Nonstatistical Unimolecular Decay of the CH<sub>2</sub>OO Criegee Intermediate in the Tunneling Regime
Yujie Qian, Thanh Lam Nguyen, Peter R. Franke, John F. Stanton, Marsha I. Lester
Abstract
Unimolecular decay of the formaldehyde oxide (CH 2 OO) Criegee intermediate proceeds via a 1,3 ring-closure pathway to dioxirane and subsequent rearrangement and/or dissociation to many products including hydroxyl (OH) radicals that are detected. Vibrational activation of jet-cooled CH 2 OO with two quanta of CH stretch (17–18 kcal mol –1 ) leads to unimolecular decay at an energy significantly below the transition state barrier of 19.46 ± 0.25 kcal mol –1, refined utilizing a high-level electronic structure method HEAT-345(Q) Λ . The observed unimolecular decay rate of 1.6 ± 0.4 × 10 6 s –1 is 2 orders of magnitude slower than that predicted by statistical unimolecular reaction theory using several different models for quantum mechanical tunneling. The nonstatistical behavior originates from excitation of a CH stretch vibration that is orthogonal to the heavy atom motions along the reaction coordinate and slow intramolecular vibrational energy redistribution due to the sparse density of states.