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  • 1
    ISSN: 1432-0649
    Keywords: PACS: 82.40.Js; 82.50.Gw
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract. The photodissociation dynamics of HNO3 in the electronic S3 (2 1 A ′ ) state leading to the fragments OH and NO2 was investigated in real time. HNO3 was prepared either in a fluorescence cell at room temperature (LIF probing of OH) or rotationally cold in a molecular beam (probing of NO2 by three-photon ionization). A 2 1 A ′ lifetime of 60–80 fs could be obtained from the experimental results, indicating essentially barrierless dissociation. In addition, secondary dissociation of internally excited nascent fragments NO2  * leading to products NO(X 2 Π) and O(3 P) with a characteristic dissociation time of 2.3 ps was observed. This time is surprisingly long when compared with dissociation lifetimes of NO2 from the literature, obtained after direct photoexcitation. The discrepancy is explained by differences in the preparation conditions of the dissociative state of NO2.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    The European physical journal 26 (1993), S. 213-216 
    ISSN: 1434-6079
    Keywords: 33.20.Lg ; 36.40.+d
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract Vibrationally resolved electronic spectra of heteroclusters C6H6-SF6 and C6H6-(SF6)2 were studied in the spectral regions near the S0-S1, 0 0 0 and 6 0 1 transitions of the benzene monomer. A nonvanishing 0 0 0 vibrational band has been observed for C6H6-SF6 with a C3v symmetry. For both clusters we have determined the ionization potentials as well as the binding energies in the electronic ground state and the ionization state. The fragmentation of larger clusters (C6H6)n(SF6)m is restricted to the loss of SF6 molecules while the emission of C6H6 molecules have not been observed.
    Type of Medium: Electronic Resource
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