Ionic Liquids in Metal, Photo-, Electro-, and (Bio) Catalysis.

Ionic liquids (ILs) have unique physicochemical properties that make them advantageous for catalysis, such as low vapor pressure, non-flammability, high thermal and chemical stabilities, and the ability to enhance the activity and stability of (bio)catalysts. ILs can improve the efficiency, selectivity, and sustainability of bio(transformations) by acting as activators of enzymes, selectively dissolving substrates and products, and reducing toxicity. They can also be recycled and reused multiple times without losing their effectiveness. ILs based on imidazolium cation are preferred for structural organization aspects, with a semiorganized layer surrounding the catalyst. ILs act as a container, providing a confined space that allows modulation of electronic and geometric effects, miscibility of reactants and products, and residence time of species. ILs can stabilize ionic and radical species and control the catalytic activity of dynamic processes. Supported IL phase (SILP) derivatives and polymeric ILs (PILs) are good options for molecular engineering of greener catalytic processes. The major factors governing metal, photo-, electro-, and biocatalysts in ILs are discussed in detail based on the vast literature available over the past two and a half decades. Catalytic reactions, ranging from hydrogenation and cross-coupling to oxidations, promoted by homogeneous and heterogeneous catalysts in both single and multiphase conditions, are extensively reviewed and discussed considering the knowledge accumulated until now.

Zwitterionic "Solutions" for Reversible CO2 Capture.

The zwitterions resulting from the covalent attachment of 3- or 4-hydroxy benzene to the 1,3-dimethylimidazolium cation represent basic compounds (pKa of 8.68 and 8.99 in aqueous solutions, respectively) that chemisorb in aqueous solutions 0.58 mol/mol of carbon dioxide at 1.3 bar (absolute) and 40 °C. Equimolar amounts of chemisorbed CO2 in these solutions are obtained at 10 bar and 40 °C. Chemisorption takes place through the formation of bicarbonate in the aqueous solution using imidazolium-containing phenolate. CO2 is liberated by simple pressure relief and heating, regenerating the base. The enthalpy of absorption was estimated to be -38 kJ/mol, which is about 30 % lower than the enthalpy of industrially employed aqueous solutions of MDEA (estimated at -53 kJ/mol using the same experimental apparatus). The physisorption of CO2 becomes relevant at higher pressures (>10 bar) in these aqueous solutions. Combined physio- and chemisorption of up to 1.3 mol/mol at 40 bar and 40 °C can be attained with these aqueous zwitterionic solutions that are thermally stable and can be recycled at least 20 times.

Thermo- and Photocatalytic Activation of CO2 in Ionic Liquids Nanodomains.

Ionic liquids (ILs) are considered to be potential material devices for CO2 capturing and conversion to energy-adducts. They form a cage (confined-space) around the catalyst providing an ionic nano-container environment which serves as physical-chemical barrier that selectively controls the diffusion of reactants, intermediates, and products to the catalytic active sites via their hydrophobicity and contact ion pairs. Hence, the electronic properties of the catalysts in ILs can be tuned by the proper choice of the IL-cations and anions that strongly influence the residence time/diffusion of the reactants, intermediates, and products in the nano-environment. On the other hand, ILs provide driving force towards photocatalytic redox process to increase the CO2 photoreduction. By combining ILs with the semiconductor, unique solid semiconductor-liquid commodities are generated that can lower the CO2 activation energy barrier by modulating the electronic properties of the semiconductor surface. This mini-review provides a brief overview of the recent advances in IL assisted thermal conversion of CO2 to hydrocarbons, formic acid, methanol, dimethyl carbonate, and cyclic carbonates as well as its photo-conversion to solar fuels.

Selective suppression of {112} anatase facets by fluorination for enhanced TiO2 particle size and phase stability at elevated temperatures.

