Facile Oxidation of Ce(III) to Ce(IV) Using Cu(I) Salts.

The synthesis, luminescence, and electrochemical properties of the Ce(III) compound, [(C5Me5)2(2,6-iPr2C6H3O)Ce(THF)], 1, were investigated. Based on the electrochemical data, treatment of 1 with CuX (X = Cl, Br, I) results in the formation of the corresponding Ce(IV) complexes, [(C5Me5)2(2,6-iPr2C6H3O)Ce(X)]. Each complex has been characterized using NMR, IR, and UV-vis spectroscopy as well as structurally determined using X-ray crystallography. Additionally, the treatment of [(C5Me5)2(2,6-iPr2C6H3O)Ce(Br)] with AgF results in the formation of the putative [(C5Me5)2(2,6-iPr2C6H3O)Ce(F)]. The electronic structure of these Ce(IV)-X complexes was investigated by bond analyses and the Ce(IV)-F moiety using quantum chemistry NMR calculations.

Evidence of a liquid-liquid transition in a glass-forming ionic liquid.

A liquid-liquid transition (LLT) is a transformation from one liquid to another through a first-order transition. The LLT is fundamental to the understanding of the liquid state and has been reported in a few materials such as silicon, phosphorus, triphenyl phosphite, and water. Furthermore, it has been suggested that the unique properties of materials such as water, which is critical for life on the planet, are linked to the existence of the LLT. However, the experimental evidence for the existence of an LLT in many molecular liquids remains controversial, due to the prevalence and high propensity of the materials to crystallize. Here, we show evidence of an LLT in a glass-forming trihexyltetradecylphosphonium borohydride ionic liquid that shows no tendency to crystallize under normal laboratory conditions. We observe a step-like increase in the static dielectric permittivity at the transition. Furthermore, the sizes of nonpolar local domains and ion-coordination numbers deduced from wide-angle X-ray scattering also change abruptly at the LLT. We independently corroborate these changes in local organization using Raman spectroscopy. The experimental access to the evolution of local order and structural dynamics across a liquid-liquid transition opens up unprecedented possibilities to understand the nature of the liquid state.

Do Ionic Liquids Slow Down in Stages?

High impact recent articles have reported on the existence of a liquid-liquid (L-L) phase transition as a function of both pressure and temperature in ionic liquids (ILs) containing the popular trihexyltetradecylphosphonium cation (P666,14+), sometimes referred to as the "universal liquifier". The work presented here reports on the structural-dynamic pathway from liquid to glass of the most well-studied IL comprising the P666,14+ cation. We present experimental and computational evidence that, on cooling, the path from the room-temperature liquid to the glass state is one of separate structural-dynamic changes. The first stage involves the slowdown of the charge network, while the apolar subcomponent is fully mobile. A second, separate stage entails the slowdown of the apolar domain. Whereas it is possible that these processes may be related to the liquid-liquid and glass transitions, more research is needed to establish this conclusively.

Deep Eutectic Solvents: A Review of Fundamentals and Applications.

Deep eutectic solvents (DESs) are an emerging class of mixtures characterized by significant depressions in melting points compared to those of the neat constituent components. These materials are promising for applications as inexpensive "designer" solvents exhibiting a host of tunable physicochemical properties. A detailed review of the current literature reveals the lack of predictive understanding of the microscopic mechanisms that govern the structure-property relationships in this class of solvents. Complex hydrogen bonding is postulated as the root cause of their melting point depressions and physicochemical properties; to understand these hydrogen bonded networks, it is imperative to study these systems as dynamic entities using both simulations and experiments. This review emphasizes recent research efforts in order to elucidate the next steps needed to develop a fundamental framework needed for a deeper understanding of DESs. It covers recent developments in DES research, frames outstanding scientific questions, and identifies promising research thrusts aligned with the advancement of the field toward predictive models and fundamental understanding of these solvents.

Coordination Polymers Constructed from Pyrogallol[4]arene-Assembled Metal-Organic Nanocapsules.

