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  • American Institute of Physics (AIP)  (545)
  • Periodicals Archive Online (PAO)
  • 11
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 93 (1990), S. 5518-5532 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A quantum mechanical treatment of a double minimum system interacting with a heat bath is presented for the purpose of interpreting experimental data on transfer kinetics in condensed hydrogen-bonded systems. The model describes the transfer motion in one or two dimensions. The heat bath is represented by a set of harmonic oscillators and the interaction by a term linear in the system coordinates and in the bath coordinates. Extending an earlier random field approach, the present treatment consistently accounts for the quantum nature of the total system. With crystalline benzoic acid dimer used as an example, the master equation for the populations of the energy levels of the hydrogen transfer motion is derived. Transition probabilities consistent with the principle of detailed balance are obtained, based on a representation with explicit off-diagonal tunnel interactions for pairs of states localized on different sides of the barrier and with diagonal terms describing the rearrangement of the heat bath as a consequence of the tunneling motion. The activation of the double minimum transfer process with increasing temperature is related to the excitation of the local vibrations in the two potential wells.
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  • 12
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 92 (1990), S. 420-427 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Total binary and tertiary quench rates have been measured for the reaction Xe (5p5np, np', n=6,7)+Cl2 at thermal temperatures. Xenon atoms are excited by state-selective, two-photon absorption with an ultraviolet laser. The time-dependent fluorescence from the excited atom in the infrared, visible, and from XeCl* (B) product near 308 nm have been measured with subnanosecond time resolution. The decay rates are measured as a function of Cl2 pressure to 20 Torr and Xe pressure to 400 Torr. The measured reaction rates (k2∼10−9 cm3 s−1) are consistent with a harpoon model described in a separate paper. We also measure large termolecular reaction rates for collisions with xenon atoms (k3∼10−28 cm6 s−1). Total product fluorescence has been examined using a gated optical multichannel analyzer. We measure unit branching fractions for high vibrational levels of XeCl* (B) with very little C state fluorescence observed.
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  • 13
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 91 (1989), S. 6195-6204 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The band-Lanczos algorithm is used to compute a few matrix elements of a resolvent, i.e., to compute 〈ψk||(ω−H)−1||ψl〉. Here H denotes a Hermitian matrix of large dimension. It is shown that the proposed method which is based on the band-Lanczos algorithm is more efficient than a method based on simple-Lanczos algorithm, e.g., than the residue algebra method. The performance of the Lanczos algorithm (both simple and band) for evaluating resolvents or other functions of H is discussed in some detail.
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  • 14
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 90 (1989), S. 4623-4625 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A new molecular beam color center laser spectrometer, which can be tuned single mode under computer control around 1.5 μm, has been used to obtain the sub-Doppler, rotationally resolved, first overtone spectrum of the nonbonded C–H stretch vibration of the HCN dimer. As for the corresponding fundamental vibration, the linewidth is instrument limited, posing a minimum limit of 11 ns to the lifetime of the excited complex.
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  • 15
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 90 (1989), S. 5566-5577 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The use of a time-dependent basis set for solving the time-dependent Schrödinger equation is proposed. The basis set is a generalization of the harmonic oscillator functions. The proposed method is similar to the approaches formulated by Lee and Heller and by Coalson and Karplus. However, in the present method the time dependence of the basis functions is determined differently. Numerical studies on the quartic oscillator and on the Morse potential are carried out to investigate the performance of the various methods.
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  • 16
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 89 (1988), S. 7112-7125 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Optical spectra of ten AX+ ions (A=B, Al, Ga, In; X=F, Cl, Br) have been observed in the visible and near UV; a total of 18 band systems were newly discovered. The emission was produced by chemiluminescent reactions A++X2 at low (2–10 eVCM) kinetic energy in a beam-gas arrangement. A position-sensitive photon counting detector with large surface area and very low dark count rate was employed, the resolution was mostly 5–50 A(ring) FWHM. Three types of band systems were observed: (1) For all AX+ combinations except BCl+ and BBr+, a very broad quasicontinuum with undulatory structure appears. On the basis of electronic state correlation arguments, photoelectron data, some ab initio calculations and, in one case, a known emission spectrum (InCl+) these band systems were identified as B 2Σ+–X 2Σ+ transitions. It is concluded that the excited state potentials are considerably displaced against the ground state, and their energetics are given. (2) For six species AX+, narrow band systems were observed in the 2500 A(ring) region. They could be clearly identified as being due to C 2Π–X 2Σ+ transitions by means of comparison with the systematics of the analogous A 2Π–X 2Σ+ transitions of the isoelectronic alkaline earth halides, by the resolved fine structure, and, in the case of AlF+, by an ab initio calculation. (3) In the GaCl+, GaBr+, and InBr+ spectra, narrow features accompany the C–X transitions. They are attributed to D 2Σ+–X 2Σ+ transitions, analogous to the alkaline earth halide B 2Σ+–X 2Σ+ band systems. Qualitative electronic state correlations are discussed, and the expected dominant configurations in different regions of the AX+ ground and excited states are given. These are in accord with recent ab initio results on AlF+.
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  • 17
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 88 (1988), S. 3475-3480 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: HCl+(A) was selectively prepared in the v'=0, 3, 5, and 6 levels using ion impact excitation. The resulting A–X spectra are largely free from band overlap. From intensity measurements on 16 bands, the electronic transition moment function M(R) was derived in the region of R=1.1–1.8 A(ring). Computer simulations based on this M(R) function were performed both for these and for additional spectra excited by electron impact. In all cases an excellent reproduction of the measured spectra was achieved. The M(R) dependence obtained in this work agrees very well with a large-scale ab initio calculation.
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  • 18
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 86 (1987), S. 7249-7249 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
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  • 19
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 94 (1991), S. 8441-8443 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The atomic force microscope has been used to record molecular structure on free-standing organic crystals. A crystal of tetracene has been imaged with molecular resolution which allows the assignment of lattice parameters to the surface layer. The intermolecular spacings on the surface of tetracene correspond remarkably closely with those in the bulk. It is even possible to distinguish between the two translationally inequivalent molecules of the unit cell. The mechanism for using force microscopy to distinguish between different molecular orientations is discussed.
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  • 20
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 93 (1990), S. 6419-6432 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: In crossed molecular-beam experiments, three type of cross sections have been measured: Total differential cross sections with well-resolved diffraction oscillations for oD2–NH3 at E=95.9 and 111.3 meV, differential energy-loss spectra for ND3–oD2 at E=118.3 meV which cover the center-of-mass (c.m.) angular range from 85° to 170° and are obtained by time-of-flight (TOF) analysis, and state-to-state integral cross sections for oNH3–H2 and pNH3–H2 at E=75 meV for many final rotational states which are detected by resonance enhanced multiphoton ionization. These data which are mainly sensitive to the anisotropy of the potential energy surface are well reproduced by quantum calculations in the coupled-states approximation. The potential is constructed by combining large basis-set self-consistent-field (SCF) calculations with damped long-range dispersion coefficients. The two free parameters of the damping function are fitted to a restricted set of configuration interaction (CI) calculations.
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