Search results for "ground"

showing 10 items of 2432 documents

Dipole moments of 4′-aminoflavonols determined using electro-optical absorption measurements or molecular Stark-effect spectroscopy

2002

The electro-optical absorption measurements (EOAM) were used to measure the dipole moments of the normal form of 4 � -(methoxy)-3hydroxyflavone (FOM), 4 � -(dimethylamino)-3-hydroxyflavone (FME), and 4 � -N-(15-azacrown-5)-3-hydroxyflavone (FCR). For these probes the excited state intramolecular proton transfer (ESIPT) takes place. For comparison, the dipole moments of 4 � -(dimethylamino)-3methoxyflavone (FME3ME), for which ESIPT is lacking, were measured. In the case of FCR, FME, and FME3ME the equilibrated ground (µg) and excited Franck–Condon state (µ FC ) electrical dipole moments are parallel to each other and also parallel to the transition dipole moment. The electrical dipole moment…

Bond dipole momentChemistryGeneral Chemical EngineeringTransition dipole momentGeneral Physics and AstronomyGeneral Chemistrysymbols.namesakeDipoleNuclear magnetic resonanceStark effectExcited statesymbolsAtomic physicsGround stateSpectroscopyExcitationJournal of Photochemistry and Photobiology A: Chemistry
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Structural symmetry breaking in octupolar tetrastyrylpyrazines and their dipole moments in equilibrium ground and Franck-Condon excited state

2018

Abstract From electrooptical absorption measurements (EOAM) follows that the dipole moment of octupolar tetrastyrylpyrazines in the equilibrium ground state is large and that the change of dipole moments upon transition to the excited Franck–Condon state is significant. Obtained results unambiguously testify to structural symmetry breaking in the studied octupolar tetrastyrylpyrazines. Molecular mechanics and semi-empirical calculations evidence that tetrastyrylpyrazines have non-planar configurations. The non-planar geometry of the molecules causes large μg values and significant change of dipole moment Δaμ after excitation. Due to large μg and Δaμ values the maxima of the first absorption…

Bond dipole momentCondensed matter physicsChemistryGeneral Chemical EngineeringTransition dipole momentGeneral Physics and Astronomy02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesMolecular physics0104 chemical sciencessymbols.namesakeDipoleAbsorption bandExcited statesymbolsSymmetry breakingPhysics::Chemical Physicsvan der Waals force0210 nano-technologyGround stateJournal of Photochemistry and Photobiology A: Chemistry
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Relativistic coupled cluster calculations of the electronic structure of KrH+, XeH+ and RnH+

2012

Potential energy curves of NgH+ cations (Ng = Kr, Xe, Rn) were obtained by using four-component relativistic CCSD(T) coupled cluster calculations. Dissociation energies, equilibrium bond lengths, electronic properties, such as dipole moments and electric field gradients at the nuclei, and the related spectroscopic parameters of the electronic ground state have been determined. The results obtained for KrH+ and XeH+ are in good agreement with available experimental data, while those for RnH+ have been determined for the first time at this level of theory.

Bond lengthDipoleCoupled clusterChemistryElectric fieldRelativistic effects Coupled cluster Protonated noble gasesElectronic structurePhysical and Theoretical ChemistryAtomic physicsGround statePotential energyDissociation (chemistry)Theoretical Chemistry Accounts
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GERMANIUM DICARBIDE: EVIDENCE FOR A T−SHAPED GROUND STATE STRUCTURE

2017

The equilibrium structure of germanium dicarbide GeC2 has been an open question since the late 1950s. Although most high-level quantum calculations predict an L-shaped geometry, a T-shaped or even a linear geometry cannot be ruled out because of the very flat potential energy surface. By recording the rotational spectrum of this dicarbide using sensitive microwave and millimeter techniques, we unambiguously establish that GeC2 adopts a vibrationally averaged T-shaped structure in its ground state. From analysis of 14 isotopologues, a precise r0 structure has been derived, yielding a Ge–C bond length of 1.952(1) A and an apex angle of 38.7(2)°.

