Search results for "ionization"

showing 10 items of 1255 documents

Stable adducts of nerve agents sarin, soman and cyclosarin with TRIS, TES and related buffer compounds—Characterization by LC-ESI-MS/MS and NMR and i…

2009

Abstract Buffering compounds like TRIS are frequently used in chemical, biochemical and biomedical applications to control pH in solution. One of the prerequisites of a buffer compound, in addition to sufficient buffering capacity and pH stability over time, is its non-reactivity with other constituents of the solution. This is especially important in the field of analytical chemistry where analytes are to be determined quantitatively. Investigating the enzymatic hydrolysis of G-type nerve agents sarin, soman and cyclosarin in buffered solution we have identified stable buffer adducts of TRIS, TES and other buffer compounds with the nerve agents. We identified the molecular structure of the…

TrisSpectrometry Mass Electrospray IonizationMagnetic Resonance SpectroscopyBicineSomanClinical BiochemistryAnalytical chemistryCyclosarinBiochemistryAnalytical Chemistrychemistry.chemical_compoundOrganophosphorus CompoundsTandem Mass SpectrometryChemical Warfare AgentsTromethamineTE bufferTBE bufferTricineAqueous solutionChromatographyChemistryCell BiologyGeneral MedicineHydrogen-Ion ConcentrationSarinMOPSModels ChemicalChromatography LiquidJournal of Chromatography B
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Stark ionization of atoms and molecules within density functional resonance theory

2013

We show that the energetics and lifetimes of resonances of finite systems under an external electric field can be captured by Kohn–Sham density functional theory (DFT) within the formalism of uniform complex scaling. Properties of resonances are calculated self-consistently in terms of complex densities, potentials, and wave functions using adapted versions of the known algorithms from DFT. We illustrate this new formalism by calculating ionization rates using the complex-scaled local density approximation and exact exchange. We consider a variety of atoms (H, He, Li, and Be) as well as the H2 molecule. Extensions are briefly discussed.

TunnelingFOS: Physical sciences02 engineering and technology01 natural sciences7. Clean energySettore FIS/03 - Fisica Della MateriaOpen quantum systemsComplex scalingPhysics - Chemical PhysicsIonizationElectric field0103 physical sciencesExcitationsPhysics::Atomic and Molecular ClustersMoleculeGeneral Materials SciencePhysical and Theoretical ChemistryPhysics::Chemical Physics010306 general physicsWave functionScalingSpectroscopyPhysicsChemical Physics (physics.chem-ph)Condensed Matter - Materials ScienceLasersAtoms in moleculesMaterials Science (cond-mat.mtrl-sci)021001 nanoscience & nanotechnologyResonancesDensity functional theoryLocal-density approximationAtomic physics0210 nano-technologyJournal of Physical Chemistry Letters
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Analysis of β2-agonists in cattle hair samples using a rapid UHPLC–ESI–MS/MS method

2016

A simple and efficient method was developed for simultaneous analysis of five illegal residual β2-agonists in cattle hair. β2-Agonists were quantified by ultra high performance liquid chromatography coupled with electrospray ionisation tandem mass spectrometry operating in positive multiple-reaction monitoring mode. The method was validated as quantitative confirmatory method according to the EU Decision 2002/657/EC: instrumental linearity, specificity, precision, recovery, decision limit (CCα) and detection capability (CCβ) were evaluated. The recovery were greater than 90% and the method appeared suitable for the control of these β2-agonists in cattle hair samples with LOQ values between …

UHPLC –ESI–MS/MSβ2-agonist0301 basic medicineElectrospray030109 nutrition & dieteticsChromatographycattle hair; Commission Decision 2002/657/EC; UHPLC–ESI–MS/MS; β2-agonists; Plant Science; Biochemistry; Analytical Chemistry; Organic ChemistryChemistryβ2 agonistsElectrospray ionization010401 analytical chemistryOrganic ChemistryPlant ScienceContaminationTandem mass spectrometry01 natural sciencesBiochemistry0104 chemical sciencesAnalytical Chemistry03 medical and health sciencesCommission Decision 2002/657/ECcattle hairAdrenergic beta-AgonistsUltra high performanceDecision limitNatural Product Research
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VEH electronic structure of Si60

1993

Abstract We present a valence effective Hamiltonian (VEH) theoretical investigation on the electronic structure of Si60. The VEH one-electron energy level distribution calculated for Si60 is used to predict the ionization potential (7.86 eV), electron affinity (6.62 eV) and HOMO-LUMO energy gap (1.24 eV) of Si60. We also report the first allowed electronic transitions of Si60. The results are compared with other theoretical levels and with those calculated for C60.

Valence (chemistry)ChemistryBand gapMechanical EngineeringMetals and AlloysElectronic structureCondensed Matter PhysicsMolecular physicsElectronic Optical and Magnetic Materialssymbols.namesakeMechanics of MaterialsAtomic electron transitionMaterials ChemistrysymbolsIonization energyAtomic physicsHamiltonian (quantum mechanics)Synthetic Metals
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A theoretical determination of the electronic spectrum of formaldehyde

1995

The electronically excited states of formaldehyde are examined by means of multiconfigurational second-order perturbation (CASPT2) theory with extended ANO-type basis sets. The calculations comprised five valence excited states plus all singlet 3s, 3p, and 3d members of the Rydberg series converging on the first ionization. The computed vertical excitation energies were found to be within 0.2 eV of the available experimental energies. Full geometry optimization has been performed for five valence excited states. Assuming a planar geometry, the “0-0” transition for the valence1A1(π → π*) state is calculated to appear near 7.9 eV, close to the (n y → 3p) region. This state is, however, not pl…

