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首页> 外文期刊>Journal of synchrotron radiation >Propagation of uncertainty in experiment: structures of Ni (II) coordination complexes
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Propagation of uncertainty in experiment: structures of Ni (II) coordination complexes

机译:不确定性在实验中的传播:Ni(II)协调复合物的结构

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摘要

Accurate experimental XAFS (X-ray absorption fine-structure) data including uncertainties are required during analysis for valid comparison of results and conclusions of hypothesis testing on structural determinations. Here an approach is developed to investigate data without standard interpolation of experimental data and with minimal loss of information content in the raw data. Nickel coordination complexes bis(i-n-propylsalicylaldiminato)nickel(II) (i-pr) and bis(N-n-propylsalicylaldiminato)nickel(II) (n-pr) are investigated. The additional physical insight afforded by the correct propagation of experimental uncertainty is used to determine newly refined structures for the innermost coordination shell. Two sets of data are investigated for each complex; one optimized for high point accuracy and one optimized for high point density. Clearly both are important and in this investigation the quality of the physical insight from each is directly provided by measured and propagated uncertainties to fairly represent the relevant accuracies. The results provide evidence for an approximate tetrahedral geometry for the i-pr Ni complex that is more symmetric than previously concluded, with our high point accuracy data yielding ligand lengths of 2.017 ± 0.006 ? and 2.022 ± 0.006 ? for Ni-N and Ni-O bonds, respectively, and an even more skewed square-planar (i.e. rhombohedral) arrangement for the n-pr complex with corresponding bond lengths of 2.133 ± 0.004 ? and 1.960 ± 0.003 ? . The ability to distinguish using hypothesis testing between the subtle differences in XAFS spectra arising from the approximate local tetrahedral and square-planar geometries of the complexes is also highlighted. The effect of standard interpolation on experimental XAFS spectra prior to fitting with theoretical model structures is investigated. While often performed as a necessary step for Fourier transformation into position space, this will nonetheless skew the fit away from actual data taken,
机译:在分析期间,在分析期间需要包括不确定性的准确实验XAFS(X射线吸收细结构)数据,以获得对结构测定的假设检测结果的有效比较和结论。这里开发了一种方法来调查没有实验数据的标准插值的数据,并且在原始数据中的信息内容丢失最小。研究了镍配合物BIS(I-N-丙基丙基丙基甲酰胺)镍(II)(I-PR)和双(N-N-丙基羟基丙基甲酰胺)镍(II)(N-PR)。通过实验性不确定性的正确传播提供的附加物理洞察力用于确定最内心的协调壳体的新精致结构。对每个复合物研究了两组数据;一种优化高点精度,并针对高点密度优化。显然,两者都很重要,并且在这项调查中,通过测量和传播的不确定性来公平地表示相关准确性的不确定性,直接提供各自的身体洞察的质量。结果为I-Pr Ni复合体的近似四面体几何形状提供了比以前得出的近似的四面体几何形状,我们的高点精度数据产生配体长度为2.017±0.006?和2.022±0.006?对于Ni-N和Ni-O键,以及用于N-PR络合物的甚至更偏斜的方形平面(即Rhombohedral)布置,相应的粘合长度为2.133±0.004? 1.960±0.003? 。还强调了在复合物的近似局部四面体和方形平面几何形状产生的XAFS光谱中的微妙差异之间区分的能力。研究了标准插值对具有理论模型结构之前实验XAFS光谱的效果。虽然经常作为傅里叶变换进入位置空间的必要步骤,但这将仍然歪斜拍摄的实际数据,

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