## Carbon -13 chemical shifts of l-phenylsulphonyl-2-phenylaziridine and several of its mand psubstituted derivatives have been determined. The substituent chemical shift (SCS) effects on the benzylic carbon C-2, and on the methylene carbon C-3 have been satisfactorily correlated with Hammett subs
Substituent effects on the 13C NMR chemical shifts of 1-hydroxyalkylphosphonic acids
✍ Scribed by Zdzisław Glowacki; Maria Hoffmann
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- English
- Weight
- 208 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
^13^C chemical shifts and ^31^P,^13^C coupling constants are reported for nine 1‐hydroxyalkylphosphonic and two additional phosphonic acids. The α‐substituent‐induced chemical shifts (α‐SCS) of the phosphonate group were calculated and their non‐additivity was observed. Good linear correlations exist between the chemical shifts and also between the α‐SCS parameters of 1‐hydroxyalkylphosphonic acids and the respective values of analogously constituted 1‐aminoalkylphosphonic acids.
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