Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Level anticrossing

Optical Nuclear Polarization (MI-ONP). Formal Equivalence of Microwave-Induced Level-Anticrossing Optical Nuclear Polarization. Extreme Values for Polarization. [Pg.294]

Level anticrossings between states with complex energies in the... [Pg.787]

The mechanism of the level-anticrossing is relatively well understood,... [Pg.374]

The level-crossing and anticrossing phenomena have been observed for the first time for hyperfine components of atomic energy levels.The level-anticrossing spectroscopy was then applied to the study of very weak singlet-triplet (or doublet-quadruplet) coupling in atoms" and in diatomic molecules (see, e.g.. Refs. 124 and 125 and references therein). [Pg.374]

The level-anticrossing techinque offers thus a unique possibility for detailed studies of electronic relaxation, because intramolecular parameters which determine the relaxation rate (the spacing of zero order ) and /) levels and of quasi-stationary a > and X) states, the mixing coefficients and vary in a well-defined way with the strength of the magnetic field. [Pg.374]

Level Anticrossing and Cross-Relaxation Effects A. The Level Anticrossing Experiment Cross-Relaxation Effects Microwave Studies Radiofrequency Studies Lifetime Measurements VI. Coherence Experiments A. The Rotating Frame Free Precession Spin Echoes... [Pg.137]

Fig. 16. Level anticrossing spectra of the lowest triplet states of 4,4 -difiuorobenzophenone, C-benzophenone, C-benzophenone, 4,4 -dichlorobenzophenone, and 4,4 -dibromobenzo-phenone in 4,4 -dibromodiphenylether with H at 1.6K. Asterisks denote weak satellites observed in the spectrum of DCBP (Mucha and Pratt, 1977b). Fig. 16. Level anticrossing spectra of the lowest triplet states of 4,4 -difiuorobenzophenone, C-benzophenone, C-benzophenone, 4,4 -dichlorobenzophenone, and 4,4 -dibromobenzo-phenone in 4,4 -dibromodiphenylether with H at 1.6K. Asterisks denote weak satellites observed in the spectrum of DCBP (Mucha and Pratt, 1977b).
Fig. 17. Cross-relaxation model, which explains satellites observed in the level anticrossing spectra of triplet benzophenones in 4,4 -dibromodiphenylether. drawn approximately to scale for C-benzophenone with H z. The solid (dashed) arrows indicate field positions at which the triplet sublevel separations are equal to the Br ( Br) nuclear quadrupole frequencies of the host (Mucha and Pratt, 1977b). Fig. 17. Cross-relaxation model, which explains satellites observed in the level anticrossing spectra of triplet benzophenones in 4,4 -dibromodiphenylether. drawn approximately to scale for C-benzophenone with H z. The solid (dashed) arrows indicate field positions at which the triplet sublevel separations are equal to the Br ( Br) nuclear quadrupole frequencies of the host (Mucha and Pratt, 1977b).

See other pages where Level anticrossing is mentioned: [Pg.235]    [Pg.258]    [Pg.191]    [Pg.284]    [Pg.315]    [Pg.339]    [Pg.682]    [Pg.318]    [Pg.374]    [Pg.374]    [Pg.375]    [Pg.376]    [Pg.35]    [Pg.203]    [Pg.204]    [Pg.204]    [Pg.204]    [Pg.213]    [Pg.361]    [Pg.9]    [Pg.613]    [Pg.1139]    [Pg.142]   


SEARCH



Anticrossings

© 2024 chempedia.info