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Combustion, Explosion and Shock Waves

2023 year, number 2

Mechanism of Formation of Four-Ring Polycyclic Aromatic Hydrocarbons in the Self-Recombination of Indenyl

V. S. Krasnoukhov1, M. V. Zagidullin1, V. N. Azyazov1, A. M. Mebel2
1Lebedev Physical Institute, Russian Academy of Sciences, Samara, 443011 Russia
2Florida International University, Miami, 33199 USA
Keywords: combustion, recombination, polycyclic aromatic hydrocarbons, PAHs, indenyl, chrysene, dibenzofulvalene, tetracene, tetraphene, dibenzoazulene

Abstract

The geometric structures, vibration frequencies and relative energies of reactants, products, intermediates, and transients involved in the self-recombination of the indenyl radical were determined using G3(MP2,CC) // B3LYP/6-311G** quantum chemical calculations. The barrierless association of a pair of indenyl radicals forms the C18H14 complex. The subsequent set of isomerizations of the complex is divided into five reaction channels, which in all cases end in H abstraction but with different four-ring isomers C18H14: in the form of condensed rings-tetraphene, tetracene, chrysene, dibenzoazulene; with an associated internal bond of the rings-dibenzofulvalene. The yield of chrysene prevails since the energy barriers encountered on the pathway of its formation are lower than the barriers on the formation pathways of other products.