## Abstract The influence of substituents on the ^13^C NMR chemical shifts of 2‐substituted 1‐methylbenzimidazoles has been investigated. The electronic effects of the substituents are transmitted to C‐4 and C‐7 mainly by the resonance mechanism, and to C‐5, C‐6 and __N__‐CH~3~, by approximately eq
Transmission of the substituent effects in 2-substituted benzimidazoles studied by 1H and 13C nuclear magnetic resonance
✍ Scribed by V. A. Lopyrev; L. I. Larina; T. I. Vakul'skaya; M. F. Larin; O. B. Nefedova; E. F. Shibanova; M. G. Voronkov
- Publisher
- John Wiley and Sons
- Year
- 1981
- Tongue
- English
- Weight
- 503 KB
- Volume
- 15
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
The substituent influence on the ^1^H and ^13^C NMR chemical shifts in 2‐substituted benzimidazoles and their anions and cations has been investigated. The transmission of the electronic effects of substituents from C‐2 to C‐5 (6) is approximately 20% less effective than that in the opposite direction. The solvent influence on the chemical shifts of protons and transmission effects in the charged forms of 2‐substituted benzimidazoles has been studied.
📜 SIMILAR VOLUMES
The iniluence of substituents on the 'H, "C and 15N NMR chemical shifts of 2-substituted 5(6)nitrobenzimidazoles and their analogues labelled with 15N in the nitro group was investigated. It was found that the substituent effects are transmitted to the carbon and hydrogen nuclei in positions 4-7 mai
H and I3C N M R studies were carried out on l-ethenylnaphthalene, Zethenylnaphthalene, 9ethenylanthracene, 9ethenylphenanthrene, l-ethenylpyrene and l-ethenylperylene. Assignments of proton and carbon resonances were made with the aid of 2D COSY, 2D HETCOR, 2D COLOC, 2D COLOCS, 3J(H,C) INAPT, and NO