Abstract
We provide a new and definitive spectral assignment for the absorption, emission, high-resolution fluorescence excitation, linear dichroism, and/or magnetic circular dichroism spectra of 32 chlorophyllides in various environments. This encompases all data used to justify previous assignments and provides a simple interpretation of unexplained complex decoherence phenomena associated with Q x → Q y relaxation. Whilst most chlorophylls conform to the Gouterman model and display two independent transitions Q x (S 2) and Q y (S 1), strong vibronic coupling inseparably mixes these states in chlorophyll-a. This spreads x-polarized absorption intensity over the entire Q-band system to influence all exciton-transport, relaxation and coherence properties of chlorophyll-based photosystems. The fraction of the total absorption intensity attributed to Q x ranges between 7% and 33%, depending on chlorophyllide and coordination, and is between 10% and 25% for chlorophyll-a. CAM-B3LYP density-functional-theory calculations of the band origins, relative intensities, vibrational Huang-Rhys factors, and vibronic coupling strengths fully support this new assignment.
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CITATION STYLE
Reimers, J. R., Cai, Z. L., Kobayashi, R., Rätsep, M., Freiberg, A., & Krausz, E. (2013). Assignment of the Q-Bands of the Chlorophylls: Coherence Loss via Q x-Q y Mixing. Scientific Reports, 3. https://doi.org/10.1038/srep02761
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