1H dynamic nuclear magnetic resonance study of hindered internal rotation in N-aroyl- and N-thioaroyl-N′- piperonylpiperazines

✍ Scribed by Rois Benassi; Ferdinando Taddei; Amedeo Leonardi; Dante Nardi

• Publisher: John Wiley and Sons
• Year: 1981
• Tongue: English
• Weight: 356 KB
• Volume: 15
• Category: Article
• ISSN: 0749-1581
• DOI: 10.1002/mrc.1270150107

✦ Synopsis

Abstract

The NMR variable temperature behaviour of N‐aroyl‐ and N‐thioaroyl‐N′‐piperonylpiperazines was investigated. The largest chemical shift separation between the exchanging methylene groups, and the highest energy barrier, is found for the thioamide compounds. Results from semi‐empirical calculations are qualitatively in line with the experimental findings, revealing that the higher barrier in the thiocarbonyl compounds compared with the carbonyl compounds is mainly connected with differences in the energies of ground states, rather than in those of transition states, of these molecules. The effect of the nature of the heterocyclic ring containing the amidic nitrogen atom on the barrier height is also discussed.