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Shift atomic

Fig. VIII-8. Surface structures (a) (1 x 1) structure on the (100) surface of a FCC crystal (from Ref. 76) (b) C(2 x 1) surface structure on the (100) surface of a FCC ciystal (from Ref. 76). In both cases the unit cell is indicated with heavy lines, and the atoms in the second layer with pluses. In (b) the shaded circles mark shifted atoms. (See also Ref. 77.)... Fig. VIII-8. Surface structures (a) (1 x 1) structure on the (100) surface of a FCC crystal (from Ref. 76) (b) C(2 x 1) surface structure on the (100) surface of a FCC ciystal (from Ref. 76). In both cases the unit cell is indicated with heavy lines, and the atoms in the second layer with pluses. In (b) the shaded circles mark shifted atoms. (See also Ref. 77.)...
Figure 14 Mechanism of oxygen elimination from the structure of BajYC Oy 0. (a) As an effect of temperature increase, atom A may jump into position A (b) As a consequence of this shift, atom B may jump into position B, C into C etc., thus causing a correlated motion of the oxygen atoms terminating with the expulsion of half oxygen atom from the structure (c) Atom C now may jump into positions C or C" generating a second cascade... Figure 14 Mechanism of oxygen elimination from the structure of BajYC Oy 0. (a) As an effect of temperature increase, atom A may jump into position A (b) As a consequence of this shift, atom B may jump into position B, C into C etc., thus causing a correlated motion of the oxygen atoms terminating with the expulsion of half oxygen atom from the structure (c) Atom C now may jump into positions C or C" generating a second cascade...
One point which such a model brings out is that if one introduces holes into the A lattice by shifting atoms from interior to surface sites, then one reduces the number of interstitial sites in the crystal available for occupation by... [Pg.48]

TABLE 17. 29Si chemical shifts atom incorporated in the ring of cyclic silanes with one silicon... [Pg.534]

The transition matrix elements in the two processes are different dipole (PES) vs. Coulomb-type (for the decay process in RPE), and each has its own molecular dynamics. These different matrix elements and the involvement of an intermediate, core-excited state in RPE often result in altered intensity ratios of the spectral features [28,29] and a different relative population of vibrational states [28]. Since core excitations are site-specific for different elements or chemically shifted atoms [30], with well-defined and separated absorption edges, RPE may supply information on the local electronic structure [31-33]. [Pg.913]

Laser pulse profile exciting an atom moving along 3 Xi+Vit. Stationary atoms experience a pulse separation of t2-tj X. The frequencies co and (O are resonant with the Doppler shifted atomic frequencies at Cl and il. ... [Pg.91]

Fig. 6-1. Transformation of displacements in linear symmetric triatomic molecule by the inversion operation, i. Note that shifted atoms (1 and 2) make no contribution to xi = —3. Fig. 6-1. Transformation of displacements in linear symmetric triatomic molecule by the inversion operation, i. Note that shifted atoms (1 and 2) make no contribution to xi = —3.
K. Heilig, A. Steudel Changes in mean square nuclear charge radii from optical isotope shifts. Atomic Data and Nuclear Data Tables 14, 613 (1974)... [Pg.352]

The coexistence of both intermediate excitons and broadened and shifted atomic lines in a rather wide density rangy is readily explained. Consider the density fluctuations in the fluid and assume that for the existence of an intermediate exciton it is essential to have a certain minimum number of atoms, near enough to each other in order to make excitation transfer between them possible (Laporte and Steinberger, 1977). This is closely connected with the work of Logan and Wolynes (1984), dealing with the localization of an excitation in a dense fluid the exciton is the de-localized entity. Clear correlation could be found... [Pg.246]

The difference between real tools and a chemist s tools, is that the latter are exquisitely refined, for they need to shift atoms around. To make a new form of matter, perhaps one that does not exist anywhere else in the universe or simply to satisfy an existing demand, a chemist needs to be able to cajole, induce, tempt, batter, urge individual atoms to leave their current partners in one substance and join those from another substance. The new linkages must also be organized in specific ways, sometimes in assemblages... [Pg.1]


See other pages where Shift atomic is mentioned: [Pg.297]    [Pg.298]    [Pg.414]    [Pg.89]    [Pg.481]    [Pg.221]    [Pg.386]    [Pg.447]    [Pg.482]    [Pg.203]    [Pg.134]    [Pg.1072]    [Pg.442]    [Pg.626]    [Pg.133]    [Pg.698]   
See also in sourсe #XX -- [ Pg.515 ]




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Amino acid, carbon atoms, chemical shifts

Atomic charges and NMR shifts

Atomic orbitals chemical shifts

Carbon atoms chemical shifts

Carbon atoms, chemical shifts effect

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Chemical shift atoms

Chemical shift hydrogen atoms

Gauge-including atomic orbital chemical shifts

Gauge-including atomic orbitals chemical shift shielding calculation

Gauge-including atomic orbitals shifts

Hydrogen atom 1,5-sigmatropic shift

Hydrogen atom 1,7-shifts thermally

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