The Journal of Physical Chemistry A · 2003 · 28 citations · 20 references
EngineeringChemistryElectronic Excited StateReaction IntermediateMolecular KineticsTime ProfilesChemical ThermodynamicsPhysicsPhotochemistryMechanistic PhotochemistryAtomic PhysicsPhysical ChemistryReactivity (Chemistry)Quantum ChemistryShock WavesLaser PhotochemistryNatural SciencesCondensed Matter PhysicsApplied PhysicsHigh Temperature ReactionExcimer Laser PhotolysisReaction ProcessChemical Kinetics
The rate constant for the reaction S + SO2 → SO + SO (1) has been investigated by measuring time profiles of S atoms behind reflected shock waves using two experimental systems: S atoms were provided by the thermal decomposition of COS in the high-temperature range (2020−2800 K) and by excimer laser photolysis of COS in the low-temperature range (T = 1120−1540 K). The results of these experiments yield the rate constant with a non-Arrhenus temperature dependence, k1 = 10-39.73T8.21 exp(4828.5/T) cm3 molecules-1 s-1, over the extended temperature range (1120−2800 K). By comparing the rate constants with that derived from a conventional transition-state theory based on the potential energy surface calculated by the G2M(CC1) methodology, a reaction mechanism including a contribution of the singlet state of the reaction intermediate S2O2 is discussed.
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Alexander M. Mebel, Keiji Morokuma, M. C. Lin · The Journal of Chemical Physics · 1995 · 466 citations