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Ultraviolet photoelectron spectrometry

Charge distributions and bonding in compounds of Cd and Hg in the solid and gaseous states can be studied by the well-established X-ray photoelectron spectrometry (XPS) and ultraviolet photoelectron spectrometry (UPS), respectively. With XPS, inner-shell electrons are removed which are indirectly influenced by the bonding, i.e., distribution of the valence electrons. UPS sees this electron distribution directly, since it measures the residual kinetic energies of electrons removed from the valence shells of the atoms, or, better, from the outer occupied orbitals of the molecules. The most detailed information accessible by UPS is obtained on gases, and it is thus applied here to volatile compounds, i.e., to the halides mainly of Hg and to organometallic compounds. [Pg.1256]

ARUPS Angle Resolved Ultraviolet Photoelectron Spectrometry... [Pg.22]

NIRMS = noble-gas-ion reflection mass spectrometry OSEE = optically stimulated exoelectron emission PES = photoelectron spectroscopy PhD = photoelectron diffraction SIMS = secondary ion mass spectroscopy UPS = ultraviolet photoelectron spectroscopy ... [Pg.398]

These sites can be studied by electron paramagnetic resonance (EPR), ultraviolet (UV) spectrometry, x-ray photoelectron spectroscopy (XPS), and other methods. Besides, a quantitative study of redox sites can be carried out with the help of a volumetric or gravimetric study of the adsorption of the oxidizing or the reducing molecules. [Pg.423]

The ultraviolet photoelectron spectra of diatomic alkali halide molecules are reviewed and interpreted. Data for lithium halide dimers, 112X2> are presented and it is shown that the dimers have significantly larger ionization thresholds than the corresponding monomers. Some historical controversies regarding the presence of dimers and their ionization energies are clarified. Photoionization mass spectrometry is used to determine the adiabatic ionization potential of lithium chloride trimer, in order to probe the trend of I.P. with cluster size. The predictions of Hartree-Fock, Xa and ionic model calculations on this point are presented. [Pg.274]

Ultraviolet photoelectron spectroscopy (UPS) of anionic C provides information on the electron affinity (EA), and electronic and vibrational structures of the corresponding neutral species. The size dependence of EAs and the vibrational fingerprints are useful to distinguish isomers when combined with mass spectrometry. In 1988 Yang et al. reported the first experimental indication of the presence of monocyclic carbon clusters C in laser vaporization of graphite in helium gas [17]. For clusters C ... [Pg.108]

Surface/interfaoe chemistry X-ray photoelectron spectros copy (XPS, ESCA) Auger electron spectroscopy (AES) Secondary ion mass spectros copy (SIMS) Rutherford backscattering spectrometry (RBS) Ultraviolet photoelectron spectroscopy (UPS) Infrared (IR) spectroscopy Raman spectroscopy... [Pg.155]

Photoelectron spectrometry is a surface analysis technique based on the detection of photoelectrons emitted from a solid sample upon irradiation with a UV (ultraviolet) discharge lamp, an X-ray tube, or a synchrotron source. By means of an electron... [Pg.5134]

Thermal scanning microscopy Temperature-time profile Time/temperature resolved pyrolysis mass spectrometry Thermal ultraviolet Thermal volatilisation analysis Thermal wave infrared imaging Transmission X-ray microscopy Total-reflection X-ray fluorescence (c/r. TRXRF) Ultrasonic force microscopy Ultraviolet photoelectron spectroscopy Ultrasound... [Pg.778]

Ultraviolet Spectroscopy. 3.5 IR Spectroscopy. 3.6 Mass Spectrometry. 3.7 Electron Spin Resonance. 3.8 Photoelectron Spectra 3.9 CD Spectra. 4 Thermodynamic Aspects. 4.1 Intermolecular Forces... [Pg.143]

Most physical properties of oxazoles have now been extensively explored. This chapter serves as an overview of the most important areas and updates the previous edition, in which the spectroscopic chapter remains relevant in aU details. NMR (surely now the single most important technique to the practicing organic chemist) is covered first and in the most detail, followed by a review of mass spectrometry, infrared and ultraviolet/visible spectroscopy, microwave spectroscopy, and other techniques. This order parallels that used in the previous edition, with some changes the proton and carbon NMR tables have been expanded, oxygen and fluorine NMR are now covered, as are microwave spectroscopy and other methods, such as photoelectron spectra. [Pg.391]


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Photoelectron spectrometry

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