Coordination polymers, commonly known as infinite crystalline lattices, are versatile networks and have diverse potential applications in the fields of gas storage, molecular separation, catalysis, optics, and drug delivery, among other areas. Secondary building blocks, mainly incorporating rigid polydentate organic linkers and metal ions or clusters, are commonly employed to construct coordination polymers. Recently, novel building blocks such as coordination polyhedra have been utilized as metal nodes to fabricate coordination polymers. Benefiting from the rigid porous structure of the coordination polyhedron, prefabricated designer "pores" can be incorporated in this type of coordinate polymer. In this Account, coordination polymers built by pyrogallol[4]arene-assembled metal-organic nanocapsules are summarized. This class of metal-organic nanocapsule possesses the following advantages that make them excellent candidates in the construction of coordination polymers: (i) Various geometrical shapes with different volumes of the inner cavities can be obtained from these capsules. Among them, the two main categories illustrated are dimeric and hexameric capsules, which comprise two and six pyrogallol[4]arenes units, respectively. (ii) A wide range of possible metal ions ranging from main group metals to transition metals and even lanthanides have been demonstrated to seam the capsules. Therefore, these coordination polymers can be endowed with fascinating functionalities such as magnetism, semiconductivity, luminescence, and radioactivity. (iii) Up to 24 metal ions have been successfully embedded on the surface of the nanocapsule, each a potential reaction site in the construction of coordination polymers, opening up pathways for the formation of multidimensional frameworks.In this Account, we focus primarily on the synthesis and the structural information on pyrogallol[4]arene-derived coordination polymers. Coordination polymers can be formed by introducing linkers with two coordination sites, using pyrogallol[4]arenes with coordination sites on the tail, or even via metal ions cross-linking with each other. Machine learning was recently developed to help us predict and screen the structures of the coordination polymers. With single crystal analysis in hand, detailed structural information provides a molecular-level perspective. Significantly, following the formation of coordination polymers, the overall shape and structure of the discrete metal-organic nanocapsules remains essentially unchanged, with full retention of the prefabricated pores. If a rigid linker is used to connect capsules, more than one lattice void with different volumes can be found within the framework. Thus, molecules with different sizes could potentially be encapsulated within these coordination polymers. In addition, flexible ligands can also be employed as linkers. For example, polymers have been employed as large linkers that transform the crystalline coordination polymers into polymer matrices, paving the way toward the synthesis of advanced functional materials. Overall, coordination polymers constructed with pyrogallol[4]arene-assembled metal-organic nanocapsules show wide diversity and tunability in structure and fascinating properties, as well as the promise of built-in functionality in the future.

Cation structure-dependence of the Pockels effect in aprotic ionic liquids.

We report on the dependence of surface charge-induced birefringence (the Pockels effect) in room temperature ionic liquids (RTILs) with different cation constituents. The induced birefringence is related to the induced free charge density gradient (ρf) in the RTIL. The RTILs are confined in a lens-shaped cell and the surface charge density of the concave cell surface is controlled by the current passed through the surface ITO film. We find that, in all cases, the induced birefringence is proportional to the surface charge density and that the change in refractive index nearest the ITO surface can be on the order of 20%. Our findings indicate that the induced birefringence depends more sensitively on the cation aliphatic substituent length than on the identity of the charge-carrying headgroup.

Cation structure-dependence of the induced free charge density gradient in imidazolium and pyrrolidinium ionic liquids.

We report on the structure-dependence and magnitude of the induced free charge density gradient (ρf) seen in room-temperature ionic liquids (RTILs) with imidazolium and pyrrolidinium cations. We characterize the spatially-resolved rotational diffusion dynamics of a trace-level cationic chromophore to characterize ρf in three different pyrrolidinium RTILs and two imidazolium RTILs. Our data show that the magnitude of ρf depends primarily on the alkyl chain length of RTIL cation and the persistence length of ρf is independent of RTILs' cation structure. These findings collectively suggest that mesoscopic structure in RTILs plays a significant role in allowing charge density gradients to form.

Ionic Liquid-Controlled Shape Transformation of Spherical to Nonspherical Polymersomes via Hierarchical Self-Assembly of a Diblock Copolymer.

