Double Intramolecular 1,2 C-H Addition of o-Methyl Groups To Form Ruthenium Pincer Double Tuck-In Complexes.

Ruthenium pincer complexes have a rich history of coordination and reaction chemistries. In this work, we report our discoveries of previously unreported Ru pincer coordination geometries. We found that mono tuck-in κ4-ArPNHPRuLCl complexes react with NaN(SiMe3)2 producing double tuck-in mer-κ5-ArPNHPRuL complexes. Interestingly, when κ4-MesPNHPRuCl is dehydrohalogenated, the resulting double tuck-in complex binds N2, forming the nitrogen complex κ5-MesPNHPRuN2. The mer-κ5-ArPNHPRuL complexes thermally isomerize to the fac-κ5-ArPNHPRuL isomers, which is an uncommon reaction for pincer complexes. The mer-κ5-ArPNHPRuL complexes react with CO and CO2 to form amide κ4-ArPNHPRu(CO)L or carbamate κ5-ArPN(CO2)PRuL complexes, respectively, supporting the hypothesis that the κ4-ArPNPRuL amide intermediates are accessible and reactive.

An Allyl Uranium(IV) Sandwich Complex: Are ϕ Bonding Interactions Possible?

A method to explore head-to-head ϕ back-bonding from uranium f-orbitals into allyl π* orbitals has been pursued. Anionic allyl groups were coordinated to uranium with tethered anilide ligands, then the products were investigated by using NMR spectroscopy, single-crystal XRD, and theoretical methods. The (allyl)silylanilide ligand, N-((dimethyl)prop-2-enylsilyl)-2,6-diisopropylaniline (LH), was used as either the fully protonated, singly deprotonated, or doubly deprotonated form, thereby highlighting the stability and versatility of the silylanilide motif. A free, neutral allyl group was observed in UI2 (L1)2 (1), which was synthesized by using the mono-deprotonated ligand [K][N-((dimethyl)prop-2-enyl)silyl)-2,6-diisopropylanilide] (L1). The desired homoleptic sandwich complex U[L2]2 (2) was prepared from all three ligand precursors, but the most consistent results came from using the dipotassium salt of the doubly deprotonated ligand [K]2 [N-((dimethyl)propenidesilyl)-2,6-diisopropylanilide] (L2). This allyl-based sandwich complex was studied by using theoretical techniques with supporting experimental spectroscopy to investigate the potential for phi (ϕ) back-bonding. The bonding between UIV and the allyl fragments is best described as ligand-to-metal electron donation from a two carbon fragment-localized electron density into empty f-orbitals.

Oxidation of uranium(iv) mixed imido-amido complexes with PhEEPh and to generate uranium(vi) bis(imido) dichalcogenolates, U(NR)2(EPh)2(L)2.

This work provides new routes for the conversion of U(iv) into U(vi) bis(imido) complexes and offers new information on the manner in which the U(vi) compounds form. Many compounds from the series described by the general formula U(NR)2(EPh)2(L)2 (R = 2,6-diisopropylphenyl, tert-butyl; E = S, Se, Te; L = py, EPh) were synthesized via oxidation of an in situ generated U(iv) amido-imido species with Ph2E2. This synthetic sequence provides a general route into bis(imido) U(vi) chalcogenolate complexes, circumventing the need to perform problematic salt metathesis reactions on U(vi) iodides. Investigation into the speciation of the U(iv) complexes that form prior to oxidation found a significant dependence on the identity of the ancillary ligands, with tBu2bpy forming the isolable imido-(bis)amido complex, U(NDipp)(NHDipp)2(tBu2bpy)2. Together, these data are consistent with the view that the bis(imido) U(vi) motif - much like the uranyl ion, UO22+- is a thermodynamic sink into which simple ligand frameworks are unable to prevent uranium from falling when in the presence of a suitable retinue of imido proligands.

Synthesis and Characterization of a Neutral U(II) Arene Sandwich Complex.

Reduction of IU(NHAriPr6)2 (AriPr6 = 2,6-(2,4,6-iPr3C6H2)2C6H3) results in a rare example of a U(II) complex, U(NHAriPr6)2, and the first example that is a neutral species. Here, we show spectroscopic and magnetic studies that suggest a 5f46d0 valence electronic configuration for uranium, along with characterization of related U(III) complexes.

A Pseudotetrahedral Uranium(V) Complex.

