Cr(2)O(7) gave [(L(OEt)Ti)(2)(mu-CrO(4))(3)] (3) that contains two L(OEt)Ti(3+) fragments bridged by three mu-CrO(4)(2-)-O,O' ligands. Complex 3 can act as a 6-electron oxidant and oxidize benzyl alcohol to give ca. 3 equiv of benzaldehyde. Treatment of [L(OEt)Ti(OTf)(3)] (OTf(-) = triflate) with [n-Bu(4)N][ReO(4)] afforded [[L(OEt)Ti(ReO(4))(2)](2)(mu-O)] (4). Treatment of [L(OEt)MF(3)] (M = Ti and Zr) with 3 equiv of [ReO(3)(OSiMe(3))] afforded [L(OEt)Ti(ReO(4))(3)] (5) and [L(OEt)Zr(ReO(4))(3)(H(2)O)] (6), respectively. Treatment of [L(OEt)MF(3)] with 2 equiv of [ReO(3)(OSiMe(3))] afforded [L(OEt)Ti(ReO(4))(2)F] (7) and [[L(OEt)Zr(ReO(4))(2)](2)(mu-F)(2)] (8), respectively, which reacted with Me(3)SiOTf to give [L(OEt)M(ReO(4))(2)(OTf)] (M = Ti (9), Zr (10)). Hydrolysis of [L(OEt)Zr(OTf)(3)] (11) with Na(2)WO(4).xH(2)O and wet CH(2)Cl(2) afforded the hydroxo-bridged complexes [[L(OEt)Zr(H(2)O)](3)(mu-OH)(3)(mu(3)-O)][OTf](4) (12) and [[L(OEt)Zr(H(2)O)(2)](2)(mu-OH)(2)][OTf](4) (13), respectively. The solid-state structures of 1-3, 6, and 11-13 have been established by X-ray crystallography. The L(OEt)Ti(IV) complexes can catalyze oxidation of methyl p-tolyl sulfide with tert-butyl hydroperoxide. The bimetallic Ti/ Re complexes 5 and 9 were found to be more active catalysts for the sulfide oxidation than other Ti(IV) complexes presumably because Re alkylperoxo species are involved as the reactive intermediates.     

Dimeric uranyl complexes with bridging perrhenates

The reaction between [UO2(ReO4)2.H(2)O] and two equivalents of either tri-n-butyl phosphine oxide (TBPO) or tri-iso-butyl phosphate (TiBP) results in the formation of [UO2(mu2-ReO4)(ReO4)(TBPO)2]2 (1) and [UO2(mu2-ReO4)(ReO4)(TiBP)2]2 (2) respectively. Both complexes crystallise as two structurally similar centrosymmetric dimers, the cores containing two uranyl moieties linked by bridging perrhenates. Two P=O donor ligands and one monodenatate perrhenate complete the pentagonal bipyramidal coordination sphere at each metal centre. Both complexes have also been characterised in the solid state by vibrational and absorption spectroscopy. Solution spectroscopic characterisation indicates that both perrhenate and phosphine oxide (1) or phosphate (2) remain coordinated, although it is not possible to state conclusively that the dimeric species remain intact. A low resolution structural study of a minor product from the reaction that yielded revealed a monomeric complex with only monodentate perrhenate coordination, [UO2(ReO4)2(H2O)(TiBP)2] (2'). These results represent the first structural evidence for the bridging coordination mode of perrhenate on coordination to an actinide and yields further insight into the possible solvent phase pertechnetate complexes that may exist in PUREX process phosphate rich solvent.     

A new series of homoleptic,paramagnetic organochromium derivatives: synthesis,characterization, and study of the magnetic properties

The synthesis and characterization of the triad of organochromium derivatives [Cr(C(6)Cl(5))(4)](n-) (n=0, 1, 2) are described. By treating [CrCl(3)(thf)(3)] with LiC(6)Cl(5) in 1:5 molar ratio, the salt [Li(thf)(4)][Cr(III)(C(6)Cl(5))(4)] (1) was obtained as a violet solid in 57 % yield. Oxidation of 1 with [N(4-BrC(6)H(4))(3)][SbCl(6)] yielded the neutral complex [Cr(IV)(C(6)Cl(5))(4)] (2) as a brown solid in 71 % yield. The arylation of [CrCl(2)(thf)] with LiC(6)Cl(5) under similar conditions as above gave [[Li(thf)(3)](2)(mu-Cl)](2)[Cr(II)(C(6)Cl(5))(4)] (3) as an extremely air- and water-sensitive red solid in 47 % yield. The crystal and molecular structures of 1 and 3 have been established by X-ray diffraction methods. Complex 3 contains the unusual cation [[Li(thf)(3)](2)(mu-Cl)](+) with an almost linear Li-Cl-Li unit (174.2(6)degrees). All four C(6)Cl(5) groups are sigma-bonded to the Cr(II) center, which is located in a square-planar environment. The local geometry around the Cr(III) center in 1 is, in turn, pseudo-octahedral, since two of the C(6)Cl(5) groups act as standard sigma-bonded monodentate ligands, while the other two act as small-bite didentate ligands coordinated through both the ipso-C and one of the ortho-Cl atoms. Compounds 1-3 are paramagnetic with maximum spin multiplicity each (EPR and magnetization measurements).     

