ISSN:
1089-7690
Source:
AIP Digital Archive
Topics:
Physics
,
Chemistry and Pharmacology
Notes:
Molecular beam depletion spectroscopy has been employed to study the dissociation of small methyl fluoride clusters upon excitation of the ν3 C–F stretch vibration at 1048.6 cm−1. Size selection has been achieved by dispersing the (CH3F)n cluster beam by a secondary rare gas beam. For the methyl fluoride dimer only very weak dissociation signals could be observed. The corresponding spectrum features a single, 13.4 cm−1 broad absorption line. This observation is explained with a symmetric dimer structure, in which both monomer units reside at equivalent positions, and an inefficient coupling of the molecular vibration to the intermolecular bond. For the trimer and tetramer very strong dissociation yields are observed. Whereas the trimer shows a complicated spectrum which is attributed to its nonsymmetric structure, the tetramer spectrum is again characterized by a single peak. In order to obtain supplementary information, dissociation spectra have also been measured for small methyl fluoride clusters residing inside or on the surface of large Arx host clusters. These matrixlike spectra are consistent with the free gas-phase cluster data. Finally, in a computational approach, the structures of the methyl fluoride dimer, trimer, and tetramer have been determined by total energy minimization. The theoretical results are in perfect agreement with the experimental findings.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1063/1.463043
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