Generally, anatase is the most desirable TiO2 polymorphic phase for photovoltaic and photocatalytic applications due to its higher photoconductivity and lower recombination rates compared to the rutile phase. However, in applications where temperatures above 500 °C are required, growing pure anatase phase nanoparticles is still a challenge, as above this temperature TiO2 crystallite sizes are larger than 35 nm which thermodynamically favors the growth of rutile crystallites. In this work, we show strong evidence, for the first time, that achieving a specific fraction (50%) of the {112} facets on the TiO2 surface is the key limiting step for anatase-to-rutile phase transition, rather than the crystallite size. By using a fluorinated ionic liquid (IL) we have obtained pure anatase phase crystallites at temperatures up to 800 °C, even after the crystallites have grown beyond their thermodynamic size limit of ca. 35 nm. While fluorination by the IL did not affect {001} growth, it stabilized the pure anatase TiO2 by suppressing the formation of {112} facets on anatase particles. By suppressing the {112} facets, using specific concentrations of fluorinated ionic liquid in the TiO2 synthesis, we controlled the anatase-to-rutile phase transition over a wide range of temperatures. This information shall help synthetic researchers to determine the appropriate material conditions for specific applications.

Introduction to celebrating Latin American talent in chemistry.

In celebration of the excellence and breadth of Latin American research achievements across the chemical sciences, we are delighted to present an introduction to the themed collection, Celebrating Latin American talent in chemistry.

Nonlinear and thermo-optical characterisation of bare imidazolium ionic liquids.

Nonlinear optical (NLO) and thermo-optical properties of two pure ionic liquids, BMIOMe.NTf2 and BMIOMe.N(CN)2, were examined in this study. This was the first nonlinear refractive index determination of a pristine ionic liquid by a standard self-refraction experiment. The NLO characterisations were performed using Z-scan and EZ-scan techniques in the thermally managed approach, with a mode-locked femtosecond laser source. Thermal properties were analysed concomitantly, and the thermo-optical coefficient, thermal characteristic time, and lens strength were characterised. These results define the parameters to be adopted in the method of nanoparticles formation by laser ablation in an ionic liquid solution and indicate that BMIOMe.NTf2 is a prominent material to be engineered for photonics applications.

Treatment and characterization of biomass of soybean and rice hulls using ionic liquids for the liberation of fermentable sugars.

We investigated the changes in the physical structure of cellulose recovered from soybean and rice hulls treated with the ionic liquids 1-butyl-3-methylimidazolium chloride ([bmim][Cl]) and 1-butyl-3-methylimidazolium acetate ([bmim][Ac]). The characterization was carried out by a combination of thermogravimetric analysis (TGA), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), and scanning electron microscopy (SEM). Regenerated cellulose from soybean hull showed loss of crystallinity and high structural disruption caused by both ionic liquid treatments as compared to the untreated material. In contrast, rice hull presented only a small structural disruption when treated with [bmim][Ac] and was practically unaffected by [bmim][Cl], showing that this biomass residue is recalcitrance towards physico-chemical treatments, possibly as a consequence of its high composition content in silica. These results suggest the use of soybean hull as a substrate to be treated with ionic liquids in the preparation of lignocellulosic hydrolysates to be used in second-generation ethanol production, whereas other methods should be considered to treat rice hull biomass.

The Nature of Carbon Dioxide in Bare Ionic Liquids.

Ionic liquids (ILs) are among the most studied and promising materials for selective CO2 capture and transformation. The high CO2 sorption capacity associated with the possibility to activate this rather stable molecule through stabilization of ionic/radical species or covalent interactions either with the cation or anion has opened new avenues for CO2 functionalization. However, recent reports have demonstrated that another simpler and plausible pathway is also involved in the sorption/activation of CO2 by ILs associated with basic anions. Bare ILs or IL solutions contain almost invariable significant amounts of water and through interaction with CO2 generate carbonates/bicarbonates rather than carbamic acids or amidates. In these cases, the IL acts as a base and not a nucleophile and yields buffer-like solutions that can be used to shift the equilibrium toward acid products in different CO2 reutilization reactions. In this Minireview, the emergence of IL buffer-like solutions as a new reactivity paradigm in CO2 capture and activation is described and analyzed critically, mainly through the evaluation of NMR data.

Catalytic Semi-Water-Gas Shift Reaction: A Simple Green Path to Formic Acid Fuel.

