# SPECTROSCOPY AND RELAXATION KINETICS OF MATRIX ISOLATED CH/D RADICALS

Please use this identifier to cite or link to this item: http://hdl.handle.net/1811/19979

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 Title: SPECTROSCOPY AND RELAXATION KINETICS OF MATRIX ISOLATED CH/D RADICALS Creators: Burroughs, Amy; Heaven, M. C. Issue Date: 2000 Publisher: Ohio State University Abstract: We have investigated the properties of matrix isolated CD and present a comparison with earlier studies of the CH radical. The CH/D radicals were formed by the microwave dissociation of methane. The products were trapped in solid Ar or Kr at 12 K and investigated using laser excitation and dispersed fluorescence techniques. The $B^{2}\Sigma - X^{2}\Pi$ and $A^{2}\Delta - X^{2}\Pi - B\rightarrow A$ nonradiative transfer. Fluorescence was not detected from CD(B), v = 0, as the the $B\rightarrow A$ transfer process was much faster than radiative decay for this isotope. Difference in the $B\rightarrow A$ energy gaps are responsible for the large difference in the transfer rates of the two isotopes. Excitation spectra yield evidence that CH/D(B) rotates in solid Ar and Kr matrices. Low frequency structure in the B-X(0,0) absorption band changed considerably on H/D isotopic substitution while it was relatively insensitive to the replacement of the matrix material. Absorption spectra for the A-X transition did not show evidence for rotation in the matrix, but it is likely that optical selection rules prevent the observation of rotational structure in this instance. Vibrational relaxation of CH/D(B) is faster for heavier isotope, indicating that vibration to rotation energy transfer is the dominant relaxation mechanism. Description: Work by the National Science Foundation Author Institution: Department of Chemistry of Chemistry, Emory University URI: http://hdl.handle.net/1811/19979 Other Identifiers: 2000-WI-06