Photochemical primary process and magnetic field effect of methyltriphenyl germane in a micelle have been investigated with the aid of a nanosecond laser-flash-photolysis technique. The germyl radical generated through triplet state was directly observed. The lifetime of the generated radical pair a
Magnetic field effect on the dynamic behavior of a radical pair involving an Sn-centered radical
β Scribed by Masanobu Wakasa; Hisaharu Hayashi
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- English
- Weight
- 433 KB
- Volume
- 229
- Category
- Article
- ISSN
- 0009-2614
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β¦ Synopsis
The photoreduction of xanthone with triethyltinhydride in a sodium dodecylsulfate solution was investigated with the aid of a time-resolved ESR and a nanosecond laser flash photolysis. Upon irradiation of xanthone with triethyltinhydride, the hydrogen abstraction occurred and the ketyl-type and cyclohexadienyl-type radicals were observed by CIDEP spectra. The escaped xanthone ketyl radical increased with increasing magnetic field strength up to 1.29 T. The observed magnetic filed effects can be interpreted by a combination of the hyperline coupling and the relaxation mechanisms in the case of a triplet radical pair.
π SIMILAR VOLUMES
The effects of fluctuating magnetic fields on the yields of chemical reactions are explored within the radical pair mechanism, for the case in which singlet and triplet radical pairs disappear at equal rates. Approximate analytical expressions and exact numerical calculations are used to discuss the
Photochemical reactions of triplet xanthone and 2,5-dimethyl-p-benzoquinone with 2-propanol, xanthene, and N,N-diethylaniline in 2-propanol were investigated at 293 K by a nanosecond laser photolysis technique under magnetic fields of 0-10 T. In the reactions with 2-propanol and xanthene hydrogen tr
A pronounced solvent viscosity and polarity dependence of the magnetic field effect was found for polymethylene-linked radical ion pairs generated by photoinduced intramolecular electron transfer in compounds of the type pyrene-(CH\*),-N,N-dimethylaniline, with n = 7-16. This is interpreted in terms