Search results for "Chemical polarity"

showing 10 items of 21 documents

Water dynamics and its role in structural hysteresis of dissolved organic matter

2016

Knowledge of structural dynamics of dissolved organic matter (DOM) is of paramount importance for understanding DOM stability and role in the fate of solubilized organic and inorganic compounds (e.g., nutrients and pollutants), either in soils or aquatic systems. In this study, fast field cycling (FFC) (1)H NMR relaxometry was applied to elucidate structural dynamics of terrestrial DOM, represented by two structurally contrasting DOM models such as Suwanee River (SRFA) and Pahokee peat (PPFA) fulvic acids purchased by the International Humic Substance Society. Measurement of NMR relaxation rate of water protons in heating-cooling cycles revealed structural hysteresis in both fulvic acids. I…

Magnetic Resonance SpectroscopyrelaxometrySettore AGR/13 - Chimica Agraria010501 environmental sciences01 natural scienceshumic substanceSoilRiversDissolved organic carbonEnvironmental ChemistryReactivity (chemistry)Benzopyrans0105 earth and related environmental sciencesChemistryHydrogen bondwater histeresiChemical polarityTemperatureSoil chemistryWaterHydrogen Bonding04 agricultural and veterinary sciencesGeneral ChemistryNuclear magnetic resonance spectroscopyEnvironmental chemistrySoil water040103 agronomy & agricultureProton NMR0401 agriculture forestry and fisheriesHydrophobic and Hydrophilic Interactions
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Adsorption Studies of Molecules on the Halloysite Surfaces: A Computational and Experimental Investigation

2017

We report the results of joint computational and experimental investigations on the adsorption capability of halloysite toward a set of common molecules (water, alcohols, halides, and carboxylic acids). The halloysite system has been modelized by means of a cluster approach choosing a portion of a spiral nanotube; it has a slight curvature, with a convex aluminic layer. The adsorption geometries are described in terms of hydrogen bond network structures; calculated interaction energies invariably indicate that the inner aluminic surface is the place for preferential adsorption of polar molecules. The presence of substitutional defects on the outer or inner surface of the halloysite model ca…

NanotubeHalideSurfaces Coatings and Film02 engineering and technologyengineering.material010402 general chemistry01 natural sciencesHalloysiteCondensed Matter::Materials ScienceAdsorptionPhysics::Atomic and Molecular ClustersCluster (physics)Organic chemistryMoleculePhysics::Chemical PhysicsPhysical and Theoretical ChemistryChemistryHydrogen bondChemical polarityElectronic Optical and Magnetic Material021001 nanoscience & nanotechnology0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsGeneral EnergyEnergy (all)Chemical physicsengineering0210 nano-technology
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Purely long-range polar molecules composed of identical lanthanide atoms

2019

International audience; Doubly polar molecules, possessing an electric dipole moment and a magnetic dipole moment, can strongly couple to both an external electric field and a magnetic field, providing unique opportunities to exert full control of the system quantum state at ultracold temperatures. We propose a method for creating a purely long-range doubly polar homonuclear molecule from a pair of strongly magnetic lanthanide atoms, one atom being in its ground level and the other in a superposition of quasi-degenerate opposite-parity excited levels [Phys. Rev. Lett. 121, 063201 (2018)]. The electric dipole moment is induced by coupling the excited levels with an external electric field. W…

PhysicsZeeman effectMagnetic moment[PHYS.PHYS.PHYS-ATOM-PH]Physics [physics]/Physics [physics]/Atomic Physics [physics.atom-ph]Atomic Physics (physics.atom-ph)Chemical polarityFOS: Physical sciences01 natural sciencesDiatomic moleculeHomonuclear molecule010305 fluids & plasmasPhysics - Atomic PhysicsElectric dipole momentsymbols.namesake[PHYS.QPHY]Physics [physics]/Quantum Physics [quant-ph]Excited stateElectric field0103 physical sciencessymbolsPhysics::Atomic Physics[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Atomic physics010306 general physics
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Functional fixedness and functional reduction as common sense reasonings in chemical equilibrium and in geometry and polarity of molecules

