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Modulation of transit

The transition from smectic A to smectic B phase is characterized by tire development of a sixfold modulation of density witliin tire smectic layers ( hexatic ordering), which can be seen from x-ray diffraction experiments where a sixfold symmetry of diffuse scattering appears. This sixfold symmetry reflects tire bond orientational order. An appropriate order parameter to describe tlie SmA-SmB phase transition is tlien [18,19 and 20]... [Pg.2560]

If the vibration does not produee a modulation of the dipole moment (e.g., as with the symmetrie streteh vibration of the CO2 moleeule), its infrared intensity vanishes beeause 0 i/3Ra) = 0. One says that sueh transitions are infrared "inaetive". [Pg.403]

Click Coached Problems for a self-study module on the geometry of transition metal complexes. [Pg.413]

The requirement I > 2 can be understood from the symmetry considerations. The case of no restoring force, 1=1, corresponds to a domain translation. Within our picture, this mode corresponds to the tunneling transition itself. The translation of the defects center of mass violates momentum conservation and thus must be accompanied by absorbing a phonon. Such resonant processes couple linearly to the lattice strain and contribute the most to the phonon absorption at the low temperatures, dominated by one-phonon processes. On the other hand, I = 0 corresponds to a uniform dilation of the shell. This mode is formally related to the domain growth at T>Tg and is described by the theory in Xia and Wolynes [ 1 ]. It is thus possible, in principle, to interpret our formalism as a multipole expansion of the interaction of the domain with the rest of the sample. Harmonics with I > 2 correspond to pure shape modulations of the membrane. [Pg.149]

Assignments. - Electric modulation of vibrational rotational bands of polar molecules included a study of phosphine.120 Ringbending (puckering) transition frequencies have been measured for the phospholene (42) for the ground and excited states.121 The PD deformation band for the sulphide (43) has been assigned.122... [Pg.405]

Figure 6.2. (I) Conventional phosphorescence spectrum of 2,3-dichloroquinoxa-line in durene at 1.6°K. (II) am-PMDR spectrum, obtained by amplitude modulation of microwave radiation that pumps the tv-t, (1.055 GHz) zf transition with the detection at the modulation frequency. Only bands whose intensities change upon microwave radiation (1.055 GHz) and thus originate from tv or rz appear in the am-PMDR spectrum. Transitions from r and rv appear with opposite sign (phase-shifted by 180°). (Hb, lie ) Polarization of the am-PMDR spectral transitions, relative to the crystal axes. The band at 0,0-490 cm-1 originates from both the r and t spin states its intensity does not change upon the 1.055-GHz saturation (no band in II) however, its polarization does rhanp. (bands in Hb and IIc ). (Reproduced with permission from M. A. El-Sayed.tt7W)... Figure 6.2. (I) Conventional phosphorescence spectrum of 2,3-dichloroquinoxa-line in durene at 1.6°K. (II) am-PMDR spectrum, obtained by amplitude modulation of microwave radiation that pumps the tv-t, (1.055 GHz) zf transition with the detection at the modulation frequency. Only bands whose intensities change upon microwave radiation (1.055 GHz) and thus originate from tv or rz appear in the am-PMDR spectrum. Transitions from r and rv appear with opposite sign (phase-shifted by 180°). (Hb, lie ) Polarization of the am-PMDR spectral transitions, relative to the crystal axes. The band at 0,0-490 cm-1 originates from both the r and t spin states its intensity does not change upon the 1.055-GHz saturation (no band in II) however, its polarization does rhanp. (bands in Hb and IIc ). (Reproduced with permission from M. A. El-Sayed.tt7W)...
The importance of peptide transmitters in the modulation of sleep and wakefulness has become apparent in recent years. Previous work had focused on the role of monoamines in the circuitry that regulates the transitions between states of vigilance. Histaminergic neurons in the tuberomammillary nucleus are known to be key players in the activation of subcortical afferents during wakefulness (Wada et al, 1991). Activity of noradrenergic neurons in the locus coeruleus correlates with the state of vigilance (Jones, 1991). The role of serotonergic neurons in rapid eye movement (REM) sleep has also been established (Lydic et al., 1987 Monti Jantos, 1992 Fabre et al., 2000). [Pg.387]

Effect of diagonal-off-diagonal dynamic disorder (D-off-DDD). The polarization fluctuations and the local vibrations give rise to variation of the electron densities in the donor and the acceptor, i.e., they lead to a modulation of the electron wave functions A and B. This leads to a modulation of the overlapping of the electron clouds of the donor and the acceptor and hence to a different transmission coefficient from that calculated in the approximation of constant electron density (ACED). This modulation may change the path of transition on the potential energy surfaces. [Pg.103]

Kinetic Parameters for the Symmetric Transition Taking Account of the Modulation of the Zeroth-Order Electron Densities (Beyond the Condon Approximation)... [Pg.115]

Based on the results obtained in the investigation of the effects of modulation of the electron density by the nuclear vibrations, a lability principle in chemical kinetics and catalysis (electrocatalysis) has been formulated in Ref. 26. This principle is formulated as follows the greater the lability of the electron, transferable atoms or atomic groups with respect to the action of external fields, local vibrations, or fluctuations of the medium polarization, the higher, as a rule, is the transition probability, all other conditions being unchanged. Note that the concept lability is more general than... [Pg.119]

The modulation of the charge of the adsorbed atom by the vibrations of heavy particles leads to a number of additional effects. In particular, it changes the electron and vibrational wave functions and the electrostatic energy of the adatom. These effects may also influence the transition probability and its dependence on the electrode potential. [Pg.141]

There are several hypotheses for a specific mechanism by which ONOO- can control the open state of the PTPC. Briefly the PTPC is regulated by primary constituents of the pore, including the inner membrane adenine nucleotide translocase (ANT) and the outer membrane protein voltage-dependent anion channel (VDAC or porin). The VDAC-ANT complex can bind to signaling proteins that modulate permeability transition, such as pro-apoptotic Bax (which opens the pore) and anti-apoptotic Bcl-2... [Pg.363]


See other pages where Modulation of transit is mentioned: [Pg.555]    [Pg.595]    [Pg.131]    [Pg.582]    [Pg.642]    [Pg.131]    [Pg.555]    [Pg.595]    [Pg.131]    [Pg.582]    [Pg.642]    [Pg.131]    [Pg.1486]    [Pg.1793]    [Pg.1981]    [Pg.30]    [Pg.729]    [Pg.327]    [Pg.215]    [Pg.421]    [Pg.834]    [Pg.39]    [Pg.255]    [Pg.186]    [Pg.22]    [Pg.281]    [Pg.601]    [Pg.391]    [Pg.114]    [Pg.143]    [Pg.163]    [Pg.551]    [Pg.200]    [Pg.347]    [Pg.600]    [Pg.1008]    [Pg.330]    [Pg.756]    [Pg.54]    [Pg.574]    [Pg.145]    [Pg.190]    [Pg.42]    [Pg.499]   
See also in sourсe #XX -- [ Pg.555 ]




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