Search results for "Tetrafluoroborate"

showing 10 items of 266 documents

Role of image charges in ionic liquid confined between metallic interfaces.

2020

The peculiar properties of ionic liquids in confinement have not only become essential for energy storage, catalysis and tribology, but still pose fundamental questions. Recently, an anomalous liquid-solid phase transition has been observed in atomic force microscopy experiments for 1-butyl-3-methylimidazolium tetrafluoroborate ([BMIM][BF4]), the transition being more pronounced for metallic surfaces. Image charges have been suggested as the key element driving the anomalous freezing. Using atomistic molecular dynamics simulations, we investigate the impact of image charges on structure, dynamics and thermodynamics of [BMIM][BF4] confined between gold electrodes. Our results not only unveil…

Phase transitionRange (particle radiation)TetrafluoroborateMaterials scienceGeneral Physics and Astronomy02 engineering and technologyTribology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesMetalMolecular dynamicschemistry.chemical_compoundchemistryChemical physicsvisual_artIonic liquidElectrodevisual_art.visual_art_mediumPhysical and Theoretical Chemistry0210 nano-technologyPhysical chemistry chemical physics : PCCP
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On the use of ionic liquids as mobile phase additives in high-performance liquid chromatography. A review.

2015

The popularity of ionic liquids (ILs) has grown during the last decades in several analytical separation techniques. Consequently, the number of reports devoted to the applications of ILs is still increasing. This review is focused on the use of ILs (mainly imidazolium-based associated to chloride and tetrafluoroborate) as mobile phase additives in high-performance liquid chromatography (HPLC). In this approach, ILs just function as salts, but keep several kinds of intermolecular interactions, which are useful for chromatographic separations. Both cation and anion can be adsorbed on the stationary phase, creating a bilayer. This gives rise to hydrophobic, electrostatic and other specific in…

TetrafluoroborateHETEROCYCLIC AROMATIC-AMINESBiochemistryHigh-performance liquid chromatographyChlorideAnalytical Chemistrychemistry.chemical_compoundSilanol suppressionAdsorptionSOLUBILIZING ABILITIES[CHIM.ANAL]Chemical Sciences/Analytical chemistryPhase (matter)medicineEnvironmental ChemistryOrganic chemistryOptimisationSpectroscopyHALF-WIDTH PLOTSMechanisms of retentionOVERLOADED BAND PROFILESANALYTICAL-CHEMISTRYSILANOL-SUPPRESSING POTENCYHYDROCARBONACEOUS STATIONARY PHASESIntermolecular forceAdditivesHigh-performance liquid chromatographyIonic liquidsSilanolROOM-TEMPERATURERETENTION MECHANISMChemical engineeringchemistryRP-HPLCIonic liquidmedicine.drugAnalytica chimica acta
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X-ray crystal structure and electronic properties of chlorobis(mepirizole)copper(II) tetrafluoroborate (mepirizole = 4-methoxy-2-(5-methoxy-3-methyl-…

1997

Abstract The crystal structure of [Cu(mep)2Cl](BF4)[mep = 4-methoxy-2-(5-methoxy-3-methyl-1H-pyrazol-1-yl)-6-methylpyrimidine] has been determined by X-ray diffraction. The crystal structure is built up of [Cu(mep)2Cl]+ cations and BF4− anions. The structure of the cation involves a five-coordinated CuN4Cl chromophore, with a stereochemistry near to a compressed trigonal bypyramid (TBP) but with a significant degree of distortion towards the square pyramidal (SP) topology. The EPR spectrum is indicative of a mixed dz2/dx2 − y2 ground state for the copper(II) ions, in agreement with the structural data.

chemistry.chemical_elementCrystal structureChromophoreCopperSquare pyramidal molecular geometryIonlaw.inventionInorganic ChemistryCopper(II) tetrafluoroboratechemistry.chemical_compoundCrystallographychemistrylawMaterials ChemistryPhysical and Theoretical ChemistryGround stateElectron paramagnetic resonancePolyhedron
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Composite Polymer Electrolytes with Improved Lithium Metal Electrode Interfacial Properties: I. Elechtrochemical Properties of Dry PEO‐LiX Systems

