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Time-resolved fluorescence-detected magnetic resonance and fluorescence studies of trialkylamines irradiated by pulse radiolysis in alkane solvents

Journal Article · · J. Phys. Chem.; (United States)
DOI:https://doi.org/10.1021/j150645a019· OSTI ID:5052169
Time-resolved fluorescence-detected magnetic resonance (FDMR) studies of irradiated alkane solutions of trialkylamines and scintillators reveal the EPR spectra of the trialkylaminium radicals, formed by scavenging solvent radical cations. A qualitative kinetic analysis indicates that the growth of the triethylaminium radical (TEA/sup +/-) FDMR signal occurs on similar time scales in both n-hexane and cyclohexane, suggesting that, in cyclohexane, TEA/sup +/- is formed by scavenging the lower mobility ''trapped'' cyclohexane radical cations. Fluorescence results indicate that TEA quenches both scintillator fluorescence and total FDMR intensities to a greater extent than is expected from amine scavenging of solvent holes. TEA also exhibits an intense, relatively long-lived fluorescence which is apparently not produced by radical ion recombination or energy transfer. 6 figures
Research Organization:
Argonne National Lab., IL
DOE Contract Number:
W-31109-ENG-38
OSTI ID:
5052169
Journal Information:
J. Phys. Chem.; (United States), Journal Name: J. Phys. Chem.; (United States) Vol. 88:1; ISSN JPCHA
Country of Publication:
United States
Language:
English