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Monitoring Crystallization Processes in Confined Porous Materials by Dynamic Nuclear Polarization Solid-State Nuclear Magnetic Resonance

机译:通过动态核偏振固态核磁共振监测狭窄多孔材料的结晶过程

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摘要

Establishing mechanistic understanding of crystallization processes at the molecular level is challenging, as it requires both the detection of transient solid phases and monitoring the evolution of both liquid and solid phases as a function of time. Here, we demonstrate the application of dynamic nuclear polarization (DNP) enhanced NMR spectroscopy to study crystallization under nanoscopic confinement, revealing a viable approach to interrogate different stages of crystallization processes. We focus on crystallization of glycine within the nanometric pores (7-8 nm) of a tailored mesoporous SBA-15 silica material with wall-embedded TEMPO radicals. The results show that the early stages of crystallization, characterized by the transition from the solution phase to the first crystalline phase, are straightforwardly observed using this experimental strategy. Importantly, the NMR sensitivity enhancement provided by DNP allows the detection of intermediate phases that would not be observable using standard solid-state NMR experiments. Our results also show that the metastable β polymorph of glycine, which has only transient existence under bulk crystallization conditions, remains trapped within the pores of the mesoporous SBA-15 silica material for more than 200 days.
机译:在分子水平上建立的结晶过程的机制理解是具有挑战性的,因为它需要瞬时固相的两个检测和监测液相和固相的演变的时间的函数。这里,我们证明动态核极化(DNP)增强NMR光谱法来研究结晶纳米下限制该应用程序,揭示一种可行的方法,以结晶过程的诘不同阶段。我们专注于与壁嵌入式TEMPO自由基的定制孔SBA-15二氧化硅材料的细孔纳米(7-8纳米)内甘氨酸结晶。结果表明,结晶的初期阶段,其特征在于通过从溶液相到第一结晶相的转变,都直接地使用该实验策略观察。重要的是,由DNP提供的NMR灵敏度增强允许中间阶段使用标准的固态NMR实验,不会可观察到的检测。我们的结果还表明,甘氨酸的亚稳态多晶型β,其中有大量结晶的条件下仅短暂存在,保持陷入内,用于200多天中孔SBA-15二氧化硅材料的孔中。

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  • 来源
    《Journal of the American Chemical Society》 |2021年第16期|6095-6103|共9页
  • 作者单位

    Aix Marseille Univ CNRS ICR 13397 Marseille France;

    Aix Marseille Univ CNRS ICR 13397 Marseille France;

    Aix Marseille Univ CNRS ICR 13397 Marseille France;

    Aix Marseille Univ CNRS Centrale Marseille FSCM 13397 Marseille France;

    Aix Marseille Univ CNRS ICR 13397 Marseille France;

    Aix Marseille Univ CNRS ICR 13397 Marseille France;

    Aix Marseille Univ CNRS ICR 13397 Marseille France Institut Universitaire de France 7S231 Paris France;

    Aix Marseille Univ CNRS ICR 13397 Marseille France;

    School of Chemistry Cardiff University Cardiff Wales CF10 3AT U. K.;

    Aix Marseille Univ CNRS ICR 13397 Marseille France;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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