1998

Several types of lithium ion conducting polymer electrolytes have been synthesized by hot-pressing homogeneous mixtures of the components, namely, poly(ethylene oxide) (PEO) as the polymer matrix, lithium trifluoromethane sulfonate (LiCF{sub 3}SO{sub 3}), and lithium tetrafluoroborate (LiBF{sub 4}), respectively, as the lithium salt, and lithium gamma-aluminate {gamma}-LiAlO{sub 2}, as a ceramic filler. This preparation procedure avoids any step including liquids so that plasticizer-free, composite polymer electrolytes can be obtained. These electrolyte have enhanced electrochemical properties, such as an ionic conductivity of the order of 10{sup {minus}4} S/cm at 80--90 C and an anodic bre…

Conductive polymerMaterials scienceRenewable Energy Sustainability and the EnvironmentInorganic chemistryLithium tetrafluoroboratechemistry.chemical_elementElectrolyteCondensed Matter PhysicsElectrochemistryLithium aluminateSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundchemistryMaterials ChemistryElectrochemistryFast ion conductorIonic conductivityLithiumJournal of The Electrochemical Society
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Direct experimental observation of mesoscopic fluorous domains in fluorinated room temperature ionic liquids

2017

Fluorinated room temperature ionic liquids (FRTILs) represent a class of solvent media that are attracting great attention due to their IL-specific properties as well as features stemming from their fluorous nature. Medium-to-long fluorous tails constitute a well-defined apolar moiety in the otherwise polar environment. Similarly to the case of alkyl tails, such chains are expected to result in the formation of self-assembled fluorous domains. So far, however, no direct experimental observation has been made of the existence of such structural heterogeneities on the nm scale. We report here the first experimental evidence of the existence of mesoscopic spatial segregation of fluorinated dom…

General Physics and AstronomyNanotechnology02 engineering and technologyNeutron scattering010402 general chemistryLAYER CAPACITOR APPLICATIONS; PERFLUOROALKYL SIDE-CHAINS; ANGLE NEUTRON-SCATTERING; PARTICLE MESH EWALD; PHYSICOCHEMICAL PROPERTIES; FORCE-FIELD; CATION SYMMETRY; STRUCTURAL-CHARACTERIZATION; AMMONIUM TETRAFLUOROBORATE; MOLECULAR SIMULATION01 natural sciencesionic liquidsionic liquids SANS nanostructuration fluorous domains NMR NOEchemistry.chemical_compoundMolecular dynamicsPhysics and Astronomy (all)nanostructurationMoietyPhysical and Theoretical ChemistryAlkylNOEchemistry.chemical_classificationfluorous domainsMesoscopic physicsSANSNuclear magnetic resonance spectroscopy021001 nanoscience & nanotechnologyNMR0104 chemical sciencesfluorinated ionic liquids neutron scattering x-ray diffraction structurechemistryChemical physicsIonic liquidPolar0210 nano-technology
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Pressure-induced hysteresis in the high spin \leftrightarrow low spin transition in bis(2,4-bis(pyridin-2-yl)thiazole) iron(II) tetrafluoroborate

2008

Studies of the spin transition behavior of the mononuclear compound [Fe(pythiaz)2](BF4)2 have been carried out under hydrostatic pressures up to 9.13 kbar in the 5–300 K temperature range. Under ambient pressure this compound exhibits an approximately half-step (incomplete) HS ↔ LS transition with T1/2 = 146 K without any thermal hysteresis. At pressures up to 4.5 kbar the behavior remains similar but with an upward displacement of T1/2 and a slight decrease in the residual high spin fraction at low T . Application of higher pressures resulted in an almost complete two-step spin transition with several unusual pressure effects. Along with the expected pressure dependence of T1/2 the surpris…

