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| Titel: |
Electron spin resonance identification of the dimer radical cation (CH3O)3P-P(OCH3)3/ in γ-irradiated trimethyl phosphite from second-order hyperfine structure |
| Auteur: |
Gillbro, Tomas Kerr, Carolyn M. L. Williams, Ffrancon |
| Verschenen in: |
Molecular physics |
| Paginering: | Jaargang 28 (1974) nr. 5 pagina's 1225-1232 |
| Jaar: |
1974-11 |
| Inhoud: |
A dimer radical possessing two anisotropically equivalent phosphorus atoms has been conclusively identified in γ-irradiated trimethyl phosphite, its E.S.R. spectrum consisting basically of four lines due to the large second-order splitting of the central component. In the powder spectrum of the γ-irradiated glass the central features are obscured by overlapping signals from other radicals. However, the downfield (1, 0) feature was clearly revealed by suppressing the formation of the interfering P(OCH3)2 radical through the inclusion of methyl bromide in the sample. The E.S.R. spectrum of a γ-irradiated single crystal is very well resolved and three complete sets of lines can be assigned unequivocally to chemically non-equivalent dimers. The spectra of two of the dimers undergo site splitting such that the symmetry elements for each pair of magnetically distinguishable sites are related. In addition, each of the lines belonging to these two dimer spectra is flanked by a pair of 'spin-flip' satellites at high microwave power. Chemical and structural evidence strongly suggests that the dimer is the centrosymmetric cation (CH3O)3P-P(OCH3)3/+, the unpaired electron occupying a σ* orbital built from the 3s and 3p orbitals of the two phosphorus atoms with a p/s hybridization ratio of approximately 2. The chemical non-equivalence of the dimers may result from slight differences in this hybridization ratio. |
| Uitgever: |
Taylor & Francis |
| Bronbestand: |
Elektronische Wetenschappelijke Tijdschriften |
Details van artikel 4 van 19 gevonden artikelen
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