Long-lived primary radical pair state detected by time-resolved fluorescence and absorption spectroscopy in an isolated Photosystem two core

1992 ◽  
Vol 34 (3) ◽  
pp. 419-431 ◽  
Author(s):  
J. De Las Rivas ◽  
B. Crystall ◽  
P. J. Booth ◽  
J. R. Durrant ◽  
S. Özer ◽  
...  
1983 ◽  
Vol 105 (9) ◽  
pp. 2903-2904 ◽  
Author(s):  
Michael R. Wasielewski ◽  
Christian H. Bock ◽  
Michael K. Bowman ◽  
James R. Norris

1990 ◽  
Vol 45 (6) ◽  
pp. 763-770 ◽  
Author(s):  
U. Eberl

AbstractTwo-step sequential and unistep, superexchange primary electron transfer form primary radical pair states which differ in the direction and magnitude of their dipole moments as revealed in the X-ray structure analysis. The direction can be measured by the excitation anisotropy of electric field induced changes of the fluorescence yield. This method determines angles between the dipole of the primary radical pair and photoselected transition moments (in absorption and emission) of cofactors in the reaction centers. Transitions particularly favourable for discrimination between the two models of primary electron transfer are discussed.


2019 ◽  
Vol 21 (9) ◽  
pp. 4839-4853 ◽  
Author(s):  
Anna Reiffers ◽  
Christian Torres Ziegenbein ◽  
Luiz Schubert ◽  
Janina Diekmann ◽  
Kristoffer A. Thom ◽  
...  

The photophysics of N-methylphthalimide (MP) in solution (cyclohexane, ethanol, acetonitrile, and water) was characterized by steady state as well as time resolved fluorescence and absorption spectroscopy.


1976 ◽  
Vol 54 (6) ◽  
pp. 979-983 ◽  
Author(s):  
Harish M. Vyas ◽  
Jeffrey K. S. Wan

The photoreduction of p-fluoranil in dioxane was studied by combined CIDNP and CIDEP techniques. It was established that the photoreactive species is the excited triplet of the quinone and the phototriplet mechanism is mainly responsible for the CIDEP observation. The CIDNP observations revealed the cage recombination of the primary radical-pair resulting in the formation of the cross-combination product from the semiquinone and the dioxane radicals. The cage recombination cannot be monitored by the conventional kinetic esr technique. The field dependent CIDNP intensity of the p-fluoranil in the photoreduction by fluorohydroquinone was also studied and a calculation based on Lawler's scheme showed that the results can be adequately explained by the radical-pair theory including both the scavenged and cage combination processes.


1997 ◽  
Vol 101 (8) ◽  
pp. 1437-1443 ◽  
Author(s):  
A. van der Est ◽  
T. Prisner ◽  
R. Bittl ◽  
P. Fromme ◽  
W. Lubitz ◽  
...  

FEBS Letters ◽  
1993 ◽  
Vol 336 (2) ◽  
pp. 357-362 ◽  
Author(s):  
Martin Volk ◽  
Matthias Gilbert ◽  
Gerhard Rousseau ◽  
Martin Richter ◽  
Alexander Ogrodnik ◽  
...  

Biochemistry ◽  
1994 ◽  
Vol 33 (11) ◽  
pp. 3185-3192 ◽  
Author(s):  
Gary Hastings ◽  
Frank A. M. Kleinherenbrink ◽  
Su Lin ◽  
Robert E. Blankenship

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