Ir(PPh3)2(H)2(ClCH2CH2Cl)][BArF4]: a well characterised transition metal dichloroethane complex

Reaction of [Ir(PPh(3))(2)(COD)][BAr(F)(4)] with H(2) in dichloroethane solution results in [Ir(PPh(3))(2)(H)(2)(ClCH(2)CH(2)Cl)][BAr(F)(4)], which has been fully characterised by X-ray crystallography, NMR spectroscopy and ESI-MS. Its activity towards alkene hydrogenation has been compared with analogous CH(2)Cl(2) complexes.     

Synthesis and characterization of pentachlorophenyl-metal derivatives with d0 and d10 electron configurations

By reaction of [TiCl(3)(thf)(3)] with LiC(6)Cl(5), the homoleptic organotitanium(III) derivative [Li(thf)(4)][Ti(III)(C(6)Cl(5))(4)] (1) has been prepared as a paramagnetic (d(1), S = 1/2, g(av) = 1.959(2)), extremely air-sensitive compound. Oxidation of 1 with [N(C(6)H(4)Br-4)(3)][SbCl(6)] gives the diamagnetic (d(0)) organotitanium(IV) species [Ti(IV)(C(6)Cl(5))(4)] (2). Compounds 1 and 2 are also electrochemically related (E(1/2) = 0.05 V). The homoleptic, diamagnetic (d(10)) compounds [N(PPh(3))(2)][Tl(C(6)Cl(5))(4)] (3) and [Sn(C(6)Cl(5))(4)] (4) have also been prepared. Nearly tetrahedral environments have been found for the d(0), d(10), and d(1) metal centers in the molecular structures of compounds 2-4 as well as in that of [Li(thf)(2)(OEt(2))(2)][Ti(III)(C(6)Cl(5))(4)].CH(2)Cl(2) (1') (X-ray diffraction). The reaction of the heavier Group 4 metal halides, MCl(4) (M = Zr, Hf) with LiC(6)Cl(5) in the presence of [NBu(4)]Br gives, in turn, the heteroleptic species [NBu(4)][M(C(6)Cl(5))(3)Cl(2)] (M = Zr (5), Hf (6)). Compounds 5 and 6 are isomorphous and isostructural, with the metal center in a trigonal-bipyramidal (TBPY-5) environment defined by two axial Cl ligands and three equatorial C(6)Cl(5) groups (X-ray diffraction). No redox features are observed for compounds 3-6 in CH(2)Cl(2) solution between -1.6 and +1.6 V.     

Uranyl and strontium salt solvation in room-temperature ionic liquids. A molecular dynamics investigation

Using molecular dynamics simulations, we compare the solvation of uranyl and strontium nitrates and uranyl chlorides in two room-temperature ionic liquids (ILs): [BMI][PF(6)] based on 1-butyl-3-methylimidazolium(+),PF(6)(-) and [EMI][TCA] based on 1-ethyl-3-methylimidazolium(+),AlCl(4)(-). Both dissociated M(2+),2NO(3)(-) and associated M(NO(3))(2) states of the salts are considered for the two cations, as well as the UO(2)Cl(2) and UO(2)Cl(4)(2)(-) uranyl complexes. In a [BMI][PF(6)] solution, the "naked" UO(2)(2+) and Sr(2+) ions are surrounded by 5.8 and 10.1 F atoms, respectively. The first-shell PF(6)(-) anions rotate markedly during the dynamics and are coordinated, on the average, monodentate to UO(2)(2+) and bidentate to Sr(2+). In an [EMI][TCA] solution, UO(2)(2+) and Sr(2+) coordinate 5.0 and 7.4 Cl atoms of AlCl(4)(-), respectively, which display more restricted motions. Four Cl atoms sit on a least motion pathway of transfer to uranyl, to form the UO(2)Cl(4)(2)(-) complex. The free NO(3)(-) anions and the UO(2)Cl(4)(2)(-) complex are surrounded by imidazolium(+) cations ( approximately 4 and 6-9, respectively). The first shell of the M(NO(3))(2) and UO(2)Cl(2) neutral complexes is mostly completed by the anionic components of the IL, with different contributions depending on the solvent, the M(2+) cation, and its counterions. Insights into energy components of solvation are given for the different systems.     

