A Study of the Stereochemistry of Sucrose and a Phenidate Derivative using the Copper Microfocus Source of the XtaLAB Synergy-i

    Application Note SMX010

    Introduction to the benefits of Cu radiation

    Cu Kα radiation is a useful source of radiation for general purpose X-ray diffraction experiments. Due to the approximate λ³ relationship with diffracted intensity, Cu Kα typically provides the strongest signal at the detector and thus enables faster experiments or easier study of small, weakly diffracting samples such as metal organic frameworks (MOFs). Due to the stronger anomalous signal obtained from Cu Kα radiation vs. other common wavelengths, it is possible to confirm the chirality for lighter atom structures—such as purely organic materials—with greater accuracy. Additionally, the longer wavelength of Cu Kα radiation can improve peak separation and consequently data quality for cases where reflection overlap is a concern; e.g., twinned crystals or long unit cell axes.

    The XtaLAB Synergy-i (Figure 1) is a cutting-edge diffractometer equipped with the latest detector technology (HyPix Bantam), optimized for its small pixel size and sensitivity, and can be configured with up to two bright microfocus sealed tube X-ray sources. Herein, two datasets are presented and their results discussed. Both datasets were collected with the PhotonJet-i Cu source.

    XtaLAB-Synergy-i with HyPix Bantam closeup

    Figure 1: The XtaLAB Synergy-i.

    Stereochemistry of sucrose

    A sucrose crystal (0.10 x 0.16 x 0.31 mm) was mounted on a nylon loop and a 5-fold redundant dataset was planned at 100 K to obtain the best possible results for this chiral molecule. The high and low angle diffraction images can be seen in Figure 2 and further details about the data collection are shown in Table 1. 

    SMX010 Figure 2 Low and high angle diffraction images

    Figure 2: The low (top) and high (bottom) angle diffraction images from the sucrose data collection.


    Table 1: Data collection details and data statistics.

    Experiment parameters
    Crystal-to-detector distance 40 mm
    Exposure time 0.2 seconds
    Total collection time 51 minutes
    Scan width / No. of frames 0.5° / 9470
    Completeness 99.9% (0.83 Å)
    Average I/σ(I) 82.17
    Redundancy [unmerged] 5.0

    Discussion

    For this 1-hour data collection a redundancy of 5 was chosen to ensure a well-determined Flack parameter was achieved. For chiral molecules, like sucrose, the Flack parameter indicates if the model has been assigned the correct chirality. The Flack parameter here was 0.02(5), indicating with high certainty that the structure has the correct handedness.

    Table 2: Data collection details and data statistics.

    Sucrose (C₁₂H₂₂O₁₁) Monoclinic, P2₁
    Rint [unmerged data] 2.40%
    R₁ [unmerged data] 1.98%
    Flack parameter 0.02 (5)
     

    SMX010 Figure 3 Sucrose molecule

    Figure 3: Sucrose molecule.

    A theo-methylphenidate salt derivative crystal

    A very thin, plate-like crystal of a theo-methylphenidate salt derivative (Figure 4) was investigated using Cu Kα radiation on the XtaLAB Synergy-i diffractometer at 100 K. The sample was weakly diffracting and required longer exposure times at high angles. Data collection details can be seen in Table 3.

    Table 3: Data collection details and data statistics.

    Detailed parameters
    Crystal-to-detector distance 40 mm
    Exposure time min/max 0.3 and 2 seconds
    Total collection time 1 h 3 min
    Scan width / No. of frames 0.5° / 2466
    Completeness 99.9% (0.83 Å)
    Average I/σ(I) 28.28
    Redundancy 2.6

    SMX010 Figure 4 Single crystal of theo-methylphenidate salt derivative

    Figure 4: Single crystal of a theo-methylphenidate salt derivative. Sample size: 0.06 x 0.19 x 0.23 mm.


    Table 4: Crystal data and refinement statistics.

    Crystal system, space group Monoclinic, C2/c
    Empirical formula C₁₅H₂₂ClNO₂
    Rint 2.19%
    R₁ 3.27%
    Largest residual peak/hole (eÅ⁻³) 0.211 / -0.249

    Discussion

    The excellent final refinement results obtained from this sample (Table 4), illustrates the high flux and good data quality that can be obtained from the Cu microfocus PhotonJet-i source of the XtaLAB Synergy-i.

    Conclusion

    The XtaLAB Synergy-i equipped with the Cu microfocus PhotonJet-i source is capable of collecting data on chiral compounds and weakly diffracting crystal samples. The high sensitivity and small pixel size of the HyPix Bantam detector ensures the reflections are being measured with greater accuracy, which thus produces better overall data quality.

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