Search results for "anion"

showing 8 items of 488 documents

STABILITY AND ORGANOCATALYTIC EFFICIENCY OF N-HETEROCYCLIC CARBENES ELECTROGENERATED IN ORGANIC SOLVENTS FROM IMIDAZOLIUM IONIC LIQUIDS

2015

The kinetic of degradation of 1-butyl-3-methylimidazole-2-ylidene (selected as model N-heterocyclic carbene - NHC), generated in organic solvents by cathodic reduction of the parent 1-butyl-3- methylimidazolium salts BMIm-X, was studied by a simple voltammetric analysis. The effect of NHC degradation rate on the efficiency of an organocatalyzed reaction (the synthesis of g-butyrolactone from cinnamaldehyde and trifluoromethylacetophenone) was investigated. The nature of the solvent and of the anion X have a remarkable effect on the stability of the NHC, the bis(trifluoromethylsulfonyl) imide anion being the best for a long lasting carbene (while acetonitrile seems to be the worst solvent). …

n-heterocyclic carbinen-heterocyclic carbeneHydrogen bondanion effect; cyclic voltammetry; ionic liquid; n-heterocyclic carbene; n-heterocyclic carbine; organocatalysisGeneral Chemical EngineeringSettore CHIM/06 - Chimica Organicacyclic voltammetryCinnamaldehydeSolventchemistry.chemical_compoundchemistryOrganocatalysisPolymer chemistryIonic liquidElectrochemistryOrganic chemistryorganocatalysiscyclic voltammetry N-heterocyclic carbene organocatalysis ionic liquid anion effectImideAcetonitrileCarbeneanion effectionic liquid
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Activation of Stainless Steel 316L Anode for Anion Exchange Membrane Water Electrolysis

2023

The increased emphasis on renewable energy has resulted in a surge of R&D efforts into hydrogen and battery research. The intensive electrochemical environment surrounding the anodic oxygen evolution reaction (OER) has plagued both the activity and stability of the catalytic layer, substrate and porous transport layer, ultimately affecting both these industries. Herein, we report the benefits of potential cycling (PC) a 316L stainless steel felt porous transport layer (PTL) for use in anion exchange membrane water electrolysis. The PC increased surface roughness and created a CrFe5Ni2-OxHy layer through the oxidation of iron as shown by SEM, EDS, XPS, XRD and Raman spectroscopy. Post-PC tes…

nianodeoxidationnifecr hydroxideporous transport layer316l stainless steelanion exchange membrane water electrolysisVDP::Teknologi: 500electrochemical impedance spectroscopyoxygen evolution reactionevolutionElectrochemistryelectrocatalystfilmspotential cycling
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New charge transfer salts of two organic π-donors of the tetrathiafulvalene type with the paramagnetic [Cr(NCS)6]3- anion

2003

cited By 9; International audience; The electrochemical combination of the paramagnetic anion [Cr(NCS)6]3- with the organic π-donors bis(ethylenedithio)tetrathiafulvalene (ET) and 4,5-bis(2-hydroxyethylthio) -4′,5′-ethylenedithiotetrathiafulvalene (DHET-EDTTTF) leads to two new radical cation salts, namely (ET)4 [Cr(NCS 6]·PhCN 1 and (DHET-EDTTTF)2 (NEt4)[Cr(NCS)6] 2. Both have been characterized by X-ray crystallography, magnetic and resistivity measurements. The structure of 1 consists of alternating inorganic layers generated by the anions and organic layers in which the PhCN molecules are inserted; the organic sub-lattice is built up from four different ET units, three of them with a ch…

organic compoundStereochemistryGeneral Chemical EngineeringDimerCrystal structure010402 general chemistry01 natural scienceschromium derivativeParamagnetismchemistry.chemical_compoundtetrathiafulvalene derivativeMolecule[CHIM]Chemical Sciencescontrolled studyradical010405 organic chemistryferromagnetic materialarticleCharge densityGeneral ChemistryanionX ray crystallographysemiconductordimerMagnetic susceptibility0104 chemical sciencescationinorganic compoundCrystallographyRadical ionchemistryelectrochemistrymagnetismchemical structureroom temperatureTetrathiafulvaleneconductanceenergy
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Unravelling the Photocatalytic Behavior of All-Inorganic Mixed Halide Perovskites: The Role of Surface Chemical States

