In this Article, we report the syntheses and comparative structural studies of lithium, sodium, and potassium anthracen-9-yl enolates, as their aggregates (Li, Na: hexamer; K: tetramer) and ligand-stabilized monomers (for Li and Na). The monomers add new members to the rare collection of group-1 metal monomeric enolates. Moreover, the series covers different group-1 metal cations (Li+, Na+ and K+) and aggregate sizes, allowing comparative structural studies to elucidate how the metal identity and aggregate size influence the enolate structure.
Given their very negative redox potential (e.g., Li+ â Li(0), -3.04 V; K+ â K(0), -2.93 V), chemical reduction of Group-1 metal cations is one of the biggest challenges in inorganic chemistry: they are widely accepted as irreducible in the synthetic chemistry regime. Their reduction usually requires harsh electrochemical conditions. Herein we suggest a new strategy: via a heterobimetallic electride intermediate and using the nonbinding "free" electron as reductant. Based on our previously reported K+[LiN(SiMe3)2]e- heterobimetallic electride, we demonstrate the reducibility of both K+ and Li+ cations. Moreover, we find that external Lewis base ligands, namely tris[2-(dimethylamino)ethyl]amine (Me6Tren) or 2,2,2-cryptand, can exert a level of reducing selectivity by preferably binding to Li+ (Me6Tren) or K+ (2,2,2-cryptand), hence pushing the electron to the other cation.
Herein we report the syntheses, structures and reactivity studies of two new monomeric alkali metal silylbenzyl complexes stabilised by a tetradentate amine ligand, tris[2-(dimethylamino)ethyl]amine (Me6Tren). The two complexes, namely [MR'(Me6Tren)] (R': CH(Ph)(SiMe3)) (2-Li: M = Li; 2-Na: M = Na), exhibit significant different coordination modes according to their metal identity (Li: σ-coordination; Na: π-coordination). Reactivity studies of 2-Li and 2-Na reveal that they are efficient in promoting a widely-used class of organic functional group interconversion: CîO bond olefination of ketones, aldehydes and amides, to produce tri-substituted internal alkenes.
Organo-alkali metal reagents are essential tools in synthetic chemistry. Alkali metal organometallics aggregate in solution and solid-state forming clusters and polymers. The structure of these aggregates and their structure-reactivity relationship have been of great interest for many decades. This Perspective will look at the strategies that have been employed to isolate low aggregates and, in particular, monomeric complexes of the most common alkali metal alkyls (M = Li-Cs, R = methyl, trimethylsilylmethyl, bis/tris(trimethylsilylmethyl), butyls and benzyl) and the relationship between level of aggregation, structure and reactivity.
Organosodium chemistry is underdeveloped compared with organolithium chemistry, and all the reported organosodium complexes exhibit similar, if not identical, reactivity patterns to their lithium counterparts. Herein, we report a rare organosodium monomeric complex, namely, [Na(CH2SiMe3)(Me6Tren)] (1-Na) (Me6Tren: tris[2-(dimethylamino)ethyl]amine) stabilized by a tetra-dentate neutral amine ligand Me6Tren. Employing organo-carbonyl substrates (ketones, aldehydes, amides, ester), we demonstrated that 1-Na features distinct reactivity patterns compared with its lithium counterpart, [Li(CH2SiMe3)(Me6Tren)] (1-Li). Based on this knowledge, we further developed a ligand-catalysis strategy to conduct ketone/aldehyde methylenations, using [NaCH2SiMe3]∞ as the CH2 feedstock, replacing the widely used but hazardous/expensive CâO methylenation methods, such as Wittig, Tebbe, Julia/Julia-Kocienski, Peterson, and so on.
