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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Rapid Communications in Mass Spectrometry 6 (1992), S. 438-448 
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: High-resolution double-charge-transfer spectroscopy has been used to measure the double-electron-capture reactions with CH4. Using kilo electron volt OH+, CI+ and F+ projectile ions it is possible in double-electron-capture reactions with CH4 molecules to populate the ground triplet state of CH42+. The energy of this state relative to the gound state of CH4 is found to be 38.2±0.4 eV, while the fiest excited triplet state is found at a double-ionization energy of 46.7±0.8 eV. In double-electron-capture reactions involving H+ projectile ions and CK4 molecules, low-lying singlet states of CH42+ are populated. The energies of the four lowest singlet states in CH42+ were measured to be 39.2±0.4, 40.5±0.4, 42.1±1 and 51.0±1 eV. High-resolution photon-induced Auger-electron spectra of the CH4 molecule have been recorded. The KLL Auger Spectrum shows four distinct structures in the 30-70 eV double-ionization evergy range centred at 40.3±0.1, 47.03, 53.2±0.3 and 6.9±0.3 eV. The previously published data on CH42+ have been reviewed.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 11 (1977), S. 317-324 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The basis set dependency of the core ionization potential of water was investigated for atomic optimized Cartesian Gaussian basis sets. Basis set parameters optimized for oxygen yielded better IP's than basis set parameters optimized for fluorine. Not much was gained by using different parameters for the ground state and for the 1s hole state.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 17 (1991), S. 94-104 
    ISSN: 0142-2421
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: High-resolution C is and O is gas-phase X-ray photoelectron spectra of methyl isobutyrate, methyl methacrylate, methyl acrylate, acrylic acid, acetic acid and formic acid have been investigated as model compounds for solid poly(methyl methacrylate) (PMMA). Secondary chemical shifts, variations in peak shapes and intensities for the different core lines were observed. It is shown that asymmetries and differences in line widths of the component peaks should be considered for a correct analysis of the solid polymer spectra. The observed intensities of the different C 1s and O is peaks in the gas-phase spectra do not follow stoichiometric ratios owing to different shake-off/shake-up probabilities. The gas-phase core electron binding energies have been compared with ab initio ΔSCF calculations where the relaxation of the core-hole state was included. Using a group shift argument, the relationship between the gas-phase model molecule shifts and the solid PMMA shifts have been discussed and applied to the analysis of the PMMA spectra.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0935-9648
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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