Formic acid (FA) is a promising CO and hydrogen energy carrier, and currently its generation is mainly centered on the hydrogenation of CO2 . However, it can also be obtained by the hydrothermal conversion of CO with H2 O at very high pressures (>100 bar) and temperatures (>200 °C), which requires days to complete. Herein, it is demonstrated that by using a nano-Ru/Fe alloy embedded in an ionic liquid (IL)-hybrid silica in the presence of the appropriate IL in water, CO can be catalytically converted into free FA (0.73 m) under very mild reactions conditions (10 bar at 80 °C) with a turnover number of up to 1269. The catalyst was prepared by simple reduction/decomposition of Ru and Fe complexes in the IL, and it was then embedded into an IL-hybrid silica {1-n-butyl-3-(3-trimethoxysilylpropyl)-imidazolium cations associated with hydrophilic (acetate, SILP-OAc) and hydrophobic [bis((trifluoromethyl)sulfonyl)amide, SILP-NTf2 ] anions}. The location of the alloy nanoparticles on the support is strongly related to the nature of the anion, that is, in the case of hydrophilic SILP-OAc, RuFe nanoparticles are more exposed to the support surface than in the case of the hydrophobic SILP-NTf2 , as determined by Rutherford backscattering spectrometry. This catalytic membrane in the presence of H2 O/CO and an appropriate IL, namely, 1,2-dimethyl-3-n-butylimidazolium 2-methyl imidazolate (BMMIm⋅MeIm), is stable and recyclable for at least five runs, yielding a total of 4.34 m of free FA.

Cerium Oxide Nanoparticles Inside Carbon Nanoreactors for Selective Allylic Oxidation of Cyclohexene.

The confinement of cerium oxide (CeO2) nanoparticles within hollow carbon nanostructures has been achieved and harnessed to control the oxidation of cyclohexene. Graphitized carbon nanofibers (GNF) have been used as the nanoscale tubular host and filled by sublimation of the Ce(tmhd)4 complex (where tmhd = tetrakis(2,2,6,6-tetramethyl-3,5-heptanedionato)) into the internal cavity, followed by a subsequent thermal decomposition to yield the hybrid nanostructure CeO2@GNF, where nanoparticles are preferentially immobilized at the internal graphitic step-edges of the GNF. Control over the size of the CeO2 nanoparticles has been demonstrated within the range of about 4-9 nm by varying the mass ratio of the Ce(tmhd)4 precursor to GNF during the synthesis. CeO2@GNF was effective in promoting the allylic oxidation of cyclohexene in high yield with time-dependent control of product selectivity at a comparatively low loading of CeO2 of 0.13 mol %. Unlike many of the reports to date where ceria catalyzes such organic transformations, we found the encapsulated CeO2 to play the key role of radical initiator due to the presence of Ce3+ included in the structure, with the nanotube acting as both a host, preserving the high performance of the CeO2 nanoparticles anchored at the GNF step-edges over multiple uses, and an electron reservoir, maintaining the balance of Ce3+ and Ce4+ centers. Spatial confinement effects ensure excellent stability and recyclability of CeO2@GNF nanoreactors.

A Cooperative Photoactive Class-I Hybrid Polyoxometalate With Benzothiadiazole-Imidazolium Cations.

An organic-inorganic hybrid species based on the Wells-Dawson polyoxotungstate [P2W18O62]6- and novel fluorescent benzothiadiazole-imidazolium cations, [BTD-4,7-ImH]2+, has been synthesized. X-ray crystallographic analysis shows that the inorganic and organic components form a hydrogen-bonded superstructure and that the cations are revealed to be non-equivalent with varying degrees of rotation between the BTD and imidazolium rings due to competition between weak intra- and intermolecular interactions. The UV-vis diffuse reflectance spectra indicate that the hybrid has a band gap of 3.13 eV, while the solid-state fluorescence properties of the cation are quenched in the hybrid material, suggesting the existence of electron transfer between the inorganic and organic components. The highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) energies of the polyoxometalate (POM) and BTD-4,7-ImH precursors, estimated through UV-vis absorption spectroscopy and cyclic voltammetry, indicate that electron transfer from the BTD cations to the POM may occur in the excited state.

Reverse Semi-Combustion Driven by Titanium Dioxide-Ionic Liquid Hybrid Photocatalyst.

Unprecedented metal-free photocatalytic CO2 conversion to CO (up to 228±48 µmol g-1 h-1) was displayed by TiO2@IL hybrid photocatalysts prepared by simple impregnation of commercially available P25-titanium dioxide with imidazolium-based ionic liquids (ILs). The high activity of TiO2@IL hybrid photocatalysts was mainly associated to (i) TiO2@IL red shift compared to the pure TiO2 absorption, and thus a modification of the TiO2 surface electronic structure; (ii) TiO2 with IL bearing imidazolate anions lowered the CO2 activation energy barrier. The reaction mechanism was postulated to occur via CO2 photoreduction to formate species by the imidazole/imidazole radical redox pair, yielding CO and water.

