The 13C NMR spectra of 48 chlorinated biphenyls are presented. The I3C shifts of the individual carbons are interpreted by the additive contributions from the substituent effect of a chlorine atom, and by the repulsive interaction of chlorine atoms substituted in a crowded relationship on the biphen
The proton chemical shifts of polychlorinated biphenyls
β Scribed by D. Welti; D. Sissons
- Publisher
- John Wiley and Sons
- Year
- 1972
- Tongue
- English
- Weight
- 410 KB
- Volume
- 4
- Category
- Article
- ISSN
- 0749-1581
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β¦ Synopsis
A 220 MHz NMR spectrometer has been used to identify the structure of polychlorinated biphenyls (PCBs). The proton chemical shifts and approximate coupling constants of PCBs fractionated from Aroclor 1254 are given in the text. The spectra of model compounds are included in the supplement. The chemical shifts are also tabulated according to the ring substitution pattern, when it can be seen that the shifts change systematically with the degree of both the total ring substitution and the substitution in the positions 'ortho' to the bridging bond between the rings. I N T R O D U C T I O N * Commercial products manufactured by Monsanto Chemicals Ltd, containing 42, 54 and 60% w/w chlorine, respectively.
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