Search results for "ORP"

showing 10 items of 15031 documents

Heterogeneous Interactions between Gas-Phase Pyruvic Acid and Hydroxylated Silica Surfaces: A Combined Experimental and Theoretical Study

2019

The adsorption of gas-phase pyruvic acid (CH3COCOOH) on hydroxylated silica particles has been investigated at 296 K using transmission Fourier transform infrared (FTIR) spectroscopy and theoretical simulations. Under dry conditions (<1% relative humidity, RH), both the trans-cis (Tc) and trans-trans (Tt) pyruvic acid conformers are observed on the surface as well as the (hydrogen bonded) pyruvic acid dimer. The detailed surface interactions were further understood through ab initio molecular dynamics simulations. Under higher relative humidity conditions (above 10% RH), adsorbed water competes for surface adsorption sites. Adsorbed water is also observed to change the relative populations …

010304 chemical physicsHydrogenChemistryDimerInorganic chemistrychemistry.chemical_element010402 general chemistry01 natural sciences0104 chemical scienceschemistry.chemical_compoundAdsorption13. Climate action0103 physical sciencesRelative humidityPyruvic acid[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Physical and Theoretical ChemistryFourier transform infrared spectroscopySpectroscopyConformational isomerismComputingMilieux_MISCELLANEOUS
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Pressure‐induced widths and shifts for the ν3 band of methane

1994

International audience; Widths and shifts of methane lines perturbed by nitrogen are calculated using a complex-valued implementation of Robert-Bonamy (RB) theory. The static intermolecular potential is described as a sum of electrostatic forces and Lennard-Jones (6-12) atom-atom terms, using literature values for all physical parameters. Vibrational dependence of the isotropic potential is obtained from the polarizability of methane assuming a dispersion interaction. The repulsive part of the Lennard-Jones accounts for the greatest part of widths, while dispersion interactions are largely responsible for shifts. Although the average error between calculated and observed linewidths (up to J…

010304 chemical physicsMathematical modelAbsorption spectroscopyIntermolecular forceIsotropyGeneral Physics and Astronomy7. Clean energy01 natural sciencesMethane010309 opticschemistry.chemical_compoundLennard-Jones potentialchemistryPolarizability0103 physical sciencesDispersion (optics)Physics::Atomic and Molecular ClustersPhysics::Chemical PhysicsPhysical and Theoretical ChemistryAtomic physicsThe Journal of Chemical Physics
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Time-resolved photoisomerization of 1,1′-di-tert-butylstilbene and 1,1′-dicyanostilbene

2016

Abstract Photoisomerization of 1,1′-di-tert-butylstilbene ( 3 ) and 1,1′-dicyanostilbene ( 4 ) is monitored with stationary and broadband transient absorption spectroscopy. The electron affinity of the substituents correlates with the shift of the absorption band. The weak extinction of 3 complicates data interpretation, but comparison with earlier measured 1,1′-dimethylstilbene ( 1 ) and 1,1′-diethylstilbene ( 2 ) helps to assign transient spectra and relaxation paths. For 3 a long-lived perpendicular state P is observed with lifetime τ P  = 134 ps in acetonitrile. For 4 τ P  = 2.1 ps in acetonitrile and 27 ps in n-hexane, the difference indicating a substantial dipole moment (∼3D) of the …

010304 chemical physicsPhotoisomerizationChemistryRelaxation (NMR)Analytical chemistryGeneral Physics and Astronomy010402 general chemistry01 natural sciences0104 chemical sciencesDipolechemistry.chemical_compoundAbsorption bandElectron affinity0103 physical sciencesUltrafast laser spectroscopyPhysical and Theoretical ChemistrySpectroscopyAcetonitrileChemical Physics Letters
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Harmonic morphisms in nonlinear potential theory

1992

This article concerns the following problem: given a family of partial differential operators with similar structure and given a continuous mapping f from an open set Ω in Rn into Rn, then when does f pull back the solutions of one equation in the family to solutions of another equation in that family? This problem is typical in the theory of differential equations when one wants to use a coordinate change to study solutions in a different environment.

010308 nuclear & particles physicsGeneral Mathematics010102 general mathematicsHarmonic (mathematics)01 natural sciencesPotential theory30C6535J60AlgebraNonlinear systemMorphism0103 physical sciences0101 mathematicsMathematicsNagoya Mathematical Journal
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Luminescent TOP Nanosensors for Simultaneously Measuring Temperature, Oxygen, and pH at a Single Excitation Wavelength

2019

Two nanosensors for simultaneous optical measurements of the bioanalytically and biologically relevant analytes temperature (“T”), oxygen (“O”), and pH (“P”) have been designed. These “TOP” nanosensors are based on 100 nm-sized silica-coated polystyrene nanoparticles (PS-NPs) doped with a near-infrared emissive oxygen- and temperature-sensitive chromium(III) complex ([Cr(ddpd)2][BPh4]3, CrBPh4) and an inert reference dye (Nile Red, NR or 5,10,15,20-tetrakis(pentafluorophenyl) porphyrin, TFPP) and are covalently labeled with pH-sensitive fluorescein isothiocyanate (FITC). These emitters can be excited at the same wavelength and reveal spectrally distinguishable emission bands, allowing for r…

010401 analytical chemistryDopingAnalytical chemistryNile redNanoparticle010402 general chemistry01 natural sciencesPorphyrinFluorescence0104 chemical sciencesAnalytical Chemistrychemistry.chemical_compoundchemistryNanosensorExcited stateLuminescenceAnalytical Chemistry
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Towards Atomically Precise Supported Catalysts from Monolayer‐Protected Clusters: The Critical Role of the Support