Bond lengthMaterials sciencechemistryPotential energy surfacechemistry.chemical_elementMillimeterIsotopologueGermaniumLinear molecular geometryGround stateMolecular physicsMicrowaveNuclear chemistryProceedings of the 72nd International Symposium on Molecular Spectroscopy
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Synthesis, crystal structure and magnetic properties of the complex [ReCl3(tppz)]·MeCN

2015

The reaction of the starting materials [ReIIICl3(MeCN)(PPh3)2] or [ReVOCl3(PPh3)2] with 2,3,5,6-tetrakis(2-pyridyl)pyrazine (tppz) in acetonitrile yielded the Re(III) complex [ReCl3(tppz)]·MeCN (1). This complex crystallizes in the monoclinic space group P21/n and its crystal structure consists of neutral mononuclear entities with meridional geometry of the chloride ligands, and the six-coordination of the Re(III) ion being completed by the tridentate tppz ligand. Each metal centre exhibits a highly distorted octahedral coordination with Re–Cl and Re–Ntppz bond lengths covering the ranges 2.3590(9)–2.3606(8) and 1.971(2)–2.096(2) A, respectively. The magnetic properties of 1 have been inves…

Bond lengthParamagnetismCrystallographyTetragonal crystal systemchemistry.chemical_compoundPyrazineChemistryGeneral Chemical EngineeringGeneral ChemistryCrystal structureGround stateMagnetic susceptibilityMonoclinic crystal systemRSC Advances
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Increasing the nuclearity and spin ground state in a new family of ferromagnetically-coupled {Ni10} disk-like complexes bearing exclusively end-on br…

2018

The synthesis of a new family of ferromagnetically-coupled {Ni10} clusters counterbalanced by various [Ln(NO3)5]2− ions is herein described. The resulting compounds are organic chelate-free and the metal ions are exclusively bridged by end-on azido ligands to stabilize a beautiful disk-like topology reminiscent of the structure of the brucite mineral.

Bridging (networking)010405 organic chemistryChemistryBruciteMetal ions in aqueous solutionMetals and AlloysGeneral Chemistryengineering.material010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsIonCrystallographyMaterials ChemistryCeramics and CompositesengineeringGround stateChemical Communications
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Tailoring the Exchange Interaction in Covalently Linked Basic Carboxylate Clusters through Bridging Ligand Selection

2012

We are reporting new dimeric units of basic carboxylates bearing the {Fe III 2M IIO} motif for M = Co and Ni, covalently bound through the tetradentate bridging (LL) 2,2′-azopyiridine (azpy) and 2,3-di(2-pyridyl)quinoxaline ligands (dpq). We structurally characterized the hexanuclear clusters, and their magnetic properties have been fully analyzed. DFT calculations have been performed as a supplementary tool. All results evidence a weak antiferromagnetic interaction through the bridging ligands between isolated spin ground states arising from intra-Fe 2MO core exchange couplings. Together with the pioneer 2,2′-bipyrimidine bridged systems, the new complexes reported constitute a family of c…

Bridging (networking)LigandStereochemistryOtras Ciencias QuímicasExchange interactionCiencias QuímicasQUANTUM INFORMATIONBridging ligandSINGLE-MOLECULE MAGNETS//purl.org/becyt/ford/1 [https]Inorganic Chemistrychemistry.chemical_compoundQuinoxalinechemistryGROUND SPIN-STATECovalent bond//purl.org/becyt/ford/1.4 [https]AntiferromagnetismCarboxylatePIVALATE COMPLEXESPhysical and Theoretical ChemistryCIENCIAS NATURALES Y EXACTASInorganic Chemistry
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First M87 Event Horizon Telescope Results. IV. Imaging the Central Supermassive Black Hole

2019

We present the first Event Horizon Telescope (EHT) images of M87, using observations from April 2017 at 1.3 mm wavelength. These images show a prominent ring with a diameter of ~40 μas, consistent with the size and shape of the lensed photon orbit encircling the "shadow" of a supermassive black hole. The ring is persistent across four observing nights and shows enhanced brightness in the south. To assess the reliability of these results, we implemented a two-stage imaging procedure. In the first stage, four teams, each blind to the others' work, produced images of M87 using both an established method (CLEAN) and a newer technique (regularized maximum likelihood). This stage allowed us to av…

