## Abstract Measurement of the ^13^C NMR spectra of the bridgehead nitro compounds __1a–5a__ has been performed. It is found that one‐bond ^13^C^15^N coupling is not necessarily a reflection of the degree of s character of the bridgehead carbon exocyclic bonding orbital. Although the magnitude of
NMR coupling of 13C and 19F with 14N in nitro compounds
✍ Scribed by Michael D. Coburn; Carlyle B. Storm; Donald W. Moore; Thomas G. Archibald
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- English
- Weight
- 426 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
The ^13^C and ^14^N NMR spectra of a variety of highly nitrated aliphatic, aromatic and heterocyclic compounds were obtained. The proton decoupled ^13^C peaks of the nitro‐substituted carbons in most of these compounds were split into the multiplets expected for coupling with spin 1 nuclei with negligible quadrupolar broadening. In addition, the ^19^F spectra of some fluoronitroaliphatic compounds showed that the ^19^F signals were also split into the expected multiplets from coupling with the ^14^N of the nitro groups.
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