Tunneling effects in confined gold nanoparticle hydrogenation catalysts.

Clean surface gold nanoparticles (AuNPs) of ∼6.6 nm that were confined in ionic liquid (IL) cages of hybrid γ-alumina (γ-Al2O3) displayed hydrogenation pathways in the reduction of trans-cinnamaldehyde distinct from those imprinted directly onto γ-Al2O3. Hydrogen activation proceeded via homolytic activation in IL-encapsulated AuNPs and via heterolytic cleavage for IL-free supported AuNPs. Higher negative apparent entropy (ΔSapp) values were obtained for the IL-confined AuNPs compared to the non-hybrid catalyst (Au/γ-Al2O3), suggesting a decrease in the number of microstates induced by the nano-confined environment. High kinetic isotope effect (KIE) values (kH/kD = 2.5-2.9 at 273 K) and Arrhenius convex curves were observed. Furthermore, differences of 5.6 and 6.2 kJ mol-1 between the apparent activation energies of the deuteration and hydrogenation reactions (E-E) associated with pre-exponential factor ratios (AD/AH) of 4.6 and 5.1 provided strong evidence of the possible involvement of a tunneling pathway in the case of the confined AuNPs.

Efficient Electrocatalytic CO2 Reduction Driven by Ionic Liquid Buffer-Like Solutions.

Electrocatalysis of CO2 reduction in aqueous electrolytes containing the ionic liquid (IL) 1-n-butyl-2,3-dimethylimidazolium acetate ([BMMIm][OAc]) and DMSO proceeded at low overpotentials (-0.9 V vs. Ag/AgCl) at commercially-available Au electrodes, with high selectivity for CO production (58 % faradaic efficiency at -1.6 V vs. Ag/AgCl). 0.43 mol CO2 per mol IL could be absorbed into the electrolyte at atmospheric pressure, forming bicarbonate and providing a constant supply of dissolved CO2 to the surface of the electrode. Electrocatalysis of CO2 reduction in the electrolyte was facilitated by stabilization of CO2 radical anions by the imidazolium cations of the IL and buffer-like effects with bicarbonate.

CO2 Electroreduction in Ionic Liquids.

CO2 electroreduction is among the most promising approaches used to transform this green-house gas into useful fuels and chemicals. Ionic liquids (ILs) have already proved to be the adequate media for CO2 dissolution, activation, and stabilization of radical and ionic electrochemical active species in aqueous solutions. In general, IL electrolytes reduce the overpotential, increase the current density, and allow for the modulation of solution pH, driving product selectivity. However, little is known about the main role of these salts in the CO2 reduction process the assumption that ILs form solvent-separated ions. However, most of the ILs in solution are better described as anisotropic fluids and display properties of an extended cooperative network of supramolecular species. That strongly reflects their mesoscopic and nanoscopic organization, inducing different processes in CO2 reduction compared to those observed in classical electrolyte solutions. The major aspects concerning the relationship between the structural organization of ILs and the electrochemical reduction of CO2 will be critically discussed considering selected recent examples.

Photocatalytic Reverse Semi-Combustion Driven by Ionic Liquids.

The simple photolysis of CO2 in aqueous solutions to generate CO and/or hydrocarbons and derivatives in the presence of a catalyst is considered to be a clean and efficient approach for utilizing CO2 as a C1 building block. Despite the huge efforts dedicated to this transformation using either semiconductors or homogeneous catalysts, only small improvements of the catalytic activity have been achieved so far. This article reports that simple aqueous solutions of organic salts-denominated as ionic liquids-can efficiently photo-reduce CO2 to CO without using photosensitizers or sacrificial agents. The system relies on the formation of the [CO2 ].- intermediate through homolytic C-C bond cleavage in a cation-CO2 adduct of imidazolium-based ionic liquids (ILs). The system continuously produced CO up to 2.88 mmol g-1 of IL after 40 h of irradiation by using an aqueous solution of 1-n-butyl-3-methylimidazolium-2-carboxylate (BMIm.CO2 ) IL, representing an apparent quantum yield of 3.9 %. The organophotocatalytic principles of our system may help to develop more simple and efficient organic materials for the production of solar fuels from CO2 under mild conditions, which represents a real alternative to those based on semiconductors and homogeneous metal-based catalysts.