2000

Many of the learning difficulties in the specific domain of chemistry are found not only in the ideas already possessed by students but in the strategic and procedural knowledge that is characteristic of everyday thinking. These defects in procedural knowledge have been described as functional fixedness and functional reduction. This article assesses the procedural difficulties of students (grade 12 and first and third year of university) based on common sense reasoning in two areas of chemistry: chemical equilibrium and geometry and polarity of molecules. In the first area, the theme of external factors affecting equilibria (temperature and concentration change) was selected because the ex…

Polarity (physics)Chemical polarityCommonsense reasoningGeometryProcedural knowledgeFunctional fixednessEducationLewis structureLe Chatelier's principlesymbols.namesakeMolecular geometryHistory and Philosophy of SciencesymbolsMathematicsScience Education
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Valence Topological Charge-Transfer Indices for Dipole Moments

2003

Valence topological charge-transfer (CT) indices are applied to the calculation of dipole moments. The dipole moments calculated by algebraic and vector semisums of the CT indices are defined. The combination of the CT indices allows the estimation of the dipole moments. The model is generalized for molecules with heteroatoms. The ability of the indices for the description of the molecular charge distribution is established by comparing them with the dipole moment of the valence-isoelectronic series of benzene and styrene. Two CT indices, μ v e c (vector semisum of vertex-pair dipole moments) and μ V v e c (valence μ v e c ) are proposed. μ v e c and μ V v e c are important for the predicti…

Protein ConformationHeteroatomPharmaceutical ScienceBiochemistryAnalytical ChemistryElectricityComputational chemistryDrug DiscoveryPhysicsvalence topological charge-transfer indexChemistryCharge densityGeneral Medicinemolecular charge distributionCondensed Matter Physicstransdermal drug deliveryChemistry (miscellaneous)Molecular MedicineAtomic physicsInformation SystemsSteric effectsBond dipole momentStatic ElectricityTransition dipole momentBiophysicsElectronsFractal dimensionMolecular physicsBiophysical PhenomenaArticleCatalysislcsh:QD241-441Inorganic Chemistrylcsh:Organic chemistryAtomic orbitalMoleculePhysical and Theoretical ChemistryMolecular BiologyStyreneTopological quantum numberDipole momentModels StatisticalValence (chemistry)Chemical polarityOrganic ChemistryBenzeneModels Theoreticalvalence topological chargetransfer indexElectric dipole momentDipolephenyl alcoholModels ChemicalMoment (physics)Electric dipole transitionMolecules
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Reversed-phase liquid chromatography with mixed micellar mobile phases of Brij-35 and sodium dodecyl sulphate: a method for the analysis of basic com…

2015

Micellar liquid chromatography (MLC) is a reversed-phase liquid chromatographic (RPLC) mode, which uses a surfactant as a modifier, with significant changes in retention and selectivity with regard to the classical RPLC mode that employs mixtures of water and organic solvent. The anionic sodium dodecyl sulphate (SDS) is the most usual surfactant in MLC, but it also requires the addition of an organic solvent to decrease the retention times and increase the efficiency. In particular, positively charged basic compounds are strongly retained by the stationary phase modified by adsorption of SDS monomers and require the addition of a strong solvent, such as propanol or pentanol. The non-ionic s…

SolventPropanolchemistry.chemical_compoundAdsorptionChromatographyPulmonary surfactantChemistryMicellar liquid chromatographyChemical polarityEnvironmental ChemistryReversed-phase chromatographySelectivityPollutionGreen Chemistry
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Molecular aggregates of quinuclidine and chlorophyll a

1991

A slightly polar molecule quinuclidine seems to form weakly bound aggregates in concentrated water solutions. Molecular dynamics simulation of a 6 mol water solution indicates clustering of quinuclidine molecules into an almost spherical structure with polar ends of the molecules pointing towards the solvent. Experimental evidence of aggregation was obtained by observing a small but obvious red shift of the o'' a absorption and a dramatic shortening of the fluorescence lifetime of the c n transition of concentrated solutions. The observed self-quenching is interpreted in terms of Frster model for energy transfer in the cluster. It is estimated that excitation may migrate on the cluster surf…

