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'Reaction Center' in keywords Facet   Publication Year 1990  [X]
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1990[X]
1Author    JonathanM. Keske, J.Malcolm Bruce, P. Leslie, D. UttonRequires cookie*
 Title    A New Method of Solvation Analysis: Applications to Quinones  
 Abstract    A new method o f analysis o f the factor contributing to solvation o f small molecules is de­ scribed. A pproxim ations o f the energetic contributions to the entry o f a molecule into water have been derived from partition coefficient data o f solutes and selected derivatives from a multiplicity o f solvents. These include taking separate account energy o f the cost o f introduction o f a molecular cavity in water, the strength o f solute-water dipolar interactions, and the strengths o f hydrogen bond formation with water o f the lone pairs and hydroxylic hydrogens associated with the molecule. In this report the solvation-free energies o f benzoquinone and hydroquinone in water are described. We also consider the solvation o f the sem iquinone anion and show it to be fundamentally different from that o f either the quinone or hydroquinone; this is discussed as a potentiality for selective binding ("solvation") o f quinone, sem iquinone and hydroquinone in sites o f redox catalysis such as those found in the photosynthetic reaction center. 
  Reference    Z. Naturforsch. 45c, 430 (1990); received December 18 1989 
  Published    1990 
  Keywords    Quinone, Ligand Binding, Reaction Centers, Solvation 
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 TEI-XML for    default:Reihe_C/45/ZNC-1990-45c-0430.pdf 
 Identifier    ZNC-1990-45c-0430 
 Volume    45 
2Author    U. Eberl, A. Ogrodnik, M. E. Michel-BeyerleRequires cookie*
 Title    Access to Primary Charge Separation Mechanism in Photosynthetic Reaction Centers: Anisotropic Excitation Spectra of Electric Field Modulated Fluorescence Yields  
 Abstract    Two-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. 
  Reference    Z. Naturforsch. 45a, 763—770 (1990); received March 17 1990 
  Published    1990 
  Keywords    Electric field effect, Anisotropy, Fluorescence, Photosynthesis, Reaction center, Pri-mary charge separation 
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 TEI-XML for    default:Reihe_A/45/ZNA-1990-45a-0763.pdf 
 Identifier    ZNA-1990-45a-0763 
 Volume    45