Rapid Structure Determination of Microcrystalline Molecular Compounds Using Electron Diffraction

被引:217
作者
Gruene, Tim [1 ]
Wennmacher, Julian T. C. [1 ]
Zaubitzer, Christan [2 ]
Holstein, Julian J. [3 ]
Heidler, Jonas [4 ]
Fecteau-Lefebvre, Ariane [5 ]
De Carlo, Sacha [6 ]
Mueller, Elisabeth [7 ]
Goldie, Kenneth N. [5 ]
Regeni, Irene [3 ]
Li, Teng [8 ]
Santiso-Quinones, Gustavo [9 ]
Steinfeld, Gunther [9 ]
Handschin, Stephan [2 ]
van Genderen, Eric [4 ]
van Bokhoven, Jeroen A. [1 ,8 ]
Clever, Guido H. [3 ]
Pantelic, Radosav [4 ,6 ]
机构
[1] Paul Scherrer Inst, Dept Energy & Environm, Forsch Str 111, CH-5232 Villigen, Switzerland
[2] Swiss Fed Inst Technol, Sci Ctr Opt & Electron Microscopy, Auguste Piccard Hof 1, CH-8093 Zurich, Switzerland
[3] TU Dortmund Univ, Dept Chem & Chem Biol, Otto Hahn Str 6, D-44227 Dortmund, Germany
[4] Paul Scherrer Inst, Dept Biol & Chem, Forsch Str 111, CH-5232 Villigen, Switzerland
[5] Univ Basel, Ctr Cellular Imaging & NanoAnalyt, Mattenstr 26, CH-4058 Basel, Switzerland
[6] DECTRIS Ltd, Taefernweg 1, CH-5405 Baden, Switzerland
[7] Paul Scherrer Inst, Electron Microscopy Facil, Forsch Str 111, CH-5232 Villigen, Switzerland
[8] Swiss Fed Inst Technol, Dept Chem & Appl Biosci, Vladimir Prelog Weg 1-5-10, CH-8093 Zurich, Switzerland
[9] Crystallise AG, Grabenstr 11a, CH-8952 Schlieren, Switzerland
基金
瑞士国家科学基金会;
关键词
chemical crystallography; electron crystallography; structure determination; methylene blue derivatives; CRYSTAL-STRUCTURE; CRYSTALLOGRAPHY; PREFERENCES; DERIVATIVES; TOMOGRAPHY; REFINEMENT; CHEMISTRY; PHASE;
D O I
10.1002/anie.201811318
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Chemists of all fields currently publish about 50000 crystal structures per year, the vast majority of which are X-ray structures. We determined two molecular structures by employing electron rather than X-ray diffraction. For this purpose, an EIGER hybrid pixel detector was fitted to a transmission electron microscope, yielding an electron diffractometer. The structure of a new methylene blue derivative was determined at 0.9 angstrom resolution from a crystal smaller than 1 x 2 mu m(2). Several thousand active pharmaceutical ingredients (APIs) are only available as submicrocrystalline powders. To illustrate the potential of electron crystallography for the pharmaceutical industry, we also determined the structure of an API from its pill. We demonstrate that electron crystallography complements X-ray crystallography and is the technique of choice for all unsolved cases in which submicrometer-sized crystals were the limiting factor.
引用
收藏
页码:16313 / 16317
页数:5
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