Don't forget the : double bond isomerism radical-acetylene growth reactions affect the primary stages of PAH and soot formation

In combustion, acetylene is a key species in molecular-weight growth reactions that form polycyclic aromatic hydrocarbons (PAHs) and ultimately soot particles. Radical addition to acetylene generates a vinyl radical intermediate, which has both trans and cis isomers. This isomerism can lead to profound changes in product distributions that are as yet insufficiently investigated. Herein, we explore acetylene addition to substituted trans -vinyl radicals, including potential rearrangement to cis structures, for eight combustion-related hydrocarbon radicals calculated using a composite method (G3X-K). Of these eight systems, the phenyl trans - and cis -Bittner-Howard HACA (hydrogen abstraction, C 2 H 2 Addition) process, where acetylene successively adds to a phenyl radical via a β-styryl intermediate, is simulated using a unified Master Equation model. Including the trans -Bittner-Howard pathway changes the products significantly at all simulated temperatures (550-1800 K) and pressures (5.33 × 10 2 -10 7 Pa), relative to a cis -only model. Typically, naphthalene remains the dominant product, but its abundance decreases at higher temperatures and pressures. For example, at 1200 K and 10 5 Pa, its branching ratio decreases from 78.5% to 62.9% when the trans pathway is included. At higher temperatures this decrease corresponds to the formation of alternative C 10 H 8 isomers, including the cis product benzofulvene with 8% maximum abundance at 1200 K and 5.33 × 10 2 Pa, and E -2-ethynyl-1-phenylethylene, a trans product with 26% maximum abundance at 1800 K, with little pressure dependence. At higher pressures, our model predicts a range of C 10 H 9 radicals, including resonance-stabilised radicals (RSRs). The impact of trans -vinyl radical chemistry in reactive environments means that they are essential to accurately describe combustion reactions and inhibit soot formation. Acetylene addition to substituted trans -vinyl radicals lead to profound changes in product distributions in HACA reactions.