Search results for "Electron ionization"

showing 10 items of 82 documents

Mass spectra of halogenated esters 5—Chloromethyl esters of aliphatic C2C12n-carboxylic acids and their monochlorinated derivatives

1984

A study has been made of the mass spectral fragmentation upon electron impact of aliphatic C2C12 chloromethyl esters and all their 66 monochlorinated derivatives. The fragmentation pathways of the parent chloromethyl esters were elucidated with the aid of the 1st FFR metastable ions. A McLafferty rearrangement gives the base peak in the C6C11 parent esters and in almost all the 4-chloro and ω-chloro isomers. The subsequent loss of HCl gives a very characteristic peak of the chloromethyl esters and their (3-ω)-chloro derivatives at m/z 72, [C3H4O2]+. The 2-chloro isomers have the corresponding chlorine-containing fragment ion at m/z 106/108. The mass spectra of 2-, 3-, 4-, 5- and ω-chloro is…

McLafferty rearrangementFragmentation (mass spectrometry)ChemistryMass spectrumMolecular MedicineOrganic chemistryAliphatic compoundInstrumentationBiochemistryMedicinal chemistrySpectroscopyElectron ionizationIonOrganic Mass Spectrometry
researchProduct

Mass spectra of halogenated esters. 7. Methyl esters of 2-chloro C2C20n-alkanoic acids

1988

The mass spectral fragmentation of a homologous series of methyl esters of 2-chloro n-alkanoic acids ranging from acetic (C2) to eicosanoic (C20) acid on electron impact has been investigated. The fragmentation pathways were elucidated with the aid of the first field-free region metastable ions, the results being presented with one compound, i.e. with ionized methyl 2-chloro-octauoate. Owing to the Cl/H exchanges and to the formation of the non-chlorinated parent esters prior to the fragmentations the spectra show the peak pairs with and without the chlorine atom. The effects become more evident with increasing chain length; shown most visually by the abundance ratios of the McLafferty rear…

McLafferty rearrangementStereochemistryBiochemistryMedicinal chemistryIonHomologous serieschemistry.chemical_compoundchemistryFragmentation (mass spectrometry)IonizationMass spectrumMolecular MedicineAliphatic compoundInstrumentationSpectroscopyElectron ionizationOrganic Mass Spectrometry
researchProduct

Mass spectra of chlorinated veratroles (1,2-dimethoxybenzenes)

1987

The behaviour of all nine chlorinated veratroles (1,2-dimethoxybenzenes) under electron impact has been investigated. The most common fragmentation processes are interpreted using metastable ion analysis and deuterium labelled compounds. For all compounds studied, the most common fragmentation route seems to be the primary loss of a methyl radical followed by loss of carbon monoxide. The ion formed has a well-known quinonoid structure and fragments by several routes elucidated by metastable ion analysis. In general, the spectra of the positional isomers are shown to be practically similar and it is apparent that e.g. the 3- and 4-chloro isomers can be differentiated only from the abundance …

Methyl radicalPhotochemistryBiochemistryIonchemistry.chemical_compoundchemistryFragmentation (mass spectrometry)DeuteriumMass spectrumStructural isomerMolecular MedicineOrganic chemistryInstrumentationSpectroscopyElectron ionizationCarbon monoxideOrganic Mass Spectrometry
researchProduct

Characterization of isomeric 1,2,4-oxadiazolyl-N-methylpyridinium salts by electrospray ionization tandem mass spectrometry.

2007

The mass spectrometric behavior of 1,2,4-oxadiazolyl- N-methylpyridinium salts has been investigated. These substances are of current interest as perspective ionic liquids, compounds used as green solvents for synthesis, and for their catalytic properties. The studies have been developed through electrospray ionization tandem mass spectrometry (ESI-MS/MS) experiments. The obtained results demonstrate a ready distinction between the two isomeric classes, 3- N-methylpyridinium- and 5- N-methylpyridinium-1,2,4-oxadiazoles, is possible through ESI-MS/MS experiments. A deeper investigation on the principal fragmentation pathways of characteristic ions has been also developed.

Models MolecularSpectrometry Mass Electrospray IonizationProtein mass spectrometry020209 energyElectrospray ionizationIonic Liquids02 engineering and technologyTandem mass spectrometrySample preparation in mass spectrometrychemistry.chemical_compoundIsomerismESI-MS ionic kiquids oxadiazolylpyridiniumComputational chemistry0202 electrical engineering electronic engineering information engineeringDirect electron ionization liquid chromatography–mass spectrometry interfaceSpectroscopyChromatographySelected reaction monitoringExtractive electrospray ionizationGeneral MedicineAtomic and Molecular Physics and OpticschemistryModels ChemicalSpectrometry Mass Matrix-Assisted Laser Desorption-IonizationIonic liquidSaltsEuropean journal of mass spectrometry (Chichester, England)
researchProduct

A compact apparatus for mass selective resonance ionization spectroscopy in a buffer gas cell

1997

Abstract An ultra-sensitive laser spectroscopic method for the investigation of transuranium nuclides has been developed based on resonance ionization in an argon buffer gas cell. This method has been combined with ion-guide extraction and mass selective direct detection of the resonantly ionized atoms. Using argon as a buffer gas, recoils of fusion reactions can be thermalized even at low pressure. The differential pumping system consists of only one roots pump and two turbo molecular pumps. The set-up has been tested with 243 Am evaporated from a filament located inside the optical gas cell. Resonance ionization is performed using a two-step excitation with an excimer-dye-laser combinatio…

