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Theory of Excitation Energy Transfer and Optical Spectra of Photosynthetic Systems

  • Thomas Renger
  • Alfred R. Holzwarth
Part of the Advances in Photosynthesis and Respiration book series (AIPH, volume 26)

In this chapter, we discuss the theories applicable for calculating energy transfer kinetics and optical spectra of photosynthetic pigment-protein complexes. The various theoretical approaches for obtaining expressions for rate constants and optical spectra are reviewed. At the extremes we distinguish weak and strong coupling between electronic excitations of the pigments. If the coupling is strong compared to the dynamic and static disorder introduced by the protein environment, then delocalized electronic states are formed after light excitation. The excitation energy relaxes between those delocalized states. In the weak coupling limit localized states are created by excitation and the excitation energy is transferred via a hopping mechanism. In general in photosynthetic antenna and reaction centers neither limit applies in a strict sense. Thus more sophisticated theories describing the intermediate cases have to be applied, and these should also account for the coupling of the excited states to the vibrational states of the environment. We discuss the recent attempts of solving the challenging problem to apply a non-perturbative description of both the pigment-pigment as well as the pigment-protein couplings. Applications of these theories to the spectroscopy of photosynthetic systems over the last decade are also reviewed.

Keywords

Exciton State Excitation Energy Transfer Site Energy Green Sulfur Bacterium Excitonic Coupling 
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 Science+Business Media B.V 2008

Authors and Affiliations

  • Thomas Renger
    • 1
  • Alfred R. Holzwarth
    • 2
  1. 1.Institut für Chemie und BiochemieFreie Universität BerlinGermany
  2. 2.Max-Planck-Institut für Bioanorganische ChemieGermany

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