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Title: Mechanism of charge transfer in the molecular DPQ complex studied by time-resolved fluorescence spectroscopy

Journal Article · · Journal of Physical Chemistry; (United States)
DOI:https://doi.org/10.1021/j100170a011· OSTI ID:7273576
; ;  [1]; ;  [2]
  1. Lomonsov Inst. of Fine Chemical Technology, Moscow (Russian Federation)
  2. Moscow State Univ. (Russian Federation)

Recent results of the X-ray analysis and femtosecond spectroscopy of photosynthetic bacteria reaction centers have contributed very much to the understanding of the primary events in photosynthesis. The pathways of charge separation in the dimethylaniline-mesoporphyrin II-naphthoquinone triad DPQ and its Zn complex were established. The rate constants of electron transfer from P and ZnP to Q were measured to be k = 1.5 {times} 10{sup 9} s{sup {minus}1} and k > 5 {times} 10{sup 10} s{sup {minus}1}, respectively, from the results of picosecond fluorescence spectroscopy. The transformation of the DPQ and DZnPQ triads to the reduced form by NaBH{sub 4} treatment results in blocking of the electron-transfer channel from both P and ZnP to Q. The role of structural and conformational changes of triads in the electron-transfer process is discussed.

OSTI ID:
7273576
Journal Information:
Journal of Physical Chemistry; (United States), Vol. 95:17; ISSN 0022-3654
Country of Publication:
United States
Language:
English