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Metal vinylidene complexes are widely encountered, or postulated, as intermediates in a range of important metal-mediated transformations of alkynes. However, fluorovinylidene complexes have rarely been described and their reactivity is largely unexplored. By making use of the novel outer-sphere electrophilic fluorination (OSEF) strategy we have developed a rapid, robust and convenient method for the preparation of fluorovinylidene and trifluoromethylvinylidene ruthenium complexes from non-fluorinated alkynes. Spectroscopic investigations (NMR and UV/Vis), coupled with TD-DFT studies, show that fluorine incorporation results in significant changes to the electronic structure of the vinylidene ligand. The reactivity of fluorovinylidene complexes shows many similarities to non-fluorinated analogues, but also some interesting differences, including a propensity to undergo unexpected C-F bond cleavage reactions. Heating fluorovinylidene complex [Ru(η(5)-C5H5)(PPh3)2(C[double bond, length as m-dash]C{F}R)][BF4] led to C-H activation of a PPh3 ligand to form an orthometallated fluorovinylphosphonium ligand. Reaction with pyridine led to nucleophilic attack at the metal-bound carbon atom of the vinylidene to form a vinyl pyridinium species, which undergoes both C-H and C-F activation to give a novel pyridylidene complex. Addition of water, in the presence of chloride, leads to anti-Markovnikov hydration of a fluorovinylidene complex to form an α-fluoroaldehyde, which slowly rearranges to its acyl fluoride isomer. Therefore, fluorovinylidenes ligands may be viewed as synthetic equivalents of 1-fluoroalkynes providing access to reactivity not possible by other routes. more...

Organofluorine chemistry plays a key role in materials science, pharmaceuticals, agrochemicals, and medical imaging. However, the formation of new carbon-fluorine bonds with controlled regiochemistry and functional group tolerance is synthetically challenging. The use of metal complexes to promote fluorination reactions is of great current interest, but even state-of-the-art approaches are limited in their substrate scope, often require activated substrates, or do not allow access to desirable functionality, such as alkenyl C(sp(2))-F or chiral C(sp(3))-F centers. Here, we report the formation of new alkenyl and alkyl C-F bonds in the coordination sphere of ruthenium via an unprecedented outer-sphere electrophilic fluorination mechanism. The organometallic species involved are derived from nonactivated substrates (pyridine and terminal alkynes), and C-F bond formation occurs with full regio- and diastereoselectivity. The fluorinated ligands that are formed are retained at the metal, which allows subsequent metal-mediated reactivity. more...

The field of ionic liquids (ILs) has shown rapid growth in recent years. Much of this work has involved the synthesis of new ILs and their application in an ever-increasing number of areas. In contrast, there have been relatively few studies that investigate and attempt to predict the fundamental physical properties of ILs, which are extremely important for their applications. The quantitative prediction of the physical properties of unknown salts remains an important goal in IL research. This will allow the design of new ILs with specific properties tailored for particular applications, without the need for time-consuming trial and error syntheses. Recently, several studies have shown that it is possible to make predictions of the physical properties of ILs e.g. melting points, conductivities, viscosities, densities, surface tensions and refractive indices. This paper gives an overview of these semi-empirical methods and makes some comparisons regarding the accuracy of their predictions and their applicability to predicting the properties of unknown salts. more...

We have used microwave dielectric relaxation spectroscopy to study the picosecond dynamics of five low-viscosity, highly conductive room temperature ionic liquids based on 1-alkyl-3-methylimidazolium cations paired with the bis((trifluoromethyl)sulfonyl)imide anion. Up to 20 GHz the dielectric response is bimodal. The longest relaxation component at the time scale of several 100 ps reveals strongly nonexponential dynamics and correlates with the viscosity in a manner consistent with hydrodynamic predictions for the diffusive reorientation of dipolar ions. Methyl substitution at the C2 position destroys this correlation. The time constants of the weak second process at the 20 ps time scale are practically the same for each salt. This intermediate process seems to correlate with similar modes in optical Kerr effect spectra, but its physical origin is unclear. The missing high-frequency portion of the spectra indicates relaxation beyond the upper cutoff frequency of 20 GHz, presumably due to subpicosecond translational and librational displacements of ions in the cage of their counterions. There is no evidence for orientational relaxation of long-lived ion pairs. more...

