Electron spin exchange in micellized radical pairs III: 13C low-field ratio 
frequency stimulated nuclear polarization spectroscopy (LF SNP)

Bagryanskaya, EG; Tarasov, VF; Avdievich, NI; Shkrob, IA

doi:10.1016/0301-0104(92)80233-L

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Electron spin exchange in micellized radical pairs III: 13C low-field ratio frequency stimulated nuclear polarization spectroscopy (LF SNP)

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https://www.sciencedirect.com/science/article/pii/030101049280233L
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Zitation

Bagryanskaya, E., Tarasov, V., Avdievich, N., & Shkrob, I. (1992). Electron spin exchange in micellized radical pairs III: 13C low-field ratio frequency stimulated nuclear polarization spectroscopy (LF SNP). Chemical Physics, 162(1), 213-223. doi:10.1016/0301-0104(92)80233-L.

Zitierlink: https://hdl.handle.net/21.11116/0000-0006-0FAE-7

Zusammenfassung

LF (low-field) SNP spectra are reported from the carbonyl carbon in dibenzyl ketone photolyzed in an aqueous micellar solution with sodium dodecyl sulfate. Spectra obtained using resonant radiofrequencies of 0.33 and 1.53 GHz are affected by adiabatic transitions within the region of ST_level-crossing of the radical pair by flip-flop transitions in the corresponding weak magnetic fields. Numerical simulation indicates that all the observable features of the spectra are accounted for by a combination of these transitions and spin relaxation induced by the electron spin exchange interaction. Unexpectedly, no additional broadening caused by the electron dipole-dipole or other anisotropic interactions is evident in them.