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Bridging-type changes facilitate successive oxidation steps at about 1 V in two binuclear manganese complexes - implications for photosynthetic water-oxidation

Magnuson, Ann (författare)
Uppsala universitet,Molekylär biomimetik
Liebisch, P. (författare)
Högblom, Joakim (författare)
Lund University,Lunds universitet,Biokemi och Strukturbiologi,Centrum för Molekylär Proteinvetenskap,Kemiska institutionen,Institutioner vid LTH,Lunds Tekniska Högskola,Biochemistry and Structural Biology,Center for Molecular Protein Science,Department of Chemistry,Departments at LTH,Faculty of Engineering, LTH
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Anderlund, M. F. (författare)
Lomoth, Reiner (författare)
Uppsala universitet,Institutionen för kemi - Ångström
Meyer-Klaucke, W. (författare)
Haumann, M. (författare)
Dau, H. (författare)
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 (creator_code:org_t)
Elsevier BV, 2006
2006
Engelska.
Ingår i: Journal of Inorganic Biochemistry. - : Elsevier BV. - 1873-3344 .- 0162-0134. ; 100:7, s. 1234-1243
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • The redox behavior of two synthetic manganese complexes illustrates a mechanistic aspect of importance for light-driven water oxidation in Photosystem 11 (PSII) and design of biomimetic systems (artificial photosynthesis). The coupling between changes in oxidation state and structural changes was investigated for two binuclear manganese complexes (1 and 2), which differ in the set of first sphere ligands to Mn (N3O3 in 1, N2O4 in 2). Both complexes were studied by electron paramagnetic resonance (EPR) and X-ray absorption spectroscopy (XAS) in three oxidation states which had been previously prepared either electro- or photochemically. The following bridging-type changes are suggested. In 1: Mn-II-(mu-OR)(mu-OCO)(2)-Mn-II double left right arrow Mn-II-(mu-OR)(mu-OCO)(2)-Mn-III double right arrow Mn-III-(mu-OR)(mu-OCO)-(mu-O)-Mn-IV. In 2: Mn-II-(mu-OR)(mu-OCO)(2)-Mn-III double left right arrow Mn-III-(mu-OR)(mu-OCO)(2)-Mn-III double right arrow Mn-III-(mu-OR)([mu-OCO)(mu-O)-Mn-IV. In both complexes, the first one-electron oxidation proceeds without bridging-type change, but involves a redox-potential increase by 0.5-1 V. The second one-electron oxidation likely is coupled to mu-oxo-bridge (or mu-OH) formation which seems to counteract a further potential increase. In both complexes, mu-O(H) bridge formation is associated with a redox transition proceeding at similar to 1 V, but the mu-O(H) bridge is observed at the Mn-2(III,III) level in I and at the Mn-III,Mn-IV level in 2, demonstrating modulation of the redox behavior by the terminal ligands. It is proposed that also in PSII bridging-type changes facilitate successive oxidation steps at approximately the same potential. (c) 2006 Elsevier Inc. All rights reserved.

Ämnesord

NATURVETENSKAP  -- Biologi -- Biokemi och molekylärbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biochemistry and Molecular Biology (hsv//eng)
NATURVETENSKAP  -- Kemi -- Oorganisk kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Inorganic Chemistry (hsv//eng)

Nyckelord

absorption spectroscopy
photosynthesis
manganese complex
biomorganic chemistry
EPR
X-ray
Kemi med inriktning mot molekylär biomimetik

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