Broadband excitation pulses for high-field solid-state nuclear magnetic resonance spectroscopy

In nuclear magnetic resonance spectroscopy, experimental limits due to the radiofrequency transmitter and/or coil means that conventional radiofrequency pulses (“hard pulses”) are sometimes not sufficiently powerful to excite magnetization uniformly over a desired range of frequencies. Effects due t...

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Bibliographic Details
Published in:Magnetic resonance in chemistry 2012-04, Vol.50 (4), p.284-288
Main Authors: Loening, Nikolaus M., van Rossum, Barth-Jan, Oschkinat, Hartmut
Format: Article
Language:English
Subjects:
broadband excitation pulses
Carbon Isotopes
Computer Simulation
Magnetic Fields
Magnetic Resonance Spectroscopy - methods
optimal control
Radio Waves
solid-state NMR
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Summary:In nuclear magnetic resonance spectroscopy, experimental limits due to the radiofrequency transmitter and/or coil means that conventional radiofrequency pulses (“hard pulses”) are sometimes not sufficiently powerful to excite magnetization uniformly over a desired range of frequencies. Effects due to nonuniform excitation are most frequently encountered at high magnetic fields for nuclei with a large range of chemical shifts. Using optimal control theory, we have designed broadband excitation pulses that are suitable for solid‐state samples under magic‐angle‐spinning conditions. These pulses are easy to implement, robust to spinning frequency variations, and radiofrequency inhomogeneities, and only four times as long as a corresponding hard pulse. The utility of these pulses for uniformly exciting 13C nuclei is demonstrated on a 900 MHz (21.1 T) spectrometer. Copyright © 2012 John Wiley & Sons, Ltd. Optimal control theory was used to design broadband excitation pulses for solid‐state NMR. For situations where RF power is limited, these pulses offer improved excitation performance in comparison to conventional pulses. We demonstrate the utility of these pulses when used for magic‐angle‐spinning experiments involving 13C on a 900 MHz (21.1 T) spectrometer.
ISSN:0749-1581
1097-458X
DOI:10.1002/mrc.3800