To understand the reactivity of resonantly stabilized radicals, often found in relevant concentrations in gaseous environments, it is important to determine their main reaction pathways. Here, it is investigated whether the fulvenallenyl radical (C 7 H 5• ) reacts preferentially with closed-shell molecules or radicals. Electronic structure calculations on the C 10 H 9 potential energy surface accessed by the reactions of C 7 H 5• with methylacetylene (CH 3 CCH) and allene (H 2 CCCH 2 ) were combined with RRKM-ME calculations of temperature-and pressure-dependent rate constants using the automated EStokTP software suite and kinetic modeling to assess the reactivity of C 7 H 5 • with closed-shell unsaturated hydrocarbons. Experimentally, the reactions were attempted in a chemical microreactor heated to 998 ± 10 K by preparing fulvenallenyl radicals via pyrolysis of trichloromethylbenzene (C 7 H 5 Cl 3 ) and seeding the radicals in methylacetylene or allene carrier gas, with product identification by means of photoionization mass spectrometry. The measured photoionization efficiency curve of m/z = 128 was assigned to a linear combination of the reference curves of two C 10 H 8 isomers, azulene (minor) and naphthalene (major), presumably resulting from the C 7 H 5• plus C 3 H 4 reactions. However, the calculations demonstrated that these reactions are too slow, and kinetic modeling of processes in the reactor allowed us to conclude that the observation of naphthalene and azulene is due to the C 7 H 5• plus C 3 H 3 • reaction, where propargyl is produced by direct hydrogen atom abstraction by chlorine (Cl) atoms from allene or methylacetylene and Cl stem from the pyrolysis of C 7 H 5 Cl 3 . Modeling results under the copyrolysis conditions of toluene and methylacetylene in high-temperature shock tube experiments confirmed the prevalence of the fulvenallenyl reaction with propargyl over its reactions with C 3 H 4 even when the concentrations of allene and methylacetylene largely exceed that of propargyl. Overall, the reactions of fulvenallenyl with both allene and methylacetylene were found to be noncompetitive in the formation of naphthalene and azulene thus attesting the inefficiency of the fulvenallenyl radical reactions with the prototype closed-shell hydrocarbon species. In the meantime, the new reaction pathways revealed, including Hassisted isomerizations between C 10 H 8 isomers and decomposition reactions of various C 10 H 9 isomers, emerge as relevant and are recommended for inclusion in combustion kinetic models for naphthalene formation.
