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Mass-selective ionization-detected stimulated Raman spectroscopy of benzene trimer and higher clusters

Journal Article · · Journal of Chemical Physics; (United States)
DOI:https://doi.org/10.1063/1.464544· OSTI ID:6873553
; ; ;  [1]
  1. Department of Chemistry and Biochemistry, University of California, Los Angeles, California 90024-1569 (United States)
We present the results of mass-selective, ionization-detected stimulated Raman spectroscopies on jet-cooled benzene clusters from the trimer to the octamer. The data pertain to the fundamentals of the totally symmetric ring-breathing ([nu][sub 1]) and C--H stretch ([nu][sub 2]) modes of benzene and provide information about geometrical structure and vibrational dynamics. For the trimer, the results indicate a species in which all three benzenes reside in equivalent sites. For the higher clusters the results point to geometries involving two or more inequivalent sites. The [nu][sub 1]-excited trimer is found to decay on a nanosecond, or longer, time scale. The [nu][sub 2]-excited trimer decays on a time scale of greater than 5 ps. Similar timescales characterize the decays of the [nu][sub 2]-excited tetramer and pentamer.
DOE Contract Number:
FG03-89ER14066
OSTI ID:
6873553
Journal Information:
Journal of Chemical Physics; (United States), Journal Name: Journal of Chemical Physics; (United States) Vol. 98:11; ISSN JCPSA6; ISSN 0021-9606
Country of Publication:
United States
Language:
English

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