Here, we report the self-assembly of poly(ethylene glycol) methyl ether-block-poly(ε-caprolactone) (PEG-b-PCL) copolymer in three ionic liquids (ILs) possessing different cations with common bis(trifluoromethylsulfonyl)imide anion. The observed polymeric nanostructures in ILs were directly visualized by room temperature conventional transmission and field emission scanning electron microscopy and were further examined for their size and shape by dynamic light scattering technique. The results show that through changes in the concentration of PEG-b-PCL and/or changing the solvent by using a different IL, we can effectively induce shape transformation of self-assembled PEG-b-PCL nanostructures in order to generate nonspherical polymersomes, such as worm-like aggregates, stomatocytes, nanotubes, large hexagonal and tubular-shaped polymersomes. These findings provide a promising platform for the design of biodegradable soft dynamic systems in the micro-/nano-motor field for cancer-targeted delivery, diagnosis and imaging-guided therapy, and controlled release of therapeutic drugs for treatment of many diseases. Non-spherical polymersome-based vaccines may be taken up more efficiently, especially against viruses for pulmonary drug delivery than the spherical polymersomes-based.

Assessing rotation and solvation dynamics in ethaline deep eutectic solvent and its solutions with methanol.

Steady-state and time-resolved fluorescence were used to investigate the solvation of coumarin 153 (C153) and coumarin 343 (C343) in methanol + ethaline binary solutions, a deep eutectic solvent composed of a 1:2 molar ratio choline chloride + ethylene glycol. In addition, time-resolved anisotropy decays were used to determine the solute's rotational reorientation time as a function of viscosity. Measurements were made in solutions covering the entire range of mole fraction. Viscosity measurements were used to characterize the bulk solvent properties, and as expected, addition of methanol resulted in an decreased viscosity, showing an exponential decrease with mole fraction, up to ∼50-fold at xMeOH = 1.0. Probe rotational reorientation times were found to be biexponential at xMeOH < 0.3 for C153 and xMeOH < 0.5 for C343 and monoexponential at richer methanol content. In proportion to viscosity, C153 and C343 average rotation times decreased ∼30-fold from xMeOH = 0 to 0.9 and showed a power law dependence of ∼η0.85. Rotation times approached the stick boundary limit on dilution with methanol. Time-resolved Stokes shifts quantified the solvation dynamics and were nearly single exponential for C153 but were clearly biexponential for C343. Solvation times also tracked with viscosity according to a power law dependence, with exponents of 0.3 and 0.4 for C153 and C343, respectively. The dilution effect of methanol was not linear in proportion to the viscosity change and alone cannot account for the change in solvation. Dilution also showed a different correlation to solvation than did temperature variations to govern the viscosity change.

Evaluation of canonical choline chloride based deep eutectic solvents as dye-sensitized solar cell electrolytes.

Deep eutectic solvents (DESs) are beginning to attract interest as electrolyte alternatives to conventional organic solvents and ionic liquids within dye-sensitized solar cells (DSSCs). The precise roles played by DES components and whether they simply represent a benign medium for mobilizing charge carriers or present beneficial functionality that impacts device performance remain unclear. To begin to address this deficiency in understanding, we performed a comprehensive characterization of the three "canonical" choline chloride-based DESs (i.e., reline, ethaline, and glyceline) as DSSC electrolytes hosting the iodide-triiodide (I-/I3 -) redox couple. The measurement of electrolyte viscosities, determination of triiodide diffusion coefficients, and photovoltaic performances assessed for water contents up to 40 wt. % allow the emergence of several important insights. A comparison to the observed photovoltaic performance arising from the individual components aids in further clarifying the impact of DES chemistry and solution viscosity on photovoltaic and charge carrier diffusion characteristics. Finally, we introduce the DES guaniline-consisting of a 1:1 molar ratio mixture of choline chloride with guanidinium thiocyanate-demonstrating it to be a superior DSSC electrolyte over those formulated from the three most widely studied canonical DESs at all water contents investigated.

Controlling Microarray Feature Spreading and Response Stability on Porous Silicon Platforms by Using Alkene-Terminal Ionic Liquids and UV Hydrosilylation.

In an attempt to develop reversible sensors based on ionic liquid/porous silicon (IL/pSi) platforms, we introduce an approach using task-specific, alkene-terminal ILs (AT-ILs) for direct grafting to the hydrogen-passivated as prepared-pSi (ap-pSi) surface via UV-hydrosilylation to address previous shortcomings associated with IL pattern impermanence (i.e., spread). By employing photoluminescence emission (PLE) and Fourier-transform infrared (FT-IR) imaging measurements, we demonstrate that the covalent grafting of AT-ILs onto the ap-pSi surface via photochemical hydrosilylation not only mitigates such feature spreading but also greatly improves PLE pattern stability. Significantly, we have discovered that, upon hydrosilylation, the resulting contact pin printed IL features remain stable to repeated challenges by toluene vapors, demonstrating the utility of AT-IL hydrosilylation for producing high-fidelity microarray features on pSi toward robust optical sensory microarrays.