Multidentate neutral amine ligands play vital roles in coordination chemistry and catalysis. In particular, these ligands are used to tune the reactivity of Group-1 metal reagents, such as organolithium reagents. Most, if not all, of these Group-1 metal reagent-mediated reactions occur in solution. However, the solution-state coordination behaviors of these ligands with Group-1 metal cations are poorly understood, compared to the plethora of solid-state structural studies based on single-crystal X-ray diffraction (SCXRD) studies. In this work, we comprehensively mapped out the coordination modes with Group-1 metal cations for three multidentate neutral amine ligands: tridentate 1,4,7-trimethyl-1,4,7-triazacyclononane (Me3TACN), tetradentate tris[2-(dimethylamino)ethyl]amine (Me6Tren), and hexadentate N,N',Nâ³-tris-(2-N-diethylaminoethyl)-1,4,7-triaza-cyclononane (DETAN). The macrocycles in the Me3TACN and DETAN are identified as the rigid structural directing motif, with the sidearms of DETAN providing flexible "on-demand" coordination sites. In comparison, the Me6Tren ligand features more robust coordination, with the sidearms less likely to undergo the decoordinating-coordinating equilibrium. This work will provide a guidance for coordination chemists in applying these three ligands, in particular, the new DETAN ligand to design metal complexes which suit their purposes.
As known, actinyl peroxides play important roles in environmental transport of actinides, and they have strategic importance in the application of nuclear industry. Compared to the most studied uranyl peroxides, the studies of transuranic counterparts are still few, and more information about these species is needed. In this work, experimentally inspired actinyl peroxide dimers ([An2O6]2+, An = U, Np, and Pu) have been studied and analyzed by using density functional theory and multireference wave function methods. This study determines that the three [An2O6]2+ have unique electronic structures and oxidation states, as [(UVIO2)2(O2)2-]2+, [(NpVIIO2)2(O2-)2]2+, and mixed-valent [(PuVI/VO2)2(O2)1-]2+. This study demonstrates the significance of two bridging oxo ligands with at most four electron holes availability in ionically directing actinyl and resulting in the unusual multiradical bonding in [(PuVI/VO2)2(O2)1-]2+. In addition, thermodynamically stable 12-crown-4 ether (12C4) chelated [(An2O6)(12C4)2]2+ complexes have been predicted, that could maintain these unique electronic structures of [An2O6]2+, where the An â O12C4 dative bonding shows a trend in binding capacity of 12C4 from κ4 (U) to κ3 (Np) and κ4 (Pu). This study reveals the interesting electronic character and bonding feature of a series of early actinide elements in peroxide complexes, which can provide insights into the intrinsic stability of An-containing species.
We report the synthesis and characterization of uranium(IV) and thorium(IV) mesoionic carbene complexes [An{N(SiMe3)2}2(CH2SiMe2NSiMe3){MIC}] (An = U, 4U and Th, 4Th; MIC = {CN(Me)C(Me)N(Me)CH}), which represent rare examples of actinide mesoionic carbene linkages and the first example of a thorium mesoionic carbene complex. Complexes 4U and 4Th were prepared via a C-H activation intramolecular cyclometallation reaction of actinide halides, with concomitant formal 1,4-proton migration of an N-heterocyclic olefin (NHO). Quantum chemical calculations suggest that the An-carbene bond comprises only a σ-component, in contrast to the uranium(III) analogue [U{N(SiMe3)2}3(MIC)] (1) where computational studies suggested that the 5f3 uranium(III) ion engages in a weak one-electron π-backbond to the MIC. This highlights the varying nature of actinide-MIC bonding as a function of actinide oxidation state. In solution, 4Th exists in equilibrium with the Th(IV) metallacycle [Th{N(SiMe3)2}2(CH2SiMe2NSiMe3)] (6Th) and free NHO (3). The thermodynamic parameters of this equilibrium were probed using variable-temperature NMR spectroscopy yielding an entropically favored but enthalpically endothermic process with an overall reaction free energy of ΔG 298.15K = 0.89 kcal mol-1. Energy decomposition analysis (EDA-NOCV) of the actinide-carbon bonds in 4U and 4Th reveals that the former is enthalpically stronger and more covalent than the latter, which accounts for the respective stabilities of these two complexes.
