Identification of a Single Light Atom within a Multinuclear Metal Cluster Using Valence-to-Core X-ray Emission Spectroscopy

被引:63
|
作者
Delgado-Jaime, Mario Ulises [1 ,2 ]
Dible, Benjamin R. [3 ]
Chiang, Karen P. [3 ]
Brennessel, William W. [3 ]
Bergmann, Uwe [4 ]
Holland, Patrick L. [3 ]
DeBeer, Serena [1 ,2 ]
机构
[1] Cornell Univ, Dept Chem & Chem Biol, Ithaca, NY 14853 USA
[2] Max Planck Inst Bioanorgan Chem, D-45470 Mulheim, Germany
[3] Univ Rochester, Dept Chem, Rochester, NY 14627 USA
[4] SLAC Natl Accelerator Lab, Linac Coherent Light Source, Menlo Pk, CA 94025 USA
关键词
ELECTRONIC-STRUCTURE; APPROXIMATION; PREDICTION; COMPLEXES; INSIGHTS; SPECTRA; ENERGY;
D O I
10.1021/ic201173j
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Iron valence-to-core Fe K beta X-ray emission spectroscopy (V2C XES) is established as a means to identify light atoms (C, N, O) within complex multimetallic frameworks. The ability to distinguish light atoms, particularly in the presence of heavier atoms, is a well-known limitation of both crystallography and EXAFS. Using the sensitivity of V2C XES to the ionization potential of the bound ligand, energetic shifts of similar to 10 eV in the ligand 2s ionization energies of bound C, N, and O may be observed. As V2C XES is a high-energy X-ray method, it is readily applicable to samples in any physical form. This method thus has great potential for application to multimetallic inorganic frameworks involved in both small molecule storage and activation.
引用
收藏
页码:10709 / 10717
页数:9
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