Collier, Martin A. and McCaffrey, John G.
The absorption and excitation spectroscopy of matrix-isolated atomic manganese: Sites of isolation in the solid rare gases.
Journal of Chemical Physics, 122.
This study collects information from absorption and luminescence excitation spectra recorded for Mn atoms isolated in the solid rare gases Ar, Kr, and Xe and presents an analysis of the site occupancy, based on the polarizabilities of the rare gases and the observed spectral shifts. Two thermally stable sites of isolation exist for atomic Mn in solid Ar and Kr, while a single thermally stable site is present in Mn/Xe. Site occupancy assignments are based on the application of a
polarizability model to the z 6P5/2Ãa 6S5/2 ; z 8P5/2Ãa 6S5/2 , and y 6P5/2Ãa 6S5/2 electronic transitions of atomic Mn. From an analysis of the observed RG matrix-to-gas phase energy shifts for PÃS type transitions, this model allows the association of certain site types occupied by metal atoms in the rare gas solids. The required condition being a linear dependence of the matrix shifts
with rare gas polarizability for those metal atoms ââtrappedââ in a particular site type. Application of
the polarizability model in conjunction with trends observed in site dominance, established a connection between the blue sites in Ar and Kr and the single site in Xe. Use of the known MgÂRG ground state bond lengths facilitated an identification of the sites of Mn atom isolation assuming the transference of the known MgÂRG bond lengths to the MnÂRG systems. Substitutional site
occupancy of atomic Mn is assigned to the blue sites in Ar and Kr and the single site in Xe, while tetra-vacancy site occupancy is assigned to the red sites in Ar and Kr. Consistent with these assignments, Mn atoms in solid Ar show a preference for trapping in tetra-vacancy sites whereas in solid Kr, single substitutional sites are preferred and in Xe, this is the only site observed.
||matrix-isolated atomic manganese, solid rare gases, spectroscopy
||Science & Engineering > Chemistry
Dr. John McCaffrey
||18 May 2007
|Journal or Publication Title:
||Journal of Chemical Physics
||American Institute of Physics
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