Since the advent of organotransuranium chemistry six decades ago, structurally verified complexes remain restricted to π-bonded carbocycle and σ-bonded hydrocarbyl derivatives. Thus, transuranium-carbon multiple or dative bonds are yet to be reported. Here, utilizing diphosphoniomethanide precursors we report the synthesis and characterization of transuranium-carbene derivatives, namely, diphosphonio-alkylidene- and N-heterocyclic carbene-neptunium(III) complexes that exhibit polarized-covalent σ2π2 multiple and dative σ2 single transuranium-carbon bond interactions, respectively. The reaction of [NpIIII3(THF)4] with [Rb(BIPMTMSH)] (BIPMTMSH = {HC(PPh2NSiMe3)2}1-) affords [(BIPMTMSH)NpIII(I)2(THF)] (3Np) in situ, and subsequent treatment with the N-heterocyclic carbene {C(NMeCMe)2} (IMe4) allows isolation of [(BIPMTMSH)NpIII(I)2(IMe4)] (4Np). Separate treatment of in situ prepared 3Np with benzyl potassium in 1,2-dimethoxyethane (DME) affords [(BIPMTMS)NpIII(I)(DME)] (5Np, BIPMTMS = {C(PPh2NSiMe3)2}2-). Analogously, addition of benzyl potassium and IMe4 to 4Np gives [(BIPMTMS)NpIII(I)(IMe4)2] (6Np). The synthesis of 3Np-6Np was facilitated by adopting a scaled-down prechoreographed approach using cerium synthetic surrogates. The thorium(III) and uranium(III) analogues of these neptunium(III) complexes are currently unavailable, meaning that the synthesis of 4Np-6Np provides an example of experimental grounding of 5f- vs 5f- and 5f- vs 4f-element bonding and reactivity comparisons being led by nonaqueous transuranium chemistry rather than thorium and uranium congeners. Computational analysis suggests that these NpIIIâC bonds are more covalent than UIIIâC, CeIIIâC, and PmIIIâC congeners but comparable to analogous UIVâC bonds in terms of bond orders and total metal contributions to the MâC bonds. A preliminary assessment of NpIIIâC reactivity has introduced multiple bond metathesis to transuranium chemistry, extending the range of known metallo-Wittig reactions to encompass actinide oxidation states III-VI.
We report the synthesis and characterisation of a series of rare-earth mesoionic carbene complexes, [RE{N(SiMe3 )2 }3 {CN(Me)C(Me)N(Me)CH}] (3RE, RE=Sc, Ce, Pr, Sm, Gd, Tb, Dy, Ho, Er, Tm, Yb, and Lu), greatly expanding the limited library of f-block mesoionic carbene complexes. These complexes were prepared by treatment of the parent RE-triamides with an N-heterocyclic olefin (NHO), where an NHO backbone proton undergoes a formal 1,4-proton migration to the NHO-methylene group. For all RE(III) metals, as expected, quantum chemical calculations suggest only a σ-component to the metal-carbene bonding, in contrast to a previously reported uranium(III) congener where the 5f3 metal engages in a weak π-back-bond to the MIC. All complexes were characterised by static variable-temperature magnetic measurements, and dynamic magnetic measurements reveal that 3Dy and 3Er are field-induced single-molecule magnets (SMMs), with Ueff energy barriers of 35 and 128â K, respectively. Complex 3Dy is, as expected, a poorly performing SMM, but conversely 3Er performs unexpectedly well.
This work comprehensively investigated the coordination chemistry of a hexa-dentate neutral amine ligand, namely, N,N',N"-tris-(2-N-diethylaminoethyl)-1,4,7-triaza-cyclononane (DETAN), with group-1 metal cations (Li+, Na+, K+, Rb+, Cs+). Versatile coordination modes were observed, from four-coordinate trigonal pyramidal to six-coordinate trigonal prismatic, depending on the metal ionic radii and metal's substituent. For comparison, the coordination chemistry of a tetra-dentate tris-[2-(dimethylamino)ethyl]amine (Me6Tren) ligand was also studied. This work defines the available coordination modes of two multidentate amine ligands (DETAN and Me6Tren), guiding future applications of these ligands for pursuing highly reactive and elusive s-block and rare-earth metal complexes.
Monomeric organolithium (LiR) complexes could provide enhanced Li-C bond reactivity and suggest mechanisms for a plethora of LiR-mediated reactions. They are highly sought-after but remain a synthetic challenge for organometallic chemists. In this work, we report the synthesis and characterisation of a monomeric (trimethylsilyl)methyl lithium complex, namely [Li(CH2SiMe3)(κ3-N,N',N''-Me6Tren)] (1), where Me6Tren is a tetradentate neutral amine ligand. The structure of 1 was comprehensively examined by single-crystal X-ray diffraction, variable temperature NMR spectroscopy and electron absorption spectroscopy. Complex 1 decomposes via ligand C-H and C-N activations to produce a Li amide complex 2. Preliminary reactivity studies of 1 reveal CîO insertion and C-H activation reaction patterns.
