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Rigid-rotator transition probabilities

Table 1. Rigid-rotator transition probabilities for four... Table 1. Rigid-rotator transition probabilities for four...
We call the correlation time it is equal to 1/6 Dj, where Dj is the rotational diffusion coefficient. The correlation time increases with increasing molecular size and with increasing solvent viscosity, equation Bl.13.11 and equation B 1.13.12 describe the rotational Brownian motion of a rigid sphere in a continuous and isotropic medium. With the Lorentzian spectral densities of equation B 1.13.12. it is simple to calculate the relevant transition probabilities. In this way, we can use e.g. equation B 1.13.5 to obtain for a carbon-13... [Pg.1504]

Under some circumstances the rotationally anisotropy may be even further simplified for T-R energy transfer of polar molecules like HF (41). To explore this quantitatively we performed additional rigid-rotator calculations in which we retained only the spherically symmetric and dipole-dipole terms of the AD potential, which yields M = 3 (see Figures 1, 3, and 4). These calculations converge more rapidly with increasing N and usually yield even less rotationally inelastic scattering. For example Table 2 compares the converged inelastic transition probabilities... [Pg.192]

In practice values of B are also often quoted in cm-1. For the simple rigid rotor the rotational quantum number J takes integral values, J = 0, 1, 2, etc. The rotational energy levels therefore have energies 0, 2B, 6B, 12B, etc. Elsewhere in this book we will describe the theory of electric dipole transition probabilities and will show that for a diatomic molecule possessing a permanent electric dipole moment, transitions between the rotational levels obey the simple selection rule A J = 1. The rotational spectrum of the simple rigid rotor therefore consists of a series of equidistant absorption lines with frequencies 2B, 4B, 6B, etc. [Pg.235]

Microcanonical transition-state theory (TST) assumes that all vibrational-rotational levels for the degrees of freedom orthogonal to the reaction coordinate have equal probabilities of being populated [12]. The quasi-classical normal-mode/rigid-rotor model described above may be used to choose Cartesian coordinates and momenta for these energy levels. Assuming a symmetric top system, the TS energy E is written as... [Pg.197]


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See also in sourсe #XX -- [ Pg.192 , Pg.194 ]




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Rotational transitions

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