Structural influences on high-resolution yttrium-89 NMR spectra of solids
β Scribed by R. Dupree; M.E. Smith
- Publisher
- Elsevier Science
- Year
- 1988
- Tongue
- English
- Weight
- 378 KB
- Volume
- 148
- Category
- Article
- ISSN
- 0009-2614
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β¦ Synopsis
Structural influences on both the isotropic NMR chemical shift and resonance linewidth of "Y are investigated by obtaining magic-angle spinning NMR spectra from a number of solid-state yttrium aluminate and silicate phases. These clearly show that the isotropic chemical shift for 89Y is dependent on the number of nearest neighbours and the nature of the next-nearest neighbours. However, unlike most other nuclei such as *%i and 27A1, the shift ranges of different nearest-neighbour coordinations significantly overlap. In the silicates the ssY spectrum becomes more shielded as the %i resonance becomes less shielded reflecting the reciprocity of the shifts.
π SIMILAR VOLUMES
High-resolution solid-state magic angle spinning (73)Ge NMR spectra of some organogermanium compounds were measured. Most tetrasubstituted germanes with identical substituents exhibited signals except for one case. Tetrasubstituted germanes with two kinds of different but somewhat similar substituen
## Abstract Highβresolution solidβstate magic angle spinning ^73^Ge NMR spectra of hexavalent germanium compounds, i.e. diiodogermylene (**1a**) and bis(1βpyrrolyl)(__meso__βtetraphenylporphyrinato)germanium (**3a**), were determined. To the best of our knowledge, this is the first example of highβ