分子
结晶
金属有机骨架
衍射
晶体结构
结晶学
化学计量学
材料科学
X射线晶体学
反常散射
溶剂
单晶
化学
化学物理
物理
物理化学
有机化学
吸附
光学
作者
Yuantao Li,Sishuang Tang,Anna Yusov,James Rose,André Nyberg Borrfors,Chunhua Tony Hu,Michael D. Ward
标识
DOI:10.1038/s41467-019-12453-6
摘要
Single crystal X-ray diffraction is arguably the most definitive method for molecular structure determination, but the inability to grow suitable single crystals can frustrate conventional X-ray diffraction analysis. We report herein an approach to molecular structure determination that relies on a versatile toolkit of guanidinium organosulfonate hydrogen-bonded host frameworks that form crystalline inclusion compounds with target molecules in a single-step crystallization, complementing the crystalline sponge method that relies on diffusion of the target into the cages of a metal-organic framework. The peculiar properties of the host frameworks enable rapid stoichiometric inclusion of a wide range of target molecules with full occupancy, typically without disorder and accompanying solvent, affording well-refined structures. Moreover, anomalous scattering by the framework sulfur atoms enables reliable assignment of absolute configuration of stereogenic centers. An ever-expanding library of organosulfonates provides a toolkit of frameworks for capturing specific target molecules for their structure determination.
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