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Spin–Spin Coupling: Two-Bond Coupling (Geminal Coupling)01:20

Spin–Spin Coupling: Two-Bond Coupling (Geminal Coupling)

1.0K
Two NMR-active nuclei bonded to a central atom can be involved in geminal or two-bond coupling. Geminal coupling is commonly seen between diastereotopic protons in chiral molecules and unsymmetrical alkenes, among others.
The central atom need not be NMR-active because its electrons are affected by the electron polarization of the spin-active atoms. However, spin information is transmitted less effectively than in one-bond coupling, and 2J values are usually weaker than 1J values. The energy of...
1.0K
Spin–Spin Coupling: Three-Bond Coupling (Vicinal Coupling)01:22

Spin–Spin Coupling: Three-Bond Coupling (Vicinal Coupling)

1.1K
Vicinal or three-bond coupling is commonly observed between protons attached to adjacent carbons. Here, nuclear spin information is primarily transferred via electron spin interactions between adjacent C‑H bond orbitals. This generally favors the antiparallel arrangement of spins, so 3J values are usually positive.
The extent of coupling depends on the C‑C bond length, the two H‑C‑C angles, any electron-withdrawing substituents, and the dihedral angle between the...
1.1K
Spin–Spin Coupling: One-Bond Coupling01:17

Spin–Spin Coupling: One-Bond Coupling

969
Coupling interactions are strongest between NMR-active nuclei bonded to each other, where spin information can be transmitted directly through the pair of bonding electrons. While nuclei polarize their electrons to the opposite spins, the bonding electron pair has opposite spins. Configurations with antiparallel nuclear spins are expected to be lower in energy. When coupling makes antiparallel states more favorable, J is considered to have a positive value. The one-bond coupling constant, 1J,...
969
¹H NMR: Long-Range Coupling01:27

¹H NMR: Long-Range Coupling

1.7K
The coupling interactions of nuclei across four or more bonds are usually weak, with J values less than 1 Hz. While these are usually not observed in spectra, the presence of multiple bonds along the coupling pathway can result in observable long-range coupling.
In alkenes, spin information is communicated via σ–π overlap, as seen in allylic (four-bond) and homoallylic (five-bond) couplings. These coupling interactions are stronger when the σ bond is parallel to the alkene...
1.7K
Spin–Spin Coupling Constant: Overview01:08

Spin–Spin Coupling Constant: Overview

921
In bromoethane, the three methyl protons are coupled to the two methylene protons that are three bonds away. In accordance with the n+1 rule, the signal from the methyl protons is split into three peaks with 1:2:1 relative intensities. The methylene protons appear as a quartet, with the relative intensities of 1:3:3:1.
Qualitatively, any spin plus-half nucleus polarizes the spins of its electrons to the minus-half state. Consequently, the paired electron in the hydrogen–carbon bond must...
921
Mutual Inductance01:24

Mutual Inductance

2.3K
Inductance is the property of a device that tells us how effectively it induces an emf in another device. In other words, it is a physical quantity that expresses the effectiveness of a given device.
When two circuits carrying time-varying currents are close to one another, the magnetic flux through each circuit varies because of the changing current in the other circuit. Consequently, an emf is induced in each circuit by the changing current in the other. Therefore, this type of emf is called...
2.3K

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相关实验视频

Updated: Jul 2, 2025

Observing the Transformation of Bodily Self-consciousness in the Squeeze-machine Experiment
07:20

Observing the Transformation of Bodily Self-consciousness in the Squeeze-machine Experiment

Published on: March 8, 2019

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有机的苏苏基-米亚拉合器

Polpum Onnuch1, Kranthikumar Ramagonolla1, Richard Y Liu1

  • 1Department of Chemistry and Chemical Biology, Harvard University, Cambridge, MA 02138, USA.

Science (New York, N.Y.)
|February 29, 2024
PubMed
概括

这项研究将烯插入木-米亚拉合物,将C-C键形成转化为C-N键形成. 这种新的方法统一了木-米亚乌拉和布赫瓦尔德-哈特维格的合途径,用于更广泛的合成应用.

科学领域:

  • 有机化学
  • 催化剂
  • 合成方法

背景情况:

  • 苏苏基-米亚乌拉合形成C-C键,而布赫瓦尔德-哈特维格合则形成C-N键.
  • 现有的方法通常需要不同的C-C和C-N键形成的起始材料.

研究的目的:

  • 开发一种新的反应, 融合了木-米亚乌拉和布赫瓦尔德-哈特维格合途径.
  • 通过统一的催化工艺从常见的原料中制造二胺.

主要方法:

  • 将正式的烯插入过程纳入苏苏基-米拉反应.
  • 使用了催化剂和一个庞大的辅助联体.
  • 使用商用氨化试剂.

主要成果:

  • 成功地将苏苏基-米亚拉产品从二基改为C-N-C结合的二基胺.
  • 通过各种烯化物,伪化物,酸和来实现有效的反应性.
  • 已证明与多种功能组和异环体的兼容性.

结论:

  • 开发的方法有效地结合了木-米亚乌拉和布赫瓦尔德-哈特维格的合策略.
  • 机理学研究显示了结合形成顺序的灵活性,表明了广泛的适用性.

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Synthesis of a Borylated Ibuprofen Derivative Through Suzuki Cross-Coupling and Alkene Boracarboxylation Reactions
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  • 发现了扩展到新的核友,电友和多组分反应的潜力.