Temperature effects on the branching dynamics in the model ambimodal (6 + 4)/(4 + 2) intramolecular cycloaddition reaction

Abstract

AbstractC14H20 (tetradecapentaene) is a simple model system exhibiting post transition‐state behavior, wherein both the (6 + 4) and (4 + 2) cycloaddition products are formed from one ambimocal transition state structure. We studied the bifurcation dynamics starting from the two ambimodal transition state structures, the chair‐form and boat‐form, using the quasi‐classical trajectory, classical molecular dynamics, and ring‐polymer molecular dynamics methods on the parameter‐optimized semiempirical GFN2‐xTB potential energy surface. It was found that the calculated branching fractions differ between the chair‐form and boat‐form due to the different nature in the IRC pathways. We also investigated the effects of temperature on bifurcation dynamics and found that, at higher temperatures, trajectories stay longer in the intermediate region of the potential energy surface.