Dealing with supramolecular structure for ionic liquids: a DOSY NMR approach.

Diffusion-ordered spectroscopy (DOSY) is arguably a powerful method for the NMR analysis of ionic liquids, since the self-diffusion coefficients for cations and anions can be measured straightforwardly. In this work, the dynamic-structural behaviour of imidazolium ionic liquids containing different anions has been investigated by experimental measurements of direct 1H diffusion coefficients in chloroform and water solutions. The influence of ion structure has been tested by using six IL salts formed by the association of different cations (1-n-butyl-3-methylimidazolium, 1,2,3-trimethylimidazolium and tetra-n-butylammonium) with different anion structures (prolinate, acetate and o-trifluoromehtylobenzoate). The influence of IL concentration (from 0.01 to 0.5 mol L-1) was also evaluated for BMI·Pro. The contact ion pairs (or aggregates) are maintained in both chloroform and water within the range of concentrations investigated. In the particular case of 1,2,3-trimethylimidazolium imidazolate (TMI·Im) containing confined water in DMSO the maintenance of the contact ion pairs depends on the water content which may even disrupt the IL supramolecular structure.

Correspondence on "Preorganization and Cooperation for Highly Efficient and Reversible Capture of Low-Concentration CO2 by Ionic Liquids".

The preorganization and cooperation mechanism of imide-based ionic liquids reported in a recent Communication was evocated to rationalize the extremely high gravimetric CO2 capture displayed by these fluids. An analysis of the reported spectroscopic evidences together with additional experiments led to the proposition of an alternative, simpler, and feasible mechanism involving the formation of bicarbonate.

Is the formation of N-heterocyclic carbenes (NHCs) a feasible mechanism for the distillation of imidazolium ionic liquids?

We describe the synthesis of two tetrachloroindate ionic liquids used as probes to study the involvement of NHCs (N-heterocyclic carbenes) in the distillation of imidazolium derivatives. Atmospheric-pressure chemical ionization mass spectrometry (APCI-MS), electrospray ionization mass spectrometry (ESI-MS), atmospheric-pressure thermal desorption ion mass spectrometry (APTDI-MS) and laser-induced acoustic desorption (LIAD) were used to depict the possibility of the involvement of NHCs during the distillation process. Each type of imidazolium derivative showed a particular mechanism of distillation, pointing firmly to the dependence of both the cation and the anion natures to distil as ion pairs or NHCs. Ionic liquid 1-n-butyl-3-methylimidazolium tetrachloroindate (1a) exhibited a preference to distil as ion pairs, whereas 3,3'-(ethane-1,2-diyl)bis(1-methyimidazolium)bis-tetrachloroindate (1b) may react with the Lewis acid anion, affording a bidentate NHC complex to distil. Thermodynamics, quantum theory of atoms in molecules (QTAIM) and natural bond orbital (NBO) analyses of the ionic liquid 1a were also conducted and helped understand the preference for ion pairs instead of NHCs. The performed theoretical calculations did not forwent the possibility of NHC formation; however, they clearly indicated the high stability of the anions (Lewis acids in nature) and also indicated that the possible reaction between NHC and the anion is not favoured. The calculated thermodynamic values were in accordance with the features observed by MS and indicated ion pairs as the feasible species for the distillation of imidazolium-based ionic liquids.

Cation-Anion-CO2 Interactions in Imidazolium-Based Ionic Liquid Sorbents.

A series of functionalized N-alkylimidazolium based ionic liquids (ImILs) were designed, through anion (carboxylates and halogenated) and cation (N-alkyl side chains) structural modifications, and studied as potential sorbents for CO2 . The sorption capacities of as prepared bare ImILs could be enhanced from 0.20 to 0.60 molar fraction by variation of cation-anion-CO2 and IL-CO2 -water interaction. By combining NMR spectroscopy with molecular dynamics simulations, a good description of interactions between ImIL and CO2 can be obtained. Three types of CO2 sorption modes have been evidenced depending on the structure of the ImIL ion pair: Physisorption, formation of bicarbonate, and covalent interaction through the nucleophilic addition of CO2 to the cation or anion. The highest CO2 sorption capacity was observed with the ImIL containing the 1-n-butyl-3-methylimidazolium cation associated with the carboxylate anions (succinate and malonate). This study provides helpful clues for better understanding the structure-activity relationship of this class of materials and the ion pair influence on CO2 capture.