Solventchemistry.chemical_compoundMolecular dynamicsMonomerChemistryChemical polarityMoleculeAbsorption (chemistry)PhotochemistryLuminescenceQuinuclidineSPIE Proceedings
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Orientation of Polar Molecules by Laser Induced Adiabatic Passage

2002

International audience; We show that two overlapping linearly polarized laser pulses of frequencies ω and its second harmonic 2ω can strongly orient linear polar molecules, by adiabatic passage along dressed states. The resulting robust orientation can be interpreted as a laser-induced localization in the effective double well potential created by the fields, which induces a preliminary molecular alignment. The direction of the orientation can be selected by the relative phase of the fields.

[PHYS.PHYS.PHYS-OPTICS] Physics [physics]/Physics [physics]/Optics [physics.optics]Physics[ PHYS.PHYS.PHYS-OPTICS ] Physics [physics]/Physics [physics]/Optics [physics.optics]Linear polarizationChemical polarityGeneral Physics and AstronomyDouble-well potentialLaserlaw.inventionlawOrientation (geometry)HarmonicAtomic physicsMolecular alignmentAdiabatic processComputer Science::Databases
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X-Ray structure, Hirshfeld analysis and DFT studies of two new hits of triazolyl-indole bearing alkylsulfanyl moieties

2021

Two new hits of triazolyl-indole containing two different alkylsulfanyl analogues named tert-butyl 2-((4-amino-5-(1H-indol-2-yl)-4H-1,2,4-triazol-3-yl)thio)acetate 2, and ethyl 2-((4-amino-5-(1H-indol-2-yl)-4H-1,2,4-triazol-3-yl)thio)acetate 3 were synthesized via reaction of 4-amino-5-(1H-indol-2-yl)-1,2,4-triazol-3(2H)-thione 1 with tert-butyl bromoacetate and ethyl chloroacetate in the presence of base (Et3N). The molecular structure of 2, and 3 was confirmed by single-crystal X-ray diffraction and 1H/13C- NMR spectroscopic techniques. In compound 2, the molecular packing depends on significant O...H (9.3%), N...H (12.4%) and S...H (3.1%) as well as relatively weak C...H (14.1%), S...C (…

aromaattiset yhdisteettriazolyl-indolereactivity descriptorsThio-Uv-Vis010402 general chemistry01 natural sciencesDFTAnalytical ChemistryInorganic Chemistrychemistry.chemical_compoundrikkiyhdisteetNBOMoleculeHirshfeld surface analysisReactivity (chemistry)Ethyl chloroacetateSpectroscopyIndole testkemiallinen synteesi010405 organic chemistryChemistryHydrogen bondChemical polarityOrganic Chemistry0104 chemical sciencesCrystallographyNatural bond orbital
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Poly(ethylene glycol) diacrylate based monolithic capillary columns for the analysis of polar small solutes by capillary electrochromatography

2018

Monolithic stationary phases based on poly(ethylene glycol) diacrylates for capillary electrochromatography were developed. Several poly(ethylene glycol) diacrylates (Mn 250, 575, and 700) were used as single monomers and the resulting columns were carefully compared. Methanol and ethyl ether were selected as porogenic solvents, and in all cases ultraviolet radiation was selected as initiation method to prepare polymeric monoliths. The influence of the monomer chain length and ratio monomer/porogen on the morphological and electrochromatographic properties of the resulting monoliths was investigated. Several families of compounds with different polarity (alkyl benzenes, organophosphorous pe…

chemistry.chemical_classificationCapillary electrochromatographyChemical polarity010401 analytical chemistryFiltration and SeparationEther02 engineering and technology021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesAnalytical Chemistrychemistry.chemical_compoundMonomerchemistryChemical engineeringMethanol0210 nano-technologyEthylene glycolAlkylBenzoic acidJournal of Separation Science
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