| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 9590676 | Journal of Molecular Structure: THEOCHEM | 2005 | 11 Pages |
Abstract
In addition, our calculations of the energies of the tautomeric forms showed that the carbonyl and thiocarbonyl tautomers are more stable than the hydroxy and mercapto forms, which is in good agreement with the experimental findings in the literature.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Physical and Theoretical Chemistry
Authors
Safiye SaÄ Erdem, Gül AltınbaÅ Ãzpınar, Melek Türker Saçan,