Amides , Lithium , Amides/chemistry , Crystallography, X-Ray , Ligands , Lithium/chemistry , Magnetic Resonance Spectroscopy
Disproportionation, where a chemical element converts its oxidation state to two different ones, one higher and one lower, underpins the fundamental chemistry of metal ions. The overwhelming majority of uranium disproportionations involve uranium(III) and (V), with a singular example of uranium(IV) to uranium(V/III) disproportionation known, involving a nitride to imido/triflate transformation. Here, we report a conceptually opposite disproportionation of uranium(IV)-imido complexes to uranium(V)-nitride/uranium(III)-amide mixtures. This is facilitated by benzene, but not toluene, since benzene engages in a redox reaction with the uranium(III)-amide product to give uranium(IV)-amide and reduced arene. These disproportionations occur with potassium, rubidium, and cesium counter cations, but not lithium or sodium, reflecting the stability of the corresponding alkali metal-arene by-products. This reveals an exceptional level of ligand- and solvent-control over a key thermodynamic property of uranium, and is complementary to isolobal uranium(V)-oxo disproportionations, suggesting a potentially wider prevalence possibly with broad implications for the chemistry of uranium.
Methyllithium (MeLi) is the parent archetypal organolithium complex. MeLi exists as aggregates in solutions and solid states. Monomeric MeLi is postulated as a highly reactive intermediate and plays a vital role in understanding MeLi-mediated reactions but has not been isolated. Herein, we report the synthesis and structure of the first monomeric MeLi complex enabled by a new hexadentate neutral amine ligand.
Actinide metal oxo clusters are of vital importance in actinide chemistry, as well as in environmental and materials sciences. They are ubiquitous in both aqueous and nonaqueous phases and play key roles in nuclear materials (e.g., nuclear fuel) and nuclear waste management. Despite their importance, our structural understanding of the actinide metal oxo clusters, particularly the transuranic ones, is very limited because of experimental challenges such as high radioactivity. Herein we report a systematic theoretical study on the structures and stabilities of seven actinide metal oxo-hydroxo clusters [AnIV6O4(OH)4L12] (1-An; An = Th-Cm; L = O2CH-) along with their group 4 (Ti, Zr, Hf, Rf) and lanthanide (Ce) counterparts [MIV6O4(OH)4L12] (1-M). The work shows the Td-symmetric structures of all of the 1-An/M clusters and suggests the positions of the -OH functional groups, which are experimentally challenging to determine. Furthermore, by removing six electrons from 1-An, we found that oxidation could happen on the AnIV metal ions, producing [AnV6O4(OH)4L12]6+ (2-An; An = Pa, U, Np), or on the O2- and OH- ligands, producing [AnIV6(Oâ¢-)4(OHâ¢)2(OH)2L12]6+ (3-An; An = Pu, Am, Cm). On the basis of 2-An, we constructed a series of tetravalent and pentavalent actinide metal oxo clusters [AnIV6O14]4- (4-An) and [AnV6O14]2+ (5-An), which proves the feasibility of the highly important pentavalent actinyl clusters, demonstrates the f orbital's structure-directing role in the formation of linear [O≡AnVâO]+ actinyl ions, and expands the concept of actinyl-actinyl interaction into pentavalent transuranic actinyl clusters.
Despite their importance as mechanistic models for heterogeneous Haber Bosch ammonia synthesis from dinitrogen and dihydrogen, homogeneous molecular terminal metal-nitrides are notoriously unreactive towards dihydrogen, and only a few electron-rich, low-coordinate variants demonstrate any hydrogenolysis chemistry. Here, we report hydrogenolysis of a terminal uranium(V)-nitride under mild conditions even though it is electron-poor and not low-coordinate. Two divergent hydrogenolysis mechanisms are found; direct 1,2-dihydrogen addition across the uranium(V)-nitride then H-atom 1,1-migratory insertion to give a uranium(III)-amide, or with trimesitylborane a Frustrated Lewis Pair (FLP) route that produces a uranium(IV)-amide with sacrificial trimesitylborane radical anion. An isostructural uranium(VI)-nitride is inert to hydrogenolysis, suggesting the 5f1 electron of the uranium(V)-nitride is not purely non-bonding. Further FLP reactivity between the uranium(IV)-amide, dihydrogen, and triphenylborane is suggested by the formation of ammonia-triphenylborane. A reactivity cycle for ammonia synthesis is demonstrated, and this work establishes a unique marriage of actinide and FLP chemistries.
