Anmelden

The spin state of an NMR-active nucleus can have a slight effect on its immediate electronic environment. This effect propagates through the intervening bonds and affects the electronic environments of NMR-active nuclei up to three bonds away; occasionally, even farther. This phenomenon is called spin–spin coupling or J-coupling. Coupling interactions are mutual and result in small changes in the absorption frequencies of both nuclei involved. While nuclei of the same element are involved in homonuclear coupling, nuclei of different elements interact in heteronuclear coupling.

Consider non-equivalent protons A and X that have excitation energies of A and X. The term J = 0 is used to indicate that they do not interact via coupling. Coupling between A and X results in the modification of their nuclear spin energy levels and is expressed as J ≠ 0. For the coupled spins of A and X, 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 antiparallel to spin X.

Tags
NMR SpectroscopySpin spin CouplingJ couplingElectronic EnvironmentAbsorption FrequenciesHomonuclear CouplingHeteronuclear CouplingNon equivalent ProtonsNuclear Spin Energy LevelsExcitation Energies

Aus Kapitel 8:

article

Now Playing

8.10 : NMR Spectroscopy: Spin–Spin Coupling

Interpreting Nuclear Magnetic Resonance Spectra

1.1K Ansichten

article

8.1 : Chemical Shift: Internal References and Solvent Effects

Interpreting Nuclear Magnetic Resonance Spectra

529 Ansichten

article

8.2 : NMR Spectroscopy: Chemical Shift Overview

Interpreting Nuclear Magnetic Resonance Spectra

1.3K Ansichten

article

8.3 : Proton (¹H) NMR: Chemical Shift

Interpreting Nuclear Magnetic Resonance Spectra

1.4K Ansichten

article

8.4 : Inductive Effects on Chemical Shift: Overview

Interpreting Nuclear Magnetic Resonance Spectra

1.0K Ansichten

article

8.5 : π Electron Effects on Chemical Shift: Overview

Interpreting Nuclear Magnetic Resonance Spectra

994 Ansichten

article

8.6 : π Electron Effects on Chemical Shift: Aromatic and Antiaromatic Compounds

Interpreting Nuclear Magnetic Resonance Spectra

1.1K Ansichten

article

8.7 : ¹H NMR Chemical Shift Equivalence: Homotopic and Heterotopic Protons

Interpreting Nuclear Magnetic Resonance Spectra

2.2K Ansichten

article

8.8 : ¹H NMR Chemical Shift Equivalence: Enantiotopic and Diastereotopic Protons

Interpreting Nuclear Magnetic Resonance Spectra

1.3K Ansichten

article

8.9 : ¹H NMR Signal Integration: Overview

Interpreting Nuclear Magnetic Resonance Spectra

1.2K Ansichten

article

8.11 : ¹H NMR Signal Multiplicity: Splitting Patterns

Interpreting Nuclear Magnetic Resonance Spectra

4.8K Ansichten

article

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

Interpreting Nuclear Magnetic Resonance Spectra

1.1K Ansichten

article

8.13 : Spin–Spin Coupling Constant: Overview

Interpreting Nuclear Magnetic Resonance Spectra

828 Ansichten

article

8.14 : Spin–Spin Coupling: One-Bond Coupling

Interpreting Nuclear Magnetic Resonance Spectra

895 Ansichten

article

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

Interpreting Nuclear Magnetic Resonance Spectra

884 Ansichten

See More

JoVE Logo

Datenschutz

Nutzungsbedingungen

Richtlinien

Forschung

Lehre

ÜBER JoVE

Copyright © 2025 MyJoVE Corporation. Alle Rechte vorbehalten