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Observation of short-lived radical ion pairs by pulse radiolysis of alkane solutions by time-resolved fluorescence-detected magnetic resonance. Electron paramagnetic resonance spectra of alkane radical cations

Journal Article · · J. Phys. Chem.; (United States)
DOI:https://doi.org/10.1021/j100219a014· OSTI ID:6497397
Time-resolved fluorescence-detected EPR studies of electron-irradiated solutions of 2,5-diphenyloxazole (PPO) in alkane solvents have shown that there are two distinct germinate radical ion pairs, distinguished by their lifetimes and EPR spectra. While the central EPR peak belongs to the aromatic radical ions, the broader components are assigned to the parent radical cation of the alkane solvent. Analysis of the resolved hyperfine structure indicates the presence of a trapped solvent hole in cyclohexane, which does not undergo unusually rapid charge exchange. The kinetic analyses of the EPR spectra show that scavenging events preserve the relative orientation of the unpaired electron spins in these geminate ion pairs.
Research Organization:
Argonne National Lab., IL
DOE Contract Number:
W-31109-ENG-38
OSTI ID:
6497397
Journal Information:
J. Phys. Chem.; (United States), Journal Name: J. Phys. Chem.; (United States) Vol. 86:22; ISSN JPCHA
Country of Publication:
United States
Language:
English