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  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Chemical Physics Letters 226 (1994), S. 178-182 
    ISSN: 0009-2614
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 110 (1999), S. 9908-9914 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The reaction D2++H2→D2H++H*(n〉1) or H2D++D*(n〉1) is studied experimentally at a relative collision energy of 20 eV. The ionic products are angle and energy analyzed in coincidence with the excited atomic products. The latter are detected by the radiation they emit, possibly after quenching in case of metastable atoms. The contour diagrams obtained for the intensity of the D2H+ or H2D+ products as functions of their center-of-mass scattering angle and velocity show the presence of these two products, with a predominance of the former. These products are essentially found in low vibrational levels and the correlated atoms are observed predominantly in n=2 states; the 2s to 2p cross section ratio is found to be nearly equal to 0.35. That the considered reaction exists was actually predicted on the basis of its analogy with the reaction He++H2→HeH++H*(n〉1). The main features of the two reactions are compared. The mechanism of the D2++H2 reaction is explained using an adaptation of the interpretation framework proposed by Dhuicq et al. [Chem. Phys. 206, 139 (1996)] for the He++H2 reaction. It involves energy level promotion, diabatic potential energy surface crossings and related electron transitions, charge transfer, and proton transfer. The discussion shows that the occurrence of this reaction and some of its characteristics stem from the Franck–Condon vibrational distribution of the D2+ reactant ions and especially to the corresponding distribution of bond distances. © 1999 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 109 (1998), S. 512-524 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The HeH+ ions produced in the He++H2 reaction at Ecm=20 eV are analyzed in coincidence with the other reaction product: either an H*(2s) metastable atom or an H*(2p) atom. The measurements are restricted to laboratory scattering angles of the HeH+ ions in the range 5°〈θ〈15° encompassing the maximum of the differential cross section for their production. The H*(2s) atoms are observed at a corresponding fixed angle around −90° relative to the incident He+ direction. The Lα radiation which is the signature of the H*(2p) atom is detected at various angles in the collision plane; this provides polarization (in particular alignment) parameters describing the H*(2p) electron cloud. The HeH+ differential cross section maximum is composed of a few peaks associated with the H*(2p or 2s) species. The H*(2s) to H*(2p) cross section ratio is around 0.1. For the HeH+ peaks at small scattering angles, the Lα radiation patterns obtained for the nascent H*(2p) electron cloud are essentially of dipolar type. The measured alignment angle relative to the final HeH+ center of mass direction lies in the range 67°–81°. A simple model is devised to relate these observations to the H*(n=2) probability amplitudes formed right after the reaction, that is, before post-reaction Stark effect in the field of the receding HeH+ ion together with Coriolis coupling modify these amplitudes. The analysis shows that contribution of the 2p⊥ state lying perpendicular to the axis joining the H* atom to the HeH+ center of charge predominates. This is attributed to a dominant role played by the 2pπu crossing between the potential energy surfaces of the (He–H2)+ compound. It also implies, in agreement with earlier predictions of Dhuicq et al. [Chem. Phys. 206, 139 (1996)] that this compound is bent when going through the important {He++H2}→{He+H2+*}→{HeH++H*} stages of the reaction at the investigated energy. At the largest angles investigated, evidence is seen for the emergence of an additional mechanism attributed to the 2sσg crossing. © 1998 American Institute of Physics.
    Type of Medium: Electronic Resource
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