## Abstract Correction of measured chemical shifts by subtracting the diamagnetic contributions caused by certain substituents on various carbons of a molecule leads to data that allow a reasonable interpretation of substituent effects on chemical shifts in ^13^C n.m.r. spectroscopy. It is shown th
Investigation of substituent effects of chalcones by 13C n.m.r. spectroscopy
✍ Scribed by E. Soĺǎniová; Š. Toma; S. Gronowitz
- Publisher
- John Wiley and Sons
- Year
- 1976
- Tongue
- English
- Weight
- 450 KB
- Volume
- 8
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
^13^C chemical shifts for 23 para‐ and meta‐substituted chalcones of the types 1 and 2 have been determined. The aromatic shieldings are compared with previous results for other aromatic derivatives. Correlations of the ^13^C chemical shifts of vinyl carbons and carbonyl carbons as well as ring carbons with Hammett σ parameters, π electron densities and the reactivity parameters of Swain and Lupton provide a consistent picture of electronic effects transmitted through the carbon framework of the compounds studied.
📜 SIMILAR VOLUMES
## Abstract The transmission of electronic effects across the ferrocene analogues of chalcones [3‐aryl‐1‐ferrocenyl‐2‐propene‐1‐ones (series 1) and 1‐aryl‐3‐ferrocenyl‐2‐propene‐1‐ones (series 2)], as well as the conformations of both types of ferrocene analogues have been studied. The ferrocene an
## Abstract Linear correlation coefficients were obtained for the substituent effect of the nitro group in primary nitroalkanes. The solvent effect of chloroform is also discussed, as well as the influence of the scalar relaxation on the half‐width of α‐carbons in ^13^C n.m.r. spectroscopy.
## Abstract ^1^H NMR spectra of 26 substituted chalcones (3‐aryl‐1 phenyl‐2‐propene‐1‐ones and 1‐aryl‐3‐phenyl‐2‐propene‐1‐ones) have been studied. The chemical shifts of the α and β protons to the carbonyl group were correlated with Hammett s̀ parameters. To gain information on the effect of the t