A series of uranium amides were synthesized from N, N, N-cyclohexyl(trimethylsilyl)lithium amide [Li][N(TMS)Cy] and uranium tetrachloride to give U(NCySiMe3) x(Cl)4- x, where x = 2, 3, or 4. The diamide was isolated as a bimetallic, bridging lithium chloride adduct ((UCl2(NCyTMS)2)2-LiCl(THF)2), and the tris(amide) was isolated as the lithium chloride adduct of the monometallic species (UCl(NCyTMS)3-LiCl(THF)2). The tetraamide complex was isolated as the four-coordinate pseudotetrahedron. Cyclic voltammetry revealed an easily accessible reversible oxidation wave, and upon chemical oxidation, the UV amido cation was isolated in near-quantitative yields. The synthesis of this family of compounds allows a direct comparison of the electronic structure and properties of isostructural UIV and UV tetraamide complexes. Spectroscopic investigations consisting of UV-vis, NIR, MCD, EPR, and U L3-edge XANES, along with density functional and wave function calculations, of the four-coordinate UIV and UV complexes have been used to understand the electronic structure of these pseudotetrahedral complexes.

Reactivity of Silanes with (tBu PONOP)Ruthenium Dichloride: Facile Synthesis of Chloro-Silyl Ruthenium Compounds and Formic Acid Decomposition.

The coordination of tBu PONOP (tBu PONOP=2,6-bis(ditert-butylphosphinito)pyridine) to different ruthenium starting materials, to generate (tBu PONOP)RuCl2 , was investigated. The resultant (tBu PONOP)RuCl2 reactivity with three different silanes was then investigated and contrasted dramatically with the reactivity of (iPr PONOP)RuCl2 (DMSO) (iPr PONOP=2,6-bis(diisopropylphosphinito)pyridine) with the same silanes. The 16-electron species (tBu PONOP)Ru(H)Cl was produced from the reaction of triethylsilane with (tBu PONOP)RuCl2 . Reactions of (tBu PONOP)RuCl2 with both phenylsilane or diphenylsilane afforded the 16-electron hydrido-silyl species (tBu PONOP)Ru(H)(PhSiCl2 ) and (tBu PONOP)Ru(H)(Ph2 SiCl), respectively. Reactions of all three of these complexes with silver triflate afforded the simple salt metathesis products of (tBu PONOP)Ru(H)(OTf), (tBu PONOP)Ru(H)(PhSiCl(OTf)), and (tBu PONOP)Ru(H)(Ph2 Si(OTf)). Formic acid dehydrogenation was performed in the presence of triethylamine (TEA), and each species proved competent for gas-pressure generation of CO2 and H2 . The hydride species (tBu PONOP)Ru(H)Cl, (tBu PONOP)Ru(H)(OTf), and (tBu PONOP)Ru(H)(PhSiCl2 ) exhibited faster catalytic activity than the other compounds tested.

Extending Stannyl Anion Chemistry to the Actinides: Synthesis and Characterization of a Uranium-Tin Bond.

We have synthesized a rare example of a uranium(IV) stannyl (κ(4)-N(CH2CH2NSi((i)Pr)3)3U(SnMe3), 1) via transmetalation with LiSnMe3. This complex has been characterized crystallographically and shown to have a U-Sn bond length of 3.3130(3) Å, substantially longer than the only other crystallographically observed U-Sn bond (3.166 Å). Computational studies suggest that the U-Sn bond in 1 is highly polarized, with significant charge transfer to the stannylate ligand. We briefly discuss plausible mechanistic scenarios for the formation of 1, which may be relevant to other transmetalation processes involving heavy main group atoms. Furthermore, we demonstrate the reducing ability of [SnMe3](-) in the absence of strongly donating ligands on U(IV).

A Linear trans-Bis(imido) Neptunium(V) Actinyl Analog: Np(V)(NDipp)2((t)Bu2bipy)2Cl (Dipp = 2,6-(i)Pr2C6H3).

The discovery that imido analogs of actinyl dioxo cations can be extended beyond uranium into the transuranic elements is presented. Synthesis of the Np(V) complex, Np(NDipp)2((t)Bu2bipy)2Cl (1), is achieved through treatment of a Np(IV) precursor with a bipyridine coligand and lithium-amide reagent. Complex 1 has been structurally characterized, analyzed by (1)H NMR and UV-vis-NIR spectroscopies, and the electronic structure evaluated by DFT calculations.

Preparation and reactivity of the versatile uranium(IV) imido complexes U(NAr)Cl2(R2bpy)2 (R = Me, (t)Bu) and U(NAr)Cl2(tppo)3.