Two rare examples of the crystal structures of large molecular clusters formed from the lithium salts of multianions are reported; the first is the dilithium salt of phenylhydrazine, which forms a tetrameric cage with a core of eight Li and eight N centres; the second is a 32-membered cage which forms from the aggregation of two [B(NNPh)3]6- hexaanions, two [NH-NPh]2- dianions and 16 Li+ cations. more...

High-yielding syntheses of complexes based around the cyclodistibazane (Sb(2)N(2)) core are described from the reaction of organoantimony(V) chlorides with varying stoichiometric amounts of lithiated primary amines, LiN(H)R. Thus, mixing Ph(3)SbCl(2) with 2 equiv of LiN(H)R (R = CH(2)Ph) produces Ph(3)Sb(mu-NR)(2)SbPh(3) (1). Mixed amido/imido complexes of formula {R(H)N}Ph(2)Sb(mu-NR)(2)SbPh(2){N(H)R} (2) (R = CH(2)Ph, 2-OMe-5-(t)()Bu-C(6)H(3), and Cy) are made from the corresponding 3:1 molar ratio combination of LiN(H)R with Ph(2)SbCl(3). A similar reaction employing only 2 equiv of LiN(H)R (R = CH(2)Ph) with 1 equiv of Ph(2)SbCl(3) yields ClPh(2)Sb(mu-NR)(2)SbPh(2)Cl (3). Compounds 2a-c and 3 possess reactive functionality which may make them useful synthetic reagents in the preparation of more complex main group imido architectures. All of the complexes have been characterized by (1)H NMR spectroscopy, elemental analysis (CHN), and X-ray crystallography. An investigation of all known crystallographically characterized Sb-N fragments from the Cambridge Structural Database highlights a series of parameters that appear to influence the observed Sb-N bond lengths. more...

A combined computational and experimental study is presented that investigates the mechanism of the anti-Markovnikov hydration of phenylacetylene by [Ru(η(5)-C5H5)(6-DPPAP)(3-DPICon)](+) (where 6-DPPAP = 6-(diphenylphosphino)-N-pivaloyl-2-aminopyridine) and 3-DPICon = 3-diphenylphosphinoisoquinolone). The proposed mechanism, modelled using density functional calculations, involves an initial alkyne-vinylidene tautomerism, which occurs via a ligand-assisted proton shuttle (LAPS) mechanism. Intramolecular ligand assistance from the 6-DPPAP and 3-DPICon ligands, particularly the basic nitrogen of 6-DPPAP, is also involved in subsequent stages of the mechanism and three LAPS processes in total are observed. The self-assembled ligand backbone helps to create a water-binding pocket close to the metal centre, which facilitates nucleophilic attack of water at the vinylidene α-carbon and mediates protonation and deprotonation of subsequent acyl and vinyl intermediates. Experimental evidence is also presented for a novel non-productive catalyst deactivation pathway, which appears to arise from an initial lactam-lactim tautomerism of the 3-DPICon ligand followed by coupling with a vinylidene. more...

The ruthenium naphthalene complex [Ru(η(5)-C5H5)(η(6)-C10H8)](+) is a catalyst precursor for the direct C-H alkenylation of pyridine and related nitrogen heterocycles by terminal alkynes. Stoichiometric studies have demonstrated that the naphthalene ligand may be displaced by either pyridine, 4-methylpyridine or dimethylaminopyridine (DMAP) to give species [Ru(η(5)-C5H5)L3](+) (L = nitrogen-based ligand). Reaction of in situ-generated [Ru(η(5)-C5H5)(py)3](+) (py = pyridine) with PPh3 results in the formation of [Ru(η(5)-C5H5)(PPh3)(py)2](+), the active catalyst for direct alkenylation, some [Ru(η(5)-C5H5)(PPh3)2(py)](+) is also formed in this reaction. A one-pot procedure is reported which has allowed for the nature of the nitrogen heterocycle and phosphine ligand to be evaluated. The sterically demanding phosphine PCy3 inhibits catalysis, and only trace amounts of product are formed when precursors containing a pentamethylcyclopentadienyl group were used. The greatest conversion was observed with PMe3 when used as co-ligand with [Ru(η(5)-C5H5)(η(6)-C10H8)](+). more...

