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Title: Vibrational overtone spectroscopy of the 4. nu. sub OH +. nu. sub OH prime combination level of HOOH via sequential local mode--local mode excitation

Journal Article · · Journal of Chemical Physics; (United States)
DOI:https://doi.org/10.1063/1.462665· OSTI ID:7234494
; ;  [1]
  1. Department of Chemistry, University of Rochester, Rochester, New York 14627 (United States)

Sequential pumping of the local OH stretch vibrations in hydrogen peroxide using infrared-optical double resonance permits spectroscopic access to the 4{nu}{sub OH}+{nu}{sub OH{prime}} combination level. Analysis of the rotationally resolved vibrational overtone spectra generated by this technique determines approximate rotational constants for this level and a value of 17 051.8{plus minus}3.4 cm{sup {minus}1} for the O--O bond dissociation energy. The linewidths of individual zeroth-order rotational transitions increase sharply with increasing {ital K} and change from smooth Lorentzian profiles to clumps of individual lines. The {ital K} dependence of the clump widths suggests that an {ital a}-axis Coriolis interaction is the primary coupling mechanism between the zeroth-order bright state and dark bath states. As a function of increasing {ital J}, each clump coalesces into a smooth Lorentzian profile. We interpret this {ital J} dependence in terms of a model that includes rotationally induced vibrational coupling among zeroth-order dark states.

OSTI ID:
7234494
Journal Information:
Journal of Chemical Physics; (United States), Vol. 96:8; ISSN 0021-9606
Country of Publication:
United States
Language:
English