2019

Within the most mesmerizing materials in the world of optoelectronics, mixed halide perovskites (MHPs) have been distinguished because of the tunability of their optoelectronic properties, balancing both the light-harvesting efficiency and the charge extraction into highly efficient solar devices. This feature has drawn the attention of analogous hot topics as photocatalysis for carrying out more efficiently the degradation of organic compounds. However, the photo-oxidation ability of perovskite depends not only on its excellent light-harvesting properties but also on the surface chemical environment provided during its synthesis. Accordingly, we studied the role of surface chemical states …

photocatalytic activityMaterials scienceIodideHalide02 engineering and technology010402 general chemistry01 natural sciences7. Clean energyiodide vacanciesSurface chemicalGeneral Materials Sciencehot-injectionPerovskite (structure)chemistry.chemical_classificationanion-exchangedegradation pathwaysIon exchangesurface chemical states021001 nanoscience & nanotechnology0104 chemical sciencesNanocrystalChemical engineeringchemistryPhotocatalysisDegradation (geology)0210 nano-technologysuperoxide ions
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Motions with Emotions? : A Phenomenological Approach to Understanding the Simulated Aliveness of a Robot Body

2019

This article examines how the interactive capabilities of companion robots, particularly their materiality and animate movements, appeal to human users and generate an image of aliveness. Building on Husserl’s phenomenological notion of a ‘double body’ and theories of emotions as affective responses, we develop a new understanding of the robots’ simulated aliveness. Analyzing empirical findings of a field study on the use of the robot Zora in care homes for older people, we suggest that the aliveness of companion robots is the result of a combination of four aspects: 1) material ingredients, 2) morphology, 3) animate movements guided by software programs and human operators as in Wizard of …

simulated alivenessmorfologiatunteetrobotitfenomenologiacompanion robotsemotions
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Surfactant self-assembling in the gas phase: bis(2-ethylhexyl)- sulfosuccinate divalent metal ion anionic aggregates

2012

RATIONALE: Investigation of fundamental aspects driving surfactant self-assembling and of the capability of including guest molecules or ions in their micellar aggregates is an exciting research field for theoretical and technological reasons. In this light, assembling and chelating properties of sodium bis(2-ethylhexyl)sulfosuccinate (AOTNa) towards divalent metal ion chlorides have been investigated in the gas phase by electrospray ionization mass spectrometry in negative ion mode, tandem mass spectrometry and energy-resolved mass spectrometry. METHODS:Water/methanol solutions of AOTNa and chloride salts of nickel, magnesium, calcium and manganese, with different AOTNa/metal salt ratios, …

surfactant self-assembling gas phase divalent metal ion anionic aggregates mass spectrometrySettore CHIM/06 - Chimica Organica
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2-Methylresorcinarene: a very high packing coefficient in a mono-anion based dimeric capsule and the X-ray crystal structure of the tetra-anion

2016

Mono- and tetra-deprotonated 2-methylresorcinarene anions (1 and 2) as their trans-1,4-diammoniumcyclohexane (TDAC)2+ inclusion complexes are reported. The mono-anion forms a fully closed dimeric capsule [1·H2O·MeOH]22− with a cavity volume of 165 Å3 and (TDAC)2+ as the guest with an extremely high packing coefficient, PC = 84.2%, while the tetra-anion forms a close-packed structure with two structurally isomeric tetra-anions 2a and 2b with a 50 : 50 ratio in the crystal lattice. peerReviewed

tetra-anionsta114biology010405 organic chemistryChemistryMetals and AlloysX-rayCapsuleGeneral ChemistryCrystal structureX-ray crystal structure010402 general chemistrybiology.organism_classification01 natural sciencesCatalysismono-anions0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsIonCrystallographyMaterials ChemistryCeramics and CompositesTetrata116
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Synthesis, Characterization, and Properties of Weakly Coordinating Anions Based on tris-Perfluoro-tert-Butoxyborane

2017

Abstract Image A convenient method for the preparation of strongly Lewis acidic tris-perfluoro-tert-butoxyborane B(ORF)3 (1), (ORF = OC(CF3)3) was developed, and its X-ray structure was determined. 1 was used as a precursor, guided by density functional theory (DFT) calculations and volume-based thermodynamics, for the synthesis of [NEt4][NCB(ORF)3] (3) and [NMe4][FB(ORF)3] (5) and the novel large and weakly coordinating anion salts [Li 15-Crown-5][B(ORF)4] (2) and [NEt4][CN{B(ORF)3}2] (4). The stability of [B(ORF)4]− was compared with that of some related known weakly coordinating anions by appropriate DFT calculations. peerReviewed

weakly coordinating anionsboranesLewis acidssynteesi
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