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多晶样品的单晶质量数据:大海捞针。

Single-crystal quality data from polycrystalline samples: finding the needle in the haystack.

作者信息

Bear Joseph Charles, Terzoudis Nikitas, Cockcroft Jeremy Karl

机构信息

School of Life Sciences, Pharmacy and Chemistry, Kingston University, Penrhyn Road, Kingston-upon-Thames, Surrey KT1 2EE, United Kingdom.

Department of Chemistry, University College London, 20 Gordon Street, London WC1H 0AJ, United Kingdom.

出版信息

IUCrJ. 2023 Nov 1;10(Pt 6):720-728. doi: 10.1107/S2052252523008163.

DOI:10.1107/S2052252523008163
PMID:37815488
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10619455/
Abstract

Multi-grain crystallography, traditionally performed at synchrotron sources in association with high-pressure studies, has new relevance with respect to laboratory single-crystal X-ray diffraction, in which crystals can be grown rapidly in situ, and a preliminary dataset analysed and solved in a matter of minutes. Subsequently, a full-sphere of IUCr-quality data can then be collected in a few hours. To demonstrate the applicability of laboratory multi-grain crystallography with Cu Kα X-rays, co-crystals of hexafluorobenzene and pyrrole were grown rapidly by cooling a 1:1 liquid mixture in an X-ray capillary on the diffractometer. The software is able to identify a single unit cell from as few as 10% of the diffraction spots from a small number of diffraction frames. Once a unit cell is identified, a full crystal structure solution is rapidly obtained by collecting a small amount of data to a resolution of ca 1 Å. The co-crystal obtained from the 1:1 mixture showed that hexafluorobenzene and pyrrole crystallize in a 3:4 ratio, in contrast to the columnar 1:1 adduct structures typified by hexafluorobenzene and benzene. The generality of our multi-grain approach for samples that are liquid at room temperature (and form a polycrystalline solid mass on cooling) is further demonstrated by investigating and solving the 1:1 co-crystal formed between hexafluorobenzene and pyridine.

摘要

多晶X射线晶体学传统上是在同步辐射源上与高压研究相结合进行的,现在对于实验室单晶X射线衍射有了新的意义,在实验室单晶X射线衍射中,晶体可以在原位快速生长,并且可以在几分钟内对初步数据集进行分析和解出结构。随后,可以在几个小时内收集到国际晶体学联盟(IUCr)质量的全球面数据。为了证明使用Cu Kα X射线进行实验室多晶X射线晶体学的适用性,通过在衍射仪上的X射线毛细管中冷却1:1的液体混合物,快速生长了六氟苯和吡咯的共晶体。该软件能够从少量衍射帧的衍射点中低至10%的衍射点识别出单个晶胞。一旦识别出晶胞,通过收集少量分辨率约为1 Å的数据,就能快速获得完整的晶体结构解。从1:1混合物中得到的共晶体表明,六氟苯和吡咯以3:4的比例结晶,这与以六氟苯和苯为典型的柱状1:1加合物结构不同。通过研究和解析六氟苯与吡啶形成的1:1共晶体,进一步证明了我们的多晶方法对于在室温下为液体(冷却后形成多晶固体块)的样品的通用性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/673a/10619455/bc4de107ea25/m-10-00720-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/673a/10619455/d9eccb61dda6/m-10-00720-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/673a/10619455/47c9560c09ed/m-10-00720-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/673a/10619455/06c5bda1dd34/m-10-00720-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/673a/10619455/bc4de107ea25/m-10-00720-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/673a/10619455/d9eccb61dda6/m-10-00720-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/673a/10619455/47c9560c09ed/m-10-00720-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/673a/10619455/06c5bda1dd34/m-10-00720-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/673a/10619455/bc4de107ea25/m-10-00720-fig4.jpg

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