Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    The European physical journal 18 (1991), S. 181-188 
    ISSN: 1434-6079
    Keywords: 36.40 ; 82.50.F
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract The infrared photodissociation spectra of C2H4 and CH3OH dimers are measured for different internal excitation energies ΔE. The dimers are size-selected in a scattering process with He and the internal energy is varied by using (1) different collision energies, (2) different scattering angles and (3) by measuring the complete energy loss spectra with and without laser radiation by time-of-flight analysis of the scattered clusters. For (CH3OH)2 the width Γ of the spectrum increases strongly with ΔE, while the cross section at the maximum is constant, a normal behaviour for an inhomogeneously broadened system. For (C2H4)2 Γ is nearly constant after a sort of threshold and the cross section increases with increasing ΔE. These results are explained by hot band excitation and the coupling to the darkv 10-mode.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    ISSN: 1434-6079
    Keywords: 36.40 ; 82.50.F
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract Infrared photodissociation spectra of (CH3NH2) n clusters were measured fromn=2 ton=6 near the monomer absorption of the C-N stretching mode at 1044 cm−1 using a cw-CO2 laser. The clusters were size-selected by scattering from a helium beam. The spectrum of cold dimers shows a red (1038 cm−1) and a blue (1048 cm−1) shifted peak which is attributed to the non-equivalent position of the C-N in the open dimer structure. The larger clusters exhibit only one peak between 1045.4 cm−1 and 1046.0 cm−1 caused by the equivalent position of the C-N in the cyclic structures of the larger clusters. Structure calculations confirm these results. Secondly, the mixed complexes C2H4-CH3COCH3 and C2H4-(CH3COCH3)2 were investigated. The dimer spectrum, measured around the monomer frequency of the out-of-plane bending mode of C2H4 at 949 cm−1, shows two peaks at 946.2 cm−1 and 961.3 cm−1. This splitting is attributed to two different isomers that are found in configuration calculations. A similar behaviour is found for the trimer.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...