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Title: Application of transient infrared spectroscopy to intramolecular energy transfer in [(phen) (CO)[sub 3]Re[sup I](NC) Ru[sup II](CN) (bpy)[sub 2]][sup +]

Journal Article · · Journal of the American Chemical Society; (United States)
DOI:https://doi.org/10.1021/ja00076a070· OSTI ID:7302072
;  [1]; ; ; ;  [2]; ;  [3]
  1. Univ. of North Carolina, Chapel Hill, NC (United States)
  2. Los Alamos National Lab., NM (United States)
  3. Universita di Ferrara (Italy)

Significant advances have been made in the design and characterization of molecular assemblies, which, when photolyzed, undergo intramolecular electron or energy transfer. Time-resolved resonance Raman spectroscopy has been successfully applied to the study of excited states and molecular assemblies, but time-resolved infrared spectroscopy is particularly well-suited for complexes containing ligands such as CO or CN. Unlike the transient Raman experiment, infrared spectroscopy does not rely on resonance enhancement in the excited state since the metal-CO and -CN stretching vibrations have high oscillator strengths, providing high sensitivity. We describe here a novel application of the technique to the elucidation of intramolecular energy transfer in the ligand-bridged complex [(phen)(CO)[sub 3]Re[sup I](NC) Ru[sup II](CN) (bpy)[sub 2]][sup +] (phen is 1, 10-phenanthroline; bpy is 2,2'-bipyridine). These results show that the transient infrared technique can be a powerful tool for the elucidation of oxidation state and mechanisms involving photochemical intermediates by direct observation of ligand vibrations. 15 refs., 2 figs.

DOE Contract Number:
FG05-86ER13633
OSTI ID:
7302072
Journal Information:
Journal of the American Chemical Society; (United States), Vol. 115:23; ISSN 0002-7863
Country of Publication:
United States
Language:
English