Shortly after their formation, transient free radicals trapped in micelles exhibit electron spin resonance (ESR) spectra with "antiphase" lineshapes, i.e. lines with their low-field halves in emission and high-field halves in absorption. It is demonstrated that this hitherto unexplained effect is co
Electron paramagnetic resonance of spin-correlated radical pairs in photosynthetic reactions
β Scribed by P.J. Hore; D.A. Hunter; C.D. McKie; A.J. Hoff
- Publisher
- Elsevier Science
- Year
- 1987
- Tongue
- English
- Weight
- 516 KB
- Volume
- 137
- Category
- Article
- ISSN
- 0009-2614
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β¦ Synopsis
Previous attempts to interpret the time-resolved electron paramagnetic resonance spectra of photosynthetic bacteria have been based on the premise that electron spin polarization arises in the primary radical pair (P+I-) formed by photoinduced charge separation. The observed spectrum is assumed to be the sum of the EPR spectra of P+ and X-, the radical produced from I-by electron transfer. Here it is argued that P+I-may be too short-lived to give rise to significant polarization and that the experimental spectrum is consistent with the rapid formation of a spin-correlated secondary radical pair.
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The spin-correlated radical pair [P+'Q~'] in protonated zinc replaced reaction centers of Rb. sphaeroides R26 is studied using electron spin echo spectroscopy. Applying a (flash-t-pulse 1-T-pulse 2-T) pulse sequence, it was found that the shape of the echo at T = ~-is influenced markedly by the dela
We demonstrate the potential of high-field (HF) time-resolved electron paramagnetic resonance (EPR) spectroscopy to reveal unique information about electron transfer processes and the structure of photosynthetic systems. The lineshapes and electron spin polarization (ESP) of spin-correlated radical