Aqueous reactions of U(VI) at high chloride concentrations: syntheses and structures of new uranyl chloride polymers

The reactions of UO(3) with acidic aqueous chloride solutions resulted in the formation of two new polymeric U(VI) compounds. Single crystals of Cs(2)[(UO(2))(3)Cl(2)(IO(3))(OH)O(2)].2H(2)O (1) were formed under hydrothermal conditions with HIO(3) and CsCl, and Li(H(2)O)(2)[(UO(2))(2)Cl(3)(O)(H(2)O)] (2) was obtained from acidic LiCl solutions under ambient temperature and pressure. Both compounds contain pentagonal bipyramidal coordination of the uranyl dication, UO(2)(2+). The structure of 1 consists of infinite [(UO(2))(3)Cl(2)(IO(3))(mu(3)-OH)(mu(3)-O)(2)](2-) ribbons that run down the b axis that are formed from edge-sharing pentagonal bipyramidal [UO(6)Cl] and [UO(5)Cl(2)] units. The Cs(+) cations separate the chains from one another and form long ionic contacts with terminal oxygen atoms from iodate ligands, uranyl oxygen atoms, water molecules, and chloride anions. In 2, edge-sharing [UO(3)Cl(4)] and [UO(5)Cl(2)] units build up tetranuclear [(UO(2))(4)(mu-Cl)(6)(mu(3)-O)(2)(H(2)O)(2)](2-) anions that are bridged by chloride to form one-dimensional chains. These chains are connected in a complex network of hydrogen bonds and interactions of uranyl oxygen atoms with Li(+) cations. Crystal data: 1, orthorhombic, space group Pnma, a = 8.2762(4) A, b = 12.4809(6) A, c = 17.1297(8) A, Z = 4; 2, triclinic, space group P1, a = 8.110(1) A, b = 8.621(1) A, c = 8.740(1) A, Z = 2.     

Synthesis, characterization, and stereochemistry of oxorhenium(V) complexes with 2-aminoethanethiolate

A series of oxorhenium(V) complexes with 2-aminoethanethiolate (aet), [ReO(aet-N,S)(D-pen-N,O,S)] (2), [[ReO(aet-N,S)(2)](2)O] (3), [ReO(Cl)(aet-N,S)(2)] (4), and [ReO(aet-N,S)(Haet-S)(2)]Cl(2) ([5]Cl(2)) was newly prepared starting from ReO(4)(-). The reaction of NH(4)ReO(4) with a 1:1 mixture of Haet.HCl and D-H(2)pen (D-penicillamine) in the presence of SnCl(2).2H(2)O in water gave 2, 3, and the known complex [ReO(D-Hpen-N,S)(D-pen-N,O,S)] (1). These complexes were fractionally precipitated by controlling the pH of the reaction solution. The complex 2 was also prepared in a higher yield by a similar reaction using methanol as a solvent. The crystal structure of 2 was determined by X-ray crystallography; 2 crystallizes in the tetragonal space group P4(3) with a = 9.621(1), c = 12.911(1) A, V = 1195.0(3) A(3), and Z = 4. The oxorhenium(V) core in 2 is coordinated by a bidentate-N,S aet ligand and a tridentate-N,O,S D-pen ligand, having a distorted octahedral geometry with a cis-N cis-S configuration in the equatorial plane perpendicular to the O-Re-O axis. The 1:2 reaction of NH(4)ReO(4) with Haet.HCl in the presence of SnCl(2).2H(2)O in methanol produced 4, which is interconvertible with 3, while the corresponding 1:3 reaction resulted in the isolation of [5]Cl(2). The complexes 4 and 5 were also structurally characterized; 4 crystallizes in the monoclinic space group P2(1)/c with a = 6.839(1), b = 10.0704(6), c = 14.1075(8) A, beta = 91.729(8) degrees, V = 971.2(2) A(3), and Z = 4, while [5]Cl(2) crystallizes in the triclinic space group P1 with a = 11.938(3), b = 12.366(3), c = 5.819(1) A, alpha = 102.71(2), beta = 101.28(2), gamma = 75.41(2) degrees, V = 802.0(3) A(3), and Z = 2. In 4, the oxorhenium(V) core is octahedrally coordinated by two bidentate-N,S aet ligands, which form a cis-N cis-S configurational equatorial plane with a Cl(-) ion trans to the oxo ligand. On the other hand, the oxorhenium(V) core in [5](2+) is coordinated by one bidenate-N,S aet and two monodentate-S Haet ligands, having a distorted trigonal-bipyramidal geometry with S and N donors at the apical positions.     

