17O chemical shifts were measured in 40 enamines activated in the b-position by CxO, COO, NO 2 , SO and groups. Data for the oxygen-containing series of o-hydroxyacyl aromatics are also included for com-SO 2 parison. Intramolecular hydrogen bonding in the enamines is discussed in terms of the accept
Relationships between 1H, 13C and 17O NMR chemical shifts and H/D isotope effects on 13C and 17O nuclear shielding in intramolecular hydrogen-bonded systems
✍ Scribed by E. Liepiņš; M. V. Petrova; E. Gudriniece; J. Pauliņš; S. L. Kuznetsov
- Publisher
- John Wiley and Sons
- Year
- 1989
- Tongue
- English
- Weight
- 698 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
The intramolecular H-bond strength in cis-enolic forms of b-diketones was investigated. The correlations between the 'H hydroxyl proton shieldings and the chemical shifts of the "C and "0 nuclei involved in the chelate ring, and the H/D isotope shifts on the latter resonances, were determined. An increase in the hydrogen bond strength leads to increasing values of H/D isotopic shifts on the "0 resonances. The results obtained are compared with quantum chemical calculations and x-ray measurements. KEY WORDS 'H, 13C, "0 NMR chemical shifts H/D isotope effects Intramolecularly hydrogen-bonded systems
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