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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 91 (1989), S. 722-731 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Direct absorption tunable difference frequency IR spectroscopy in a slit jet supersonic expansion has been used to observe complexes of Ne with HF for the first time. Spectra of both the weak HF stretch fundamental (1000)←(0000) and the 10–20 fold more intense bend and stretch combination band (111e,f0)←(0000) transitions are observed, and illustrate several interesting dynamical features. The large ratio of combination band to fundamental intensity is evidence for a highly isotropic potential with respect to HF rotation. The HF bend vibration is thus better thought of as nearly free internal rotor motion with a nearly good space fixed quantum number, jHF =1. Weak anisotropy in the potential permits the jHF=1 (Πebend) levels to relax intramolecularly to jHF =0 (Σ) levels, leading to predissociative line broadening in the sub-Doppler slit jet spectra. This observed dissociation of NeHF with 44 cm−1 of internal excitation provides a rigorous upper limit to the binding energy. The Πfbend levels, on the other hand, have no lower energy internal rotor states of the correct parity to relax into, and thus the (111f0) ←(0000) spectra exhibit linewidths limited by the apparatus resolution. The internal relaxation of the jHF=1 (Πebend) levels results from Coriolis mixing with the Σbend states (1200) by overall rotation of the NeHF complex, and thus the lifetimes depend dramatically on J. The J-dependent predissociation rates observed are in remarkably quantitative agreement with quantum scattering calculations on the CEPA ab initio surface of ONeil and co-workers.
    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 82 (1985), S. 2884-2895 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Energy resolved photodissociation studies of CO3−⋅(H2O)n, n=1,2,3 are reported for photon energies ranging from 1.95 to 2.2 eV. The only dissociation channel observed is the loss of all attached water molecules to give unclustered CO3− as the sole photofragment ion. The cross section for this mechanism is substantially higher than that for the bare ion, and the sharp structure observed in the spectrum of the bare ion is nearly lost in the clusters. Analysis of the kinetic energy distributions for the photofragment ions places an upper limit of 20 μs on the lifetime of the excited clusters, and demonstrates that approximately 95% of the excess energy in the cluster remains in the CO3− containing fragment rather than being partitioned into relative translation of the photofragments or into internal motion of the water fragments. The dissociation mechanism begins with a bound–bound 2A1←2B1 transition within the core CO3− ion. Internal conversion returns the core ion to the electronic ground state with substantial vibrational excitation; redistribution of this vibrational energy results in vibrational predissociation of the cluster. The relations of this mechanism to those that occur in the bare ion and to other vibrational predissociation experiments on clusters are discussed.
    Type of Medium: Electronic Resource
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