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1-Ethyl-3-methylimidazolium tetrafluoroborate ≥98% (HPLC); CAS Number: 143314-16-3; Synonyms: EMIMBF4; find Sigma-Aldrich-711721 MSDS, related peer-reviewed papers, technical documents, similar products & more at Sigma-Aldrich

1-Ethyl-3-methylimidazolium tetrafluoroborate ≥98% (HPLC) | Sigma-Aldrich

1-Ethyl-3-methylimidazolium tetrafluoroborate &#8805;98% (HPLC)

1-Ethyl-3-methylimidazolium tetrafluoroborate

Flexible Asymmetric Supercapacitor Based on Structure?Optimized Mn3O4/Reduced Graphene Oxide Nanohybrid Paper with High Energy and Power Density

Efficient, halide free synthesis of new, low cost ionic liquids: 1, 3-dialkylimidazolium salts containing methyl-and ethyl-sulfate anions

Solubility of carbon dioxide in 1-ethyl-3-methylimidazolium tetrafluoroborate

Crystal structures of frozen room temperature ionic liquids, 1-ethyl-3-methylimidazolium tetrafluoroborate (EMImBF 4), hexafluoroniobate (EMImNbF 6) and hexafluorotantalate (EMImTaF 6), determined by low-temperature X-ray diffraction

Viscosity Measurements for Binary Mixtures of 1-Ethyl-3-Methylimidazolium Tetrafluoroborate with Acetonitrile, Ethylene Glycol, and Methanol

Rapid Preparation of Room Temperature Ionic Liquids with Low Water Content as Characterized with a ta-C: N Electrode.

NMR evidence of hydrogen bonding in 1-ethyl-3-methylimidazolium-tetrafluoroborate room temperature ionic liquid

Densities and viscosities of binary liquid mixtures of 1-ethyl-3-methylimidazolium tetrafluoroborate with acetone, methyl ethyl ketone, and N-methyl-2-pyrrolidone

The phase behaviour of 1-alkyl-3-methylimidazolium tetrafluoroborates; ionic liquids and ionic liquid crystals.

Physical and electrochemical properties of ionic liquids 1-ethyl-3-methylimidazolium tetrafluoroborate, 1-butyl-3-methylimidazolium trifluoromethanesulfonate and 1-butyl-1-methylpyrrolidinium bis (trifluoromethylsulfonyl) imide

Density and Viscosity Measurements for Binary Mixtures of 1-Ethyl-3-methylimidazolium Tetrafluoroborate ([Emim][BF4]) with Dimethylacetamide, Dimethylformamide, and Dimethyl Sulfoxide

To measure electrophysiological signals from the human body, it is essential to establish stable, gentle and nonallergic contacts between the targeted biological tissue and the electrical probes. However, it is difficult to form a stable interface between the two for long periods, especially when the surface of the biological tissue is wet and/or the tissue exhibits motion. Here we resolve this difficulty by designing and fabricating smart, stress-absorbing electronic devices that can adhere to wet and complex tissue surfaces and allow for reliable, long-term measurements of vital signals. We demonstrate a multielectrode array, which can be attached to the surface of a rat heart, resulting in good conformal contact for more than 3 h. Furthermore, we demonstrate arrays of highly sensitive, stretchable strain sensors using a similar design. Ultra-flexible electronics with enhanced adhesion to tissue could enable future applications in chronic in vivo monitoring of biological signals.

A strain-absorbing design for tissue-machine interfaces using a tunable adhesive gel.

The influence of the structure of ionic liquids on the crystallinity of aluminum hydroxide (Al(OH)3) prepared by a sol-gel process with aluminum isopropoxide (Al(OPr(i))3) in imidazolium-based ionic liquids was investigated. When Al(OH)3 was prepared in ionic liquids having long alkyl chains, such as 1-butyl-3-methylimidazolium salts and 1-methyl-3-octylimidazolium salts, highly crystalline products were obtained. In contrast, Al(OH)3 obtained using the 1-ethyl-3-methylimidazolium salt was an amorphous material, indicating that hydrophobic interaction of the alkyl tail of the imidazolium cation of the ionic liquid strongly affects the crystallinity of sol-gel products and the local structure of the ionic liquid. Moreover, the crystallinity of Al(OH)3 prepared in ionic liquids increased relative to the amount of additional water (ionic liquid/water = 1.28/2.0-3.5/0.2, w/w). In the case of addition of a small amount of water (ionic liquid/water = 3.5/0.2, w/w), the product was amorphous. These results implied that the presence of an ionic liquid and a sufficient amount of water was crucial for the successful synthesis of sol-gel products with high crystallinity. (1)H NMR analyses revealed a shift of the peak associated with the imidazolium cation upon addition of water, which suggested that the molecular orientation of the ionic liquid was similar to that of a micelle.

Influence of the molecular-oriented structure of ionic liquids on the crystallinity of aluminum hydroxide prepared by a sol-gel process in ionic liquids.

Sputtering of noble metals, such as Au, Ag, Pd, and Pt, onto room-temperature ionic liquids (RTILs) enabled the formation of monoparticle films composed of spherical noble metal nanoparticles on the liquid surface only when the RTILs used contained hydroxyl-functionalized cations as a component. Sputter deposition of these metals under the same conditions simply produced well-dispersed metal particles without the formation of any films on the solution surface when pure RTILs with non-functionalized cations were employed. Anionic species, even those containing a hydroxyl group, did not significantly affect the formation of the particle film on the RTIL surface or dispersion of particles in the solution. The size of Au particles could be controlled by varying the sputtering condition regardless of the two-dimensional particle density, which was determined by the composition of RTILs used. An Au monoparticle film on the RTIL surface was easily transferred onto various solid substrates via the horizontal liftoff method without large aggregation even when the substrate surface was highly curved.

Single-step preparation of two-dimensionally organized gold particles via ionic liquid/metal sputter deposition.

In reversed-phase liquid chromatography in the absence of additives, cationic basic compounds give rise to broad and asymmetrical peaks as a result of ionic interactions with residual free silanols on silica-based stationary phases. Ionic liquids (ILs), added to the mobile phase, have been suggested as alternatives to amines to block the activity of silanols. However, the dual character of ILs should be considered: both cation and anion may be adsorbed on the stationary phase, thereby creating a double asymmetrical layer positively or negatively charged, depending on the relative adsorption of both ions. In this work, a study of the performance of six imidazolium-based ILs (the chlorides and tetrafluoroborates of 1-ethyl-, 1-butyl- and 1-hexyl-3-methylimidazolium) as modifiers of the chromatographic behaviour of a group of 10 β-blockers is performed, and compared with triethylamine and dimethyloctylamine. In order to gain more insight in the behaviour of ILs in RPLC, the changes in the nature of the chromatographic system, at increasing concentration of the additives, were followed based on retention and peak shape modelling. The multiple interactions that amines and ILs experience inside the chromatographic system suggest that the suppressing potency should be measured based on the shape of chromatographic peaks and not on the changes in retention. The ILs 1-hexyl-3-methyl-imidazolium chloride and tetrafluoroborate offered the most interesting features for the separation of the basic drugs.

Gaining insight in the behaviour of imidazolium-based ionic liquids as additives in reversed-phase liquid chromatography for the analysis of basic compounds.

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1-Ethyl-3-methylimidazolium tetrafluoroborate

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