Effect of ionic liquid on the fluorescence of an intramolecular exciplex forming probe.

The effects of ionic liquid addition on the spectroscopic properties of a pyrene-tryptophan-containing fluorescent intramolecular complex in polar-aprotic and polar-protic solvents, specifically, acetonitrile and ethanol, are assessed. Two ionic liquid sets, consisting of seven different ionic liquids, were explored; set 1 comprised three imidazolium-containing ionic liquids paired with different anions while set 2 consisted of varying cations, namely, imidazolium, pyrrolidinium, ammonium, and pyridinium, partnered with a common anion, bis(trifluoromethylsulfonyl)imide ([Tf2N-]). The results provided herein reveal that all ionic liquids explored behave as quenchers, however, the imidazolium-, pyrrolidinium-, and ammonium-containing ionic liquids selectively quenched the fluorescence from the exciplex while the monomer emission from pyrene was largely unaffected relative to exciplex emission. Conversely, the pyridinium ionic liquid, significantly quenched the fluorescence from both the pyrene monomer and the pyrene-tryptophan exciplex, as was expected. The observed quenching is demonstrated to originate from the cations of the ionic liquids and is, in general, more efficient for an imidazolium ionic liquid that contains an acidic proton in the C2 position. Stern-Volmer plots of the exciplex quenching demonstrate a complex quenching mechanism that does not appear to follow any conventional quenching models with the data best fit to an exponential equation. Furthermore, time-resolved fluorescence measurements reveal that the quenching is not dynamic in nature as the recovered decay times do not systematically decrease with increasing ionic liquid concentration, suggesting a possible static quenching mechanism. Thus, the formation of a "dark" ensemble is proposed, in which the ionic liquid cations complex with or crowd around the exciplex, quenching the intramolecular energy transfer.

QCM Sensor Arrays, Electroanalytical Techniques and NIR Spectroscopy Coupled to Multivariate Analysis for Quality Assessment of Food Products, Raw Materials, Ingredients and Foodborne Pathogen Detection: Challenges and Breakthroughs.

Quality checks, assessments, and the assurance of food products, raw materials, and food ingredients is critically important to ensure the safeguard of foods of high quality for safety and public health. Nevertheless, quality checks, assessments, and the assurance of food products along distribution and supply chains is impacted by various challenges. For instance, the development of portable, sensitive, low-cost, and robust instrumentation that is capable of real-time, accurate, and sensitive analysis, quality checks, assessments, and the assurance of food products in the field and/or in the production line in a food manufacturing industry is a major technological and analytical challenge. Other significant challenges include analytical method development, method validation strategies, and the non-availability of reference materials and/or standards for emerging food contaminants. The simplicity, portability, non-invasive, non-destructive properties, and low-cost of NIR spectrometers, make them appealing and desirable instruments of choice for rapid quality checks, assessments and assurances of food products, raw materials, and ingredients. This review article surveys literature and examines current challenges and breakthroughs in quality checks and the assessment of a variety of food products, raw materials, and ingredients. Specifically, recent technological innovations and notable advances in quartz crystal microbalances (QCM), electroanalytical techniques, and near infrared (NIR) spectroscopic instrument development in the quality assessment of selected food products, and the analysis of food raw materials and ingredients for foodborne pathogen detection between January 2019 and July 2020 are highlighted. In addition, chemometric approaches and multivariate analyses of spectral data for NIR instrumental calibration and sample analyses for quality assessments and assurances of selected food products and electrochemical methods for foodborne pathogen detection are discussed. Moreover, this review provides insight into the future trajectory of innovative technological developments in QCM, electroanalytical techniques, NIR spectroscopy, and multivariate analyses relating to general applications for the quality assessment of food products.

An Indium-Seamed Hexameric Metal-Organic Cage as an Example of a Hexameric Pyrogallol[4]arene Capsule Conjoined Exclusively by Trivalent Metal Ions.