Distorted equatorial coordination environments and weakening of U=O bonds in uranyl complexes containing NCN and NPN ligands

Treatment of [UO(2)Cl(2)(thf)(3)] in thf with 2 equiv of Na[PhC(NSiMe(3))(2)] (Na[NCN]) or Na[Ph(2)P(NSiMe(3))(2)] (Na[NPN]) gives uranyl complex [UO(2)(NCN)(2)(thf)] (1) or [UO(2)(NPN)(2)] (3), respectively. Each complex is a rare example of out-of-plane equatorial nitrogen ligand coordination; the latter contains a significantly bent O=U=O unit and represents the first example of a uranyl ion within a quadrilateral-faced monocapped trigonal prismatic geometry. Removal of the thf in 1 gives [UO(2)(NCN)(2)] (2) with in-plane N donor ligands. Addition of 3 equiv of Na[NCN] gives the tris complex [Na(thf)(2)PhCN][[UO(2)(NCN)(3)] (4.PhCN) with elongation and weakening of one U=O bond through coordination to Na(+). Hydrolysis of 4 provides the oxo-bridged dimer [Na(thf)UO(2)(NCN)(2)](2)(micro(2)-O) (6), a complex with the lowest reported O=U=O symmetrical stretching frequency (nu(1) = 757 cm(-)(1)) for a dinuclear uranyl complex. The anion in complex 4 is unstable in solution but can be stabilized by the introduction of 18-crown-6 to give [Na(18-crown-6)][UO(2)(NCN)(3)] (5). The structures of 1-4 and 6 have been determined by crystallography, and all except 2 show significant deviations of the N ligand atoms from the equatorial plane, driven by the steric bulk of the NCN and NPN ligands. Despite the unusual geometries, these distortions in structure do not appear to have any direct effect on the bonding and electronic structure of the uranyl ion. The main influences toward lowering the U=O bond stretching frequency (nu(1)) are the donating ability of the equatorial ligands, overall charge of the complex, and U=O.Na-type interactions. The intense orange/red colors of these compounds are because of low-energy ligand-to-metal charge-transfer electronic transitions.     

Synthesis and characterization of uranyl compounds with iminodiacetate and oxydiacetate displaying variable denticity

Eight uranyl compounds containing the dicarboxylate ligands iminodiacetate (IDA) or oxydiacetate (ODA) have been characterized in the solid state. The published polymeric structures for [UO(2)(C(4)H(6)NO(4))(2)] and [UO(2)(C(4)H(4)O(5))](n) have been confirmed, while Ba[UO(2)(C(4)H(5)NO(4))(2)] x 3H(2)O, [(CH(3))(2)NH(CH(2))(2)NH(CH(3))(2)][UO(2)(C(4)H(4)O(5))(2)] [orthorhombic space group Pnma, a = 10.996(5) A, b = 21.42(1) A, c = 8.700(3) A, Z = 4], and [C(2)H(5)NH(2)(CH(2))(2)NH(2)C(2)H(5)][UO(2)(C(4)H(4)O(5))(2)] [monoclinic space group P2(1)/n, a = 6.857(3) A, b = 9.209(5) A, c = 16.410(7) A, beta = 91.69(3), Z = 2] contain monomeric anions. The distance from the uranium atom to the central heteroatom (O or N) in the ligand varies. Crystallographic study shows that U-heteroatom (O/N) distances fall into two groups, one 2.6-2.7 A in length and one 3.1-3.2 A, the latter implying no bonding interaction. By contrast, EXAFS analysis of bulk samples suggests that either a long U-heteroatom (O/N) distance (2.9 A) or a range of distances may be present. Three possible structural types, two symmetric and one asymmetric, are identified on the basis of these results and on solid-state (13)C NMR spectroscopy. The two ligands in the complex can be 1,4,7-tridentate, giving five-membered rings, or 1,7-bidentate, to form an eight-membered ring. (C(4)H(12)N(2))[(UO(2))(2)(C(4)H(5)NO(4))(2)(OH)(2)] x 8H(2)O [monoclinic space group P2(1)/a, a = 7.955(9) A, b = 24.050(8) A, c = 8.223(6) A, beta = 112.24(6), Z = 2], (C(2)H(10)N(2))[(UO(2))(2)(C(4)H(5)NO(4))(2)(OH)(2)] x 4H(2)O, and (C(6)H(13)N(4))(2)[(UO(2))(2)(C(4)H(4)O(5))(2)(OH)(2)] x 2H(2)O [monoclinic space group C2/m, a = 19.024(9) A, b = 7.462(4) A, c = 2.467(6) A, beta = 107.75(4), Z = 4] have a dimeric structure with two capping tridentate ligands and two mu(2)-hydroxo bridges, giving edge-sharing pentagonal bipyramids.