Issue 17, 2023

Residual proton line width under refocused frequency-switched Lee-Goldburg decoupling in MAS NMR

Abstract

Despite many decades of research, homonuclear decoupling in solid-state NMR under magic-angle spinning (MAS) has yet to reach a point where the achievable proton line widths become comparable to the resolution obtained in solution-state NMR. This makes the precise determination of isotropic chemical shifts difficult and thus presents a limiting factor in the application of proton solid-state NMR to biomolecules and small molecules. In this publication we analyze the sources of the residual line width in refocused homonuclear-decoupled spectra in detail by comparing numerical simulations and experimental data. Using a hybrid analytical/numerical approach based on Floquet theory, we find that third-order effective Hamiltonian terms are required to realistically characterize the line shape and line width under frequency-switched Lee-Goldburg (FSLG) decoupling under MAS. Increasing the radio-frequency field amplitude enhances the influence of experimental rf imperfections such as pulse transients and the MAS-modulated radial rf-field inhomogeneity. While second- and third-order terms are, as expected, reduced in size at higher rf-field amplitudes, the line width becomes dominated by first-order terms which severely limits the achievable line width. We expect, therefore, that significant improvements in the line width of FSLG-decoupled spectra can only be achieved by reducing the influence of MAS-modulated rf-field inhomogeneity and pulse transients.

Graphical abstract: Residual proton line width under refocused frequency-switched Lee-Goldburg decoupling in MAS NMR

Supplementary files

Article information

Article type
Paper
Submitted
26 Jan 2023
Accepted
16 Mar 2023
First published
17 Mar 2023
This article is Open Access
Creative Commons BY license

Phys. Chem. Chem. Phys., 2023,25, 11959-11970

Residual proton line width under refocused frequency-switched Lee-Goldburg decoupling in MAS NMR

K. Aebischer and M. Ernst, Phys. Chem. Chem. Phys., 2023, 25, 11959 DOI: 10.1039/D3CP00414G

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