A combined experimental and theoretical study has demonstrated that [Ru(η(5)-C(5)H(5))(py)(2)(PPh(3))](+) is a key intermediate, and active catalyst for, the formation of 2-substituted E-styrylpyridines from pyridine and terminal alkynes HC≡CR (R = Ph, C(6)H(4)-4-CF(3)) in a 100% atom efficient manner under mild conditions. A catalyst deactivation pathway involving formation of the pyridylidene-containing complex [Ru(η(5)-C(5)H(5))(κ(3)-C(3)-C(5)H(4)NCH═CHR)(PPh(3))](+) and subsequently a 1-ruthanaindolizine complex has been identified. Mechanistic studies using (13)C- and D-labeling and DFT calculations suggest that a vinylidene-containing intermediate [Ru(η(5)-C(5)H(5))(py)(═C═CHR)(PPh(3))](+) is formed, which can then proceed to the pyridylidene-containing deactivation product or the desired product depending on the reaction conditions. Nucleophilic attack by free pyridine at the α-carbon in this complex subsequently leads to formation of a C-H agostic complex that is the branching point for the productive and unproductive pathways. The formation of the desired products relies on C-H bond cleavage from this agostic complex in the presence of free pyridine to give the pyridyl complex [Ru(η(5)-C(5)H(5))(C(5)H(4)N)(═C═CHR)(PPh(3))]. Migration of the pyridyl ligand (or its pyridylidene tautomer) to the α-carbon of the vinylidene, followed by protonation, results in the formation of the 2-styrylpyridine. These studies demonstrate that pyridylidene ligands play an important role in both the productive and nonproductive pathways in this catalyst system. more...

Copper and silver form coordination complexes with P4 whereas gold forms a homoleptic [Au(P4)2]+ cation.

A series of bis(trifluoromethylsulfonyl)imide ionic liquids (ILs) with classical as well as mildly functionalized cations was prepared and their viscosities and conductivities were determined as a function of the temperature. Both were analyzed with respect to Arrhenius, Litovitz and Vogel-Fulcher-Tammann (VFT) behaviors, as well as in the context of their molecular volume (V(m)). Their viscosity and conductivity are highly correlated with V(m)/T or related expressions (R(2) ≥0.94). With the knowledge of V(m) of new cations, these correlations allow the temperature-dependent prediction of the viscosity and conductivity of hitherto unknown, non- or mildly functionalized ILs with low error bars (0.05 and 0.04 log units, respectively). The influence of the cation structure and mild functionalization on the physical properties was studied with systematically altered cations, in which V(m) remained similar. The T(o) parameter obtained from the VFT fits was compared to the experimental glass temperature (T(g)) and the T(g)/T(o) ratio for each IL was calculated using both experimental values and Angell's relationship. With Walden plots we investigated the IL ionicity and interpreted it in relation to the cation effects on the physical IL properties. We checked the validity of these V(m)/T relations by also including the recently published variable temperature viscosity and conductivity data of the [Al(OR(F))(4)](-) ILs with R(F) =C(H)(CF(3))(2) (error bars for the prediction: 0.09 and 0.10 log units, respectively). more...

Collisions of hyperthermal oxygen atoms, with an average translational energy of 520 kJ mol−1, on continuously refreshed ionic liquids, 1‐ethyl‐3‐methylimidazolium bis(trifluoromethylsulfonyl) imide ([emim][NTf2]) and 1‐dodecyl‐3‐methylimidazolium bis(trifluoromethylsulfonyl) imide ([C12mim][NTf2]), were studied with the use of a beam‐surface scattering technique. Time‐of‐flight and angular distributions of inelastically scattered O and reactively scattered OH and H2O were collected for various angles of incidence with the use of a rotatable mass spectrometer detector. For both O and OH, two distinct scattering processes were identified, which can be empirically categorized as thermal and non‐thermal. Non‐thermal scattering is more probable for both O and OH products. The observation of OH confirms that at least some reactive sites, presumably alkyl groups, must be exposed at the surface. The ionic liquid with the longer alkyl chain, [C12mim][NTf2], is substantially more reactive than the liquid with the ... more...

