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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Accounts of chemical research 22 (1989), S. 139-144 
    ISSN: 1520-4898
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Accounts of chemical research 25 (1992), S. 71-76 
    ISSN: 1520-4898
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1520-510X
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 116 (1994), S. 8673-8680 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
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  • 5
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Accounts of chemical research 16 (1983), S. 88-95 
    ISSN: 1520-4898
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
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  • 6
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 94 (1991), S. 7810-7818 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Measurements of ion-velocity distributions of CO+ in a He buffer gas are presented as a function of an applied electric field. The distributions are obtained by single frequency, laser-induced fluorescence from various initial rotational states with the laser beam propagating parallel and perpendicular to the drift velocity vector. All distributions are well represented by a Maxwellian for the observed E/N range of 0–13 Td. The reduced mobilities, calculated from the shift of the mean velocity as a function of electric field, increase from 18.7±1.0 cm2 V−1 s−1 at very low fields to 26.4±0.7 cm2 V−1 s−1 at 13 Td. From the width of the Doppler profiles, translational "temperatures'' are calculated, which are compared to simple attractive and repulsive Maxwell models as a function of the field. The measured values disagree with the predictions, which are well established for atomic ion systems. The differences are discussed in terms of rotationally inelastic energy transfer in the collisions, which is predicted by kinetic theory models. This argument is strengthened by the fact that even though the rotational states rapidly equilibrate, measurements on different lines yield higher temperatures for higher rotational levels. Finally, the small influence of selective quenching of the electronically excited CO+ on the Doppler profiles is demonstrated by measuring effective lifetimes as a function of the applied drift field.
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  • 7
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 93 (1990), S. 6554-6559 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A general method is developed for determination of cylindrically symmetric velocity distributions from Doppler profile measurements. This method applies Kinsey's Fourier transform Doppler spectroscopy [J. L. Kinsey, J. Chem. Phys. 66, 2560 (1977)] to distributions arising from photodissociation and uses an orthogonal polynomial expansion to perform the integral transforms analytically. This method is shown to offer an improvement in stability over direct numerical solution of the integral equation and to have applicability to distributions which are not "separable,'' that is, which cannot be separated into a product of speed- and angle-dependent factors. The method is applied to experimental measurements of the collisional relaxation of a fast anisotropic distribution of I[2P1/2] atoms in a thermal bath (preceding paper). It is shown that the nascent distribution is separable, but the distribution does not remain separable throughout the relaxation process.
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  • 8
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Time-resolved Fourier transform infrared (FTIR) emission is used to study the formation of CCH in the photodissociation of C2H2 at 193 nm. Excitation of C2H2 at 193 nm is known to populate the 10ν3 level of the trans–bent electronically excited state of acetylene, which undergoes decomposition. State-resolved infrared emission is obtained from the CCH radicals that are produced. Only vibronic levels which originate or borrow oscillator strength from the low-lying electronically excited state of CCH, A˜ 2Π, are observed in this study. The relative intensities of these bands are measured and the rotational state distribution for the A˜(010) state is obtained. The observed average rotational energy of CCH is ∼156 cm−1, which is less than the average rotational energy of the acetylene precursor. A kinematic model which can account for a rotational cooling effect in the A˜(010) state is described. The model incorporates the angular momentum generated by the impulsive kick due to the release of the H atom and the cooling due to the orbital angular momentum carried away by the tangential velocity of the H atom, which is imparted by the initial C2H2 rotation.
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  • 9
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 90 (1989), S. 964-976 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: State-specific total quenching rate constants are measured for selected rotational levels of Br2 under single collision conditions with argon at 296 K. A strict criterion is used to obtain single collision conditions in a cell experiment. A 0.04 cm−1 bandwidth, etalon-narrowed pulsed dye laser excites single rovibronic transitions of the B 3Π(0+u) state, and fluorescence decay traces with and without the argon collision partner are analyzed at early times to extract total quenching rate constants. The rotational levels that are initially prepared are J'=26, 32, 37, 41, 46, and 58. The total quenching rate constants dramatically decrease with increasing J': for J'=26/32/37/41, respectively, they are =8.7×10−11/4.4×10−11/3.3×10−11/7.6×10−12 cm3 molecule−1 s−1. The effect of rotational excitation on the quenching is interpreted to be due to the decreased probability of forming collision complexes. In contrast to the levels J'〈41, negative quenching rate constants are observed for J'〉41, i.e., the decay rates with Ar are slower than those without. This result can be explained by taking into account the possibility of R↔V energy transfer processes in which a high rotational level is transferred to a lower rotational state in the next higher vibration and the lower rotational state has a much slower spontaneous predissociation rate.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 89 (1988), S. 302-308 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Rotational relaxation rates for HF(v=0, J=13) colliding with rare gases (He, Ne, Ar, Kr, Xe), H2, and D2 are measured using a transient-absorption double-resonance technique. The relaxation rate constants with rare gases (rotation-to-translation, R–T) decrease dramatically through the series He–Ne–Ar, then increase substantially through the series Ar–Kr–Xe, revealing the increased effectiveness of either highly impulsive or highly attractive collisions. Rate constants at 298 K are: (He), 1.3±0.2×10−11; (Ne), 2.2±0.4×10−12; (Ar), 9.3±0.9×10−13; (Kr), 4.4±0.5×10−12; (Xe), 6.2±0.6×10−12 cm3 molecule−1 s−1. The fact that the rate constants with hydrogen (1.1±0.2×10−10 cm3 molecule−1 s−1) and deuterium (1.2±0.2×10−10 cm3/molecule−1 s−1) are ten times faster than with helium underscores the importance of rotation-to-rotation (R–R) transfer in the rotational relaxation process. The decrease in rates from He to Ar can be understood by an impulsive-type model, analogous to the Schwartz, Slawsky, and Herzfeld (SSH) treatment of vibration-to-translation transfer. However, the increasing trend from Ar to Xe, while clearly due to the increasing magnitude of the attractive interaction, is not easily modeled.
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