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Ionization energies for

The ionization energy for hydrogen is the minimum amount of energy that is required to bring about the reaction... [Pg.76]

The ionization energy for hydrogen (or other hydrogen-like systems) can be found from the Rydberg equation... [Pg.76]

The simplest, and perhaps the most important, information derived from photoelectron spectra is the ionization energies for valence and core electrons. Before the development of photoelectron spectroscopy very few of these were known, especially for polyatomic molecules. For core electrons ionization energies were previously unobtainable and illustrate the extent to which core orbitals differ from the pure atomic orbitals pictured in simple valence theory. [Pg.297]

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]

Optical absorption measurements give band-gap data for cubic sihcon carbide as 2.2 eV and for the a-form as 2.86 eV at 300 K (55). In the region of low absorption coefficients, optical transitions are indirect whereas direct transitions predominate for quantum energies above 6 eV. The electron affinity is about 4 eV. The electronic bonding in sihcon carbide is considered to be predominantiy covalent in nature, but with some ionic character (55). In a Raman scattering study of vahey-orbit transitions in 6H-sihcon carbide, three electron transitions were observed, one for each of the inequivalent nitrogen donor sites in the sihcon carbide lattice (56). The donor ionization energy for the three sites had values of 0.105, 0.140, and 0.143 eV (57). [Pg.465]

Table 3 Vertical Ionization Energies for some Thiiranes and Thiirenes... Table 3 Vertical Ionization Energies for some Thiiranes and Thiirenes...
ESCA has been used to determine the molecular structure of the fluoride lon-induced tnmenzation product of perfluorocyclobutene [74] and the products of the sodium borohydnde reduction of perfluoromdene [75] ESCA is also used to analyze and optimize gas-phase reactions, such as the bromination of trifluoro-methane to produce bromotrifluoromethane, a valuable fire suppression agent [76] The ionization energies for several hundred fluorme-containing compounds are summarized in a recent review [77]... [Pg.1033]

Figure 10.1 Suecessive ionization energies for Group 14 elements showing the influence of the Sd shell between Si and Ge and the 4f shell between Sn and Pb. Figure 10.1 Suecessive ionization energies for Group 14 elements showing the influence of the Sd shell between Si and Ge and the 4f shell between Sn and Pb.
The diagonal elements of the HF-LCAO matrix are taken to be the negatives of the valence shell ionization energy for the orbital in question. These can be determined from a study of atomic spectra. [Pg.130]

Between sodium and chlorine, there is a slow rise in ionization energy. For magnesium and aluminum the ionization energy is still rather low. Hence electrons are readily lost and positive ions can be expected to be important in the... [Pg.269]

From the following bond energy data and the ionization energies given in Table 15-111, calculate the entries in the last two columns of Table 16-111 for the compounds LiF and LiBr. The ionization energy, (, for bromine atom is 273 kcal/mole. [Pg.290]

Write out the electron configuration of sodium, magnesium, and aluminum and find the ionization energies for all their valence electrons (Table 20-IV, p. 374). Account for the trend in the heats of vaporization and boiling points (Table 20-1) of these elements. Compare your discussion with that given in Section 17-1.3. [Pg.365]

Ionization energies usually increase on going from left to right across the periodic table. The ionization energy for oxygen, however, is lower than that of either nitrogen or fluorine. Explain this anomaly. [Pg.178]

PIE curves for ra/z = 72 (C4H8O) measured in four butanol flames. The accepted ionization energies for species identified by the observed ionization thresholds are indicated. (From Yang, B. et at. Combust. Flame, 148,198, 2007. With permission.)... [Pg.11]

A multielectron atom can lose more than one electron, but ionization becomes more difficult as cationic charge increases. The first three ionization energies for a magnesium atom in the gas phase provide an illustration. (Ionization energies are measured on gaseous elements to ensure that the atoms are isolated from one another.)... [Pg.539]

Appendix C gives the first three ionization energies for the first 36 elements. [Pg.539]

Ionizing sodium atoms requires that energy be supplied, the amount being the first ionization energy for sodium Na(g) Na (g) +e AE = E — 495.5 kJ/mol... [Pg.546]

The chemistry of the transition metals is determined in part by their atomic ionization energies. Metals of the 3d and 4d series show a gradual increase in ionization energy with atomic number (Z), whereas the trend for the 5d series is more pronounced (Figure 20-3). First ionization energies for transition metals in the 3d and 4d series are between 650 and 750 kJ/mol, somewhat higher than the values for Group 2 alkaline earth metals but lower than the typical values for nonmetals in the p block. [Pg.1431]

The graph shows the first ionization energy for elements with atomic numbers 3-20. According to the graph, what is the approximate first ionization energy for the element with atomic number 16 ... [Pg.12]

A large nnmber of the measured ionization energies for stable neutral molecules come from electron impact appearance energy studies, but it has also been adapted for the direct study of reactive neutral molecules. If the reactant molecule is RH, then the appearance energy for R+ from RH, designated AE(R+, RH),... [Pg.215]

Few positive ion methods are generally applicable to the investigation of triradicals because of the problem of measuring ionization energies for di- and triradicals and... [Pg.233]

This energy is not likely to be repaid during compound formation. The reason for such a high second ionization energy for lithium is because the electron configuration of Li+ is Is2 which has a filled s orbital. It is the special stability of the filled s orbital which prevents the formation of Li2+ ions. Also, the formation of Li2+ requires 14 times more energy than the formation of Li+ and so is much less likely. [Pg.80]

TABLE 11. Calculated ionization energies for SnCp2 (38) and experimental ionization energies for SnCp2 (38), PbCp2 (39), SnCp 2 (40) and PbCp 2 (41). Reprinted with permission from Reference 140. Copyright (1982) American Chemical Society... [Pg.330]


See other pages where Ionization energies for is mentioned: [Pg.91]    [Pg.389]    [Pg.307]    [Pg.26]    [Pg.201]    [Pg.14]    [Pg.83]    [Pg.113]    [Pg.553]    [Pg.268]    [Pg.103]    [Pg.177]    [Pg.178]    [Pg.955]    [Pg.505]    [Pg.549]    [Pg.743]    [Pg.334]    [Pg.351]    [Pg.165]    [Pg.220]    [Pg.223]    [Pg.180]    [Pg.23]    [Pg.88]    [Pg.207]    [Pg.200]   
See also in sourсe #XX -- [ Pg.27 ]




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Ionization energy

Ionizing energy

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