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  • 1
    Call number: S 04.0048(18)
    In: Geological Survey of Denmark and Greenland bulletin
    Type of Medium: Series available for loan
    Pages: 126 S. Ill., graph. Darst., Kt. + 1 Kt.-Beil.
    Edition: 2nd ed.
    ISBN: 9878778712585
    Series Statement: Geological Survey of Denmark and Greenland bulletin 18
    Location: Lower compact magazine
    Branch Library: GFZ Library
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  • 2
    Series available for loan
    Series available for loan
    Copenhagen : Geological Surv. of Denmark and Greenland, Ministry of Environment and Energy
    Associated volumes
    Call number: S 98.0089(185)
    In: Geology of Greenland Survey bulletin
    Type of Medium: Series available for loan
    Pages: 93 S. + 1 Kt.-Beil.
    ISBN: 8778710693
    Series Statement: Geology of Greenland Survey bulletin 185
    Classification:
    Regional Geology
    Location: Lower compact magazine
    Branch Library: GFZ Library
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  • 3
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 91 (1989), S. 4700-4713 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We present an approach to quantum dynamics, based entirely on Cartesian coordinates, which covers vibrational as well as rotational motion. The initial state is represented in terms of multidimensional Gaussian wave packets. Rotational adaptation to angular momentum eigenstates is done by using angular momentum projection operators. This gives an initial state represented as a weighted superposition of Gaussians with different average orientation in space. It is shown that the subsequent dynamics can be determined from the dynamics of Gaussians corresponding to just one of these orientations. An application to the 3D photodissociation dynamics of ICN is presented. All six degrees of freedom which describe the internal motion of the triatomic are included, the only approximation introduced in the present calculation being the thawed Gaussian wave packet approximation for the dynamics. The total absorption spectrum out of vibrational–rotational eigenstates of ICN as well as fully resolved final product distributions are calculated.
    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 89 (1988), S. 5607-5613 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We examine the relation between photodissociation dynamics and the form of the total absorption spectrum for H2O in the first absorption band. Application of an exact time dependent formalism gives a direct and intuitive relation between molecular motion and spectral features. We show that the series of weak structures on top of the broad continuum is due to symmetric stretch motion in the excited state. The spacing between the structures is, essentially, given by the frequency associated with this motion. In addition, we present some excited state eigenfunctions, which provide a direct connection between the structured spectrum, the final product distributions, and the dynamics.
    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 113 (2000), S. 10477-10485 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We consider the relation between observed pump–probe signals in the femtosecond regime and the kinetics of unimolecular reactions, that is, the exponential decay of reactants and the exponential rise of the product population, respectively. It is shown that the signals cannot be fully accounted for within standard approaches of unimolecular decay, conventionally used in the past, since interference effects between the quasi-bound vibrational states within the bandwidth of the pump laser cannot be neglected. When these effects are included, all features of the signals can be accounted for. We apply this theoretical treatment of coherent interference to examine the dynamics and kinetics of the quasi-bound transition configurations, and relate them to the decay rates of individual quasi-bound resonance states. The signals show multi-exponential behavior, reflecting the different decay rates of the resonance states, with an average rate constant (within the bandwidth of the pump laser) which can be extracted directly from the signals. The persistence of coherence is evident in the observed signals. The predissociation of NaI is used as a prototype for numerical illustration. © 2000 American Institute of Physics.
    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 102 (1995), S. 5387-5395 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We derive an expression for a short-time phase space propagator. We use it in a new propagation scheme and demonstrate that it works for a Morse potential. The propagation scheme is used to propagate classical distributions which do not obey the Heisenberg uncertainty principle. It is shown that the simple classical deterministic motion breaks down surprisingly fast in an anharmonic potential. Finally, we discuss the possibility of using the scheme as a useful approach to quantum dynamics in many dimensions. To that end we present a Monte Carlo integration scheme using the norm of the propagator as a part of the sampling function. © 1995 American Institute of Physics.
    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 111 (1999), S. 10469-10475 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We consider pump–probe frequency integrated fluorescence signals. These transients, in general, arise from wave packets where the intrinsic dynamics and the response to the pump pulse is entangled in a complicated way. The signal from an infinitely short δ-pump pulse is the only exception. However, if the pump–probe signal is integrated over the frequencies of the pump laser, the signal can be expressed as a convolution of the pulse envelope with the signal obtained from a δ-pulse excitation. We consider the deconvolution of the pulse envelope and demonstrate that the signal corresponding to a δ-pump pulse can be recovered exactly from signals using pump pulses of finite temporal width. Numerical examples are presented for asymptotic fragment detection in the reaction, ICN→I+CN. © 1999 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 98 (1994), S. 3272-3279 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 105 (1996), S. 9115-9120 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We elaborate on a two-pulse (pump-pump) laser control scheme for selective bond-breaking in molecules [Amstrup and Henriksen, J. Chem. Phys. 97, 8285 (1992)]. We show, in particular, that with this scheme one can overcome the obstacle of intramolecular vibrational relaxation. As an example, we consider an ozone molecule with isotopic substitution, that is, 16O16O18O. It is shown that asymmetric bond stretching can be created in simple (intense) laser fields. We predict that an alternating high selectivity between the channels 16O+16O18O and 16O16O+18O can be obtained when such a non-stationary vibrating ozone molecule is photodissociated with short laser pulses (∼10–15 fs) with a time delay corresponding to half a vibrational period (∼17 fs). © 1996 American Institute of Physics.
    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 109 (1998), S. 4335-4341 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We study theoretically the electronic and nuclear dynamics in NaI. After a femtosecond pulse has prepared a wave packet in the first excited state, we consider the adiabatic and the nonadiabatic electronic dynamics and demonstrate explicitly that a nonstationary electron is created in NaI corresponding to electron transfer between Na and I. The electronic motion is introduced via nuclear motion, more specifically, through nonadiabatic curve crossing and the electronic motion is here on the same time scale as the nuclear motion. We show that the branching ratio between the channels Na+I and Na++I− depends on the electron distribution (i.e., where the electron "sits") prior to the time where the bond is broken by a subpicosecond half-cycle unipolar electromagnetic pulse. Thus we control, in real time, which nucleus one of the valence electrons will follow after the bond is broken. © 1998 American Institute of Physics.
    Type of Medium: Electronic Resource
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