## Abstract Carbon‐13, carbon‐13 coupling constants and carbon‐13 chemical shifts have been measured in a series of phenyl substituted ethylenes and aromatics all doubly labelled with ^13^C at the olefinic positions (α,β‐) or at neighbouring aromatic positions, tetraphenylcyclopentadienone labelled
13C, 13C coupling constants in anthracene, 9,10-dihydroanthracene and phthalic acid derivatives. Determination of signs by the symmetrical double labelling (SDL) method V
✍ Scribed by P. E. Hansen; A. Berg
- Publisher
- John Wiley and Sons
- Year
- 1979
- Tongue
- English
- Weight
- 543 KB
- Volume
- 12
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
Carbon‐13, carbon‐13 one‐bound and long‐range coupling constants are determined for anthracene and 9,10‐dihydroanthracene labelled in the 9,10‐positions, and for thiophthalic anhydride and phthalimide, labelled in both carbonyl groups. Relative signs are determined by the SDL method. Signs in naphthalene, anthracene and pyrene derivatives are discussed. The general trends observed in many aromatic compounds, ^3^J|>|^2^J|>|^4^J| and ^2^J positive, ^3^J positive, ^4^J negative are mostly confirmed. However, evidence suggests that two‐bond couplings between carbon atoms in the same ring in aromatic hydrocarbons are negative.
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