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0 Is spectra

Figure 23 (a) C Is and 0 Is spectra of Cr(CO)6 (b) Schematic energy level diagram for a neutral metal CO system and two ionic states with a 2a (C Is) core hole... [Pg.3840]

The angular variation exhibited by the deposition products, particularly in the F Is and 0 Is spectra, indicates a fairly abrupt interface between the polymer and metallization reaction products. [Pg.137]

Fig. 21. C Is and 0 Is spectra from the surface of a thermally pressed poly(ethylene-co-methyl acrylate) film containing 23.4% methyl acrylate (45° take-off angle). Reproduced from Ref 13. Fig. 21. C Is and 0 Is spectra from the surface of a thermally pressed poly(ethylene-co-methyl acrylate) film containing 23.4% methyl acrylate (45° take-off angle). Reproduced from Ref 13.
Figure Bl.16.20. FTEPR spectra of photogenerated DQ m TXlOO solution for delay times between laser excitation of ZnTPPS and microwave pulse ranging from 20 ns to 11 ps. The central hyperfme line (M= 0) is at s - 4.5 MHz. Reprinted from [63]. Figure Bl.16.20. FTEPR spectra of photogenerated DQ m TXlOO solution for delay times between laser excitation of ZnTPPS and microwave pulse ranging from 20 ns to 11 ps. The central hyperfme line (M= 0) is at s - 4.5 MHz. Reprinted from [63].
The one-electron reduction of thiazole in aqueous solution has been studied by the technique of pulse radiolysis and kinetic absorption spectrophotometry (514). The acetone ketyl radical (CH ljCOH and the solvated electron e were used as one-electron reducing agents. The reaction rate constant of with thiazole determined at pH 8.0 is fe = 2.1 X 10 mole sec in agreement with 2.5 x 10 mole sec" , the value given by the National Bureau of Standards (513). It is considerably higher than that for thiophene (6.5 x 10" mole" sec" ) (513) and pyrrole (6.0 X10 mole sec ) (513). The reaction rate constant of acetone ketyl radical with thiazolium ion determined at pH 0.8 is lc = 6.2=10 mole sec" . Relatively strong transient absorption spectra are observed from these one-electron reactions they show (nm) and e... [Pg.135]

In spin relaxation theory (see, e.g., Zweers and Brom[1977]) this quantity is equal to the correlation time of two-level Zeeman system (r,). The states A and E have total spins of protons f and 2, respectively. The diagram of Zeeman splitting of the lowest tunneling AE octet n = 0 is shown in fig. 51. Since the spin wavefunction belongs to the same symmetry group as that of the hindered rotation, the spin and rotational states are fully correlated, and the transitions observed in the NMR spectra Am = + 1 and Am = 2 include, aside from the Zeeman frequencies, sidebands shifted by A. The special technique of dipole-dipole driven low-field NMR in the time and frequency domain [Weitenkamp et al. 1983 Clough et al. 1985] has allowed one to detect these sidebands directly. [Pg.116]

The XPS survey spectrum of a 75 nm thick film of plasma polymerized acetylene that was deposited onto a polished steel substrate is shown in Fig. 18 [22]. This film consisted mostly of carbon and a small amount of oxygen. Thus, the main peaks in the spectrum were attributed to C(ls) electrons near 284.6 eV and 0(ls) electrons near 533.2 eV. Additional weak peaks due to X-ray-induced O(KVV) and C(KLL) Auger electrons were also observed. High-resolution C(ls) and 0(ls) spectra are shown in Fig. 19. The C(ls) peak was highly symmetric. [Pg.268]

In the case where x and y are the same, C (r) is called an autocorrelation function, if they are different, it is called a cross-correlation function. For an autocorrelation function, the initial value at t = to is 1, and it approaches 0 as t oo. How fast it approaches 0 is measured by the relaxation time. The Fourier transforms of such correlation functions are often related to experimentally observed spectra, the far infrared spectrum of a solvent, for example, is the Foiuier transform of the dipole autocorrelation function. ... [Pg.380]

Figure 5.35. Effect of electrochemical O2- pumping on the O Is spectrum of Pt/YSZ6 (A-C). XPS spectra at 400°C (A) AUWR=0, 1=0 (B) AUWr=1-2 V, 1=40 pA (C) 0 Is difference spectrum.6 Reprinted with permission from the American Chemical Society. Figure 5.35. Effect of electrochemical O2- pumping on the O Is spectrum of Pt/YSZ6 (A-C). XPS spectra at 400°C (A) AUWR=0, 1=0 (B) AUWr=1-2 V, 1=40 pA (C) 0 Is difference spectrum.6 Reprinted with permission from the American Chemical Society.
The technique of SPEM allows one to obtain XPS spectra from extremely small (-0.02 pm2) surface areas and thus one can study O Is spectra obtained from small (-0.02 pm2) spots on the Pt surface.67... [Pg.252]