Uranium tetrachloride undergoes facile reactions with 4,4'-dialkyl-2,2'-bipyridine, resulting in the generation of UCl4(R2bpy)2, R = Me, (t)Bu. These precursors, as well as the known UCl4(tppo)2 (tppo = triphenylphosphine oxide), react with 2 equiv of lithium 2,6-di-isopropylphenylamide to provide the versatile uranium(IV) imido complexes, U(NDipp)Cl2(L)n (L = R2bpy, n = 2; L = tppo, n = 3). Interestingly, U(NDipp)Cl2(R2bpy)2 can be used to generate the uranium(V) and uranium(VI) bisimido compounds, U(NDipp)2X(R2bpy)2, X = Cl, Br, I, and U(NDipp)2I2((t)Bu2bpy), which establishes these uranium(IV) precursors as potential intermediates in the syntheses of high-valent bis(imido) complexes from UCl4. The monoimido species also react with 4-methylmorpholine-N-oxide to yield uranium(VI) oxo-imido products, U(NDipp)(O)Cl2(L)n (L = (t)Bu2bpy, n = 1; L = tppo, n = 2). The aforementioned molecules have been characterized by a combination of NMR spectroscopy, X-ray crystallography, and elemental analysis. The chemical reactivity studies presented herein demonstrate that Lewis base adducts of uranium tetrachloride function as excellent sources of U(IV), U(V), and U(VI) imido species.

Energy landscape of self-assembled superlattices of PbSe nanocrystals.

Self-assembly of nanocrystals (NCs) into superlattices is an intriguing multiscale phenomenon that may lead to materials with novel collective properties, in addition to the unique properties of individual NCs compared with their bulk counterparts. By using different dispersion solvents, we synthesized three types of PbSe NC superlattices--body-centered cubic (bcc), body-centered tetragonal (bct), and face-centered cubic (fcc)--as confirmed by synchrotron small-angle X-ray scattering. Solution calorimetric measurements in hexane show that the enthalpy of formation of the superlattice from dispersed NCs is on the order of -2 kJ/mol. The calorimetric measurements reveal that the bcc superlattice is the energetically most stable polymorph, with the bct being 0.32 and the fcc 0.55 kJ/mol higher in enthalpy. This stability sequence is consistent with the decreased packing efficiency of PbSe NCs from bcc (17.2%) to bct (16.0%) and to fcc (15.2%). The small enthalpy differences among the three polymorphs confirm a closely spaced energy landscape and explain the ease of formation of different NC superlattices at slightly different synthesis conditions.

Tetrahalide complexes of the [U(NR)2]2+ ion: synthesis, theory, and chlorine K-edge X-ray absorption spectroscopy.

Synthetic routes to salts containing uranium bis-imido tetrahalide anions [U(NR)(2)X(4)](2-) (X = Cl(-), Br(-)) and non-coordinating NEt(4)(+) and PPh(4)(+) countercations are reported. In general, these compounds can be prepared from U(NR)(2)I(2)(THF)(x) (x = 2 and R = (t)Bu, Ph; x = 3 and R = Me) upon addition of excess halide. In addition to providing stable coordination complexes with Cl(-), the [U(NMe)(2)](2+) cation also reacts with Br(-) to form stable [NEt(4)](2)[U(NMe)(2)Br(4)] complexes. These materials were used as a platform to compare electronic structure and bonding in [U(NR)(2)](2+) with [UO(2)](2+). Specifically, Cl K-edge X-ray absorption spectroscopy (XAS) and both ground-state and time-dependent hybrid density functional theory (DFT and TDDFT) were used to probe U-Cl bonding interactions in [PPh(4)](2)[U(N(t)Bu)(2)Cl(4)] and [PPh(4)](2)[UO(2)Cl(4)]. The DFT and XAS results show the total amount of Cl 3p character mixed with the U 5f orbitals was roughly 7-10% per U-Cl bond for both compounds, which shows that moving from oxo to imido has little effect on orbital mixing between the U 5f and equatorial Cl 3p orbitals. The results are presented in the context of recent Cl K-edge XAS and DFT studies on other hexavalent uranium chloride systems with fewer oxo or imido ligands.

Phototriggered DNA phosphoramidate ligation in a tandem 5'-amine deprotection/3'-imidazole activated phosphate coupling reaction.

