| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 10734087 | Radiation Physics and Chemistry | 2005 | 6 Pages |
Abstract
Hydroxyphthalimide, hydroxysuccinimide, and hydroxybenzotriazole were irradiated in methanol, ethanol, 2-propanol, and acetonitrile. All the hydroxy compounds, R-NOH, changed to R-NH in acetonitrile, though hydroxyphthalimide in methanol and hydroxysuccinimide in the alcohol solutions were not decomposed. The decomposition of R-NOH is caused by electron attachment. It seems that the strong hydrogen bonding between the solvent alcohol and the solute prevent the electron attachment to hydroxysuccinimide. The molecular structure of the hydroxy compounds will affect the extent of the hydrogen bonding.
Related Topics
Physical Sciences and Engineering
Physics and Astronomy
Radiation
Authors
Seiko Nakagawa,