Bibliothek

feed icon rss

Ihre E-Mail wurde erfolgreich gesendet. Bitte prüfen Sie Ihren Maileingang.

Leider ist ein Fehler beim E-Mail-Versand aufgetreten. Bitte versuchen Sie es erneut.

Vorgang fortführen?

Exportieren
Filter
Materialart
Erscheinungszeitraum
  • 1
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 113 (2000), S. 5302-5310 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: Using a pump–probe technique, the reactions of Mg(4 1S0 and 3 1D2) with H2 have been measured to yield similar rotational distributions of MgH(v=0 and 1) as that obtained for the reaction of the Mg(3 1P1) state with H2. A series of measurements is conducted to clarify that the reactions are initiated directly by these higher states, rather than occurring from the lower 3 1P1 state following radiative and collisional relaxation. The reactivity of the Mg 4 1S0 state with H2 is found to be comparable to that of the 3 1P1 state, but about three times larger than that of the 3 1D2 state. The Mg(4 1S0, 3 1D2)–H2 reactions proceed via a harpoon-type process, and are closely associated with the Mg(3 1P1)–H2 reaction coordinate through evolution of a series of surface crossings. To support our suggestion that the harpoon mechanism is involved, the cross sections of collisional deactivation by H2 for various excited states are measured. The ratios of cross sections observed for the 3 1P1, 4 1S0, and 5 1S0 state, equal to 1:2.85:4.3, are consistent with the calculated prediction of 1:2.62:4.24. The calculated cross sections are based on a simple hard sphere model with effective radii evaluated differently. Here, the effective radii for the higher states are determined from the crossing of ionic and covalent curves, while the Mg(3 1P1)–H2 radius is estimated from the nonadiabatic crossing between the reactive 1 1B2 state and the ground state. Consistency between observation and prediction confirms that the harpoon mechanism proposed in this work is plausible. © 2000 American Institute of Physics.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 2
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 111 (1999), S. 5277-5278 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: We have obtained for the first time the nascent rotational population distributions of CaH(v=0 and 1) in the reaction of Ca(4s4p 1P1) with H2. The rotational, vibrational, and translational fractions of product energy disposal may accordingly be evaluated to be 0.19±0.02, 0.33±0.02, and 0.48±0.02, respectively. Compared to the prior prediction, the low rotational and high vibrational fractions obtained suggest that the reaction mechanism should favor the collinear approach. © 1999 American Institute of Physics.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 3
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 110 (1999), S. 4402-4409 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: Forty-two vibrational (v=2–43) levels of the 7LiH C 1Σ+ excited electronic state have been observed by a pulsed optical–optical double resonance fluorescence depletion spectroscopic technique. The absolute vibrational numbering of the C 1Σ+ state is identified with the measurements of the isotopic shifts between 7LiH and 6LiH among several rotation-vibration bands of the C 1Σ+−A 1Σ+ electronic system, and it is further demonstrated by the consistency between observed spectral intensities and calculated ones. The highest observed quasi bound rotational level for the v=43 level is J=8. The spectral term values for those vibrational levels lying above v=33 occur in an irregular order. The level of v=34 lies mainly in the inner, tiny well. The term values for the observed rovibrational levels (2≤v≤32, 0≤J≤11) in the outer ionic well are described by a set of Dunham-type coefficients, with which a Rydberg–Klein–Rees (RKR) potential energy curve is constructed. This RKR potential is combined with an ab initio potential to construct an effective hybrid potential. The calculated electronic transition moment function for the C-A transition is also given. © 1999 American Institute of Physics.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 4
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 114 (2001), S. 9395-9401 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: By using a pump-probe technique, we have observed the nascent rotational population distribution of LiH (v=0) in the Li (2 2PJ) with a H2 reaction, which is endothermic by 1680 cm−1. The LiH (v=0) distribution yields a single rotational temperature at ∼770 K, but the population in the v=1 level is not detectable. According to the potential energy surface (PES) calculations, the insertion mechanism in (near) C2v collision geometry is favored. The Li (2 2PJ)–H2 collision is initially along the 2A′ surface in the entrance channel and then diabatically couples to the ground 1A′ surface, from which the products are formed. From the temperature dependence measurement, the activation energy is evaluated to be 1280±46 cm−1, indicating that the energy required for the occurrence of the reaction is approximately the endothermicity. As Li is excited to higher states (3 2S or 3 2P), we cannot detect any LiH product. From a theoretical point of view, the 4A′ surface, correlating with the Li 3 2S state, may feasibly couple to a repulsive 3A′ surface, from which the collision complex will rapidly break apart into Li (2 2PJ) and H2. The probability for further surface hopping to the 2A′ or 1A′ surfaces is negligible, since the 3A′ and 2A′ surfaces are too far separated to allow for an efficient coupling. The Li (3 2P) state is expected to behave similarly. The observation also provides indirect evidence that the harpoon mechanism is not applicable to this system. © 2001 American Institute of Physics.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
Schließen ⊗
Diese Webseite nutzt Cookies und das Analyse-Tool Matomo. Weitere Informationen finden Sie hier...