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Ionization energies spectra

Figure Bl.6.12 Ionization-energy spectrum of carbonyl sulphide obtained by dipole (e, 2e) spectroscopy [18], The incident-electron energy was 3.5 keV, the scattered incident electron was detected in the forward direction and the ejected (ionized) electron detected in coincidence at 54.7° (angular anisotropies cancel at this magic angle ). The energy of the two outgoing electrons was scaimed keeping the net energy loss fixed at 40 eV so that the spectrum is essentially identical to the 40 eV photoabsorption spectrum. Peaks are identified with ionization of valence electrons from the indicated molecular orbitals. Figure Bl.6.12 Ionization-energy spectrum of carbonyl sulphide obtained by dipole (e, 2e) spectroscopy [18], The incident-electron energy was 3.5 keV, the scattered incident electron was detected in the forward direction and the ejected (ionized) electron detected in coincidence at 54.7° (angular anisotropies cancel at this magic angle ). The energy of the two outgoing electrons was scaimed keeping the net energy loss fixed at 40 eV so that the spectrum is essentially identical to the 40 eV photoabsorption spectrum. Peaks are identified with ionization of valence electrons from the indicated molecular orbitals.
There are several methods of producing gas-phase inorganic ions, the starting materials in mass spectrometric studies. The properties of the source of the ions required for study are important in the choice of ionization method. The production of bare metal ions from an involatile nonmolecular source requires a large amount of energy deposited on the surface of the material. The processes that occur after the initial ionization process may also affect the ions finally observed (e.g., clustering). At the other end of the ionization energy spectrum, gas-phase ions of a complexity similar to those observed in the condensed phases require a soft ionization process. A brief description of some of the ionization methods follows. [Pg.352]

Time-of-flight mass spectrometers have been used as detectors in a wider variety of experiments tlian any other mass spectrometer. This is especially true of spectroscopic applications, many of which are discussed in this encyclopedia. Unlike the other instruments described in this chapter, the TOP mass spectrometer is usually used for one purpose, to acquire the mass spectrum of a compound. They caimot generally be used for the kinds of ion-molecule chemistry discussed in this chapter, or structural characterization experiments such as collision-induced dissociation. Plowever, they are easily used as detectors for spectroscopic applications such as multi-photoionization (for the spectroscopy of molecular excited states) [38], zero kinetic energy electron spectroscopy [39] (ZEKE, for the precise measurement of ionization energies) and comcidence measurements (such as photoelectron-photoion coincidence spectroscopy [40] for the measurement of ion fragmentation breakdown diagrams). [Pg.1354]

Procedure. Use Mathcad, QLLSQ, or TableCurve (or, preferably, all three) to determine a value of the ionization energy of hydrogen from the wave numbers in Table 3-4 taken from spectroscopic studies of the Lyman series of the hydrogen spectrum where ni = 1. [Pg.76]

This point is illustrated in Figure 8.13 which shows the X-ray photoelectron spectrum of a 2 1 mixture of CO and CO2 gases obtained with MgXa (1253.7 eV) source radiation. The ionization energy for removal of an electron from the s orbital on a carbon atom, referred to as the C s ionization energy, is 295.8 eV in CO and 297.8 eV in CO2, these being quite comfortably resolved. The O s ionization energy is 541.1 eV in CO and 539.8 eV in CO2, which are also resolved. [Pg.307]

Figure 8.14 The monochromatized AlATa carbon Is X-ray photoelectron spectrum of ethyltrifluoroacetate showing the chemical shifts relative to an ionization energy of 291.2 eV (Reproduced, with permission, from Gelius, U., Basilier, E., Svensson, S., Bergmark, T. and Siegbahn, K., J. Electron Spectrosc., 2, 405, 1974)... Figure 8.14 The monochromatized AlATa carbon Is X-ray photoelectron spectrum of ethyltrifluoroacetate showing the chemical shifts relative to an ionization energy of 291.2 eV (Reproduced, with permission, from Gelius, U., Basilier, E., Svensson, S., Bergmark, T. and Siegbahn, K., J. Electron Spectrosc., 2, 405, 1974)...
Indazoles have been subjected to certain theoretical calculations. Kamiya (70BCJ3344) has used the semiempirical Pariser-Parr-Pople method with configuration interaction for calculation of the electronic spectrum, ionization energy, tt-electron distribution and total 7T-energy of indazole (36) and isoindazole (37). The tt-densities and bond orders are collected in Figure 5 the molecular diagrams for the lowest (77,77 ) singlet and (77,77 ) triplet states have also been calculated they show that the isomerization (36) -> (37) is easier in the excited state. [Pg.175]

The photoelectron spectrum of gaseous 82 has been measured and analyzed it provided the value of the ionization energy of this ion as 1.67 eV [135]. [Pg.147]

Figure 8. Photoelectron spectrum (PES) and Penning ionization electron spectrum (PIES) of nitric oxide radical. Average vibrational energy spacing of the first band amounts to 285 and 284 cm", respectively (104). Figure 8. Photoelectron spectrum (PES) and Penning ionization electron spectrum (PIES) of nitric oxide radical. Average vibrational energy spacing of the first band amounts to 285 and 284 cm", respectively (104).
Comparison between flame-sampled PIE curves for (a) m/z = 90 (C H ) and (b) m/z = 92 (C Hg) with the PIE spectra simulated based on a Franck-Condon factor analysis and the cold-flow PIE spectrum of toluene. Calculated ionization energies of some isomers are indicated. (From Hansen, N. et al., /. Phys. Chem. A, 2007. With permission.)... [Pg.9]

If the work function is smaller than the ionization potential of metastable state (see. Fig. 5.18b), then the process of resonance ionization becomes impossible and the major way of de-excitation is a direct Auger-deactivation process similar to the Penning Effect ionization a valence electron of metal moves to an unoccupied orbital of the atom ground state, and the excited electron from a higher orbital of the atom is ejected into the gaseous phase. The energy spectrum of secondary electrons is characterized by a marked maximum corresponding to the... [Pg.320]

The bonding in solids is similar to that in molecules except that the gap in the bonding energy spectrum is the minimum energy band gap. By analogy with molecules, the chemical hardness for covalent solids equals half the band gap. For metals there is no gap, but in the special case of the alkali metals, the electron affinity is very small, so the hardness is half the ionization energy. [Pg.193]


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See also in sourсe #XX -- [ Pg.436 ]




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