A hexameric metal-organic nanocapsule is assembled from pyrogallol[4]arene units, which are stitched together with indium ions. This indium-seamed capsule is the first instance of a M24 L6 type hexameric coordination cage held together exclusively by trivalent metal ions. Explicitly, unlike previously reported pyrogallol[4]arene-based metal-seamed capsules, the current In3+ seamed capsule is entirely supported by O→In coordinate bonds. This work demonstrates the important proof of concept of the ability of pyrogallol[4]arene to react with metals in higher oxidation states to assemble into atomically-precise hexameric coordination cages. As such, these results open up exciting avenues toward the assembly of previously unanticipated metal-organic capsules, for example offering inspiration for tackling metals exhibiting high valence states such as in the lanthanide and actinide series.

Vascular endothelial function is improved after active mattress use.

OBJECTIVE: Active mattresses are used to prevent, treat and relieve pressure ulcers (PU) by intermittent contact pressure/relief. However, no studies have directly assessed the vascular endothelial response to long-term active mattress use. This study investigated the hypothesis that eight weeks use of an active mattress would lead to improvements in vascular endothelial function in healthy participants. METHODS: Physiological parameters of baseline skin temperature (BskT), resting blood flow (RBF) and endothelial function as measured using post-occlusive reactive hyperaemia (PORH), were assessed at baseline (week 0); following eight weeks of sleeping on an active mattress, and after an eight week washout period (at week 16). RESULTS: We recruited 10 healthy participants (four male, age 52.7±8.5 years, six female age 51.8±17.5 years). Following active mattress use RBF, PORH and BskT at the hallux pulp increased by 336%, 197% and 3.5ºC, respectively. Mean values increased from 24.3±38.3 perfusion units to 106.0±100.3 perfusion units (p=0.021) and from 13,456±10,225 to 40,252±23,995 perfusion units x seconds (p=0.003) and from 22.9±2.5ºC to 26.4±1.9ºC (p<0.001), respectively. CONCLUSION: Active mattress use for eight weeks leads to significant improvements in RBF, PORH, and BskT. These results suggest that active mattress use can improve endothelial function. Future research is required to explore the potential of active mattress use in the treatment and management of diseases and conditions that would benefit from an improved endothelial function.

Formation of Water Channels in the Crystalline Hydrates of Macrocyclic Compounds.

Crystalline hydrates of macrocyclic compounds such as pyroagllol[4]arenes (PgCs) and resorcin[4]arenes (RsCs) are rare owing to their lower water solubility. Functionalization of these macrocyclic compounds is an affordable way to enhance water solubility. However, functionalization also encounters the formation of multiple conformers and subsequent difficulty in purification of the product. Herein, four novel crystalline hydrates of functionalized PgCs and RsCs were synthesized. Formation of water channels and the effects of intermolecular interactions on the physical properties of these novel hydrates are discussed.

Exploiting the Inherent Photophysical Properties of the Major Tirapazamine Metabolite in the Development of Profluorescent Substrates for Enzymes That Catalyze the Bioreductive Activation of Hypoxia-Selective Anticancer Prodrugs.

Hypoxia-selective cytotoxins (HSCs) seek to exploit the oxygen-poor nature of tumor tissue for therapeutic gain. Typically, HSCs require activation by one-electron bioreductive enzymes such as NADPH:cytochrome P450 reductase (CYPOR). Thus, successful clinical deployment of HSCs may be facilitated by the development and implementation of diagnostic probes that detect the presence of relevant bioreductive enzymes in tumor tissue. The work described here develops analogues of the well-studied HSC tirapazamine (3-amino-1,2,4-benzotriazine 1,4-di- N-oxide, TPZ) as profluorescent substrates of the one-electron reductases involved in bioactivation of HSCs. Hypoxic metabolism of TPZ or 7-fluoro-TPZ by one-electron reductases releases inherently fluorescent mono- N-oxide metabolites that may serve as indicators, probes, markers, or stains for the detection of the enzymes involved in the bioactivation of HSCs. In particular, profluorescent compounds of this type can provide a foundation for fluorescence-based bioassays that help identify tumors responsive to HSCs.

Tandem copper and gold nanoclusters for two-color ratiometric explosives detection.

