The NMR relaxation times of the "C(O) nuclei of formanilide, acetanilide, benzamide, benzoic acid, the benzoate anion and glycine were measured for four different magnetic field values, allowing the determination of the contribution of the shielding anisotropy mechanism to the total relaxation rate.
A multinuclear NMR (13C, 15N and 29Si) study of the SiN bond in silylamines: (p – d) π interaction
✍ Scribed by M. L. Filleux-Blanchard; Nguyen Dinh An
- Publisher
- John Wiley and Sons
- Year
- 1979
- Tongue
- English
- Weight
- 409 KB
- Volume
- 12
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
A series of variously substituted aminosilanes was investigated by ^15^N NMR spectroscopy to obtain further information on the controversial problem of pπ‐dπ interaction in these systems. The ^15^N NMR data are consistent with the ^13^C and ^29^Si results and suggest that the (p‐d)π backbonding is not negligible in these systems. The values of the ^15^N chemical shifts and the ^13^C parameters [δ^13^C and J(^13^CH)] are discussed in terms of nitrogen lone‐pair delocalization and provide a good basis for explaining the variations of the ^29^Si chemical shifts with the nature of the nitrogen atom substituents.
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