## Abstract The chemical shifts and coupling constants for the ring protons of nine disubstituted naphthalenes (mainly halogenonitre compounds) in carbon tetrachloride solutions have been obtained by analysis and computer simulation of their 100 MHz magnetic resonance spectra. Substituent effects a
Proton magnetic resonance spectra of monosubstituted naphthalenes
β Scribed by Vittorio Lucchini; Peter R. Wells
- Publisher
- John Wiley and Sons
- Year
- 1976
- Tongue
- English
- Weight
- 377 KB
- Volume
- 8
- Category
- Article
- ISSN
- 0749-1581
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β¦ Synopsis
Abstract
The chemical shifts and coupling constants for the ring protons of fourteen monosubstituted naphthalenes in carbon tetrachloride solution have been obtained by analysis and computer simulation of their 100 MHz magnetic resonance spectra. Studies at several concentrations have enabled shifts extrapolated to infinite dilution to be obtained and concentration effects arising from soluteβsolute interactions to be determined.
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