Search results for " molecule"

showing 10 items of 1523 documents

Enhanced nanoscopy of individual CsPbBr3 perovskite nanocrystals using dielectric sub-micrometric antennas

2020

We demonstrate an efficient, simple, and low-cost approach for enhanced nanoscopy in individual green emitting perovskite (CsPbBr3) nanocrystals via TiO2 dielectric nanoantenna. The observed three- to five-fold emission enhancement is attributed to near-field effects and emission steering promoted by the coupling between the perovskite nanocrystals and the dielectric sub-micrometric antennas. The dark-field scattering configuration is then exploited for surface-enhanced absorption measurements, showing a large increase in detection sensitivity, leading to the detection of individual nanocrystals. Due to the broadband spectral response of the Mie sub-micrometric antennas, the method can be e…

Detection sensitivityMaterials sciencelcsh:BiotechnologyCesium compoundsPhysics::Optics02 engineering and technologyDielectricPerovskiteLead compoundsperovskite solar cells01 natural sciences7. Clean energyCondensed Matter::Materials Sciencenanocrystalslcsh:TP248.13-248.650103 physical sciencesEnhanced absorptionSemiconductor quantum dotsElectronic transitionGeneral Materials Science[SPI.NANO]Engineering Sciences [physics]/Micro and nanotechnologies/MicroelectronicsAbsorption (electromagnetic radiation)perovskitePerovskite (structure)010302 applied physicsScatteringbusiness.industryGeneral Engineering021001 nanoscience & nanotechnologylcsh:QC1-999NanocrystalsNear field effectNanocrystalAtomic electron transitionQuantum dotOptoelectronicsTitanium dioxideAntennasDark-field scatteringsLow cost approachPhotonics0210 nano-technologybusinessOrganic moleculeslcsh:PhysicsBromine compoundsEmission enhancement
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Combined proton NMR wideline and NMR relaxometry to study SOM-water interactions of cation-treated soils

2013

Abstract Focusing on the idea that multivalent cations affect SOM matrix and surface, we treated peat and soil samples by solutions of NaCl, CaCl2 or AlCl3. Water binding was characterized with low field 1H-NMR-relaxometry (20 MHz) and 1H wideline NMR spectroscopy (400 MHz) and compared to contact angles. From 1H wideline, we distinguished mobile water and water involved in water molecule bridges (WaMB). Large part of cation bridges (CaB) between SOM functional groups are associated with WaMB. Unexpectedly, 1H NMRrelaxometry relaxation rates suggest that cross-linking in the Al-containing peat is not stronger than that by Ca. The relation between percentage of mobile water and WaMB water in…

Dewey Decimal Classification::500 | Naturwissenschaften::550 | GeowissenschaftenDewey Decimal Classification::500 | Naturwissenschaften::570 | Biowissenschaften BiologieDewey Decimal Classification::600 | Technik::630 | Landwirtschaft VeterinärmedizinAnalytical chemistrySoil organic matter (SOM); Low field 1H NMR relaxometry; 1H wideline NMR spectroscopy; Contact angle; Cation bridges; Water molecule bridges.TA Engineering (General). Civil engineering (General)soil organic matter (som)Low field H-1 NMR relaxometrystateContact angleNuclear magnetic resonancewater molecule bridgesddc:550ddc:630natural organic-mattercontact angleWater Science and TechnologyFluid Flow and Transfer Processeschemistry.chemical_classificationhumic substancesWater molecule bridges.Nuclear magnetic resonance spectroscopycation bridgesCation bridgemultiexponential decay datanuclear-magnetic-resonanceH-1 wideline NMR spectroscopyProton NMRWater bindingTC1-978Relaxometryuniform-penalty inversionlow field 1h nmr relaxometrySettore AGR/13 - Chimica AgrariaContext (language use)1h wideline nmr spectroscopyforest soilsCation bridgesddc:570sandy soilOrganic mattercontact-angleContact angleSoil organic matter (SOM)repellencyMechanical EngineeringHydraulic engineeringchemistrySoil waterWater molecule bridgesJournal of Hydrology and Hydromechanics
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Analytic first and second derivatives for the CCSDT-n (n = 1–3) models: a first step towards the efficient calculation of CCSDT properties

2000

Analytic first and second derivatives of the energy are implemented for closed-shell systems described by the CCSDT-n (n=1, 1b, 2 and 3) and CC3 electron correlation models. A detailed discussion of the computational requirements of these calculations is given, along with diagrammatic formulas for all relevant quantities. The method is applied to calculate the nuclear magnetic shielding of H2O, CO and N2O and the structure and properties of propadienylidene.

