Kinetic Study by EPR of the Production and Decay of SO(1
) in the Reaction of O2(1
g) with SO(3
−)
J. Chem. Phys. 56, 465 (1972); doi:10.1063/1.1676891
Issue Date: 1 January 1972
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The existence of the reaction of O2(1
g) with ground-state SO(3
−) to produce SO(1
) and ground-state O2(3
g−) has been confirmed using a fast-flow system and electron paramagnetic resonance detection of all four species. A kinetic study of this reaction has resulted in the determination of the absolute value of the rate constant: (2.12±0.22×108)litermole−1·sec.−1 The reaction is therefore faster, by an order of magnitude, than any quenching process by a neutral species yet reported for O2(1
g) in the gas phase, reaction or deactivation. The rapid rate is in rough accord with predictions derived from observations of similar atomic processes by other workers, indicating that the reactive process probably involves simple spin-allowed transfer of electronic energy in which a resonance situation is approximated. The mechanism for the decay of the SO(1
) produced in the reaction has also been determined. It is shown that SO(1
) is heterogeneously deactivated to SO(3
−) at the reaction vessel walls with an efficiency about four orders of magnitude greater than that observed for deactivation of O2(1
g) to O2(3
). Such a high wall deactivation efficiency may explain the spectroscopic observations by other workers of SO(3
−) but not the expected SO(1
) in the pyrolysis products of ethylene episulfoxide.
©1972 The American Institute of Physics
g) with ground-state SO(3
−) to produce SO(1
) and ground-state O2(3
g−) has been confirmed using a fast-flow system and electron paramagnetic resonance detection of all four species. A kinetic study of this reaction has resulted in the determination of the absolute value of the rate constant: (2.12±0.22×108)litermole−1·sec.−1 The reaction is therefore faster, by an order of magnitude, than any quenching process by a neutral species yet reported for O2(1
g) in the gas phase, reaction or deactivation. The rapid rate is in rough accord with predictions derived from observations of similar atomic processes by other workers, indicating that the reactive process probably involves simple spin-allowed transfer of electronic energy in which a resonance situation is approximated. The mechanism for the decay of the SO(1
) produced in the reaction has also been determined. It is shown that SO(1
) is heterogeneously deactivated to SO(3
−) at the reaction vessel walls with an efficiency about four orders of magnitude greater than that observed for deactivation of O2(1
g) to O2(3
−) but not the expected SO(1
) in the pyrolysis products of ethylene episulfoxide.
©1972 The American Institute of Physics
| History: | Received 28 June 1971 |
| Permalink: |
http://link.aip.org/link/?JCPSA6/56/465/1 |
PUBLICATION DATA
0021-9606 (print)
1089-7690 (online)
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