The ruthenium bis-acetate complex Ru(κ(2)-OAc)(2)(PPh(3))(2) reacts with HC≡CPh to afford the vinylidene-containing species Ru(κ(1)-OAc)(κ(2)-OAc)(=C=CHPh)(PPh(3))(2). An experimental study has demonstrated that this reaction occurs under very mild conditions, with significant conversion being observed at 255 K. At lower temperatures, evidence for a transient metallo-enol ester species Ru(κ(1)-OAc)(OC{Me}O-C=CHPh)(PPh(3))(2) was obtained. A comprehensive theoretical study to probe the nature of the alkyne/vinylidene tautomerisation has been undertaken using Density Functional Theory. Calculations based on a number of isomers of the model system Ru(κ(1)-OAc)(κ(2)-OAc)(=C=CHMe)(PH(3))(2) demonstrate that both the η(2)(CC) alkyne complex Ru(κ(1)-OAc)(κ(2)-OAc)(η(2)-HC≡CMe)(PH(3))(2) and the C-H agostic σ-complex Ru(κ(1)-OAc)(κ(2)-OAc)(η(2){CH}-HC≡CMe)(PH(3))(2) are minima on the potential energy surface. The lowest energy pathway for the formation of the vinylidene complex involves the intramolecular deprotonation of the σ-complex by an acetate ligand followed by reprotonation of the subsequently formed alkynyl ligand. This process is thus termed a Ligand-Assisted Proton Shuttle (LAPS). Calculations performed on the full experimental system Ru(κ(1)-OAc)(κ(2)-OAc)(=C=CHPh)(PPh(3))(2) reinforce the notion that lowest energy pathway involves the deprotonation/reprotonation of the alkyne by an acetate ligand. Inclusion of the full ligand substituents in the calculations are necessary to reproduce the experimental observation of Ru(κ(1)-OAc)(κ(2)-OAc)(=C=CHPh)(PPh(3))(2) as the thermodynamic product. more...

We have investigated the reactivity of photolytically generated ground-state, gas-phase atomic oxygen O(3P) with the surfaces of two related ionic liquids, 1-ethyl-3-methylimidazolium ([emim]) bis(trifluoromethyl-sulfonyl)imide ([NTf2]) and 1-dodecyl-3-methylimidazolium ([C12mim]) [NTf2]. The liquids differ only in the length of the alkyl side-chain on the cation. Laser-induced fluorescence was used to detect the gas-phase OH radicals formed at the gas-liquid interface. The considerable yield of OH from [C12mim][NTf2] in comparison to the undetectable amount from [emim][NTf2] cannot simply be explained by the difference in stoichiometry. We propose that this "chemical probe" method therefore provides strong evidence for the preferential accumulation of longer alkyl chains at the gas-liquid interface. © 2009 American Chemical Society. more...

A range of N-donor ligands based on the 1H-pyridin-(2E)-ylidene (PYE) motif have been prepared, including achiral and chiral examples. The ligands incorporate one to three PYE groups that coordinate to a metal through the exocyclic nitrogen atom of each PYE moiety, and the resulting metal complexes have been characterised by methods including single-crystal X-ray diffraction and NMR spectroscopy to examine metal-ligand bonding and ligand dynamics. Upon coordination of a PYE ligand to a proton or metal-complex fragment, the solid-state structures, NMR spectroscopy and DFT studies indicate that charge redistribution occurs within the PYE heterocyclic ring to give a contribution from a pyridinium-amido-type resonance structure. Additional IR spectroscopy and computational studies suggest that PYE ligands are strong donor ligands. NMR spectroscopy shows that for metal complexes there is restricted motion about the exocyclic C-N bond, which projects the heterocyclic N-substituent in the vicinity of the metal atom causing restricted motion in chelating-ligand derivatives. Solid-state structures and DFT calculations also show significant steric congestion and secondary metal-ligand interactions between the metal and ligand C-H bonds. more...

Ionic π-acidic alkene ligands based on chalcone and benzylidene acetone frameworks have been “doped” into ionic liquids to provide functional reaction media for Pd-catalysed cross-couplings of a cyclohexenyl carbonate with aryl siloxanes that allow simple product isolation, free from Pd ( more...

The conversion of the alkyne complex RhCl(PPr(i)3)2(eta2-PhC[triple bond]CH) into its vinylidene isomer RhCl(PPr(i)3)2(=C=CPhH) has been monitored via NMR spectroscopy in a range of solvents. In THF and hexane solution the reaction was observed to proceed via the alkynyl hydride complex Rh(H)Cl(PPr(i)3)2(-C[triple bond]CPh). The kinetic profile of the reaction demonstrates that this species is an intermediate in the formation of the vinylidene complex. more...

