Abstract
The 4-quinolinone derivatives present a keto-enol tautomerism, which can be studied using different analytical techniques, including NMR. In this work, the spectroscopic study in solution of numerous derivatives with different substitution patterns in positions 1–4 of the quinolone rings, and their correlation with simulated spectra by density functional theory-gauge independent atomic orbitals method (DFT-GIAO) approximation is presented. Polyfunctionalized derivatives where the tautomeric equilibrium is blocked by N- or O-substitution allow us to observe the different behavior in chemical shifts by NMR. The study of some derivatives in the solid state by ss-NMR and X-ray Crystallography is also included.
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