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We consider a mixture of a diatomic photolytic precursor AX and a reagent BC that undergoes the photoinitiated reaction AX + hν → A + X followed by A + BC → AB + C. In the limit that AX is stationary relative to BC, we show that the three-dimensional velocity distribution of the AB product in a specified quantum state can be related to the differential cross section of the A + BC reaction by a simple, invertable, closed-form expression. With a favorable choice of kinematics, we demonstrate that it is possible to extract the full state-to-state differential cross section from a measurement of the velocity distribution of the AB product in the laboratory frame.
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Shafer et al. (1993) studied this question.
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