Abstract
The ability to investigate ultrafast photophysics and photochemistry of reaction centers and antenna pigments of photosynthetic bacteria and of bacteriorhodopsin is a direct result of the advancing technology for the generation and the amplification of ultrashort light pulses [1]. The dual-beam femtosecond absorption spectrometer with which the data discussed here were obtained is described in detail elsewhere [2]. For our investigations of reaction centers and antenna pigments of photosynthetic bacteria, a tunable excitation beam was obtained by amplification [2–4] of a selected portion of a white-light continuum. For systems with several interacting chromophores, such as reaction centers, tunability of the excitation and the probe beams is equally as important as temporal resolution [3,5].
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Petrich, J.W., Breton, J., Martin, J.L. (1987). Femtosecond Absorption Studies of the Primary Events in Bacterial Photosynthesis and Light- and Dark-Adapted Bacteriorhodopsin. In: Kobayashi, T. (eds) Primary Processes in Photobiology. Springer Proceedings in Physics, vol 20. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-72835-8_6
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DOI: https://doi.org/10.1007/978-3-642-72835-8_6
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