Structure of L-arginine and detection of trace DL-arginine by 3D ED.

IF 0.7 4区 化学 Q4 CHEMISTRY, MULTIDISCIPLINARY
Krishna P Khakurel, Sohail Mahmoudi
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引用次数: 0

Abstract

3D electron crystallography has emerged as a method with great potential for the structure determination of small molecules and macromolecules complementing traditional single-crystal X-ray crystallography and powder X-ray diffraction (PXRD). It offers the unique capability of determining the structures of small molecules and macromolecules from micro- and nanocrystals. In this study, using 3D electron diffraction (3D ED), we determined the single-crystal structure of commercially sourced arginine directly from its bottle. The 3D ED analysis of micro-sized single crystals identified two distinct forms: the L-arginine enantiomer and the racemic mixture DL-arginine. At the time of writing, neither the Cambridge Structural Database nor the Crystallographic Open Database contain a single-crystal structure of isolated L-arginine (sum formula C6H14N4O2), which has been solved in this work by 3D ED. We also present a comparison of the structures of these molecules solved by 3D ED and PXRD.

l -精氨酸的结构及痕量l -精氨酸的3D ED检测。
三维电子晶体学作为传统的单晶x射线晶体学和粉末x射线衍射(PXRD)的补充,在小分子和大分子的结构测定方面具有很大的潜力。它提供了从微晶体和纳米晶体中确定小分子和大分子结构的独特能力。在这项研究中,我们使用3D电子衍射(3D ED),直接从其瓶子中确定了商业来源的精氨酸的单晶结构。微尺寸单晶的3D ED分析确定了两种不同的形式:l -精氨酸对映体和外消旋混合物dl -精氨酸。在撰写本文时,剑桥结构数据库和晶体学开放数据库都没有包含分离l -精氨酸的单晶结构(和式C6H14N4O2),这在本工作中已被3D ED解决。我们还比较了3D ED和PXRD解决的这些分子的结构。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Acta Crystallographica Section C Structural Chemistry
Acta Crystallographica Section C Structural Chemistry CHEMISTRY, MULTIDISCIPLINARYCRYSTALLOGRAPH-CRYSTALLOGRAPHY
CiteScore
1.60
自引率
12.50%
发文量
148
期刊介绍: Acta Crystallographica Section C: Structural Chemistry is continuing its transition to a journal that publishes exciting science with structural content, in particular, important results relating to the chemical sciences. Section C is the journal of choice for the rapid publication of articles that highlight interesting research facilitated by the determination, calculation or analysis of structures of any type, other than macromolecular structures. Articles that emphasize the science and the outcomes that were enabled by the study are particularly welcomed. Authors are encouraged to include mainstream science in their papers, thereby producing manuscripts that are substantial scientific well-rounded contributions that appeal to a broad community of readers and increase the profile of the authors.
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