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相关概念视频

NMR Spectrometers: Overview01:20

NMR Spectrometers: Overview

NMR spectrometers consist of a strong magnet, a radiofrequency transmitter, and a detector attached to a computer console for recording spectra of samples containing NMR-active nuclei. In first-generation NMR instruments called continuous-wave spectrometers, the resonance frequencies of the nuclei are determined by frequency-sweep or field-sweep methods. The magnetic field strength is fixed and the rf signal is swept in the former, while the radiofrequency signal is fixed and the magnetic field...
Two-Dimensional (2D) NMR: Overview01:12

Two-Dimensional (2D) NMR: Overview

The 1D NMR spectrum of large and complex molecules like natural products has complicated splitting patterns and overlapping signals, which can be easily interpreted using 2-dimensional (2D) NMR. Unlike 1D NMR, 2D NMR has two frequency axes that provide the coupling information between the nucleus A and nucleus B in a molecule. The process from which 2D spectra are obtained has four steps.
The first step is the preparation period, during which nucleus A is excited with a radiofrequency pulse.
2D NMR: Heteronuclear Single-Quantum Correlation Spectroscopy (HSQC)01:19

2D NMR: Heteronuclear Single-Quantum Correlation Spectroscopy (HSQC)

Heteronuclear single-quantum correlation spectroscopy (HSQC) is a 2D NMR technique that reveals one-bond correlations between hydrogen and a heteronucleus. The HSQC experiment is similar to the heteronuclear correlation experiment (HETCOR) but is more sensitive. In the HSQC spectrum, the proton chemical shift is plotted on the horizontal F2 axis, while the 13C chemical shift is plotted on the vertical F1 axis. The corresponding proton and 13C spectra are also shown. The HSQC contour plot does...
NMR Spectroscopy of Aromatic Compounds01:14

NMR Spectroscopy of Aromatic Compounds

Aromatic compounds can be identified or analyzed using proton NMR and carbon‐13 NMR. Typically, aromatic hydrogens or hydrogens directly bonded to the aromatic rings are strongly deshielded by the aromatic ring current. Therefore, they absorb in the range of 6.5–8.0 ppm in proton NMR spectra. For instance, aromatic hydrogens directly bonded to the benzene ring absorb at 7.3 ppm. However, aromatic hydrogens of larger rings absorb farther upfield or downfield than the ideal range. Consider...
NMR Spectroscopy: Chemical Shift Overview01:15

NMR Spectroscopy: Chemical Shift Overview

The position of the absorption signal of a sample is reported relative to the position of the signal of tetramethylsilane (TMS), which is added as an internal reference while recording spectra. The difference between the absorption frequencies of the sample and TMS (in Hz) is divided by the spectrometer operating frequency (in MHz) to obtain a dimensionless quantity called the chemical shift. It is reported on the δ (delta) scale and expressed in parts per million.
For instance, the proton...
NMR Spectrometers: Radiofrequency Pulses and Pulse Sequences01:17

NMR Spectrometers: Radiofrequency Pulses and Pulse Sequences

A pulse is a short burst of radio waves distributed over a range of frequencies that simultaneously excites all the nuclei in the sample. Upon passing a radio frequency pulse along the x-axis, the nuclei absorb energy corresponding to their Larmor frequencies and achieve resonance. This shifts the net magnetization vector from the z-axis toward the transverse plane. This angle of rotation of the magnetization vector, or the flip angle, is proportional to the duration and intensity of the pulse.

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相关实验视频

Updated: Jun 25, 2026

Rapid Scan Electron Paramagnetic Resonance Opens New Avenues for Imaging Physiologically Important Parameters In Vivo
08:01

Rapid Scan Electron Paramagnetic Resonance Opens New Avenues for Imaging Physiologically Important Parameters In Vivo

Published on: September 26, 2016

在任意尺寸的单扫描NMR光谱学.

Yoav Shrot1, Lucio Frydman

  • 1Department of Chemical Physics, Weizmann Institute of Science, 76100 Rehovot, Israel.

Journal of the American Chemical Society
|October 14, 2005
PubMed
概括

超快的多维核磁共振 (NMR) 加快了数据采集. 这种新方法使得在单个瞬态中收集完整的n维NMR光谱,大大缩短了实验时间.

科学领域:

  • 分析化学 分析化学
  • 生物化学 生物化学
  • 频谱学是一种光谱学.

背景情况:

  • 多维核磁共振 (NMR) 对于分析复杂的分子结构和动态至关重要.
  • 传统的NMR实验需要大量的采集时间,特别是对于更高的维度 (2D,3D等). ) 的情况.
  • 目前的方法涉及连续的数据收集,限制了实验速度.

研究的目的:

  • 将以前开发的并行二维NMR数据采集方法扩展到n维.
  • 介绍和描述超快的n维NMR的原理.
  • 为了证明快速获得复杂的NMR光谱的可行性.

主要方法:

  • 开发和应用一个平行数据采集策略,用于多维NMR.
  • 将二维NMR并行化技术扩展到任意数量的维度 (n维NMR).
  • 用于光谱重建的时间域信号的富里埃分析.

主要成果:

  • 一个超快的n维NMR方法的演示.
  • 成功收集了完整的3D和4DNMR光谱.
  • 在几分之一秒内获取光谱,大大减少了实验持续时间.

结论:

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NMR 15N Relaxation Experiments for the Investigation of Picosecond to Nanoseconds Structural Dynamics of Proteins

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  • 拟议的超快的n维NMR方法显著加速光谱采集.
  • 这种方法可以快速阐明复杂分子的结构和动态.
  • 该技术适用于同核和异核NMR实验.