Origin of the residual line width under frequency-switched Lee–Goldburg decoupling in MAS solid-state NMR
-
Published:2020-02-19
Issue:1
Volume:1
Page:13-25
-
ISSN:2699-0016
-
Container-title:Magnetic Resonance
-
language:en
-
Short-container-title:Magn. Reson.
Author:
Hellwagner Johannes, Grunwald LiamORCID, Ochsner Manuel, Zindel Daniel, Meier Beat H.ORCID, Ernst MatthiasORCID
Abstract
Abstract. Homonuclear decoupling sequences in solid-state nuclear magnetic resonance (NMR) under
magic-angle spinning (MAS) show experimentally significantly larger residual
line width than expected from Floquet theory to second order. We present an
in-depth theoretical and experimental analysis of the origin of the residual
line width under decoupling
based on frequency-switched Lee–Goldburg (FSLG) sequences. We analyze the effect of experimental pulse-shape errors (e.g., pulse
transients and B1-field inhomogeneities) and use a Floquet-theory-based
description of higher-order error terms that arise from the interference
between the MAS rotation and the pulse sequence. It is shown that the
magnitude of the third-order auto term of a single homo- or heteronuclear
coupled spin pair is important and leads to significant line broadening
under FSLG decoupling. Furthermore, we show the dependence of these
third-order error terms on the angle of the effective field with the
B0 field. An analysis of second-order cross terms is presented that
shows that the influence of three-spin terms is small since they are
averaged by the pulse sequence. The importance of the inhomogeneity of the radio-frequency (rf) field
is discussed and shown to be the main source of residual line broadening
while pulse transients do not seem to play an important role.
Experimentally, the influence of the combination of these error terms is
shown by using restricted samples and pulse-transient compensation. The
results show that all terms are additive but the major contribution to the
residual line width comes from the rf-field inhomogeneity for the standard
implementation of FSLG sequences, which is significant even for samples with
a restricted volume.
Funder
European Research Council Eidgenössische Technische Hochschule Zürich Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
Publisher
Copernicus GmbH
Reference66 articles.
1. Agarwal, V., Penzel, S., Szekely, K., Cadalbert, R., Testori, E., Oss, A.,
Past, J., Samoson, A., Ernst, M., Böckmann, A., and Meier, B. H.: DeNovo
3-D Structure Determination from Sub-milligram Protein Samples by Solid-State
100 kHz MAS NMR Spectroscopy, Angew. Chem. Int. Ed., 53, 12253–12256,
https://doi.org/10.1002/anie.201405730, 2014. 2. Andreas, L. B., Jaudzems, K., Stanek, J., Lalli, D., Bertarello, A., Le
Marchand, T., Cala-De Paepe, D., Kotelovica, S., Akopjana, I., Knott, B.,
Wegner, S., Engelke, F., Lesage, A., Emsley, L., Tars, K., Herrmann, T., and
Pintacuda, G.: Structure of fully protonated proteins by proton-detected
magic-angle spinning NMR, P. Natl. Acad. Sci. USA, 113, 9187–9192,
https://doi.org/10.1073/pnas.1602248113, 2016. 3. Barbara, T. M., Martin, J. F., and Wurl, J. G.: Phase transients in NMR probe
circuits, J. Magn. Reson., 93, 497–508,
https://doi.org/10.1016/0022-2364(91)90078-8, 1991. 4. Barfield, M.: Structural dependencies of interresidue scalar coupling h3JNC'
and donor 1H chemical shifts in the hydrogen bonding regions of proteins, J.
Am. Chem. Soc., 124, 4158–4168, https://doi.org/10.1021/ja012674v, 2002. 5. Berglund, B. and Vaughan, R. W.: Correlations between proton chemical shift
tensors, deuterium quadrupole couplings, and bond distances for hydrogen
bonds in solids, J. Chem. Phys., 73, 2037–2043, https://doi.org/10.1063/1.440423,
1980.
Cited by
9 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
|
|