In continuation of recent work on the dielectric response of imidazolium-based ionic liquids (ILs) (J. Phys. Chem. B, 2006, 110, 12682), we report on the effect of cation variation on the frequency-dependent dielectric permittivity up to 20 GHz of ionic liquids. The salts are comprised of pyrrolidinium, pyridinium, tetraalkylammonium, and triethylsulfonium cations combined with the bis-((trifluoromethyl)sulfonyl)imide anion. The dielectric spectra resemble those observed for imidazolium salts with the same anion. In all cases, the major contribution results from a diffusive low-frequency response on the time scale of several 100 ps, which shows a broadly distributed kinetics similar to that of spatially heterogeneous states in supercooled and glassy systems rather than that observed in fluid systems. There is evidence for a weak secondary process near 10-20 ps. Perhaps the most interesting difference to imidazolium salts is founded in the missing portions of the spectra due to processes beyond the upper cutoff frequency of 20 GHz. These are lower than that observed for imidazolium-based salts and seem to vanish for tetraalkylammonium and triethylsulfonium salts. As for imidazolium salts, the extrapolated static dielectric constants are on the order of epsilon(S) congruent with 10-13, classifying these ILs as solvents of moderate polarity. more...

We have developed a simple and quantitative explanation for the relatively low melting temperatures of ionic liquids (ILs). The basic concept was to assess the Gibbs free energy of fusion (Delta(fus)G) for the process IL(s) --IL(l), which relates to the melting point of the IL. This was done using a suitable Born-Fajans-Haber cycle that was closed by the lattice (i.e., IL(s) --IL(g)) Gibbs energy and the solvation (i.e., IL(g) --IL(l)) Gibbs energies of the constituent ions in the molten salt. As part of this project we synthesized and determined accurate melting points (by DSC) and dielectric constants (by dielectric spectroscopy) for 14 ionic liquids based on four common anions and nine common cations. Lattice free energies (Delta(latt)G) were estimated using a combination of Volume Based Thermodynamics (VBT) and quantum chemical calculations. Free energies of solvation (Delta(solv)G) of each ion in the bulk molten salt were calculated using the COSMO solvation model and the experimental dielectric constants. Under standard ambient conditions (298.15 K and 10(5) Pa) Delta(fus)G degrees was found to be negative for all the ILs studied, as expected for liquid samples. Thus, these ILs are liquid under standard ambient conditions because the liquid state is thermodynamically favorable, due to the large size and conformational flexibility of the ions involved, which leads to small lattice enthalpies and large entropy changes that favor melting. This model can be used to predict the melting temperatures and dielectric constants of ILs with good accuracy. A comparison of the predicted vs experimental melting points for nine of the ILs (excluding those where no melting transition was observed and two outliers that were not well described by the model) gave a standard error of the estimate (s(est)) of 8 degrees C. A similar comparison for dielectric constant predictions gave s(est) as 2.5 units. Thus, from very little experimental and computational data it is possible to predict fundamental properties such as melting points and dielectric constants of ionic liquids. more...

Treatment of the diborane(4) compound B(2)(NMe(2))(4) with aniline or 2,6-dimethylaniline results in the primary amido compounds B(2)(NHR)(4)(R = Ph, 2,6-Me(2)C(6)H(3)); subsequent treatment with n-BuLi in toluene in each case affords the first examples of anionic imidodiborates namely Li(4)(thf)(6)B(2)(NPh)(4) and Li(4)(thf)(4)B(2)(N-2,6-Me(2)C(6)H(3))(4); all complexes have been characterised crystallographically. more...

Building pyramids: The first P-C cluster, namely, the novel nido species 2, is readily prepared from 1 (• = CtBu), which is also an excellent precursor for the selective synthesis of the anion 3. DFT calculations show that there is a switch in the global minimum, on the introduction of three P atoms (CH) into the [C5H5]+ ion, from cyclic-unsaturated to saturated cage species, such as 2. more...

Recent studies concerning p-block imido anion chemistry have tended to focus on imido compounds where the central atom is from groups 15 or 16. The imido anions of group 13 are less well investigat... more...

