EPR studies of the formation and transformation of isomeric radicals [C3H5O](center dot). Rearrangement of the allyloxyl radical in non-aqueous solution involving a formal 1,2-hydrogen-atom shift promoted by alcohols
Elford, PE; Roberts, BP
| HERO ID | 4144981 |
|---|---|
| In Press | No |
| Year | 1996 |
| Title | EPR studies of the formation and transformation of isomeric radicals [C3H5O](center dot). Rearrangement of the allyloxyl radical in non-aqueous solution involving a formal 1,2-hydrogen-atom shift promoted by alcohols |
| Authors | Elford, PE; Roberts, BP |
| Journal | Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry |
| Issue | 11 |
| Page Numbers | 2247-2256 |
| Abstract | At 220 K in cyclopropane solvent, hydrogen-atom abstraction from allyl alcohol by Bu(1)O(.), EtO(.), PhMe(2)CO(.), (Me(3)Si)(2)N-. or triplet-state acetone gives the 1-hydroxyallyl radical 3 as a ca. 3:1 mixture of the syn- and anti-isomers. In contrast, the allyloxyl radical does not react with allyl alcohol to bring about abstraction of hydrogen, but instead undergoes a more rapid alcohol-promoted rearrangement to give 3 as a ca. 1:1 mixture of the syn- and anti-forms. 2-Methylallyl alcohol, ethanol and propan-2-ol also induce this formal 1,2-H-atom shift in the allyloxyl radical. In the presence of ethan[H-2]ol, both 3 and (3-OD) are formed and as [EtOD] is increased from 0.3 to 3.6 mol dm(-3) [3-OD]/[3] first passes through a maximum value of ca. 1 and then decreases to 0.38. It is proposed that there is more than one mechanism for the alcohol-induced rearrangement of the allyloxyl radical, one that involves assisted migration of hydrogen from the alpha-carbon atom to the oxygen atom and another that results in incorporation of deuterium from the EtOD. The importance of the latter mechanism decreases at high alcohol concentrations and this behaviour is thought to be related to the extent of association of the alcohol by hydrogen-bonding. The allyloxyl radical was generated by UV photolysis of:allyl tert-butyl peroxide and by ring opening of the oxiranylmethyl radical, derived from epibromohydrin or epichlorohydrin by halogen-atom abstraction. Ab initio molecular orbital calculations predict that an unassisted 1,2-H-atom shift in the allyloxyl radical will involve a very large activation energy. The alcohol is believed to serve a dual function in promoting the rearrangement: first, to increase the acidity of the alpha-CH2 group by hydrogen-bonding to the oxygen atom of the allyloxyl radical and, secondly, to provide a basic oxygen atom to facilitate the transfer/removal of a protic alpha-hydrogen atom. |
| Doi | 10.1039/p29960002247 |
| Wosid | WOS:A1996VT28800003 |
| Is Certified Translation | No |
| Dupe Override | No |
| Is Public | Yes |