We report the preparation and use of an N-methyl picolinium carbamate protecting group for applications in a phototriggered nonenzymatic DNA phosphoramidate ligation reaction. Selective 5'-amino protection of a modified 13-mer oligonucleotide is achieved in aqueous solution by reaction with an N-methyl-4-picolinium carbonyl imidazole triflate protecting group precursor. Deprotection is carried out by photoinduced electron transfer from Ru(bpy)(3)(2+) using visible light photolysis and ascorbic acid as a sacrificial electron donor. Phototriggered 5'- amino oligonucleotide deprotection is used to initiate a nonenzymatic ligation of the 13-mer to an imidazole activated 3'-phospho-hairpin template to generate a ligated product with a phosphoramidate linkage. We demonstrate that this methodology offers a simple way to exert control over reaction initiation and rates in nonenzymatic DNA ligation for potential applications in the study of model protocellular systems and prebiotic nucleic acid synthesis.

A direct route to bis(imido)uranium(V) halides via metathesis of uranium tetrachloride.

Metathesis reactions between uranium tetrachloride and lithium 2,6-diisopropylphenylamide in the presence of 4,4'-dialkyl-2,2'-bipyridyl (R(2)bpy; R = Me, (t)Bu) or triphenylphosphine oxide (tppo) appear to generate bis(imido)uranium(IV) in situ. These extremely reactive complexes abstract chloride from dichloromethane to generate U(NDipp)(2)Cl(R(2)bpy)(2) or U(NDipp)(2)Cl(tppo)(3) (Dipp = 2,6-(i)Pr(2)C(6)H(3)). The preparation of the bromide and iodide analogues U(NDipp)(2)X(R(2)bpy)(2) was achieved by addition of CH(2)X(2) (X = Br, I) to the uranium(IV) solutions. The uranium(V) halides were characterized by X-ray crystallography and found to exhibit linear N-U-N units and short U-N bonds. Electrochemical measurements were made on the chloride bipyridine species, which reacts readily with iodine or ferrocenium to generate bis(imido)uranium(VI) cations.

Photorelease of primary aliphatic and aromatic amines by visible-light-induced electron transfer.

Visible-light-absorbing tris(bipyridyl)ruthenium(II) has been used to mediate electron transfer to N-methylpicolinium carbamates that undergo C-O bond fragmentation followed by spontaneous carbon dioxide release to give free amines. Release of several aliphatic and aromatic primary amines has been demonstrated under mild conditions using visible light.

A general and modular synthesis of monoimidouranium(IV) dihalides.

The conproportionation reaction between the dimeric diimidouranium(V) species [U(N(t)Bu)(2)(I)((t)Bu(2)bpy)](2) ((t)Bu(2)bpy = 4,4'-di-tert-butyl-2,2'-bipyridyl) and UI(3)(THF)(4) in the presence of additional (t)Bu(2)bpy yields U(N(t)Bu)(I)(2)((t)Bu(2)bpy)(THF)(2) (2), an unprecedented example of a monoimidouranium(IV) dihalide complex. The general synthesis of this family of uranium(IV) derivatives can be achieved more readily by adding 2 equiv of MN(H)R (M = Li, K; R = (t)Bu, 2,6-(i)PrC(6)H(3), 2-(t)BuC(6)H(4)) to UX(4) in the presence of coordinating Lewis bases to give complexes with the general formula U(NR)(X)(2)(L)(n) (X = Cl, I; L = (t)Bu(2)bpy, n = 1; L = THF, n = 2). The complexes were characterized by (1)H NMR spectroscopy and single-crystal X-ray diffraction analysis of compounds 2 and {U[N(2,6-(i)PrC(6)H(3))](Cl)(2)(THF)(2)}(2) (4). (The X-ray structures of 5 and 6 are reported in the Supporting Information.)

Interactions between catalysts and amphiphilic structures and their implications for a protocell model.

One of the essential elements of any cell, including primitive ancestors, is a structural component that protects and confines the metabolism and genes while allowing access to essential nutrients. For the targeted protocell model, bilayers of decanoic acid, a single-chain fatty acid amphiphile, are used as the container. These bilayers interact with a ruthenium-nucleobase complex, the metabolic complex, to convert amphiphile precursors into more amphiphiles. These interactions are dependent on non-covalent bonding. The initial rate of conversion of an oily precursor molecule into fatty acid was examined as a function of these interactions. It is shown that the precursor molecule associates strongly with decanoic acid structures. This results in a high dependence of conversion rates on the interaction of the catalyst with the self-assembled structures. The observed rate logically increases when a tight interaction between catalyst complex and container exists. A strong association between the metabolic complex and the container was achieved by bonding a sufficiently long hydrocarbon tail to the complex. Surprisingly, the rate enhancement was nearly as strong when the ruthenium and nucleobase elements of the complex were each given their own hydrocarbon tail and existed as separate molecules, as when the two elements were covalently bonded to each other and the resulting molecule was given a hydrocarbon tail. These results provide insights into the possibilities and constraints of such a reaction system in relation to building the ultimate protocell.

