J. Friedrich, D. Haarer
The Journal of Chemical Physics
We have shown that both the native C-phycocyanin and its corresponding free biline chromophore undergo reversible, low-temperature photochemistry. We attribute this photochemistry to reversible proton-transfer processes and utilize the observed photoreaction for photochemical hole burning (PHB). Using narrow-band PHB experiments, we have been able to perform high-resolution optical studies and show that the protein-chromophore assembly forms a very rigid structure. The results lead to the conclusion that the light-induced proton transfer occurs most probably in the triplet state. © 1981, American Chemical Society. All rights reserved.
J. Friedrich, D. Haarer
The Journal of Chemical Physics
J. Friedrich, D. Haarer
Chemical Physics Letters
J. Friedrich, H. Scheer, et al.
The Journal of Chemical Physics
J. Friedrich, H. Wolfrum, et al.
The Journal of Chemical Physics