The Journal of Chemical Physics · 1993 · 125 citations · 30 references
Natural SciencesChemistryPhysicsMolecular PhysicsPhysical ChemistryQuantum ChemistryAtomic ExcitationHydrogen AtomMolecular Excited StatesMolecular VibrationReaction MechanismsVibrational StructureBimolecular Reaction KineticsExcitationQuantum Wave FunctionSelectivityVibrational ModesVibrationally Excited Reaction Pathways
We have determined the branching ratio for the reaction of hydrogen atoms and HOD with either the O–H bond excited or the O–D bond excited. In both cases, the initially excited bond reacts preferentially. Excitation of the third O–H stretching overtone, 4νOH, favors breaking the O–H bond by a factor of ∼200, and excitation of the fourth O–D stretching overtone, 5νOD, favors breaking the O–D bond by a factor of ∼220. Thus vibrational excitation can control the H+HOD reaction to produce either product almost exclusively. A simple model using the calculated wave function for each state and the measured reaction cross section for a particular vibrational excitation predicts the high selectivity observed for the two reactions.
30
Classical Electrodynamics (2nd edn)
M. G. Brereton · Physics Bulletin · 1976 · 2.5K citations
Evaluated Kinetic Data for Combustion Modelling
D. L. Baulch, Carlos J. Cobos, R. A. Cox et al. · Journal of Physical and Chemical Reference Data · 1992 · 2.1K citations · Full text
<i>Molecular Reaction Dynamics and Chemical Reactivity</i>
R. D. Levine, Richard B. Bernstein, Yuan T. Lee · Physics Today · 1988 · 1.4K citations
The HITRAN database: 1986 edition
Laurence S. Rothman, Robert R. Gamache, Alan S. Goldman et al. · Applied Optics · 1987 · 977 citations