On the relation of protein dynamics and exciton relaxation in pigment–protein complexes: An estimation of the spectral density and a theory for the calculation of optical spectra
By Thomas Renger, R. Marcus. 2002
314 citations recorded by the source corpus.
Subfields: Atomic and Molecular Physics, and Optics, Cellular and Molecular Neuroscience, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/99ce6af828dc06309bab23b55224afc4ba453c50
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In Atomic and Molecular Physics, and Optics
- Seogjoo J. Jang
- Benedetta Mennucci
- Akihito Ishizaki
- Graham R. Fleming
- Julian Adolphs
- Thomas Renger
- G. Engel
- Gitt Panitchayangkoon
In Cellular and Molecular Neuroscience
- Benedetta Mennucci
- Seogjoo J. Jang
- Akihito Ishizaki
- Graham R. Fleming
- Julian Adolphs
- Thomas Renger
- K. Birgitta Whaley
- Mohan Sarovar
In Molecular Biology
- Seogjoo J. Jang
- Benedetta Mennucci
- Akihito Ishizaki
- Graham R. Fleming
- Julian Adolphs
- Thomas Renger
- G. Engel
- Gitt Panitchayangkoon
Citations in the corpus
- Delocalized excitons in natural light-harvesting complexes (2018, methodology): “To this end, an exciton-bath model (Jang and Silbey, 2003a) incorporating the bath spectral density (Renger and Marcus, 2002) extracted from spectroscopic data was developed.”
- Theoretical examination of quantum coherence in a photosynthetic system at physiological temperature (2009, methodology): “On the other hand, in the fastest relaxation case in the literature, τc = 35 fs (35), numerical results with Eq.”
- Long-lived quantum coherence in photosynthetic complexes at physiological temperature (2010, result): “energy (35 cm-1 ) and ω c is the cut-off frequency (150 cm -1) (7). The observed linear relationship demonstrates that an Ohmic spectral density is a reasonable approximation for modeling this complex(28). Furthermore, the slope from the linear regression fit is 0.52 ± 0.07 cm-1/K, agreeing with the”
- How proteins trigger excitation energy transfer in the FMO complex of green sulfur bacteria. (2006, methodology): “The linear absorption a(v) is obtained from the dipoledipole correlation function as explained in detail in Renger and Marcus (26), aðvÞ} + M j~mMj 2 DMðvÞ dis ; (13) where DM(v) is the lineshape function and Æ ædis denotes an average over static disorder in site energies.”