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  • 1995-1999  (2)
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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 106 (1997), S. 5943-5946 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The photodissociation of acetyl and propionyl radicals at 248 and 266 nm has been studied by time-resolved Fourier transform infrared spectroscopy. A vibrationally excited product CO(v≤8) was observed in the emission spectra. The vibrational temperatures of the nascent CO products were about 7400 K for the acetyl radical and 6930 K for the propionyl radical. The vibrational energy partitioning of the CO fragments fits a soft impulsive model. © 1997 American Institute of Physics.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 105 (1996), S. 5377-5379 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The internal conversion and intramolecular vibrational relaxation processes of nitro-tri-tert-butylphthalocyanine, tetra-phenylporphyrin (TPP), and tetra-tert-butylphthalocyanine (BuPc) in chloroform solution were investigated with an ultrafast time-resolved fluorescence depletion method. A regular fluorescence depletion was observed, indicating that the vibrational relaxation in the S1 state takes a few hundred femtoseconds to several picoseconds. For TPP and BuPc, an additional sharp dip superposes on the regular depletion. It is explained by an ultrafast internal conversion process from the S2 state to the S1 state with a time of a few tens of femtoseconds. © 1996 American Institute of Physics.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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