| DOI | Resolve DOI: https://doi.org/10.1021/jo7014592 |
|---|
| Author | Search for: DiLabio, Gino A.1; Search for: Ingold, Keith U.2; Search for: Walton, John C. |
|---|
| Affiliation | - National Research Council of Canada. National Institute for Nanotechnology
- National Research Council of Canada. NRC Steacie Institute for Molecular Sciences
|
|---|
| Format | Text, Article |
|---|
| Abstract | Spectroscopic data are consistent with computations that show that, in their most stable conformations, the peroxyl moiety is equatorial in cyclohexylperoxyl radicals and axial in oxa- and most polyoxacyclohexyl-2-peroxyl radicals. |
|---|
| Publication date | 2007-09-13 |
|---|
| In | |
|---|
| Language | English |
|---|
| NRC number | 520 |
|---|
| NPARC number | 12327482 |
|---|
| Export citation | Export as RIS |
|---|
| Report a correction | Report a correction (opens in a new tab) |
|---|
| Record identifier | e0051c3d-b7f0-456f-871f-1003d9405af0 |
|---|
| Record created | 2009-09-10 |
|---|
| Record modified | 2020-05-10 |
|---|