2020

Abstract Controlling the size and uniformity of metal clusters with atomic precision is essential for fine‐tuning their catalytic properties, however for clusters deposited on supports, such control is challenging. Here, by combining X‐ray absorption spectroscopy and density functional theory calculations, it is shown that supports play a crucial role in the evolution of monolayer‐protected clusters into catalysts. Based on the acidic nature of the support, cluster‐support interactions lead either to fragmentation of the cluster into isolated Au–ligand species or ligand‐free metallic Au0 clusters. On Lewis acidic supports that bind metals strongly, the latter transformation occurs while pre…

010402 general chemistry01 natural sciencesgold clustersNanomaterials | Hot PaperCatalysiskultaCatalysisNanomaterialsmonolayer-protected clustersMetalklusteritnoncovalent interactionskatalyytitMonolayerCluster (physics)Non-covalent interactionschemistry.chemical_classificationX-ray absorption spectroscopyFull Paper010405 organic chemistryOrganic ChemistryX-ray absorption spectroscopyGeneral ChemistryFull Papersgold0104 chemical sciencesX-Ray Absorption SpectroscopychemistryChemical physicsvisual_artdensity functional calculationsvisual_art.visual_art_mediumDensity functional theorynanohiukkasetcluster-support interactionChemistry (Weinheim an Der Bergstrasse, Germany)
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Unveiling the Occurrence of Co(III) in NiCo Layered Electroactive Hydroxides: The Role of Distorted Environments

2020

Co- and Ni-based layered hydroxides constitute a unique class of two-dimensional inorganic materials with exceptional chemical diversity, physicochemical properties and outstanding performance as supercapacitors and overall water splitting catalysts. Recently, the occurrence of Co(III) in these phases has been proposed as a key factor that enhance their electrochemical performance. However, the origin of this centers and control over its contents remains as an open question. We employed the Epoxide Route to synthesize a whole set of α-NiCo layered hydroxides. The PXRD and XAS characterization alert about the occurrence of Co(III) as a consequence of the increment in the Ni content. DFT+U si…

010402 general chemistryElectrochemistry01 natural sciencesRedoxCatalysisCatalysis//purl.org/becyt/ford/1 [https]symbols.namesake//purl.org/becyt/ford/1.4 [https]LAYERED HYDROXIDESX-ray absorption spectroscopy2D MATERIALS010405 organic chemistryChemistryOrganic ChemistryFermi levelGeneral Chemistry0104 chemical sciencesCharacterization (materials science)Chemical engineeringOctahedronWATER SPLITTINGsymbolsWater splittingENERGY STORAGESUPERCAPACITANCEChemistry – A European Journal
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2,4,5-Triaryl imidazole probes for the selective chromo-fluorogenic detection of Cu(II). Prospective use of the Cu(II) complexes for the optical reco…

2019

The sensing behaviour toward metal cations and biothiols of two 2,4,5-triarylimidazole probes (3a and 3b) is tested in acetonitrile and in acetonitrile-water. In acetonitrile the two probes present charge-transfer absorption bands in the 320-350 nm interval. Among all cations tested only Cu(11) is able to induce bathochromic shifts of the absorption band in the two probes, which is reflected in marked colour changes. Colour modulations are ascribed to the formation of 1:1 Cu(II)-probe complexes in which the cation interacts with the imidazole acceptor heterocycle. Besides, the two probes present intense emission bands (at 404 and 437 nm for 3a and 3b respectively) in acetonitrile that are q…

010402 general chemistryPhotochemistryCu(II) detection01 natural sciencesCu(II) imagingInorganic ChemistryMetalchemistry.chemical_compoundBathochromic shiftMaterials ChemistryImidazolePhysical and Theoretical ChemistryAcetonitrileImidazole-based probesAqueous solutionScience & Technology010405 organic chemistryGSH imagingAcceptor0104 chemical sciences3. Good healthchemistryAbsorption bandvisual_artvisual_art.visual_art_mediumHypsochromic shiftBiothiols recognition
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Gold(II) Porphyrins in Photoinduced Electron Transfer Reactions

2019

Chemistry - a European journal 25(23), 5940 - 5949 (2019). doi:10.1002/chem.201900050

010405 organic chemistryArylOrganic ChemistryPhotoredox catalysisGeneral Chemistry010402 general chemistryPhotochemistry54001 natural sciencesRedoxPorphyrinCatalysisPhotoinduced electron transfer0104 chemical scienceslaw.inventionchemistry.chemical_compoundElectron transferchemistrylawddc:540AzideElectron paramagnetic resonance
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A Cationic Oligomer as an Organic Template for Direct Synthesis of Aluminosilicate ITH Zeolite

2020

There are a large number of zeolites, such as ITH, that cannot be prepared in the aluminosilicate form. Now, the successful synthesis of aluminosilicate ITH zeolite using a simple cationic oligomer as an organic template is presented. Key to the success is that the cationic oligomer has a strong complexation ability with aluminum species combined with a structural directing ability for the ITH structure similar to that of the conventional organic template. The aluminosilicate ITH zeolite has very high crystallinity, nanosheet-like crystal morphology, large surface area, fully four-coordinated Al species, and abundant acidic sites. Methanol-to-propylene (MTP) tests reveal that the Al-ITH zeo…

010405 organic chemistryChemistryCationic polymerizationchemistry.chemical_elementGeneral MedicineGeneral Chemistry010402 general chemistryCrystal morphology01 natural sciencesOligomerCatalysis0104 chemical scienceschemistry.chemical_compoundCrystallinityChemical engineeringAluminosilicateAluminiumZeoliteSelectivityAngewandte Chemie International Edition
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