We report a sensory platform for the determination of common explosive species (e.g., TNT, PETN, RDX) based on the differential response from two different luminescent metal nanoclusters. In particular, whereas the red emission from bovine serum albumin-protected gold nanoclusters was strongly quenched by nitro-, nitrate-, and nitroamine-containing explosive organic molecules, blue-emitting glutathione-capped copper nanoclusters proved inert to quenching by these same analytes, instead showing evidence for aggregation-induced emission enhancement (AIEE). As a result, this discrete gold/copper nanocluster pairing provides a dual-probe, ratiometric (red-to-blue) system signaling the presence of TNT and other common explosives. This strategy opens up new potential for nanocluster-based analyte signaling, with implications to fluorescence resonance energy transfer (FRET) strategies as well.

Ionic liquid inspired alkalinochromic salts based on Reichardt's dyes for the solution phase and vapochromic detection of amines.

Chromogenic salts based on the negatively solvatochromic pyridinium N-phenolate betaines 2,6-diphenyl-4-(2,4,6-triphenyl-N-pyridino)-phenolate (Reichardt's dye 30) and 2,6-dichloro-4-(2,4,6-triphenyl-N-pyridino)-phenolate (Reichardt's dye 33) proved to be promising probes for the colorimetric detection of bases, including hydroxide ion, ammonia, and aliphatic amines. Specifically, the protonated halide forms of these two dyes were ion exchanged to generate lipophilic bis(trifluoromethylsulfonyl)imide derivatives, denoted [ET(30)][Tf2N] and [ET(33)][Tf2N], respectively. When dissolved in 95 vol% EtOH, these essentially colorless solutions displayed dramatic "alkalinochromic" color-on switching due to phenolic deprotonation to generate the zwitterionic form of the dyes with their characteristic charge-transfer absorption. The extent of the colorimetric response varied with the base strength for the aliphatic amines tested (i.e., propylamine, ethanolamine, ethylenediamine, diethylenetriamine, triethylamine, triethanolamine), being loosely correlated with the pKb of the amine. In addition, we demonstrated proof of concept for the vapochromic detection of ammonia and aliphatic amines by dissolution of the chromogenic probes in the ionic liquid 1-propyl-1-methylpyrrolidinium bis(trifluoromethylsulfonyl)imide. We also showed that the dyed ionic liquid can be successfully immobilized within silica sol-gel ionogels to generate more practical and robust sensory platforms. This strategy represents a useful addition to existing colorimetric sensor arrays targeting amines and other basic species. In particular, the differential response of the two different probes offers a measure of chemical selectivity which will be of interest for detecting biogenic amines in food safety applications, among other areas.

NMR relaxometric probing of ionic liquid dynamics and diffusion under mesoscopic confinement within bacterial cellulose ionogels.

Bacterial cellulose ionogels (BCIGs) represent a new class of material comprising a significant content of entrapped ionic liquid (IL) within a porous network formed from crystalline cellulose microfibrils. BCIGs suggest unique opportunities in separations, optically active materials, solid electrolytes, and drug delivery due to the fact that they can contain as much as 99% of an IL phase by weight, coupled with an inherent flexibility, high optical transparency, and the ability to control ionogel cross-sectional shape and size. To allow for the tailoring of BCIGs for a multitude of applications, it is necessary to better understand the underlying principles of the mesoscopic confinement within these ionogels. Toward this, we present a study of the structural, relaxation, and diffusional properties of the ILs, 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ([emim][Tf2N]) and 1-butyl-1-methylpyrrolidinium bis(trifluoromethylsulfonyl)imide ([bmpy][Tf2N]), using 1H and 19F NMR T1 relaxation times, rotational correlation times, and diffusion ordered spectroscopy (DOSY) diffusion coefficients, accompanied by molecular dynamics (MD) simulations. We observed that the cation methyl groups in both ILs were primary points of interaction with the cellulose chains and, while the pore size in cellulose is rather large, [emim]+ diffusion was slowed by ∼2-fold, whereas [Tf2N]- diffusion was unencumbered by incorporation in the ionogel. While MD simulations of [bmpy][Tf2N] confinement at the interface showed a diffusion coefficient decrease roughly 3-fold compared to the bulk liquid, DOSY measurements did not reveal any significant changes in diffusion. This suggests that the [bmpy][Tf2N] alkyl chains dominate diffusion through formation of apolar domains. This is in contrast to [emim][Tf2N] where delocalized charge appears to preclude apolar domain formation, allowing interfacial effects to be manifested at a longer range in [emim][Tf2N].