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Ultrafast Magic Angle Spinning Solid-State NMR Spectroscopy: Advances in Methodology and Applications.超快魔角旋转固态核磁共振波谱学:方法学和应用的进展。
Chem Rev. 2023 Feb 8;123(3):918-988. doi: 10.1021/acs.chemrev.2c00197. Epub 2022 Dec 21.
2
H-Detected Biomolecular NMR under Fast Magic-Angle Spinning.在快速魔角旋转下的 H 检测生物分子 NMR。
Chem Rev. 2022 May 25;122(10):9943-10018. doi: 10.1021/acs.chemrev.1c00918. Epub 2022 May 10.
3
Extension and improvement of the methanol-d NMR thermometer calibration.甲醇-dNMR 温度计校准的扩展和改进。
Magn Reson Chem. 2022 Feb;60(2):203-209. doi: 10.1002/mrc.5216. Epub 2021 Sep 25.
4
Setting the magic angle for fast magic-angle spinning probes.为快速魔角旋转探头设置魔角。
J Magn Reson. 2018 Aug;293:115-122. doi: 10.1016/j.jmr.2018.06.002. Epub 2018 Jun 15.
5
Influences of Dilute Organic Adsorbates on the Hydration of Low-Surface-Area Silicates.稀释有机吸附物对低比表面积硅酸盐水合作用的影响。
J Am Chem Soc. 2015 Jul 1;137(25):8096-112. doi: 10.1021/jacs.5b00622. Epub 2015 Jun 19.
6
Origins of linewidth in 1H magic-angle spinning NMR.氢核磁共振魔角旋转中谱线宽度的起源
J Chem Phys. 2006 Oct 14;125(14):144508. doi: 10.1063/1.2357602.
7
Chemical shift referencing in MAS solid state NMR.魔角旋转固态核磁共振中的化学位移参考
J Magn Reson. 2003 Jun;162(2):479-86. doi: 10.1016/s1090-7807(03)00082-x.
8
Recommendations for the presentation of NMR structures of proteins and nucleic acids. IUPAC-IUBMB-IUPAB Inter-Union Task Group on the Standardization of Data Bases of Protein and Nucleic Acid Structures Determined by NMR Spectroscopy.蛋白质和核酸核磁共振结构的呈现建议。国际纯粹与应用化学联合会-国际生物化学与分子生物学联盟-国际纯粹与应用生物学联合会蛋白质和核酸结构数据库标准化联合任务组(由核磁共振光谱法测定)
J Biomol NMR. 1998 Jul;12(1):1-23. doi: 10.1023/a:1008290618449.
9
High-speed magic-angle spinning 13C MAS NMR spectra of adamantane: self-decoupling of the heteronuclear scalar interaction and proton spin diffusion.金刚烷的高速魔角旋转13C MAS NMR谱:异核标量相互作用的自去耦和质子自旋扩散
J Magn Reson. 1998 Feb;130(2):176-85. doi: 10.1006/jmre.1997.1311.

四(三甲基硅基)硅烷作为快速旋转固体核磁共振实验的标准化合物。

Tetrakis(trimethylsilyl)silane as a standard compound for fast spinning Solid-State NMR experiments.

作者信息

Han Ruixian, Paterson Alexander L, Milchberg Moses H, Pang Yuanchi, Vanderloop Boden H, Rienstra Chad M

机构信息

Department of Chemistry, University of Wisconsin-Madison, Madison, WI, United States.

National Magnetic Resonance Facility at Madison (NMRFAM), University of Wisconsin-Madison, Madison, WI, United States.

出版信息

J Magn Reson. 2024 Oct;367:107747. doi: 10.1016/j.jmr.2024.107747. Epub 2024 Aug 5.

DOI:10.1016/j.jmr.2024.107747
PMID:39178749
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11408081/
Abstract

The development of magic angle spinning (MAS) at rates ranging from 30 kHz to greater than 100 kHz has substantially advanced solid-state nuclear magnetic resonance (SSNMR) spectroscopy H-detection methods. The small rotors required for such MAS rates have a limited sample volume and low C-detection sensitivity, rendering the traditional set of standard compounds for SSNMR insufficient or highly inconvenient for shimming and magic-angle calibration. Additionally, the reproducibility of magic angle setting, chemical shift referencing, and probe position can be especially critical for SSNMR experiments at high fields. These conditions suggest the need for a high signal-to-noise ratio (SNR) H-detection standard compound, which is preferably multi-purpose, to simplify instrument set up for ultra-fast MAS SSNMR instruments at high magnetic fields. In this study, we present the results for setting magic angle and shimming using tetrakis(trimethylsilyl)silane (TTMSS, or TKS), a tetramethylsilane (TMS) analogue, at near 40 kHz and demonstrate that we can achieve favorable results in less time but with equal or superior precision as traditional KBr and adamantane standards. The high SNR and TMS-like chemical shift of TKS also opens the possibilities for using TKS as an internal standard with biological samples. A single rotor containing a four-component mixture of TKS, adamantane, uniformly C, N-labeled N-acetyl valine and KBr was used to perform a complete configuration and calibration of a SSNMR probe without sample changes. We anticipate TKS as a standard compound to be especially effective at very high MAS conditions and to greatly simplify the instrument set up for high and ultra-high field SSNMR instruments.

摘要

魔角旋转(MAS)技术在30kHz至大于100kHz的速率范围内的发展极大地推动了固态核磁共振(SSNMR)光谱H检测方法的进步。如此高MAS速率所需的小转子样品体积有限且C检测灵敏度低,使得用于SSNMR的传统标准化合物集对于匀场和魔角校准而言不足或极不方便。此外,对于高场下的SSNMR实验,魔角设置、化学位移参考和探头位置的可重复性可能尤为关键。这些情况表明需要一种高信噪比(SNR)的H检测标准化合物,最好是多功能的,以简化高磁场下超快MAS SSNMR仪器的仪器设置。在本研究中,我们展示了使用四(三甲基硅基)硅烷(TTMSS,或TKS)(一种四甲基硅烷(TMS)类似物)在接近40kHz时进行魔角设置和匀场的结果,并证明我们可以在更短的时间内获得良好的结果,且精度与传统的KBr和金刚烷标准相当或更高。TKS的高SNR和类似TMS的化学位移也为将TKS用作生物样品的内标开辟了可能性。使用一个包含TKS、金刚烷、均匀C、N标记的N-乙酰缬氨酸和KBr四组分混合物的转子,无需更换样品即可对SSNMR探头进行完整的配置和校准。我们预计TKS作为标准化合物在非常高的MAS条件下会特别有效,并将极大地简化高场和超高场SSNMR仪器的仪器设置。