Diagrammatic reasoningElectronic correlationComputational chemistryChemistryTriatomic moleculeElectromagnetic shieldingStructure (category theory)General Physics and AstronomyApplied mathematicsPhysical and Theoretical ChemistryPropadienylideneDiatomic moleculeSecond derivativePhysical Chemistry Chemical Physics
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Selected dissociation‐ and correlation‐consistent configuration interaction by a perturbative criterion

1990

We propose a perturbative criterion to select the most important dissociation‐ or correlation‐consistent type of contributions to perform generalized valence bond‐configuration interaction (GVB‐CI) calculations, dissociation‐consistent configuration interaction (DCCI) or correlation‐consistent configuration interaction (CCCI) approach, respectively. The procedure presented is computationally less demanding than the CCCI proposed by Goddard and co‐workers. To ensure the distance consistency of the MOs used, the nonvalence virtual orbitals are obtained by a projection technique. The results obtained for a few test calculations show the ability of the suggested approach to get close results to…

Diatomic MoleculesValence (chemistry)ChemistryConfiguration Interaction ; Electronic Structure ; Dissociation Energy ; Perturbation Theory ; Diatomic Molecules ; Polyatomic MoleculesGeneral Physics and AstronomyDissociation EnergyElectronic structureConfiguration interactionBond-dissociation energyDiatomic moleculeDissociation (chemistry)Polyatomic MoleculesUNESCO::FÍSICA::Química físicaConfiguration InteractionElectronic StructureAtomic orbitalComputational chemistryPerturbation TheoryPerturbation theory (quantum mechanics)Statistical physicsPhysical and Theoretical Chemistry:FÍSICA::Química física [UNESCO]The Journal of Chemical Physics
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Fourier-transform spectroscopy, direct-potential-fit, and electronic structure calculations on the entirely perturbed (4)1Π state of RbCs

2018

We performed a high-resolution Fourier-transform spectroscopic study of the (4)1Π state of the RbCs molecule by applying two-step (4)1Π ← A1Σ+ ∼ b3Π ← X1Σ+ optical excitation followed by observation of the (4)1Π → X1Σ+ laser induced fluorescence (LIF) spectra. In many LIF progressions the collision-induced satellite rotational lines were observed thus increasing the amount of term values and allowing to estimate the Λ-doubling effect in the (4)1Π state. The Direct-Potential-Fit (DPF) of experimental term values of 777 rovibronic levels of both 85RbCs and 87RbCs isotopologues has been performed by means of the robust weighted non-linear least squares method. The PFanalysis based on adiabatic…

Diatomic moleculeselectronic structure calculations:NATURAL SCIENCES::Physics [Research Subject Categories]Fourier transform spectroscopy
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Atom- and Bond-Based 2D TOMOCOMD-CARDD Approach and Ligand-Based Virtual Screening for the Drug Discovery of New Tyrosinase Inhibitors

2008

Two-dimensional atom- and bond-based TOMOCOMD-CARDD descriptors and linear discriminant analysis (LDA) are used in this report to perform a quantitative structure-activity relationship (QSAR) study of tyrosinase-inhibitory activity. A database of inhibitors of the enzyme is collected for this study, within 246 highly dissimilar molecules presenting antityrosinase activity. In total, 7 discriminant functions are obtained by using the whole set of atom- and bond-based 2D indices. All the LDA-based QSAR models show accuracies above 90% in the training set and values of the Matthews correlation coefficient (C) varying from 0.85 to 0.90. The external validation set shows globally good classifica…

DicumarolQuantitative structure–activity relationshipStereochemistryTyrosinaseQuantitative Structure-Activity RelationshipLigandsBiochemistryAnalytical ChemistrySmall Molecule Librarieschemistry.chemical_compoundDrug DiscoveryCluster AnalysisVirtual screeningDrug discoveryChemistryComputational BiologyDiscriminant AnalysisReproducibility of ResultsMatthews correlation coefficientLigand (biochemistry)Linear discriminant analysisCombinatorial chemistryMolecular MedicinePeptidesKojic acidBiotechnologySLAS Discovery
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Anisotropic lattice distortions in biogenic calcite induced by intra-crystalline organic molecules.

