Title: Reaction of phenyl radicals with propyne
Authors: Vereecken, Luc ×
Peeters, Jozef
Bettinger, HF
Kaiser, RI
Schleyer, PV
Schaefer, HF #
Issue Date: 20-Mar-2002
Publisher: Amer chemical soc
Series Title: Journal of the American Chemical Society vol:124 issue:11 pages:2781-2789
Abstract: The potential energy surface (PES) for the phenyl + propyne reaction, which might contribute to the growth of polycyclic aromatic hydrocarbons (PAHs) under a wide variety of reaction conditions, is described. The PES was characterized at the B3LYP-DFT/6-31 G(d) and B3LYP-DFT/6-311 +G(d,p) levels of theory. The energies of the entrance transition states, a direct hydrogen-transfer channel and two addition reactions leading to chemically activated C9H9+ intermediates, were also evaluated at the QCISD(T)/6-311 G(d,p) and CCSD(T)/6-311 G(d,p) levels of theory. An extensive set of unimolecular reactions was examined for these activated C9H9 intermediates, comprising 70 equilibrium structures and over 150 transition states, and product formation channels leading to substituted acetylenes and allenes such as PhCCH, PhCCCH3, and PhCHCCH2 were identified. The lowest energy pathway leads to indene, a prototype PAH molecule containing a five-membered ring. The title reaction thus is an example of possible direct formation of a PAH containing a five-membered ring, necessary to explain formation of nonplanar PAH structures, from an aromatic radical unit and an unsaturated hydrocarbon bearing an odd number of carbons. Extensive Supporting Information is available.
ISSN: 0002-7863
Publication status: published
KU Leuven publication type: IT
Appears in Collections:Quantum Chemistry and Physical Chemistry Section
× corresponding author
# (joint) last author

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