TetrafluoroborateCondensed matter physicsSpin transitionAtmospheric temperature rangeCondensed Matter Physicschemistry.chemical_compoundCrystallographyHysteresischemistryStructural changeGeneral Materials ScienceThiazoleAmbient pressureSpin-½Journal of Physics: Condensed Matter
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Synthesis, characterization, crystal structures and magnetic exchange in dinuclear copper complexes with 3-amino-1-propanol as terminal and bridging …

1990

Abstract The synthesis, X-ray structures and spectroscopic and magnetic properties are described for two groups of dinuclear Cu(II) compounds with the ligand 3-amino-1-propanol (Hap). The formulae of the compounds are for group A: [Cu(ap)(anion)]2, in which ap is the dehydronated Hap and the anions are formate, nitrate, chloride and bromide and for group B: [Cu(ap)(Hap)]2(anion)2, with anion = iodide, bromide, chloride, nitrate and tetrafluoroborate. The structure of group A compounds consists of dinuclear units with the co-planar centrosymmetric chromophore ANCuOO′CuNA, in which the A ligands (anions) bridge to neighbouring units as axial ligands, thereby forming infinite chains. Dimer Cu……

TetrafluoroborateCoordination sphereChemistryHydrogen bondStereochemistryLigandDimerBridging ligandCrystal structureSquare pyramidal molecular geometryInorganic Chemistrychemistry.chemical_compoundCrystallographyMaterials ChemistryPhysical and Theoretical ChemistryInorganica Chimica Acta
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Resorcinarene Podand with Amine-Functionalized Side Arms – Synthesis, Structure, and Binding Properties of a Neutral Anion Receptor

2009

The synthesis and structure of a neutral resorcinarene host bearing four amine-functionalized side arms is described. The anion binding properties were investigated in solution by 1H NMR spectroscopic titration and diffusion experiments and in the gas phase by mass spectrometric studies. It was observed that in solution 1:2 (host/guest) complexes were formed between the resorcinarene host and the basic fluoride and acetate anions, whereas in the gas phase 1:1 complexes with other anions (Cl–, HCOO–, NO3–, and BF4–) were detected additionally. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)

TetrafluoroborateStereochemistryOrganic ChemistrySupramolecular chemistryResorcinareneChemical synthesisInclusion compoundchemistry.chemical_compoundchemistryPolymer chemistryTitrationAmine gas treatingPhysical and Theoretical ChemistryAnion bindingEuropean Journal of Organic Chemistry
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Synthesis and characterization of catalytic iridium nanoparticles in imidazolium ionic liquids

2006

Abstract The reduction of [Ir(cod)Cl]2 (cod = 1,5-cyclooctadiene) dissolved in 1-n-butyl-3-methyl tetrafluoroborate, hexafluorophosphate and trifluoromethane sulphonate ionic liquids in the presence of 1-decene by molecular hydrogen produces Ir(0) nanoparticles. The formation of these nanoparticles follows the two-step [A → B, A + B → 2B ( k 1 , k 2 )] autocatalytic mechanism. The same mean diameter values of around 2–3 nm were estimated from in situ TEM and SAXS analyses of the Ir(0) nanoparticles dispersed in the ionic liquids and by XRD of the isolated material. XPS and EXAFS analyses clearly show the interactions of the ionic liquid with the metal surface demonstrating the formation of …

TetrafluoroborateInorganic chemistryAnalytical chemistrychemistry.chemical_elementNanoparticleSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsIonBiomaterialsMetalchemistry.chemical_compoundColloid and Surface ChemistrychemistryTransition metalHexafluorophosphatevisual_artIonic liquidvisual_art.visual_art_mediumIridiumJournal of Colloid and Interface Science
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ChemInform Abstract: 1,4-Regioselective Iodofunctionalizations of 1,3-Butadiene.

1989

1,3-Butadiene (I) is treated with a iodonium tetrafluoroborate in the presence of HBF4 and aqueous acetonitrile (II) or benzene (IV), yielding the 1,4-adducts (III) or (V).

chemistry.chemical_compoundTetrafluoroborateAqueous solutionchemistryRegioselectivity13-ButadieneGeneral MedicineAcetonitrileBenzeneMedicinal chemistryChemInform
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