Войдите в систему

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. Similarly, if A has three neighbors (AX3 spin system), four possible electronic environments result in a quartet of peaks with the relative intensities 1:3:3:1.

Empirically, a proton coupled to n equivalent neighbors yields a multiplet signal split into n + 1 peaks. The relative intensities of the peaks in a multiplet can be predicted using Pascal's triangle, which is an array where each entry is the sum of the entries to its left and right in the row above it.

Теги

1H NMRSignal Splittingn 1 RuleAX Proton Spin SystemDoublet NMR SignalTriplet SignalQuartet PeaksRelative IntensitiesMultiplet SignalChemical ShiftElectronic EnvironmentsPascal s Triangle

Из главы 8:

article

Now Playing

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

Interpreting Nuclear Magnetic Resonance Spectra

1.1K Просмотры

article

8.1 : Chemical Shift: Internal References and Solvent Effects

Interpreting Nuclear Magnetic Resonance Spectra

535 Просмотры

article

8.2 : NMR Spectroscopy: Chemical Shift Overview

Interpreting Nuclear Magnetic Resonance Spectra

1.3K Просмотры

article

8.3 : Proton (¹H) NMR: Chemical Shift

Interpreting Nuclear Magnetic Resonance Spectra

1.4K Просмотры

article

8.4 : Inductive Effects on Chemical Shift: Overview

Interpreting Nuclear Magnetic Resonance Spectra

1.0K Просмотры

article

8.5 : π Electron Effects on Chemical Shift: Overview

Interpreting Nuclear Magnetic Resonance Spectra

1.0K Просмотры

article

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

Interpreting Nuclear Magnetic Resonance Spectra

1.1K Просмотры

article

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

Interpreting Nuclear Magnetic Resonance Spectra

2.2K Просмотры

article

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

Interpreting Nuclear Magnetic Resonance Spectra

1.3K Просмотры

article

8.9 : ¹H NMR Signal Integration: Overview

Interpreting Nuclear Magnetic Resonance Spectra

1.2K Просмотры

article

8.10 : NMR Spectroscopy: Spin–Spin Coupling

Interpreting Nuclear Magnetic Resonance Spectra

1.1K Просмотры

article

8.11 : ¹H NMR Signal Multiplicity: Splitting Patterns

Interpreting Nuclear Magnetic Resonance Spectra

4.8K Просмотры

article

8.13 : Spin–Spin Coupling Constant: Overview

Interpreting Nuclear Magnetic Resonance Spectra

838 Просмотры

article

8.14 : Spin–Spin Coupling: One-Bond Coupling

Interpreting Nuclear Magnetic Resonance Spectra

900 Просмотры

article

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

Interpreting Nuclear Magnetic Resonance Spectra

894 Просмотры

See More

JoVE Logo

Исследования

Образование

О JoVE

Авторские права © 2025 MyJoVE Corporation. Все права защищены