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関連する概念動画

¹H NMR: Complex Splitting01:13

¹H NMR: Complex Splitting

A proton M that is coupled to a proton X results in doublet signals for M. However, NMR-active nuclei can be simultaneously coupled to more than one nonequivalent nucleus. When M is coupled to a second proton A, such as in styrene oxide, each peak in the doublet is split into another doublet.
Splitting diagrams or splitting tree diagrams are routinely used to depict such complex couplings. While drawing splitting diagrams, the splitting with the larger coupling constant is usually applied first.
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.
¹H NMR Signal Multiplicity: Splitting Patterns01:13

¹H NMR Signal Multiplicity: Splitting Patterns

When protons A and X are coupled, their nuclear spin energy levels are slightly modified. This is because the energy required to excite proton A to a spin state parallel to proton X is slightly different from the energy required for it to become anti-parallel to spin X. Consequently, there are two possible excitation frequencies for A (A1 and A2), depending on the spin state of X, and vice versa. The mutual nature of coupling implies that the difference between frequencies A1 and A2, indicated...
Interpreting ¹H NMR Signal Splitting: The (n + 1) Rule01:10

Interpreting ¹H NMR Signal Splitting: The (n + 1) Rule

In the AX proton spin system, proton A can sense the two spin states of a coupled proton X, resulting in a doublet NMR signal with two peaks of equal (1:1) intensity. When proton A is coupled to two equivalent protons (AX2 spin system), the spin states of each X can be aligned with or against the external field, creating three possible scenarios. This results in a 1:2:1  triplet signal, where the central peak corresponds to the chemical shift of A and is twice as large or intense as the others.
¹H NMR of Conformationally Flexible Molecules: Variable-Temperature NMR01:15

¹H NMR of Conformationally Flexible Molecules: Variable-Temperature NMR

The axial and equatorial protons in cyclohexane can be distinguished by performing a variable-temperature NMR experiment. In this process, except for one proton, the remaining eleven protons are replaced by deuterium. The deuterium substitution avoids the possible peak splitting caused by the spin-spin coupling between the adjacent protons. The remaining proton flips between the axial and equatorial positions.
¹³C NMR: ¹H–¹³C Decoupling01:04

¹³C NMR: ¹H–¹³C Decoupling

The probability of having two carbon-13 atoms next to each other is negligible because of the low natural abundance of carbon-13. Consequently, peak splitting due to carbon-carbon spin-spin coupling is not observed in spectra. However, protons up to three sigma bonds away split the carbon signal according to the n+1 rule, resulting in complicated spectra.
A broadband decoupling technique is used to simplify these complex, sometimes overlapping, signals. Broadband decoupling relies on a...

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関連する実験動画

Updated: Jul 12, 2026

Nuclear Magnetic Resonance Spectroscopy for the Identification of Multiple Phosphorylations of Intrinsically Disordered Proteins
12:47

Nuclear Magnetic Resonance Spectroscopy for the Identification of Multiple Phosphorylations of Intrinsically Disordered Proteins

Published on: December 27, 2016

半整数四極核の分離局域NMRスペクトロスコーピーは,半整数四極核を対象としています.

Julia Grinshtein1, Christopher V Grant, Lucio Frydman

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

Journal of the American Chemical Society
|November 7, 2002
PubMed
まとめ

隔離された局所フィールドスペクトロスコピーを用いた新しい固体NMR方法は,四極核を特徴付けます. これらのテクニックは,共振を割り当て,固体の動態を研究するためにスペクトルパターンを相関させます.

科学分野:

  • 固体核磁共振 (NMR) スペクトロスコーピーは,固体核磁共振 (NMR) スペクトロスコーピーを用います.
  • マテリアルサイエンス 材料科学
  • 物理化学 物理化学

背景:

  • 半整数四極核の固体状態NMRスペクトロスコピーの共振を特徴づけるのは,課題を提示する.
  • 既存の方法は,複雑な固体材料における不等価な位置または動態を完全に解決できない可能性があります.

研究 の 目的:

  • 半整数四極核の固体状態NMRにおける共振を特徴付けるための新しいアプローチを探求する.
  • 特定の構造環境に共鳴を割り当て,分子動態を調査するための高度なNMR技術を開発する.

主な方法:

  • 回転する固体上の異核分離局域スペクトルの取得.
  • 二次四極MAS粉末パターンを二極MASサイドバンドパターンと相関させる二次元 (2D) 実験の開発.
  • 同位体次元に沿って不等価な化学部位を分離するための3次元 (3D) NMR 配列への拡張.

主要な成果:

  • 特定の化学サイトにおける二極 MAS サイドバンドパターンと四極 MAS 粉末パターンの相関を示した.
  • アニゾトロプ的相関スペクトルに基づく3D NMR配列を用いて不等価な共振を成功裏に分離した.
  • モノヌクレオチドの1H-23Na再結合実験でこれらの方法の適用を図解した.

さらに関連する動画

Atomic Scale Structural Studies of Macromolecular Assemblies by Solid-state Nuclear Magnetic Resonance Spectroscopy
14:55

Atomic Scale Structural Studies of Macromolecular Assemblies by Solid-state Nuclear Magnetic Resonance Spectroscopy

Published on: September 17, 2017

A New Straightforward Method for Lipophilicity (logP) Measurement using 19F NMR Spectroscopy
09:32

A New Straightforward Method for Lipophilicity (logP) Measurement using 19F NMR Spectroscopy

Published on: January 30, 2019

関連する実験動画

Last Updated: Jul 12, 2026

Nuclear Magnetic Resonance Spectroscopy for the Identification of Multiple Phosphorylations of Intrinsically Disordered Proteins
12:47

Nuclear Magnetic Resonance Spectroscopy for the Identification of Multiple Phosphorylations of Intrinsically Disordered Proteins

Published on: December 27, 2016

Atomic Scale Structural Studies of Macromolecular Assemblies by Solid-state Nuclear Magnetic Resonance Spectroscopy
14:55

Atomic Scale Structural Studies of Macromolecular Assemblies by Solid-state Nuclear Magnetic Resonance Spectroscopy

Published on: September 17, 2017

A New Straightforward Method for Lipophilicity (logP) Measurement using 19F NMR Spectroscopy
09:32

A New Straightforward Method for Lipophilicity (logP) Measurement using 19F NMR Spectroscopy

Published on: January 30, 2019

結論:

  • 拡張された分離された局所フィールドのNMRは四極核に近づき,特定の構造的環境への共振割り当てを容易にします.
  • 固体材料のダイナミクスの調査のための新しいツールを提供しました.
  • これらの2Dおよび3DNMR実験の有用性を実用的な応用を通じて検証しました.