Nuclear and High Energy PhysicsArgonBuffer gasAnalytical chemistrychemistry.chemical_elementMass spectrometryIon sourceAtmospheric-pressure laser ionizationchemistryIonizationAtomic physicsInstrumentationQuadrupole mass analyzerElectron ionizationNuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms
researchProduct

Selective laser ionization of radioactive Ni-isotopes

1997

Abstract A chemically selective laser ion source based on resonance ionization of atoms in a hot cavity has been applied in the study of Ni-isotopes at the CERN-ISOLDE on-line isotope separator. Laser ionization enhanced the yields of long-lived Ni-isotopes almost four orders of magnitude when compared to the yields obtained with the surface ionization mode of the source. As a result, high yields of long-lived Ni-isotopes were obtained. Separation efficiencies of 0.3 and 0.8% were obtained for Ni produced in uranium-carbide, produced from uranium-di-pthalocyanine, and Ta-foil targets, respectively. Ni was found to be released very slowly from the present target and ion source combination.

Nuclear and High Energy PhysicsChemical ionizationMatrix-assisted laser desorption electrospray ionizationChemistryRadiochemistryAnalytical chemistryThermal ionizationIon sourceAtmospheric-pressure laser ionizationIonizationPhysics::Atomic PhysicsNuclear ExperimentInstrumentationElectron ionizationAmbient ionizationNuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms
researchProduct

Time profiles of ions produced in a hot-cavity resonant ionization laser ion source

2011

Abstract The time profiles of Cu, Sn, and Ni ions extracted from a hot-cavity resonant ionization laser ion source are investigated. The ions are produced in the ion source by three-photon resonant ionization with pulsed Ti:Sapphire lasers. Measurements show that the time spread of these ions generated within laser pulses of about 30 ns duration could be larger than 100 μs when the ions are extracted from the ion source. A one-dimensional ion-transport model using the Monte Carlo method is developed to simulate the time dependence of the ion pulses. The prediction of the model agrees reasonably well with the experimental data. To reproduce the observed ion time profiles, we find it necessar…

Nuclear and High Energy PhysicsChemistryIon gunCharged particleIon sourcelaw.inventionIonIon beam depositionPhysics::Plasma PhysicsReflectronlawIonizationAtomic physicsInstrumentationElectron ionizationNuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms
researchProduct

Production of molecular sideband radioisotope beams at CERN-ISOLDE using a Helicon-type plasma ion source

2013

In order to account for the increasing demand for strong molecular beams for nuclear physics experiments at ISOLDE, a new radioactive ion source concept based on an RE discharge in a magnetized plasma was developed at CERN. Experimental studies at the ISOLDE offline separator show that the optimum conditions for CO+ and CO2+ ion production are given when the ion source is operated with He plasma, in line with expectations based on their electron impact ionization cross-sections. At optimum tuning, ionization efficiencies of 2.5% and 4% were measured for CO+ and Ar+, respectively. The capability of the Helicon ion source prototype for ISOL operation was evaluated during two online runs at th…

Nuclear and High Energy PhysicsIon beam depositionLarge Hadron ColliderHeliconta114ChemistryIonizationPlasmaAtomic physicsInstrumentationIon sourceElectron ionizationIonNuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms
researchProduct

Development of resonance ionization in a supersonic gas-jet for studies of short-lived and long-lived radioactive nuclei

2013

High-resolution resonance ionization spectroscopy (RIS) is required for laser spectroscopy and trace analysis of short-lived and long-lived radioactive nuclei. We have proposed high-resolution resonance ionization spectroscopy in a gas jet combined with a narrow band-width injection-locked Ti:Sapphire laser. Resonance ionization of stable 93Nb in a gas jet was demonstrated using a broad bandwidth Ti:Sapphire laser. In addition, a setup for high-resolution RIS in a gas-jet was designed using numerical simulations of the gas-jet conditions based on computational fluid dynamics.

Nuclear and High Energy PhysicsJet (fluid)ta114ChemistryThermal ionizationInstrumental chemistryIon sourceAtmospheric-pressure laser ionizationPhysics::Atomic PhysicsAtomic physicsSpectroscopyInstrumentationElectron ionizationAmbient ionizationNuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms
researchProduct

Spin Polarization of Electrons by Resonance Scattering from Mercury

1980

Hg- compound ion states formed by electron impact with neutral mercury atoms at collision energies of 4.55, 4.71, 4.94, and 5.51 eV show up in the 2S1/2, 2D3/2, 2D5/2, and 2D5/2 scattering states in order of increasing energy. This identification is supported by the observed energy dependence of (i) elastic (e-, Hg) differential cross section, of (ii) 63P0 excitation of mercury by electron impact, and of (iii) spin polarization of electrons scattered elastically from mercury.

Nuclear magnetic resonanceX-ray Raman scatteringMaterials scienceSpin polarizationchemistryScatteringchemistry.chemical_elementElectronMott scatteringAtomic physicsElectron ionizationMercury (element)Ion
researchProduct