Spin trapping of radicals formed during radiolysis of aqueous solutions. Direct electron spin resonance observations

1976 ◽  
Vol 54 (2) ◽  
pp. 275-279 ◽  
Author(s):  
Frederick Peter Sargent ◽  
Edward Michael Gardy

It is shown that esolv, H•, and OH formed by the radiolysis of water by 3 MeV electrons are trapped by nitroso and nitrone compounds to give nitroxides with well defined esr spectra. Three spin trapping agents were used, nitroso-t-butane, phenyl-t-butyl nitrone, and 5,5′-dimethyl pyrroline-1-oxide. The latter was shown to be an excellent compound for these studies. Complications due to the instability of some of the nitroxides were overcome by coupling the electron accelerator to the esr spectrometer to permit direct observation of the spectra.

1982 ◽  
Vol 60 (12) ◽  
pp. 1597-1597 ◽  
Author(s):  
Walter Kremers ◽  
Grant W Koroll ◽  
Ajit Singh

Azide radicals (N3·) are formed in aqueous solutions by the reaction of hydroxyl radicals (·OH) with azide anions (N3aq−). Azide radicals have been spin trapped with three nitroso spin traps: nitrosodurene (ND), 2,6-dideutero-3,5-dibromo-4-nitrosobenzene sulfonate (DDNBS), and 2-methyl-2-nitrosopropane (MNP). The electron spin resonance (esr) spectra show the presence of two molecules of the spin traps in the spin-trapped species.


1982 ◽  
Vol 60 (12) ◽  
pp. 1542-1548 ◽  
Author(s):  
Uwe M Oehler ◽  
Edward G Janzen

A computer program written in BASIC is presented for the simulation of isotropic esr spectra using a microprocessor. Since BASIC is the most common microprocessor language, this program can easily be adapted to most microprocessors. Through the use of more efficient methods the capabilities of much larger FORTRAN programs, run on mainframe computers, are retained in the more restricted environment of the microprocessor. As a result, most spin trapping results can be dealt with easily. A number of sample simulations illustrate the program’s features.


1975 ◽  
Vol 53 (20) ◽  
pp. 3128-3132 ◽  
Author(s):  
Frederick Peter Sargent ◽  
Edward Michael Gardy

Intermediates formed during radioylsis of benzyl alcohol have been identified by an e.s.r. and spin trapping method. Solutions of tert-BuNO in benzyl alcohol were irradiated insitu with 3 MeV electrons and the e.s.r. spectra of the resulting nitroxides directly recorded.[Formula: see text]These demonstrated that benzyl, PhCH2.,and hydroxybenzyl, PhĊHOH, radicals are formed in the radiolysis. By an examination of the effects of the addition of electron scavengers, it was shown that the benzyl radicals are probably directly formed from the reaction of electrons with benzyl alcohol. Since these scavengers had no effect on the yield of PhĊHOH trapped, this radical is not derived from the reactions of electrons. It is suggested that it is partly produced by reaction of the alkoxy radical, PhCH2O.,with the solvent benzyl alcohol.[Formula: see text]


Sign in / Sign up

Export Citation Format

Share Document