Static and magic angle spinning 51V NMR spectra of were recorded at three di †erent Ðeld BiVO 4 strengths (2.3, 9.4 and 14.1 T) and give evidence of the relative e †ects of the quadrupolar interaction and electronic shielding at the nucleus. The experimental powder spectra were Ðtted to ascertain bo
Determination of chemical-shift tensor orientations in methylene groups by separated-local-field NMR
✍ Scribed by K. Schmidt-Rohr; M. Wilhelm; A. Johansson; H. W. Spiess
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 566 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The ^13^C chemical‐shift tensor orientations in the OCH~2~CH~2~O moieties of poly(ethylene oxide) (PEO) and poly(ethylene terephthalate) (PET) were determined by means of ^1^H^13^C separated‐local‐field NMR spectroscopy, and the literature values for the shift tensors in polyethylene (PE) and polyoxymethylene (POM) were improved. An angular resolution of ± 4° was attained on standard equipment with 90° pulse lengths exceeding 4 μs. Relatively high uniformity of the methylene tensor orientations, complying with local molecular symmetry, was found.
📜 SIMILAR VOLUMES
The orientations of the 13C chemical shift tensors in undoped cis-and tram-polyacetylene have been determined from the chemical shift-dipolar two-dimensional powder patterns observed in rotating samples.
The potential of heteronuclear MAS NMR spectroscopy for the characterization of (15)N chemical shift (CS) tensors in multiply labeled systems has been illustrated, in one of the first studies of this type, by a measurement of the chemical shift tensor magnitude and orientation in the molecular frame
The magnitudes and orientations of the 15 N chemical shift tensor of [1-15 N]-2-deoxyguanosine were determined from a polycrystalline sample using the two-dimensional PISEMA experiment. The magnitudes of the principal values of the 15 N chemical shift tensor of the N1 nitrogen of [1-15 N]-2-deoxygua
We demonstrate a dipolar-chemical shift correlation technique for sign-sensitive determination of the torsion angle in solid peptides and proteins under magic-angle spinning. The indirect dimension of the experiment is obtained by separate but synchronous evolution of the magnetization under the 15