Reproducible proton chemical shifts in the porphyrin series are obtained when the spectrum is measured in chloroform using the zinc (11) complex of the porphyrin in the presence of an excess of pyrrolidine. This method is specifically demonstrated for the case of 2,4-dicyanodeuteroporphyrin-M dimeth
The proton resonance spectra of heterocycles—VI: The correlation of substituent effects on chemical shifts in bicyclic compounds
✍ Scribed by A. R. Katritzky; Y. Takeuchi; B. Ternai; G. J. T. Tiddy
- Publisher
- John Wiley and Sons
- Year
- 1970
- Tongue
- English
- Weight
- 477 KB
- Volume
- 2
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
The proton chemical shifts are reported for monosubstituted naphthalenes, quinolines and quinoxalines. Together with literature data, these chemical shifts are compared with the parent compounds and substituent effects evaluated statistically. The effect of substituents parallels that in benzenes, but is modified by bond fixation, steric hindrance and other effects which can, at least qualitatively be understood. The treatment enables estimation of likely chemical shifts for ABC spectra in fused aromatic systems which should facilitate the solution of such spectra.
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