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Excited State Structure and Relaxation Dynamics of Polypyridyl Complexes of Low Spin d6 Metal Ions by Means of Step-Scan FTIR Time-Resolved Spectroscopy (S2FT-IR TRS)

  • Richard A. Palmer
  • Pingyun Chen
  • Susan E. Plunkett
  • James L. Chao
Conference paper
Part of the Mikrochimica Acta Supplement book series (MIKROCHIMICA, volume 14)

Abstract

Time-resolved infrared spectroscopy has been applied to study the excited state dynamics of many biological molecules and transition metal complexes following laser-flash excitation [1–6]. The short lifetimes of the excited states involved in these processes require very high time resolution. Until recently, fast time-resolved IR measurements have typically utilized tunable IR diode lasers as the probe source. The limited tunability of these IR lasers limited the studies to systems that contain CO or CN groups as a “reporter” ligand.

Keywords

Excited State Difference Spectrum Transient Absorption Relaxation Dynamics High Time Resolution 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© Springer-Verlag Wien 1997

Authors and Affiliations

  • Richard A. Palmer
    • 1
  • Pingyun Chen
    • 1
  • Susan E. Plunkett
    • 1
  • James L. Chao
    • 2
  1. 1.Department of ChemistryDuke UniversityDurhamUSA
  2. 2.Research Triangle ParkIBM CorporationUSA

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