Valence (chemistry)ChemistryEnergy minimizationsymbols.namesakeExcited stateIonizationRydberg formulasymbolsChiropracticsSinglet statePhysical and Theoretical ChemistryAtomic physicsAdiabatic processExcitationTheoretica Chimica Acta
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Theoretical study of the electronic spectrum of p-benzoquinone

1999

The electronic excited states of p-benzoquinone have been studied using multiconfigurational second-order perturbation theory (CASPT2) and extended atomic natural orbital (ANO) basis sets. The calculation of the singlet–singlet and singlet–triplet transition energies comprises 19 valence singlet excited states, 4 valence triplet states, and the singlet 3s,3p, and 3d members of the Rydberg series converging to the first four ionization limits. The computed vertical excitation energies are found to be in agreement with the available experimental data. Conclusive assignments to both valence and Rydberg states have been performed. The main features of the electronic spectrum correspond to the π…

Valence (chemistry)ChemistryExcited statesGeneral Physics and AstronomyPerturbation theoryTriplet stateRydberg statesSpectral lineUNESCO::FÍSICA::Química físicaOrbital calculationssymbols.namesakeOrganic compounds Spectra ; Excited states ; Perturbation theory ; Triplet state ; Rydberg states ; Orbital calculationsOrganic compounds SpectraExcited stateIonizationRydberg formulasymbolsSinglet statePhysical and Theoretical ChemistryAtomic physicsTriplet state:FÍSICA::Química física [UNESCO]Excitation
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Full configuration interaction calculation of the low lying valence and Rydberg states of BeH

2007

The all-electron full configuration interaction (FCI) vertical excitation energies for some low lying valence and Rydberg excited states of BeH are presented in this article. A basis set of valence atomic natural orbitals has been augmented with a series of Rydberg orbitals that have been generated as centered onto the Be atom. The resulting basis set can be described as 4s2p1d/2s1p (Be/H) + 4s4p3d. It allows to calculate Rydberg states up to n= {3,4,5} of the s, p, and d series of Rydberg states. The FCI vertical ionization potential for the same basis set and geometry amounts to 8.298 eV. Other properties such as FCI electric dipole and quadrupole moments and FCI transition dipole and qua…

Valence (chemistry)ChemistryGeneral ChemistryFull configuration interactionComputational Mathematicssymbols.namesakeDipoleExcited stateRydberg atomRydberg formulasymbolsPhysics::Atomic PhysicsIonization energyAtomic physicsBasis setJournal of Computational Chemistry
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Electronic Excitation in a Saturated Chain:  An MS-CASPT2 Treatment of the Anti Conformer of n-Tetrasilane

2000

The singlet−singlet electronic spectrum of the anti conformer of n-tetrasilane has been studied using multiconfigurational wave functions (CASSCF), second-order perturbation theory (CASPT2), and its multi-state extension (MS-CASPT2), in conjunction with large ANO-type basis sets including Rydberg functions. The calculations include the 4s, 4p, and 3d members of the Rydberg series converging on the first ionization. Mixing of valence and Rydberg states observed in the CASSCF wave functions is not fully rectified by single-reference CASPT2 theory, whereas the MS-CASPT2 method separates the valence and Rydberg states effectively. At the MS-CASPT2 level, six valence excited states have been fou…

Valence (chemistry)Chemistrysymbols.namesakeAtomic orbitalIonizationExcited stateRydberg formulasymbolsPhysics::Atomic PhysicsPhysical and Theoretical ChemistryAtomic physicsWave functionConformational isomerismExcitationThe Journal of Physical Chemistry A
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On the dissociation energy of Cu2 and CuH using a differential correlation approach

1990

The energy contributions involved in the “dissociation-consistent configuration interaction” (DCCI) scheme proposed by Goddard and co-workers plus the dispersion effects associated with the valence MOs adjacent to the bond (DISP) are evaluated for the Cu2 and CuH systems, following the “configuration interaction by perturbation with multiconfigurational zeroth-order wavefunction selected by iterative process” (CIPSI) algorithm. Using a relativistic pseudopotential to represent the neon core of copper, and a flexible basis set for the valence shell, the results obtained with the CIPSI/DCCI (+ DISP) approach shows a good agreement with previous theoretical results employing basis sets of simi…

Valence (chemistry)Electronic correlationChemistryGeneral Physics and AstronomyConfiguration interactionBond-dissociation energyMolecular physicsPseudopotentialComputational chemistryPhysics::Atomic and Molecular ClustersPhysical and Theoretical ChemistryIonization energyValence electronBasis setChemical Physics
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Electronic Transitions in Tetrathiafulvalene and Its Radical Cation:  A Theoretical Contribution

2001

The low-lying electronic states of tetrathiafulvalene (TTF) and its radical cation (TTF+) have been studied using the multistate extension of a multiconfigurational second-order perturbation method (MS−CASPT2). The minimum-energy equilibrium geometries optimized at the CASSCF level have a boatlike conformation for the neutral molecule, with no significant barrier toward planarity. A more aromatic planar structure is, however, found for the ionic system. For TTF, the calculations of the vertical excitation energies comprise valence singlet and triplet states as well as the lowest members of the Rydberg series converging to the first ionization limit. Valence doublet states have been consider…

Valence (chemistry)Ionic bondingMolecular physicschemistry.chemical_compoundsymbols.namesakechemistryRadical ionComputational chemistryIonizationPhysics::Atomic and Molecular ClustersRydberg formulasymbolsCondensed Matter::Strongly Correlated ElectronsSinglet statePhysical and Theoretical ChemistryIonization energyTetrathiafulvaleneThe Journal of Physical Chemistry A
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