2006

9 pages; International audience; We have performed precise structural measurements on five different calcitic seashells by high-resolution X-ray powder diffraction on a synchrotron beam line and by laboratory single crystal X-ray diffraction. The unit cell parameters a and c of biogenic calcite were found to be systematically larger than those measured in the non-biogenic calcite. The maximum lattice distortion (about 2.10(-3)) was detected along the c-axis. Under heat treatment above 200 degrees C, a pronounced lattice relaxation was observed, which allowed us to conclude that anisotropic lattice swelling in biogenic calcite is induced by organic macromolecules incorporated within the sing…

DiffractionBiomineralizationMESH : Calcium CarbonateMESH: Bivalvia02 engineering and technologyCrystallography X-Ray01 natural scienceslaw.inventionchemistry.chemical_compoundStructural BiologylawMESH : BivalviaOstreaMESH : AnisotropyMESH: AnimalsOrganic ChemicalsCrystallizationAnisotropyMESH: CrystallizationCalciteMESH: OstreaSynchrotron radiationCalciteCrystal growth and nucleationMESH : Organic Chemicals021001 nanoscience & nanotechnologyMESH: Calcium CarbonateMESH : CrystallizationX-ray crystallographyCrystallization0210 nano-technologyMaterials scienceMESH : Crassostrea010402 general chemistryCalcium CarbonateAnimalsCrassostreaIntra-crystalline organic molecules[SDV.IB.BIO]Life Sciences [q-bio]/Bioengineering/BiomaterialsBiogenic crystalsMESH : OstreaMESH: Organic ChemicalsMESH: Crystallography X-Ray[ SDV.IB.BIO ] Life Sciences [q-bio]/Bioengineering/BiomaterialsBivalvia0104 chemical sciencesX-ray diffractionCrystallographyMESH: CrassostreachemistryMESH: AnisotropyAnisotropyMESH : AnimalsMESH : Crystallography X-RaySingle crystalPowder diffractionBiomineralization
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QTAIM View of Metal-Metal Bonding in Di- and Trinuclear Disulfido Carbonyl Clusters

2012

The experimental and theoretical charge densities in the sulfido-bridged cluster compounds Fe2(μ-S2)(CO)6 (1), Fe3(μ3-S)2(CO)9 (2), Mn2(μ-S2)(μ-CO)(CO)6 (3), and Fe2(μ-S2)(CO)5(PPh3) (4) have been studied using the quantum theory of atoms in molecules (QTAIM) methodology. High-resolution X-ray diffraction data have been measured for compounds 2–4 at 100 K. The topological analyses show that only in compounds 1 and 4 is there any evidence for metal–metal bonding in terms of the presence of a bond path. For compound 1, the topology of the Fe2S2 cage is highly dependent on the Fe–Fe separation, and the deformation along this vector is an extremely soft mode. The experimentally observed topolog…

DiffractionChemistryOrganic ChemistryAtoms in moleculesCharge (physics)Soft modesDecompositionInorganic ChemistryCrystallographyDelocalized electronComputational chemistryCluster (physics)Physical and Theoretical Chemistryta116Topology (chemistry)Organometallics
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Revisiting the charge density analysis of 2,5-dichloro-1,4-benzoquinone at 20 K

2017

A high-resolution X-ray diffraction measurement of 2,5-dichloro-1,4-benzoquinone (DCBQ) at 20 K was carried out. The experimental charge density was modeled using the Hansen–Coppens multipolar expansion and the topology of the electron density was analyzed in terms of the quantum theory of atoms in molecules (QTAIM). Two different multipole models, predominantly differentiated by the treatment of the chlorine atom, were obtained. The experimental results have been compared to theoretical results in the form of a multipolar refinement against theoretical structure factors and through direct topological analysis of the electron density obtained from the optimized periodic wavefunction. The si…

DiffractionElectron density202 engineering and technology010402 general chemistry01 natural sciencesMolecular physics14-Benzoquinonechemistry.chemical_compound5-di­chloro-1Materials Chemistryelectron densityWave functionIntermolecular forceAtoms in moleculesMetals and AlloysCharge density021001 nanoscience & nanotechnologyAtomic and Molecular Physics and Optics0104 chemical sciencesElectronic Optical and Magnetic MaterialsQTAIMchemistry4-benzo­quinonemultipole models0210 nano-technologyMultipole expansionActa Crystallographica Section B Structural Science, Crystal Engineering and Materials
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The Significance of Ionic Bonding in Sulfur Dioxide: Bond Orders from X-ray Diffraction Data

2012

A novel refinement technique for X‐ray diffraction data has been employed to derive S-O bond orders in sulfur dioxide experimentally. The results show that ionic S-O bonding dominates over hypervalency.

DiffractionSulfonylchemistry.chemical_classificationMolecular StructureChemistryInorganic chemistryHypervalent moleculeIonic bondingGeneral ChemistryBond orderCatalysischemistry.chemical_compoundX-Ray DiffractionX-ray crystallography540 ChemistryHumansSulfur DioxideMoleculePhysical chemistry570 Life sciences; biologySulfur dioxide
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