The reaction kinetics of the ground and first two excited states of atomic phosphorus, P, with atmospherically relevant species were studied at temperatures ranging from ?200 to 750 K using a pulsed laser photolysis-laser-induced fluorescence technique. The temperature dependence of the rate coefficients is parametrized as follows (units: cm3 molecule?1 s?1, 1? errors): k(P(2P)+O2)(189 ? T/K ? 701) = (7.10 ? 1.03) ? 10?12 ? (T/298)1.42?0.13 ? exp[(374 ? 41)/T]; k(P(2D)+O2)(188 ? T/K ? 714) = (1.20 ? 0.29) ? 10?11 ? (T/298)0.821?0.207 ? exp[(177 ? 70)/T]; k(P(2D)+CO2)(296 ? T/K ? 748) = (5.68 ? 0.36) ? 10?12 ? (T/298)0.800?0.103; k(P(2D)+N2)(188 ? T/K ? 748) = (1.42 ? 0.03) ? 10?12 ? (T/298)1.36?0.04; k(P(4S)+O2)(187 ? T/K ? 732) = (3.08 ? 0.31) ? 10?13 ? (T/298)2.24?0.29. Electronic structure theory combined with RRKM calculations have been used to explain the unusual temperature dependence of P(4S) + O2. The small pre-exponential factor for the reaction results from a tight steric constraint, together with the requirement that the reaction occurs on doublet rather than sextet electronic surfaces.
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Douglas et al. (2019) studied this question.
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