Exploring the coordination modes of pyrrolyl ligands in bis(imido) uranium(VI) complexes.

The preparation of a family of bis(imido) uranium(VI) complexes stabilized by mono- and bidentate pyrrolyl ancillary ligands is described. X-ray crystallographic studies of dipyrrolylmethane (dpm) derivatives show that the pyrrolyl coordination mode in these uranium(VI) ions is unexpected in comparison to analogous transition metal and lanthanide chemistry. The ability of the coordinated pyrrolyl moieties to undergo pyrrolyl isomerization has also been explored and demonstrates reactivity that is unique from structurally similar uranium(VI)-bis(cyclopentadienyl) derivatives.

Oxidative addition to U(V)-U(V) dimers: facile routes to uranium(VI) bis(imido) complexes.

The ability of dimeric bis(imido) uranium(V) complexes with the general formula [U(N(t)Bu)(2)(Y)((t)Bu(2)bpy)](2) (Y = I (1), SPh (2); (t)Bu(2)bpy = 4,4'-di-tert-butyl-2,2'-bipyridyl) to behave as two-electron reducing agents was examined with I(2), AgX (X = Cl, Br), PhEEPh (E = S, Se, Te), and chalcogen (O, S, Se) atom transfer reagents. The addition of I(2) and AgX to 1 leads to the formation of uranium(VI) dihalide complexes with the general formula U(N(t)Bu)(2)(I)(X)((t)Bu(2)bpy) (X = I (3), Cl (4), Br (5)). Complexes 1 and 2 can also reduce PhEEPh to generate uranium(VI) complexes with the general formula U(N(t)Bu)(2)(X)(EPh)((t)Bu(2)bpy) (X = I, E = S (6), Se (8), Te (10); X = SPh, E = S (7), Se (12)). These unsymmetrical complexes appear to be in equilibrium with the uranium(VI) complexes U(N(t)Bu)(2)(X)(2)((t)Bu(2)bpy) and U(N(t)Bu)(2)(EPh)(2)((t)Bu(2)bpy) (E = Se (9), Te (11)) and suggest that both U-I and U-E bonds possess a labile nature in bis(imido) uranium(VI) complexes. Complex 1 also reacts as a two-electron reductant toward chalcogen atom transfer reagents such as 4-methylmorpholine N-oxide, S(8), and Se to produce dimeric bis(imido) uranium(VI) complexes with the general formula [U(N(t)Bu)(2)(I)((t)Bu(2)bpy)](2)(mu-E) (E = O (13), S (14), Se (15)) and [U(N(t)Bu)(2)(I)((t)Bu(2)bpy)](2)(mu-eta(2):eta(2)-E(4)) (E = S (16), Se (17)). Density functional theory studies performed on a model complex of 13 indicate the presence of multiple bonding in the bridging U-O bond.

Cation-cation interactions, magnetic communication, and reactivity of the pentavalent uranium ion [U(NtBu)2]+.

Communication is important: The dimeric bis(imido) uranium complex [{U(NtBu)(2)(I)(tBu(2)bpy)}(2)] (see picture; U green, N blue, I red) has cation-cation interactions between [U(NR)(2)](+) ions. This f(1)-f(1) system also displays f orbital communication between uranium(V) centers at low temperatures, and can be oxidized to generate uranium(VI) bis(imido) complexes.

Uranium(VI) bis(imido) chalcogenate complexes: synthesis and density functional theory analysis.

Bis(imido) uranium(VI) trans- and cis-dichalcogenate complexes with the general formula U(N(t)Bu)(2)(EAr)(2)(OPPh(3))(2) (EAr = O-2-(t)BuC(6)H(4), SPh, SePh, TePh) and U(N(t)Bu)(2)(EAr)(2)(R(2)bpy) (EAr = SPh, SePh, TePh) (R(2)bpy = 4,4'-disubstituted-2,2'-bipyridyl, R = Me, (t)Bu) have been prepared. This family of complexes includes the first reported monodentate selenolate and tellurolate complexes of uranium(VI). Density functional theory calculations show that covalent interactions in the U-E bond increase in the trans-dichalcogenate series U(N(t)Bu)(2)(EAr)(2)(OPPh(3))(2) as the size of the chalcogenate donor increases and that both 5f and 6d orbital participation is important in the M-E bonds of U-S, U-Se, and U-Te complexes.