## Abstract Nitrogen and carbon electron densities of the toluidines and xylidines have been recalculated by the INDO method; previously published errors have been corrected. Although the nitrogen‐15 chemical shifts of these compounds still display the earlier suggested correlation with σ and total
Deuterium nuclear magnetic resonance spectroscopy. 1—Larmor frequency ratio, referencing and chemical shift
✍ Scribed by Jasim M. A. Al-Rawi; George Q. Behnam; Nihad I. Taha
- Publisher
- John Wiley and Sons
- Year
- 1981
- Tongue
- English
- Weight
- 339 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Precise values for the ratio of the Larmor frequencies, w~1H~/w~2H~, were measured at constant field for various organic compounds. The values of the Larmor frequency ratio depend on carbon‐hydrogen bond hybridization. The best ratio for the ghost referencing of ^2^H NMR spectra was then determined (6.514399862). This value enables an accurate ghost reference for any ^2^H NMR spectrum to be derived from the observed ^1^H NMR frequency of the normal internal reference. Deuterium and proton chemical shifts measured from internal, partially deuteriated TMS under the same conditions are shown to be the same.
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