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Limitation energy transfers

Intramolecular proton-transfer (ESIPT) dyes can be combined independently with limited energy transfer by the special properties of the ESIPT system. 121... [Pg.36]

Oiffiision-limited energy transfer has also been applied to membrane-bound luoro diores, but to a case different fiom lateral diffiision (Eq. [15.22]). One example, shown in the bottom panel of Figure 15.16, is for donors tirgrped within a vesicle of radius b. The acceptors are at a brown surface density (Oa in molecules/A located at a distance re below the surface. The diffiision-limited transfra rate is given by... [Pg.437]

Muller, J.G., U. Lemmer, G. Raschke, M. Anni, U. Scherf, J.M. Lupton, and J. Feldmann. 2003. Linewidth-limited energy transfer in single conjugated polymer molecules. Phys Rev Lett 91 267403. [Pg.740]

Straub J E and Berne B J 1986 Energy diffusion in many dimensional Markovian systems the consequences of the competition between inter- and intra-molecular vibrational energy transfer J. Chem. Phys. 85 2999 Straub J E, Borkovec M and Berne B J 1987 Numerical simulation of rate constants for a two degree of freedom system in the weak collision limit J. Chem. Phys. 86 4296... [Pg.897]

Note that in the low pressure limit of iinimolecular reactions (chapter A3,4). the unimolecular rate constant /fu is entirely dominated by energy transfer processes, even though the relaxation and incubation rates... [Pg.1053]

CFIDF end group, no selective reaction would occur on time scales above 10 s. Figure B2.5.18. In contrast to IVR processes, which can be very fast, the miennolecular energy transfer processes, which may reduce intennolecular selectivity, are generally much slower, since they proceed via bimolecular energy exchange, which is limited by the collision frequency (see chapter A3.13). [Pg.2137]

Brown N J and Miller J A 1984 Collisional energy transfer in the low-pressure-limit unimoleoular dissooiation of FIO2 J. Chem. Rhys. 80 5568-80... [Pg.3016]

For the case of intramolecular energy transfer from excited vibrational states, a mixed quantum-classical treatment was given by Gerber et al. already in 1982 [101]. These authors used a time-dependent self-consistent field (TDSCF) approximation. In the classical limit of TDSCF averages over wave functions are replaced by averages over bundles of trajectories, each obtained by SCF methods. [Pg.16]

As described above, quantum restrictions limit tire contribution of tire free electrons in metals to the heat capacity to a vety small effect. These same electrons dominate the thermal conduction of metals acting as efficient energy transfer media in metallic materials. The contribution of free electrons to thermal transport is very closely related to their role in the transport of electric current tlrrough a metal, and this major effect is described through the Wiedemann-Franz ratio which, in the Lorenz modification, states that... [Pg.167]

For fixed values of R and V, a selection of a value of tt2 (corresponding to a value of stagger angle) fixes a limiting value of o. from cascade data. Thus the blade speed, u, is determined and then the energy transfer E is found. [Pg.233]

Research Opportunities. The presence of a long-lived fluorescing state following either 532 nm or 1064 nm excitation of PuF6(g) provides a valuable opportunity to study the extent to which electronic energy in a 5f electron state is available in photochemical and energy transfer reactions. Such gas phase bimolecular reactions would occur in a weak interaction limit governed by van der Waals forces. Seen from the perspective of potential photochemical separations in fluoride volatility... [Pg.171]

Steady-State Fluorescence Depolarization Spectroscopy. For steady state depolarization measurements, the sample is excited with linearly polarized lig t of constant intensity. Observed values of P depend on the angle between the absorption and emission dipole moment vectors. In equation 2 (9), Po is the limiting value of polarization for a dilute solution of fluorophores randomly oriented in a rigid medium that permits no rotation and no energy transfer to other fluorophores ... [Pg.183]

Discuss and compare the mechanisms of energy transfer using high-pressure steam, microwaves and ultrasound. Discuss the role and limitations of solvents for carrying out a chemical reaction using these energy sources. [Pg.233]

The method of exchange-luminescence [46, 47] is based on the phenomenon of energy transfer from the metastable levels of EEPs to the resonance levels of atoms and molecules of de-exciter. The EEP concentration in this case is evaluated by the intensity of de-exciter luminescence. This technique features sensitivity up to-10 particle/cm, but its application is limited by flow system having a high flow velocity, with which the counterdiffusion phenomenon may be neglected. Moreover, this technique permits EEP concentration to be estimated only at a fixed point of the setup, a factor that interferes much with the survey of heterogeneous processes associated with taking measurements of EEP spatial distribution. [Pg.294]


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