scholarly journals Photoprotection and triplet energy transfer in higher plants: the role of electronic and nuclear fluctuations

2016 ◽  
Vol 18 (16) ◽  
pp. 11288-11296 ◽  
Author(s):  
Lorenzo Cupellini ◽  
Sandro Jurinovich ◽  
Ingrid G. Prandi ◽  
Stefano Caprasecca ◽  
Benedetta Mennucci

Photosynthetic organisms employ several photoprotection strategies to avoid damage due to the excess energy in high light conditions.

1988 ◽  
Vol 48 (3) ◽  
pp. 318-322 ◽  
Author(s):  
N. Kh. Ibraev ◽  
G. A. Ketsle ◽  
L. V. Levshin ◽  
Yu. A. Soinikov

2017 ◽  
Vol 114 (28) ◽  
pp. E5513-E5521 ◽  
Author(s):  
Junming Ho ◽  
Elizabeth Kish ◽  
Dalvin D. Méndez-Hernández ◽  
Katherine WongCarter ◽  
Smitha Pillai ◽  
...  

In photosynthetic organisms, protection against photooxidative stress due to singlet oxygen is provided by carotenoid molecules, which quench chlorophyll triplet species before they can sensitize singlet oxygen formation. In anoxygenic photosynthetic organisms, in which exposure to oxygen is low, chlorophyll-to-carotenoid triplet–triplet energy transfer (T-TET) is slow, in the tens of nanoseconds range, whereas it is ultrafast in the oxygen-rich chloroplasts of oxygen-evolving photosynthetic organisms. To better understand the structural features and resulting electronic coupling that leads to T-TET dynamics adapted to ambient oxygen activity, we have carried out experimental and theoretical studies of two isomeric carotenoporphyrin molecular dyads having different conformations and therefore different interchromophore electronic interactions. This pair of dyads reproduces the characteristics of fast and slow T-TET, including a resonance Raman-based spectroscopic marker of strong electronic coupling and fast T-TET that has been observed in photosynthesis. As identified by density functional theory (DFT) calculations, the spectroscopic marker associated with fast T-TET is due primarily to a geometrical perturbation of the carotenoid backbone in the triplet state induced by the interchromophore interaction. This is also the case for the natural systems, as demonstrated by the hybrid quantum mechanics/molecular mechanics (QM/MM) simulations of light-harvesting proteins from oxygenic (LHCII) and anoxygenic organisms (LH2). Both DFT and electron paramagnetic resonance (EPR) analyses further indicate that, upon T-TET, the triplet wave function is localized on the carotenoid in both dyads.


1983 ◽  
Vol 38 (10) ◽  
pp. 1146-1148
Author(s):  
M. Zander

Abstract The intermolecular triplet-triplet energy transfer system benzophenone (donor)/naphthalene (acceptor) was studied in various rigid glasses at 77 K. It is shown that energy transfer is much more efficient if the donor is present in the form of microcrystals than in the case where both donor and acceptor compound are in true solution.


2002 ◽  
Vol 106 (29) ◽  
pp. 6702-6709 ◽  
Author(s):  
Jacques Lalevée ◽  
Xavier Allonas ◽  
Frédéric Louërat ◽  
Jean Pierre Fouassier

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