Conversely, under p-polarization (Fig. 8B), a splitting of the optical spectra with increasing 0 is observed One of the peaks is shifted toward high energy compared to that of isolated spherical particles, whereas the second one is at lower energy. [Pg.324]

The relaxation rates of the individual nuclei can be either measured or estimated by comparison with other related molecules. If a molecule has a very slow-relaxing proton, then it may be convenient not to adjust the delay time with reference to that proton and to tolerate the resulting inaccuracy in its intensity but adjust it according to the average relaxation rates of the other protons. In 2D spectra, where 90 pulses are often used, the delay between pulses is typically adjusted to 3T] or 4Ti (where T] is the spin-lattice relaxation time) to ensure no residual transverse magnetization from the previous pulse that could yield artifact signals. In ID proton NMR spectra, on the other hand, the tip angle 0 is usually kept at 30°-40°. [Pg.54]

Fig. 4.3 Ranges of isomer shifts observed for Fe compounds relative to metallic iron at room temperature (adapted from [24] and complemented with recent data). The high values above 1.4-2 mm s were obtained from Co emission experiments with insulators like NaCl, MgO or Ti02 [25-28], which yielded complex multi-component spectra. However, the assignment of subspectra for Fe(I) to Fe(III) in different spin states has never been confirmed by applied-field measurements, or other means. More recent examples of structurally characterized molecular Fe (I)-diketiminate and tris(phosphino)borate complexes with three-coordinate iron show values around 0.45-0.57 mm s [29-31]. The usual low-spin state for Fe(IV) with 3d configuration is 5 = 1 for quasi-octahedral or tetrahedral coordination. The low-low-spin state with S = 0 is found for distorted trigonal-prismatic sites with three strong ligands [30, 32]. Occurs only in ferrates. There is only one example of a molecular iron(VI) complex it is six-coordinate and has spin S = 0 [33]... Fig. 4.3 Ranges of isomer shifts observed for Fe compounds relative to metallic iron at room temperature (adapted from [24] and complemented with recent data). The high values above 1.4-2 mm s were obtained from Co emission experiments with insulators like NaCl, MgO or Ti02 [25-28], which yielded complex multi-component spectra. However, the assignment of subspectra for Fe(I) to Fe(III) in different spin states has never been confirmed by applied-field measurements, or other means. More recent examples of structurally characterized molecular Fe (I)-diketiminate and tris(phosphino)borate complexes with three-coordinate iron show values around 0.45-0.57 mm s [29-31]. The usual low-spin state for Fe(IV) with 3d configuration is 5 = 1 for quasi-octahedral or tetrahedral coordination. The low-low-spin state with S = 0 is found for distorted trigonal-prismatic sites with three strong ligands [30, 32]. Occurs only in ferrates. There is only one example of a molecular iron(VI) complex it is six-coordinate and has spin S = 0 [33]...
Fig. 4.14 Magnetically perturbed quadrupole spectra simulated for powder distributions of the EFG (Vzz > 0) with an applied field B = 4T which is fixed in the laboratory system perpendicular to the y-beam/ The value of the quadrupole splitting is kept constant at AEq = +4 mm s For negative quadrupole splitting (V z < 0), the spectra would be inverted on the velocity scale. Note the difference in relative intensities for the spectrum for ry = 0 and the single-crystal type spectrum given in Fig. 4.13. Similar patterns are obtained for B y... Fig. 4.14 Magnetically perturbed quadrupole spectra simulated for powder distributions of the EFG (Vzz > 0) with an applied field B = 4T which is fixed in the laboratory system perpendicular to the y-beam/ The value of the quadrupole splitting is kept constant at AEq = +4 mm s For negative quadrupole splitting (V z < 0), the spectra would be inverted on the velocity scale. Note the difference in relative intensities for the spectrum for ry = 0 and the single-crystal type spectrum given in Fig. 4.13. Similar patterns are obtained for B y...
Fig. 3. Amide F FTIR (left) and VCD (right) of effectively fully disordered systems, unblocked (L-Lys)2 (bottom) and (L-Lys)3 (top) in D2O, having one and two amide groups, respectively. The large deflection to low wavenumber is due to the terminal COO- group. The breadth of the K3 spectrum is due to different environments for the two C=0 groups. Spectra are offset for clarity, and the actual signals measured are roughly at our detection limits for reasonable S/N (A A 5 x 10-6). Fig. 3. Amide F FTIR (left) and VCD (right) of effectively fully disordered systems, unblocked (L-Lys)2 (bottom) and (L-Lys)3 (top) in D2O, having one and two amide groups, respectively. The large deflection to low wavenumber is due to the terminal COO- group. The breadth of the K3 spectrum is due to different environments for the two C=0 groups. Spectra are offset for clarity, and the actual signals measured are roughly at our detection limits for reasonable S/N (A A 5 x 10-6).

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See also in sourсe #XX -- [ Pg.163 , Pg.165 , Pg.166 ]




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