Zaloguj się

Spin systems where the difference in chemical shifts of the coupled nuclei is greater than ten times J are called first-order spin systems. These nuclei are weakly coupled, and their chemical shifts and coupling constant can generally be estimated from the well-separated signals in the spectrum.

As Δν decreases and the signals move closer, the doublets appear increasingly distorted. The intensities of the inner lines increase at the cost of those of the outer lines as the signals are slanted or roofed towards each other. When Δν/J is less than 10, the spins are said to be strongly coupled, and the spectra show second-order effects.

Peaks may overlap completely and appear deceptively simple, similar to first-order spectra. Second-order effects can also result in shoulders and multiplets that cannot be interpreted. Accordingly, chemical shifts and coupling constants in these spectra are often identified by computer simulation methods. Because Δν increases with spectrometer frequency and J remains constant, second-order effects decrease when spectra are recorded using higher-field instruments.

Tagi
1H NMRSpin SystemFirst orderWeak CouplingChemical ShiftCoupling ConstantSecond orderStrong CouplingDistortionOverlapSimulation

Z rozdziału 8:

article

Now Playing

8.20 : ¹H NMR: Interpreting Distorted and Overlapping Signals

Interpreting Nuclear Magnetic Resonance Spectra

909 Wyświetleń

article

8.1 : Chemical Shift: Internal References and Solvent Effects

Interpreting Nuclear Magnetic Resonance Spectra

530 Wyświetleń

article

8.2 : NMR Spectroscopy: Chemical Shift Overview

Interpreting Nuclear Magnetic Resonance Spectra

1.3K Wyświetleń

article

8.3 : Proton (¹H) NMR: Chemical Shift

Interpreting Nuclear Magnetic Resonance Spectra

1.4K Wyświetleń

article

8.4 : Inductive Effects on Chemical Shift: Overview

Interpreting Nuclear Magnetic Resonance Spectra

1.0K Wyświetleń

article

8.5 : π Electron Effects on Chemical Shift: Overview

Interpreting Nuclear Magnetic Resonance Spectra

995 Wyświetleń

article

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

Interpreting Nuclear Magnetic Resonance Spectra

1.1K Wyświetleń

article

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

Interpreting Nuclear Magnetic Resonance Spectra

2.2K Wyświetleń

article

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

Interpreting Nuclear Magnetic Resonance Spectra

1.3K Wyświetleń

article

8.9 : ¹H NMR Signal Integration: Overview

Interpreting Nuclear Magnetic Resonance Spectra

1.2K Wyświetleń

article

8.10 : NMR Spectroscopy: Spin–Spin Coupling

Interpreting Nuclear Magnetic Resonance Spectra

1.1K Wyświetleń

article

8.11 : ¹H NMR Signal Multiplicity: Splitting Patterns

Interpreting Nuclear Magnetic Resonance Spectra

4.8K Wyświetleń

article

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

Interpreting Nuclear Magnetic Resonance Spectra

1.1K Wyświetleń

article

8.13 : Spin–Spin Coupling Constant: Overview

Interpreting Nuclear Magnetic Resonance Spectra

829 Wyświetleń

article

8.14 : Spin–Spin Coupling: One-Bond Coupling

Interpreting Nuclear Magnetic Resonance Spectra

897 Wyświetleń

See More

JoVE Logo

Prywatność

Warunki Korzystania

Zasady

Badania

Edukacja

O JoVE

Copyright © 2025 MyJoVE Corporation. Wszelkie prawa zastrzeżone