An information-rich and non-destructive analytical tool, nuclear magnetic resonance (NMR) spectroscopy uses the inherent magnetic properties of specific atomic nuclei to reveal the structure, identity, concentration, and behavior of molecules in solid or liquid samples.
Research and quality assurance laboratories across various fields of study rely on NMR to:
A wealth of established methods make NMR easier to use than ever before, while also flexible enough to study targets from small molecules to RNA hundreds of nucleotides long. Recent advances in technology and software have made NMR compact and approachable enough for use in most analytical labs, with more powerful options for targeted research applications. NMR spectrometers range from cost-conscious benchtop systems to sophisticated research spectrometers with high-field magnets to maximize sensitivity and resolution.
NMR provides unique analytical capabilities:
Here’s a high-level overview of the process:
The sample – typically a liquid or a solid dissolved in solvent – may be degassed and particles removed before analysis.
A thin-walled glass vial containing the sample is placed inside an electronic coil, or resonator, which in turn sits inside a powerful magnet at the heart of the NMR spectrometer. The magnet causes susceptible atomic nuclei within the sample to align with its field, giving them a consistent resting alignment.
NMR specifically applies to nuclei that contain an odd number of protons and/or neutrons, for example, 1H or 13C. These nuclei exhibit a built-in magnetic moment and angular momentum that together give the nuclei a property called “spin.” A strong enough magnet will cause these nuclei to align their spins with its field.
The resonator coil releases one or more radio-frequency pulses at the right frequency to perturb specific nuclei, then detects the energy released as the nuclei “relax” back to their resting alignments in a process called free-induction decay (FID). Because the FID signal is typically very small relative to background noise, multiple acquisitions are generally averaged. That signal is then converted by Fourier transformation into an NMR spectrum showing the frequencies at which the nuclei responded.
Well-characterized differences in the response frequencies for a given isotope reveal the electromagnetic influences of neighboring electrons (“chemical shift”). Splitting of peaks into two or more subpeaks indicate magnetic influences of neighboring nuclei (“spin coupling”). The figures below show each effect, using the NMR spectrum for ethanol based on either carbon (top) or hydrogen (bottom) nuclei.
Customized sequences of RF pulses tease out specific details about a sample, sometimes probing multiple nuclei. Advanced software can simplify analysis and interpretation, and automate many aspects of data acquisition, analysis, and reporting.
This application can also be used with our benchtop NMR system, the Fourier 80