Brightness010504 meteorology & atmospheric sciencesgalaxies: jetAstronomyblack hole physicsFOS: Physical sciencesgalaxies: individualtechniques: image processingAstrophysicsGeneral Relativity and Quantum Cosmology (gr-qc)galaxies: individual: M8701 natural sciencesSynthetic dataGeneral Relativity and Quantum Cosmologygalaxies: individual (M87)0103 physical sciencesimage processing [Techniques]010303 astronomy & astrophysicsInstrumentation and Methods for Astrophysics (astro-ph.IM)0105 earth and related environmental sciencesEvent Horizon TelescopePhysicsGround truthSupermassive black holetechniques: high angular resolutionAstronomy and AstrophysicsBlack hole physicsgalaxies: jetsindividual (M87) [Galaxies]Astrophysics - Astrophysics of Galaxiesblack hole physic3. Good healthOrbitInterferometryhigh angular resolution [Techniques]Space and Planetary Sciencetechniques: interferometricAstrophysics of Galaxies (astro-ph.GA)interferometric [Techniques]jets [Galaxies]Deconvolution[PHYS.ASTR]Physics [physics]/Astrophysics [astro-ph]Astrophysics - Instrumentation and Methods for Astrophysics
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Three-Dimensional Calibration for Routine Analyses of Bromide and Nitrate Ions as Indicators of Groundwater Quality in Coastal Territories

2019

Nitrate and bromide ions are generally considered indicators of anthropogenic pollution and seawater intrusion, respectively, in the groundwater of coastal territories. The analysis of these species is generally carried out with routine chromatographic analyses which generally afford partially merged or poorly resolved peaks. In the present paper a simple method for the correct evaluation of their concentration in water is reported. This method does not imply utilization of other instruments or technologies, only the mathematical elaboration of the data obtained from routine analysis of standard solutions containing the two species. Standard binary solutions of nitrate and bromide ions at d…

Bromidespeak separationpoor resolved peaksHealth Toxicology and MutagenesisIon chromatographyAnalytical chemistrylcsh:MedicineChemical010501 environmental sciencesStandard solutionNitrate01 natural sciencesArticleIonPeak separationchemistry.chemical_compoundNitrateGroundwater qualityBromide3D calibration; Bromide; Groundwater quality; Nitrate; Peak separation; Poor resolved peaks; Bromides; Calibration; Environmental Monitoring; Groundwater; Nitrates; Water Pollutants Chemical; Water QualitynitrateWater QualityCalibrationPoor resolved peaksWater PollutantsWater pollutionGroundwater0105 earth and related environmental sciencesbromideNitrates010405 organic chemistrylcsh:RPublic Health Environmental and Occupational Health0104 chemical scienceschemistryPoor resolved peakBromideCalibrationEnvironmental scienceGroundwaterWater Pollutants ChemicalEnvironmental Monitoring3D calibrationInternational Journal of Environmental Research and Public Health
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Theoretical study of the low‐lying states of trans‐1,3‐butadiene

1992

We present extensive ab initio calculations on the low‐lying electronic states of trans‐1,3‐butadiene within the multireference configuration interaction (MRCI) framework by selecting the configurations with a perturbative criterion. The X 1Ag ground state and 1 3Bu, 1 3Ag, 2 1Ag, and 1 1Bu valence excited states have been calculated at a fixed geometry. The results obtained are in good agreement with previous experimental and calculated values, and could help to understand polyene spectroscopy, photochemistry, and photophysics. The advantages of a MRCI method where the most important contributions to the total MRCI wave function, perturbatively selected, are treated variationally, and the …

ButadieneElectronic correlationChemistryGeneral Physics and AstronomyMultireference configuration interactionPolyenesConfiguration interactionChromophoresUNESCO::FÍSICA::Química físicaConfiguration InteractionComputational chemistryAb initio quantum chemistry methodsExcited stateButadiene ; Ab Initio Calculations ; Configuration Interaction ; Perturbation Theory ; Energy Levels ; Molecular Orbital Method ; Polyenes ; Biology ; ChromophoresEnergy LevelsPerturbation TheoryPerturbation theory (quantum mechanics)Molecular Orbital MethodPhysical and Theoretical ChemistryAtomic physicsGround stateWave function:FÍSICA::Química física [UNESCO]Ab Initio CalculationsBiology
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