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Extended X-ray Absorption Fine Structure of Copper(II) Complexes at the Air-Water Interface by a Polarized Total-Reflection X-ray Absorption Technique

机译:通过偏振全反射X射线吸收技术扩展空气 - 水界面铜(II)配合物的X射线吸收精细结构

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摘要

Copper(II) complexes spread on an aqueous solution surface were studied by a polarized total-reflection X-ray absorption fine structure (TR-XAFS) technique. The polarized TR-XAFS spectra at the Cu-K edge for copper(II) porphyrins and copper(II) chlorophyllin in a monolayer were measured in situ at the air-water interface. The polarization dependences of X-ray absorption near-edge structure (XANES) involving a 1s→4pz transition allowed us to estimate the molecular orientation and the local coordination structure around the copper(II) atom in the polarization plane selectively. The extended X-ray absorption fine structure (EXAFS) region of the polarized TR-XAFS spectra for the metal complexes present at the air-water interface was successfully analyzed for the first time. The relative coordination number for the copper center evaluated from the EXAFS analysis indicated larger values in the vertical polarization than in the horizontal one, in agreement with the standing-up molecular orientation at the air-water interface estimated from the XANES region.
机译:通过极化全反射X射线吸收精细结构(TR-XAFS)技术研究了散布在水溶液表面的铜(II)配合物。在空气-水界面处原位测量了铜(II)卟啉和叶绿素铜(II)在Cu-K边缘的极化TR-XAFS光谱。涉及1s→4pz跃迁的X射线吸收近边缘结构(XANES)的偏振相关性使我们能够选择性地估计偏振平面中铜(II)原子周围的分子取向和局部配位结构。首次成功地分析了空气-水界面处存在的金属配合物的极化TR-XAFS光谱的扩展X射线吸收精细结构(EXAFS)区域。通过EXAFS分析评估的铜中心的相对配位数表明,垂直极化的值大于水平极化的值,这与XANES区域估算的气水界面处的立式分子取向一致。

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