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Double Resonance Techniques: Overview01:12

Double Resonance Techniques: Overview

Double resonance techniques in Nuclear Magnetic Resonance (NMR) spectroscopy involve the simultaneous application of two different frequencies or radiofrequency pulses to manipulate and observe two distinct nuclear spins. One important application of double resonance is spin decoupling, which selectively suppresses coupling with one type of nucleus while observing the NMR signal from another nucleus, simplifying the spectrum and enhancing resolution.
Spin decoupling is usually achieved by...
Standing Waves in a Cavity01:28

Standing Waves in a Cavity

A household microwave and lasers are examples of standing electromagnetic waves in a cavity. When two conducting metal plates are placed parallel at the nodal planes, it creates a cavity where standing waves are formed. The cavity between the two planes is analogous to a stretched string held at the points x = 0 and x = L. Here, the distance 'L' between the two planes must be an integer multiple of half of the wavelength. The wavelengths that satisfy this condition are given by:
Spectroscopy of Carboxylic Acid Derivatives01:26

Spectroscopy of Carboxylic Acid Derivatives

Infrared spectroscopy is primarily used to determine the types of bonds and functional groups. In carboxylic acid derivatives, a typical carbonyl bond absorption is observed around 1650–1850 cm−1. For esters, the absorption is recorded at around 1740 cm−1, while acid halides show the absorption at about 1800 cm−1. Another acid derivative, the acid anhydrides, exhibit two carbonyl absorption around 1760 cm−1 and 1820 cm−1, arising from the symmetrical and unsymmetrical carbonyl vibration.
In the...
¹³C NMR: Distortionless Enhancement by Polarization Transfer (DEPT)01:20

¹³C NMR: Distortionless Enhancement by Polarization Transfer (DEPT)

When proton-coupled carbon-13 spectra are simplified by a broadband proton decoupling technique, structural information about the coupled protons is lost. Distortionless enhancement by polarization transfer (DEPT) is a technique that provides information on the number of hydrogens attached to each carbon in a molecule. While the DEPT experiment utilizes complex pulse sequences, the pulse delay and flip angle are specifically manipulated. The resulting signals have different phases depending on...
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...
2D NMR: Heteronuclear Single-Quantum Correlation Spectroscopy (HSQC)01:19

2D NMR: Heteronuclear Single-Quantum Correlation Spectroscopy (HSQC)

Heteronuclear single-quantum correlation spectroscopy (HSQC) is a 2D NMR technique that reveals one-bond correlations between hydrogen and a heteronucleus. The HSQC experiment is similar to the heteronuclear correlation experiment (HETCOR) but is more sensitive. In the HSQC spectrum, the proton chemical shift is plotted on the horizontal F2 axis, while the 13C chemical shift is plotted on the vertical F1 axis. The corresponding proton and 13C spectra are also shown. The HSQC contour plot does...

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Related Experiment Video

Updated: Jun 6, 2026

Differential Imaging of Biological Structures with Doubly-resonant Coherent Anti-stokes Raman Scattering (CARS)
12:56

Differential Imaging of Biological Structures with Doubly-resonant Coherent Anti-stokes Raman Scattering (CARS)

Published on: October 17, 2010

Doubly labeled water analysis using cavity ring-down spectroscopy.

Thomas Thorsen1, Timothy Shriver, Natalie Racine

  • 1Nutritional Sciences, University of Wisconsin-Madison, Madison, WI 60637, USA.

Rapid Communications in Mass Spectrometry : RCM
|December 15, 2010
PubMed
Summary

Cavity-ring down spectroscopy (CRDS) offers a cost-effective alternative to isotope ratio mass spectrometry for measuring total energy expenditure using the doubly labeled water method. While CRDS shows comparable accuracy, memory effects require careful management for reliable results.

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Fabrication of a Dipole-assisted Solid Phase Extraction Microchip for Trace Metal Analysis in Water Samples
09:42

Fabrication of a Dipole-assisted Solid Phase Extraction Microchip for Trace Metal Analysis in Water Samples

Published on: August 7, 2016

Related Experiment Videos

Last Updated: Jun 6, 2026

Differential Imaging of Biological Structures with Doubly-resonant Coherent Anti-stokes Raman Scattering (CARS)
12:56

Differential Imaging of Biological Structures with Doubly-resonant Coherent Anti-stokes Raman Scattering (CARS)

Published on: October 17, 2010

Fabrication of a Dipole-assisted Solid Phase Extraction Microchip for Trace Metal Analysis in Water Samples
09:42

Fabrication of a Dipole-assisted Solid Phase Extraction Microchip for Trace Metal Analysis in Water Samples

Published on: August 7, 2016

Area of Science:

  • Human Physiology
  • Analytical Chemistry
  • Biotechnology

Background:

  • The doubly labeled water method is the gold standard for measuring total energy expenditure in free-living individuals.
  • Isotope ratio mass spectrometry (IRMS) is currently required for precise isotopic analysis, but it is expensive.
  • Cavity-ring down spectroscopy (CRDS) presents a potentially more affordable alternative for isotopic measurements.

Purpose of the Study:

  • To compare the precision and accuracy of CRDS with IRMS for total energy expenditure measurements.
  • To evaluate CRDS as a viable, less expensive alternative to IRMS in the context of doubly labeled water analysis.
  • To identify and address potential limitations of CRDS, such as memory effects, in urine specimen analysis.

Main Methods:

  • Urine specimens from 14 human subjects were analyzed using both CRDS and IRMS.
  • Measurements focused on isotopic abundance of oxygen-18 ((18)O) and deuterium ((2)H).
  • CRDS performance was assessed for accuracy, precision, and the presence of memory effects between samples.

Main Results:

  • CRDS demonstrated comparable accuracy and precision to IRMS for isotope abundance measurements in urine.
  • Relative accuracy for total body water was 0.5 ± 1%, and for total energy expenditure was 0.5 ± 6%.
  • Significant memory effects were observed in the CRDS instrument for both (18)O (5%) and (2)H (9%), necessitating specific protocols to mitigate their impact.

Conclusions:

  • CRDS can provide accurate and precise measurements for doubly labeled water analysis, comparable to IRMS.
  • Memory effects in CRDS require careful specimen handling and data correction, limiting throughput.
  • Further development to reduce CRDS memory effects is recommended to enhance its utility for new laboratories.