Locating Organic Guests in Inorganic Host Materials from X-ray Powder Diffraction Data
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- 作者：Stef Smeets ; Lynne B. McCusker ; Christian Baerlocher ; Saleh Elomari ; Dan Xie ; Stacey I. Zones
- 刊名：Journal of the American Chemical Society
- 出版年：2016
- 出版时间：June 8, 2016
- 年：2016
- 卷：138
- 期：22
- 页码：7099-7106
- 全文大小：554K
- 年卷期：0
- ISSN：1520-5126
文摘
Can the location of the organic structure-directing agent (SDA) inside the channel system of a zeolite be determined experimentally in a systematic manner? In an attempt to answer this question, we investigated six borosilicate zeolites of known framework structure (SSZ-53, SSZ-55, SSZ-56, SSZ-58, SSZ-59, and SSZ-60), where the location of the SDA had only been simulated using molecular modeling techniques in previous studies. From synchrotron powder diffraction data, we were able to retrieve reliable experimental positions for the SDA by using a combination of simulated annealing (global optimization) and Rietveld refinement. In this way, problems arising from data quality and only partially compatible framework and SDA symmetries, which can lead to indecipherable electron density maps, can be overcome. Rietveld refinement using geometric restraints were then performed to optimize the positions and conformations of the SDAs. With these improved models, it was possible to go on to determine the location of the B atoms in the framework structure. That is, two pieces of information that are key to the understanding of zeolite synthesis—the location of the organic SDA in the channel system and of the positions adopted by heteroatoms in the silicate framework—can be extracted from experimental data using a systematic strategy. In most cases, the locations of the SDAs determined experimentally compare well with those simulated with molecular modeling, but there are also some clear differences, and the reason for these differences can be understood. The approach is generally applicable, and has also been used to locate organic guests, linkers, and ligands in metal–organic compounds.