Literature DB >> 16161579

Through-space contributions to two-dimensional double-quantum J correlation NMR spectra of magic-angle-spinning solids.

Franck Fayon1, Dominique Massiot, Malcolm H Levitt, Jeremy J Titman, Duncan H Gregory, Luminita Duma, Lyndon Emsley, Steven P Brown.   

Abstract

A routinely used assumption when interpreting two-dimensional NMR spectra obtained with a commonly used double-quantum (DQ) magic-angle-spining (MAS) pulse sequence referred to as the refocused incredible natural abundance double-quantum transfer experiment (INADEQUATE) [A. Lesage, M. Bardet, and L. Emsley, J. Am. Chem. Soc. 121, 10987 (1999)] has been that correlation peaks are only observed for pairs of nuclei with a through-bond connectivity. The validity of this assumption is addressed here by theory, experiment, and computer simulations. If the isotropic chemical shifts of the two nuclei are different and the MAS frequency is far from rotational resonance, the theoretical description demonstrates that DQ correlation peaks are indeed indicative of a J coupling. However, if the isotropic chemical shifts are the same, it is shown that DQ peaks can appear for pairs of nuclei even in the absence of a through-bond J coupling. These peaks appear in the specific case of a pair of nuclei with a nonzero through-space dipole-dipole coupling and chemical shift anisotropy tensors having different principal magnitudes or orientations, provided that the MAS frequency is comparable to or smaller than the chemical shift anisotropies. Experimental 31P spectra recorded on a sample of TiP2O7 and computer simulations show that the magnitude of these anomalous peaks increases with increasing B0 magnetic field and that they decrease with increasing MAS frequency. This behavior is explained theoretically.

Entities:  

Year:  2005        PMID: 16161579     DOI: 10.1063/1.1898219

Source DB:  PubMed          Journal:  J Chem Phys        ISSN: 0021-9606            Impact factor:   3.488


  6 in total

1.  Revealing weak histidine 15N homonuclear scalar couplings using Solid-State Magic-Angle-Spinning NMR spectroscopy.

Authors:  Chunhua Tan; Yuquan Chen; Xinhua Peng; Zhong Chen; Shuhui Cai; Timothy A Cross; Riqiang Fu
Journal:  J Magn Reson       Date:  2020-06-01       Impact factor: 2.229

Review 2.  Tailoring NMR experiments for structural characterization of amorphous biological solids: A practical guide.

Authors:  John E Kelly; Christine Chrissian; Ruth E Stark
Journal:  Solid State Nucl Magn Reson       Date:  2020-08-27       Impact factor: 2.293

3.  Folding of xylan onto cellulose fibrils in plant cell walls revealed by solid-state NMR.

Authors:  Thomas J Simmons; Jenny C Mortimer; Oigres D Bernardinelli; Ann-Christin Pöppler; Steven P Brown; Eduardo R deAzevedo; Ray Dupree; Paul Dupree
Journal:  Nat Commun       Date:  2016-12-21       Impact factor: 14.919

4.  Solid-State Nuclear Magnetic Resonance as a Tool to Probe the Impact of Mechanical Preprocessing on the Structure and Arrangement of Plant Cell Wall Polymers.

Authors:  Coyla R Munson; Yu Gao; Jenny C Mortimer; Dylan T Murray
Journal:  Front Plant Sci       Date:  2022-01-12       Impact factor: 5.753

5.  Identification and Quantification of Glycans in Whole Cells: Architecture of Microalgal Polysaccharides Described by Solid-State Nuclear Magnetic Resonance.

Authors:  Alexandre Poulhazan; Malitha C Dickwella Widanage; Artur Muszyński; Alexandre A Arnold; Dror E Warschawski; Parastoo Azadi; Isabelle Marcotte; Tuo Wang
Journal:  J Am Chem Soc       Date:  2021-11-04       Impact factor: 15.419

6.  Structure of In Vitro-Synthesized Cellulose Fibrils Viewed by Cryo-Electron Tomography and 13C Natural-Abundance Dynamic Nuclear Polarization Solid-State NMR.

Authors:  Fabien Deligey; Mark A Frank; Sung Hyun Cho; Alex Kirui; Frederic Mentink-Vigier; Matthew T Swulius; B Tracy Nixon; Tuo Wang
Journal:  Biomacromolecules       Date:  2022-03-26       Impact factor: 6.978

  6 in total

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