The electronic structure of Mn in oxides, coordination complexes, and the oxygen-evolving complex of photosystem II studied by resonant inelastic X-ray scattering

被引:158
作者
Glatzel, P [1 ]
Bergmann, U
Yano, J
Visser, H
Robblee, JH
Gu, WW
de Groot, FMF
Christou, G
Pecoraro, VL
Cramer, SP
Yachandra, VK
机构
[1] Univ Calif Davis, Dept Appl Sci, Davis, CA 95616 USA
[2] Univ Utrecht, Debye Inst, Dept Inorgan Chem & Catalysis, NL-3584 CA Utrecht, Netherlands
[3] Univ Florida, Dept Chem, Gainesville, FL 32611 USA
[4] Univ Michigan, Dept Chem, Ann Arbor, MI 48109 USA
[5] Univ Calif Berkeley, Lawrence Berkeley Lab, Melvin Calvin Lab, Phys Biosci Div, Berkeley, CA 94720 USA
关键词
D O I
10.1021/ja038579z
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Resonant inelastic X-ray scattering (RIXS) was used to collect Mn K pre-edge spectra and to study the electronic structure in oxides, molecular coordination complexes, as well as the S-1 and S-2 states of the oxygen-evolving complex (OEC) of photosystem II (PS II). The RIXS data yield two-dimensional plots that can be interpreted along the incident (absorption) energy or the energy transfer axis. The second energy dimension separates the pre-edge (predominantly 1s to 3d transitions) from the main K-edge, and a detailed analysis is thus possible. The 1s2p RIXS final-state electron configuration along the energy transfer axis is identical to conventional L-edge absorption spectroscopy, and the RIXS spectra are therefore sensitive to the Mn spin state. This new technique thus yields information on the electronic structure that is not accessible in conventional K-edge absorption spectroscopy. The line splittings can be understood within a ligand field multiplet model, i.e., (3d,3d) and (2p,3d) two-electron interactions are crucial to describe the spectral shapes in all systems. We propose to explain the shift of the K pre-edge absorption energy upon Mn oxidation in terms of the effective number of 3d electrons (fractional 3d orbital population). The spectral changes in the Mn 1s2p(3/2) RIXS spectra between the PS II S, and S2 states are small compared to that of the oxides and two of the coordination complexes (Mn-III(acac)(3) and Mn-IV(sal)(2)(bipy)). We conclude that the electron in the step from S-1 to S-2 is transferred from a strongly delocalized orbital.
引用
收藏
页码:9946 / 9959
页数:14
相关论文
共 76 条
  • [1] [Anonymous], 1996, ADV PHOTOSYNTH
  • [2] [Anonymous], 1967, INTERSCIENCE
  • [3] BALLHAUSEN CJ, 1964, MOL ORBITAL THEORY
  • [4] Characterization of the Mn oxidation states in photosystem II by Kβ X-ray fluorescence spectroscopy
    Bergmann, U
    Grush, MM
    Horne, CR
    DeMarois, P
    Penner-Hahn, JE
    Yocum, CF
    Wright, DW
    Dubé, CE
    Armstrong, WH
    Christou, G
    Eppley, HJ
    Cramer, SP
    [J]. JOURNAL OF PHYSICAL CHEMISTRY B, 1998, 102 (42): : 8350 - 8352
  • [5] A high-resolution large-acceptance analyzer for X-ray fluorescence and Raman spectroscopy
    Bergmann, U
    Cramer, SP
    [J]. CRYSTAL AND MULTILAYER OPTICS, 1998, 3448 : 198 - 209
  • [6] A HIGHLY RESOLVED, OXYGEN-EVOLVING PHOTOSYSTEM-II PREPARATION FROM SPINACH THYLAKOID MEMBRANES - ELECTRON-PARAMAGNETIC-RES AND ELECTRON-TRANSPORT PROPERTIES
    BERTHOLD, DA
    BABCOCK, GT
    YOCUM, CF
    [J]. FEBS LETTERS, 1981, 134 (02) : 231 - 234
  • [7] ATOMIC INNER-SHELL LEVEL ENERGIES DETERMINED BY ABSORPTION SPECTROMETRY WITH SYNCHROTRON RADIATION
    BREINIG, M
    CHEN, MH
    ICE, GE
    PARENTE, F
    CRASEMANN, B
    [J]. PHYSICAL REVIEW A, 1980, 22 (02): : 520 - 528
  • [8] Pulsed and parallel-polarization EPR characterization of the photosystem II oxygen-evolving complex
    Britt, RD
    Peloquin, JM
    Campbell, KA
    [J]. ANNUAL REVIEW OF BIOPHYSICS AND BIOMOLECULAR STRUCTURE, 2000, 29 : 463 - 495
  • [9] BRITT RD, 1996, OXYGENIC PHOTOSYNTHE, V4, P137
  • [10] THE EFFECT OF TEMPERATURE ON THE FORMATION AND DECAY OF THE MULTILINE ELECTRON-PARAMAGNETIC-RES SIGNAL SPECIES ASSOCIATED WITH PHOTOSYNTHETIC OXYGEN EVOLUTION
    BRUDVIG, GW
    CASEY, JL
    SAUER, K
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA, 1983, 723 (03) : 366 - 371