Dichotomous Disorder versus Excitonic Splitting of the B800 Band of Allochromatium vinosum
Journal Article
·
· Journal of Physical Chemistry Letters
- Kansas State Univ., Manhattan, KS (United States); Kansas State University
- Kansas State Univ., Manhattan, KS (United States)
The purple bacterium of Allochromatium vinosum has a distinct double peak structure of the 800 nm band (B800). Several hypotheses were proposed in the literature to explain its origin. Although recent 77 K two-dimensional electronic spectroscopy (2DES) data could neither refute or validate previous findings that the two B800 sub-bands are due to different site-energies (most likely due weakly and strongly hydrogen bonded B800 BChls [A. Kell et al., J. Phys. Chem. B 2017, 121, 9999]), the authors concluded that strong excitonic coupling of dimerized bacteriochlorophylls (BChls) within the B800 ring is largely responsible for the B800 split [M. Schroter et al., J. Phys. Chem. Lett. 2018, 9, 1340]. Here it is demonstrated that the latter is incorrect and excitonic interactions between BChls in the B800 ring, though present, are weak. This conclusion is based on an exciton model with dichotomous protein conformation disorder. We show that complementary data provided by hole burning (HB) spectroscopy, 2DES, and modeling studies provide a more comprehensive picture on the origin of the B800 band split. Energy transfer pathways from B800B → B800R, B800B → B850 and B800R → B850 revealed by HB spectroscopy are compared to those obtained via 2DES.
- Research Organization:
- Kansas State Univ., Manhattan, KS (United States)
- Sponsoring Organization:
- USDOE Office of Science (SC), Basic Energy Sciences (BES)
- Grant/Contract Number:
- SC0006678
- OSTI ID:
- 1539331
- Journal Information:
- Journal of Physical Chemistry Letters, Journal Name: Journal of Physical Chemistry Letters Journal Issue: 14 Vol. 9; ISSN 1948-7185
- Publisher:
- American Chemical SocietyCopyright Statement
- Country of Publication:
- United States
- Language:
- English
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