Please use this identifier to cite or link to this item:
http://repo.lib.jfn.ac.lk/ujrr/handle/123456789/164| Title: | Theoretical study of hydroxamic acids |
| Authors: | Fitzpatrick, N.J Mageswaran, R |
| Issue Date: | 1989 |
| Abstract: | Ab initio molecular orbital calculations on formohydroxamic and acetohydroxamic acids give stabilities in the order: E-keto ≫ Z-keto ≫ Z-enol ≫ E-enol. However, on hydration the E-keto and Z-keto order is reversed, in agreement with NMR results. Methyl substituted forms are also considered, and the importance of hydrogen bonding is noted. |
| URI: | http://repo.lib.jfn.ac.lk/ujrr/handle/123456789/164 |
| ISSN: | 02775387 |
| Appears in Collections: | Chemistry |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| Fitzpatrick-Theoretical_study_of_hydroxamic_acids.pdf | 298.28 kB | Adobe PDF |  View/Open |
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