In the present contribution, results concerning the role of small amounts of water in the 1-butyl-3-methylimidazolium bis 2-ethylhexyl sulfosuccinate ([bmim][AOT]) based 1-butyl-3-methylimidazolium tetrafluoroborate ([bmim][BF4])-in-benzene reverse microemulsions are emphasized. The microemulsion aggregates have demonstrated features in common with traditional aqueous systems, such as a normal microemulsion droplet size and decreased stability due to the addition of a polar component. Dynamic light scattering (DLS) showed that the size change of microemulsion with added water depends on the loaded [bmim][BF4] content in the microemulsion: when the [bmim][BF4] content is low, the microemulsion diameter first decreases and then increases, while the size remains about the same for microemulsions with a moderate [bmim][BF4] loading and a successive increase in size was found for high-loaded [bmim][BF4] microemulsions. (1)H NMR along with two-dimensional rotating frame nuclear Overhauser effect (NOE) experiments (ROESY) revealed that water molecules formed wide interactions with both 1-butyl-3-methylimidazolium ([bmim]) and bis 2-ethylhexyl sulfosuccinate ([AOT]), leading to a decrease in the headgroup area of [bmim][AOT], i.e. α value, which will decrease the microemulsion size. On the other hand, addition of water can simultaneously swell the microemulsions, causing an increase in the diameter. It is also deduced that the Coulomb forces between the [AOT] and [bmim] should be one of the main driving forces for the formation of [bmim][BF4]-in-benzene microemulsions. more...

An environmentally benign and convenient amine-functionalized ionic liquid (IL) catalytic system was explored for the preparation of α,α′-bis(substituted benzylidene)cyclopentanones by the cross-aldol condensation of aromatic aldehydes with cyclopentanone. High yields were obtained without using any organic solvents. The condensation products can be separated easily and the ILs can be recovered and reused at least five times without apparently loss of activity. The potential mechanism of the cross-aldol condensation reaction in this IL catalytic system is discussed. more...

Attempted metallation of a triamidoaluminane gives a complex containing the [R′Al(NR) 3 ] 4− anion whose formal tetranegative charge is the highest charge observed crystallographically for a simple mononuclear imido main group anion system. more...

Reaction of equimolar quantities of MX (M = Au, Cu, X = Cl; M = Ag, X = OTf) and GaCl(3) in CH(2)Cl(2) with P(4) leads to phosphorus ligating a cationic coinage metal centre. For Cu and Ag, ion-contacted coordination polymers are formed; for Au, an ion-separated complex is observed that features the [Au(η(2)-P(4))(2)](+) cation, which is the first homoleptic Au-P(4) complex to be characterised in the condensed phase. more...

A series of 16 symmetric, dimeric, dicationic liquid-crystalline ionic liquids with mesogenic 3,4,5-tris(alkyloxy)benzyl moieties tethered to two bridged imidazolium cations were designed and synthesised. As a comparison, 12 monocationic imidazolium liquid crystals with the same mesogens were also prepared. The mesomorphic properties of these ionic liquids were characterised in terms of polarised optical microscopy (POM) and differential scanning calorimetry (DSC), while thermal stabilities were obtained by thermogravimetric analysis (TGA). All compounds having chloride (Cl−) and tetrafluoroborate (BF4−) anions exhibit hexagonal columnar (Colh) liquid crystal mesophases, with the dimeric materials showing mesophases over an extended temperature range. The effect of the linking chain, alkyl substituents, and anion type on the thermal properties of these dimers was examined and showed a significant influence. For example, Colh mesophases were only observed for ionic liquids having Cl− and BF4− anions, whereas systems with the bis(trifluoromethylsulfonyl)imide (Tf2N−) anion melted directly to an isotropic liquid. A shorter spacer paired with longer alkoxy chains tends to give rise to broad-temperature-range Colh ionic liquid crystal phases. more...

Stable salts of the first homoleptic Cu-phosphorus and Cu-ethene complexes, [Cu(eta2-P4)2]+ and [Cu(eta2-C2H4)3]+, isolated by the aid of the weakly coordinating anion (WCA) [Al(OC(CF3)3)4]-, were obtained. more...

Reaction of AsCl3 with 3 equivalents of (2-OPh)C6H4NH2 in toluene/NEt3, followed by metallation with 3 equivalents of BunLi produces a bis(imido)organoarsenate dianion as a lithium salt which co-complexes BunLi to form a dimeric cage with a 14 membered core. more...

The mol. vol. Vm (i.e., the sum of the ionic vols. Vion of the constituent ions) of an ionic liq. (IL) in combination with an anion-dependent empirical relationship is all one needs to predict phys. properties such as viscosity, cond., and d. of [N(CN)2]-, [BF4]-, [PF6]-, and [N(SO2CF3)2]- ionic liqs., including those which may as yet only exist on paper. more...