## 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
Investigation of substituent effects on the 1H and 13C NMR spectra of ferrocene analogues of chalcones
✍ Scribed by E. Solčániová; S. Toma; A. Fiedlerová
- Publisher
- John Wiley and Sons
- Year
- 1980
- Tongue
- English
- Weight
- 414 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
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 analogues of chalcones of series 1 were found to be in a non‐planar conformation. Their H‐α and C‐α chemical shifts are more sensitive to the resonance than to the inductive effects of substituents. The C‐α chemical shifts of the ferrocene analogues of chalcones of series 2 are more sensitive to the inductive than to the resonance effects of substituents. The transmission of the substituent effects to the ferrocene moiety is also briefly discussed.
📜 SIMILAR VOLUMES
a See footnote d in Table 1. 'H and "C NMR Spectra of 4 4 - ## Substituted Chalcones KIKUKO HAYAMIZU (to whom correspondence should be addressed), MASARU YANAGISAWA, TETSUKO ISHII,
## 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
## Abstract ^1^H and ^13^C nmr spectra of several __N__‐ and C‐substituted carbazoles (Series 1, 2, 3 and 4) were measured. Correlations between chemical shifts and substituent constants show that these parameters describe properly the substituent effect on the nmr phenomena. Atomic charge densitie
## Abstract Correlations with reactivity constants and quantum chemical parameters were used to characterize the substituent effects on the ^1^H NMR spectra of a series of __N__,__N__‐dimethylanilines and __N__,__N__‐diethylanilines. The results indicate that the variations of the chemical shifts o