The mechanism of formation of stable radical pairs by photolysis of 2,6-di-tert-butylbenzoquinone diazide in crystals of 2,6-di-tert-butyl-4-methylphenol
- 1 July 1991
- journal article
- Published by Elsevier in Chemical Physics Letters
- Vol. 181 (6) , 512-516
- https://doi.org/10.1016/0009-2614(91)80304-g
Abstract
No abstract availableKeywords
This publication has 3 references indexed in Scilit:
- Stable radical pairs under the photolysis of 2,6-di-t-butyl quinone diazide in the single crystals of sterically hindered phenols: New type of double-spin probesChemical Physics Letters, 1990
- Calculation of the geometry of the complex of spatially hindered quinones and phenols from E.S.R. spectra of radical pairsMolecular Physics, 1978
- Structure cristalline de trois phénols encombrés: le diméthyl-2,3 phénol, le méthyl-2 bromo-3 phénol et le ditertiobutyl-2,6 méthyl-4 phénolActa Crystallographica Section B: Structural Science, Crystal Engineering and Materials, 1973