Little is known about the chemistry of the 2-arsaethynolate anion, but to date it has exclusively undergone fragmentation reactions when reduced. Herein, we report the synthesis of [U(TrenTIPS )(OCAs)] (2, TrenTIPS =N(CH2 CH2 NSiiPr3 )3 ), which is the first isolable actinide-2-arsaethynolate linkage. UV-photolysis of 2 results in decarbonylation, but the putative [U(TrenTIPS )(As)] product was not isolated and instead only [{U(TrenTIPS )}2 (µ-η2 :η2 -As2 H2 )] (3) was formed. In contrast, reduction of 2 with [U(TrenTIPS )] gave the mixed-valence arsenido [{U(TrenTIPS )}2 (µ-As)] (4) in very low yield. Complex 4 is unstable which precluded full characterisation, but these photolytic and reductive reactions testify to the tendency of 2-arsaethynolate to fragment with CO release and As transfer. However, addition of 2 to an electride mixture of potassium-graphite and 2,2,2-cryptand gives [{U(TrenTIPS )}2 {µ-η2 (OAs):η2 (CAs)-OCAs}][K(2,2,2-cryptand)] (5). The coordination mode of the trapped 2-arsaethynolate in 5 is unique, and derives from a new highly reduced and bent form of this ligand with the most acute O-C-As angle in any complex to date (O-C-As â ≈128°). The trapping rather than fragmentation of this highly reduced O-C-As unit is unprecedented, and quantum chemical calculations reveal that reduction confers donor-acceptor character to the O-C-As unit.
Despite continuing and burgeoning interest in f-block complexes and their bonding chemistry in recent years, investigations of the electronic structures and oxidation states of heterobimetallic complexes, and their bonding features between transition-metals (TMs) and f-elements remain relatively less explored. Here, we report a quantum chemical computational study on the series of TM-actinide and -neodymium complexes [TMAn(L)] and [TMNd(L)] [An = U, Np, Pu; TM = Cr, Mn, Fe; L = {N(o-[NCH2P(CH3)2]C6H4)3}3-] in order to explore periodic trend, generalities and differences in the electronic structure and metal-metal bonding between f-block and d-block elements. Based on the calculations, we find up to five-fold covalent multiple bonding between actinide and transition metal ions, which is in sharp contrast with a single bond between neodymium and transition metals. From a comparative study, a general trend of strength of the An-TM interaction emerges in accordance with the atomic number of the actinide metal, which relates to the nature, energy level, and spatial arrangement of their frontier orbitals. The trend presents a valuable insight for future experimental endeavour searching for isolable complexes with strong and multiple An-TM bonding interactions, especially for the experimentally challenging transuranic elements that require targeted research due to their radioactive nature.
A fundamental bonding model in coordination and organometallic chemistry is the synergic, donor-acceptor interaction between a metal and a neutral π-acceptor ligand, in which the ligand σ donates to the metal, which π back-bonds to the ligand. This interaction typically involves a metal with an electron-rich, mid-, low- or even negative oxidation state and a ligand with a π* orbital. Here, we report that treatment of a uranium-carbene complex with an organoazide produces a uranium(V)-bis(imido)-dinitrogen complex, stabilized by a lithium counterion. This complex, which was isolated in a crystalline form, involves an electron-poor, high-oxidation-state uranium(V) 5f1 ion that is π back-bonded to the poor π-acceptor ligand dinitrogen. We propose that this is made possible by a combination of cooperative heterobimetallic uranium-lithium effects and the presence of suitable ancillary ligands that render the uranium ion unusually electron rich. This electron-poor back-bonding could have implications for the field of dinitrogen activation.
