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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 105 (1996), S. 111-117 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Ionization probabilities of NO molecules electronically excited in the A 2Σ+ and B 2Π states have been determined by (1+1) resonance-enhanced, two-photon ionization. Various vibrational levels within these states have been excited prior to ionization. Measurements of the unsaturated ionization signal yields accurate values for the relative detection probabilities of NO of 1:(0.70±0.07): (0.67±0.11) for excitation via the γ(0−0), γ(1−1), and γ(2−2) bands, respectively, and (3.7±0.36)×10−7 and (5.8±0.65)×10−4 for ionization through β(0−0) and β(2−1) bands, respectively. Applying published data for the γ- and β-band transition probabilities allows the deduction of the ionization cross section of A 2Σ+ and B 2Π vibrational states. The respective ionization cross sections are (7.0±0.9)×10−19 cm2, (8.5±0.8)×10−19 cm2, (6.0±1.0)×10−19 cm2 for A 2Σ+(v′=0, 1, and 2) and (5.0±0.5)×10−21 cm2 and (1.7±0.2)×10−20 cm2 for B 2Π(v′=0 and 2). These values are based on the experimentally determined cross section for A 2Σ+(v′=0). Using a larger theoretical cross section for this state the other cross sections scale accordingly, within the experimental uncertainties. © 1996 American Institute of 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 84 (1986), S. 7058-7058 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    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 83 (1985), S. 4360-4363 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Selective photoionization from single rotational states of the B 1Σ+u(v'=0 and 3) excited state of the H2 molecule has been investigated with fixed frequency and tunable laser radiation around λ=266 nm. State selection of the B-state levels was achieved by tunable VUV laser excitation around λ=110 and 106 nm, respectively. The ionization cross section has been determined for different states, and found to be critically dependent upon the initial rotational quantum state and to show pronounced spectral structure with the ionization wavelength. At λI=266.05 nm the cross section varies between 0.23×10−18 and 1.2×10−18 cm2, depending on the initial state.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 85 (1986), S. 2599-2608 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Single rotational states were populated in vibrationally excited hydrogen by stimulated Raman pumping. The population in H2 X 1∑+g(v″=0,1) and D2 X 1∑+g(v″=0,1) was probed state selectively by tunable vacuum ultraviolet (VUV) laser radiation around λ=110 nm, and the fluorescence induced when exciting the hydrogen molecules in the (0–0), (1–0), (2–0), (3–1), and (4–1) Lyman bands of the (B 1∑+u←X 1∑+g) transition monitored. From a comparison of line heights, the stimulated Raman pumping efficiency is estimated to be 30%–50% in the focal volume. Rotational transitions in X 1∑+g(v″=1) were induced in collisions with H2, D2, and He. State-to-state rotational relaxation rates were measured for the (J″=1→J″=3) transition in H2(v″=1) and for the (J″=2→J″=0,4) transitions in D2(v″=1). These rates were found to be generally higher than the corresponding previously determined ones in ground state hydrogen, in qualitative accord with recent theoretical calculations. A comparison with available theoretical state-to-state cross sections shows that the rates obtained with these cross sections are generally lower than the relaxation rates directly measured in this work.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 83 (1985), S. 4831-4844 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Rotational state selective fluorescence excitation and two-color resonantly enhanced ionization of nitric oxide has been investigated under collision free conditions. Single photon absorption from a tunable VUV laser source prepared the molecules in the intermediate B 2Π, C 2Π, and D 2Σ+ states energetically close to the dissociation limit of NO. The dissociation of C 2Π(v'=0) at J'=2.5(2Π3/2) and J'=3.5(2Π1/2) as well as B 2Π(v'=7) at J'=4.5(2Π3/2) and J'=7.5 (2Π1/2) was clearly established. Time delayed photoionization was used to measure the lifetimes of stable and weakly predissociative states. Photoionization cross sections of single rotational levels in the electronically excited states have been determined by saturating the ionization step.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 99 (1993), S. 4864-4866 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Rotational alignment in a polyatomic molecule is produced by stimulated S-branch Raman pumping. This technique, applied to pump the (ν2‘=1) vibration of acetylene, generates a nearly perfect quadrupole aligned MJ distribution (A0(2)=−1) for Jf=2. First results concerning the collisional alignment decay rate constant are reported.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 101 (1994), S. 5804-5817 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A complete set of state-to-state rotational energy transfer rate constants has been measured for acetylene–acetylene collisions at room temperature under single collision conditions. Initial rotational states (Ji=5,7,...,25) were prepared and final states (Jf=1,...,25) interrogated. The measurements were carried out in a typical gas phase pump and probe arrangement. The initial vibrationally excited state was prepared by stimulated Raman pumping using strong Q-branch transitions. State preparation via this branch produces an isotropic spatial distribution of the excited state which is important for data analysis. Narrow bandwidth lasers ensure single rotational state selectivity. The rotational distribution after collisions is monitored by time-delayed laser-induced fluorescence via the A˜ 1Au(ν3' = 1)←X˜ 1Σg(ν2‘ = 1) transition. In general, the rate constants decrease exponentially with the transferred rotational energy. The complete rate constant matrix can consistently be described by a simple parameter set within the dynamical infinite order sudden power approximation. In addition to this general behavior a significant ΔJ propensity of the rate constants is observed. Using the energy corrected sudden approximation with a power law basis an excellent match, reproducing the ΔJ propensities, to the rate constant matrix is obtained, again with a single set of parameters.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    New blackfriars 20 (1939), S. 0 
    ISSN: 1741-2005
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Theology and Religious Studies
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    New blackfriars 16 (1935), S. 0 
    ISSN: 1741-2005
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Theology and Religious Studies
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    New blackfriars 16 (1935), S. 0 
    ISSN: 1741-2005
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Theology and Religious Studies
    Type of Medium: Electronic Resource
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