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★声明:本文仅代表个人观点,笔者学识有限,资料整理过程中难免存在疏漏谬误,请不吝指正。 原子非正定处理案例6(CAP调整mu和r乘积) 案例来源:碳酸镉,Cadmiumcarbonate, CdCO3. CAS:513-78-0. CCDC [1]: 2589924. DOI [2]: 10.5517/ccdc.csd.cc2sy0yq. ▲图1 正常还原解析结果 >>步骤1:打开Finalize弹窗 在CAP软件右上角点击Data Reduction(或将鼠标悬停在Data Reduction处),在弹窗菜单中点击Finalize,如图2所示。 ▲图2 Data Reduction>>Finalize 或者,在CAP软件界面左上角点击如图3所示红色箭头所指按钮(Inspect data reduction results and refinalize with usercorrections)。 ▲图3 Inspect data reduction results and refinalize with usercorrections按钮 在弹出的对话框中,点击左下角的Refinalize按钮,如图4红色箭头所指。 ▲图4 Refinalize按钮 >>步骤2:修改μr乘积值 经步骤1后,打开Finalize对话框,如图5所示,Corrections下默认是Empirical correction的Automated,此时点击Numerical absorption右侧的Sphere(红色箭头所指)。 ▲图5 Finalize>>Corrections>>Empiricalcorrection>>Sphere 然后,界面展开如图6所示,点击Numerical absorption右侧的Advanced(高级)按钮(红色箭头所指)。 ▲图6 Finalize>>Corrections>>Empiricalcorrection>>Manual>>Advanced 当前μr值为0.689,对应的等效半径为0.400 mm,如图7红色方框所示。 ▲图7 当前μr值及等效半径 解析完成,分子式为CdCO3,此时打开CIF [9]文件,找到记录吸收吸收系数μ的条目_exptl_absorpt_coefficient_mu(参阅推文“CIF核心词典-EXPTL”),其μ值为74.537 mm–1,如图8所示。 ▲图8 CIF中记录的吸收系数 该晶体尺寸大约为0.09 mm ×0.10 mm × 0.11 mm,半径r值可取0.10 mm的一半,即0.05 mm,则μr = 74.537 mm–1 × 0.05 mm = 3.72685,将其填入μr处,等效半径自动更新为2.1650 mm,如图9所示,然后点击该界面右下角的OK按钮。 ▲图9 修改的μr值 然后,点击Finalize对话框右下角的OK按钮,如图10红色箭头所指。 ▲图10 修改μr值后返回的Finalize界面 程序根据输入的μr进行Numerical absorption,然后弹出对话框让选择空间群,选择对应的空间群后,点击右下角OK按钮,如图11红色箭头所指。 ▲图11 空间群选择 随后利用新的hkl文件进行精修,结果如图12所示,原子恢复成正常椭球形(即不再是非正定状态),A级警报PLAT203和PLAT211均消失。 ▲图12 重新校正后的结果 相关视频: 单晶结构解析练习795(CAP数据还原-非预期结构-非正定):https://www.bilibili.com/video/BV1RhaP6JEi2 相关阅读: 推文: 视频: 参考文献 [1] (a)Allen, F. H. The Cambridge Structural Database: A Quarter of a Million CrystalStructures and Rising. Acta Cryst. 2002, B58, 380–388. DOI:10.1107/S0108768102003890. (b) Groom, C. R.; Bruno, I. J.; Lightfoot, M.P.; Ward, S. C. The Cambridge Structural Database. Acta Cryst. 2016, B72, 171–179. DOI:10.1107/S2052520616003954. (c) Mitchell, J.; Robertson, J. H.; Raithby,P. R. Cambridge Crystallographic Data Centre (CCDC). Comprehensive Coordination Chemistry III 2021, 413–437. DOI:10.1016/B978-0-12-409547-2.14829-2. [2] (a)International Organization for Standardization (2012). ISO 26324:2012. Information and Documentation – DigitalObject Identifier System. http://www.iso.org/iso/catalogue_detail.htm?csnumber=43506. (b) McDonald J. D.;Levine-Clark, M. Encyclopedia of Libraryand Information Sciences. Fourth Edition, CRC Press, 2017. DOI: 10.1081/e-elis4. (c) Liu, J. Digital ObjectIdentifier (DOI) and DOI Services: An Overview. Libri 2021, 71, 349‒360. DOI:10.1515/libri-2020-0018. (d) International Organization forStandardization (2022). ISO 26324:2022. Informationand Documentation – Digital Object Identifier System. https://www.iso.org/standard/81599.html[3] RigakuOxford Diffraction, (2025), CrysAlisPro Software System, version1.171.44.91a, Rigaku Corporation, Wroclaw, Poland. [4] Dolomanov,O. V.; Bourhis, L. J.; Gildea, R. J.; Howard, J. A. K.; Puschmann, H. OLEX2: A Complete Structure Solution,Refinement and Analysis Program. J. Appl. Cryst. 2009, 42, 339–341. DOI: 10.1107/S0021889808042726. [5] Sheldrick,G. M. SHELXT – Integrated Space-Groupand Crystal Structure Determination. ActaCryst. 2015, A71, 3–8. DOI:10.1107/S2053273314026370. [6] (a) Sheldrick, G. M. SHELXL-2025/1, Program for Crystal Structure Refinement, University of Göttingen,Germany, 2019. (b)Sheldrick, G. M. A Short History of SHELX.Acta Cryst. 2008, A64, 112–122. DOI:10.1107/S0108767307043930. (c) Sheldrick, G. M. Crystal Structure Refinement with SHELXL. Acta Cryst. 2015, C71, 3–8. DOI: 10.1107/S2053229614024218.(d) Lübben, J.; Wandtke, C. M.;Hübschle, C. B.; Ruf, M.; Sheldrick, G. M.; Dittrich, B. Aspherical ScatteringFactors for SHELXL – Model,Implementation and Application. ActaCryst. 2019, A75, 50–62. DOI:10.1107/S2053273318013840. [7] (a) Spek, A. L. Single-CrystalStructure Validation with the Program PLATON.J. Appl. Cryst. 2003, 36, 7–13. DOI: 10.1107/S0021889802022112.(b) Spek, A. L. StructureValidation in Chemical Crystallography. ActaCryst. 2009, D65, 148–155. DOI:10.1107/S090744490804362X. (c) Spek, A. L. What Makes a Crystal Structure Report Valid? Inorg. Chim. Acta 2018, 470, 232–237. DOI:10.1016/j.ica.2017.04.036. (d) Spek, A. L. checkCIFValidation ALERTS: What They Mean and How to Respond. Acta Cryst. 2020, E76, 1–11. DOI: 10.1107/S2056989019016244. [8] Bruker(2024). APEX6 (Version 2025.6-0). Program for Data Collection on AreaDetectors. Bruker AXS Inc., Madison, Wisconsin, USA. [9] (a)Hall, S. R.; Allen, F. H. Brown, I. D. The Crystallographic Information File(CIF): A New Standard Archive File for Crystallography. Acta Cryst. 1991, A47, 655–685. DOI:10.1107/S010876739101067X. (b) Hall, S. R. The STAR File: A New Formatfor Electronic Data Transfer and Archiving. J.Chem. Inf. Comput. Sci. 1991, 31, 326–333. DOI:10.1021/ci00002a020. (c) Hall, S. R.; Spadaccini, N. The STAR File:Detailed Specifications. J. Chem. Inf.Comput. Sci. 1994, 34, 505–508. DOI:10.1021/ci00019a005.
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