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-Reference-Cited by-同舟云学术

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

Published:1991-07 Issue:6 Volume:181 Page:512-516
ISSN:0009-2614
Container-title:Chemical Physics Letters
language:en
Short-container-title:Chemical Physics Letters

Author:

Lazarev G.G.,Kuskov V.L.,Lebedev Ya.S.,Rieker A.

Publisher

Elsevier BV

Subject

Physical and Theoretical Chemistry,General Physics and Astronomy

Reference8 articles.

1. 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 probes

2. Calculation of the geometry of the complex of spatially hindered quinones and phenols from E.S.R. spectra of radical pairs

3. Structure cristalline de trois phénols encombrés: le diméthyl-2,3 phénol, le méthyl-2 bromo-3 phénol et le ditertiobutyl-2,6 méthyl-4 phénol

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1. Effect of donor and acceptor on the mechanism of a photochemical reaction in doped single crystals for radical pairs in 4-bromo-2,6-di-tert-butylphenol single crystal doped with 2,6-di-tert-butyl-p-quinone;Kinetics and Catalysis;2001

2. Convenient unimolecular sources of aryloxyl radicals. III - photolysis of bis(aryloxy)phosphine azides;Tetrahedron Letters;1994-06

3. The role of dopant geometry in the photoinduced formation of radical pairs in crystals of 2,6-di-tert-butyl-4-methylphenol and 2,6-di-tert-butylphenol;Chemical Physics Letters;1993-09

4. Radical pairs during photolysis of an iminoquinone in single crystals of 2,6-di-tert-butyl-4-methylphenol;Chemical Physics Letters;1992-10

5. Mechanism of Radical Pair Formation During the Photolysis of 2,6-Di-tert-butylquinonediazide in Single Crystals of 2,6-Di-tert-butylphenol;Zeitschrift für Physikalische Chemie;1992-01-01