Introduction of a fluorine substituent into an aromatic ring of [2.2]paracyclophane causes distinct shielding and deshielding effects at the anti -and syn-protons, respectively, of the adjacent bridge methylene group. A recent contradictory claim in the literature was disproved by 2D H,H-NOESY, long
Structural investigation on phenyl- and pyridin-2-ylamino(methylene)naphthalen-2(3H)-one. Substituent effects on the NMR chemical shifts
✍ Scribed by Taracad K. Venkatachalam; Gregory K. Pierens; Marc R. Campitelli; David C. Reutens
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 195 KB
- Volume
- 48
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.2626
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Schiff bases bearing phenyl and pyridyl groups were synthesized by condensation of appropriate amines with 2‐hydroxynaphthaldehyde. These Schiff bases were obtained as colored crystalline solids. The proton NMR spectra of these compounds showed a doublet for the NH protons indicating a keto tautomer for these Schiff bases. The pyridyl‐substituted Schiff bases containing hydroxyl moiety were found to show the most downfield shift for the NH protons in DMSO solvent, and this was rationalized due to the formation of a six‐ and five‐membered ring using hydrogen bonds for these two compounds. Correspondingly, the olefinic proton of the Schiff bases is also found to be a doublet due to coupling to the amine proton. These Schiff bases exhibited thermochromic properties. Detailed NMR spectral analysis for both the phenyl‐ and pyridyl‐substituted Schiff bases is presented. Copyright © 2010 John Wiley & Sons, Ltd.
📜 SIMILAR VOLUMES
## Abstract Substituent effects on the ^13^C and ^1^H chemical shifts have been studied for derivatives of 3‐benzylidene‐2, 4‐pentanedione. A significant correlation has been found between chemical shifts of the __Z__ carbonyl group (C‐2) and Hammett constants, while no correlation has been found f
## Abstract The synthesis and assignment of ^15^N and ^13^C NMR signals of the 1,3,4‐oxathiazol‐2‐one ring in a series of __para__‐substituted 5‐phenyl derivatives are reported. DFT calculations of ^15^N and ^13^C chemical shifts correspond closely to observed values. Substituent effects are interp
The 13C chemical shifts of 2-R-3-methylbenzothiazolium quaternary salts and the corresponding ZRbenzothiazoles are presented. ## KEY WORDS I3C NMR Substituent effects 2-R-3-methylbenzothiazoliurn quaternary salts 2-R-benzothiazoles reveal some systematic trends in the 13C data for these comr>ound
## Abstract The influence of substituents on ^1^H and ^13^C NMR chemical shifts of 2‐substituted 1,3‐dimethylbenzimidazolium perchlorates in different solvents has been investigated. It has been shown that the transmission of the electronic effects of the substituents in benzimidazoles and their qu