Combined Experimental and Computational Investigation of the Elementary Reaction of Ground State Atomic Carbon (C; 3Pj) with Pyridine (C5H5N; X1A1) via Ring Expansion and Ring Degradation Pathways
- Univ. of Hawaii at Manoa, Honolulu, HI (United States)
- Samara Univ. (Russia)
- Florida International Univ., Miami, FL (United States); Samara Univ. (Russia)
In t his work, we explored the elementary reaction of atomic carbon (C; 3Pj) with pyridine (C5H5N; X1A1) at a collision energy of 34 ± 4 kJ mol-1 utilizing the crossed molecular beams technique. Forwardconvolution fitting of the data was combined with high-level electronic structure calculations and statistical (RRKM) calculations on the triplet C6H5N potential energy surface (PES). These investigations reveal that the reaction dynamics are indirect and dominated by large range reactive impact parameters leading via barrier-less addition to the nitrogen atom and to two chemically non-equivalent ‘aromatic’ carbon-carbon bonds forming three distinct collision complexes. At least two reaction pathways through atomic hydrogen loss were identified on the triplet surface. These channels involve multiple isomerization steps of the initial collision complexes via ring-opening and ring expansion forming an acyclic 1-ethynyl-3-isocyanoallyl radical (P1; 2A”) and a hitherto unreported seven-membered 1-aza-2-dehydrocyclohepta-2,4,6-trien-4-yl radical isomer (P3; 2A), respectively. For RRKM calculations at zero collision energy, representing conditions in cold molecular clouds, the ring expansion product P3 is formed nearly exclusively for the atomic hydrogen loss channel. Based on the computations, the molecular fragmentation channel eliminating acetylene (C2H2) plus 3-cyano-2-propen-1-ylidene (P6; 3A”) plays also an important role the reaction of atomic carbon with pyridine proposing a probable destruction pathway of interstellar pyridine. Lastly, these results are also discussed in light of the isoelectronic carbon – benzene (C6H6; X1A1) system with important implications to the rapid degradation of nitrogen-bearing polycyclic aromatic hydrocarbons (NPAHs) in the interstellar medium compared to mass growth processes of PAH counterparts through ring expansion.
- Research Organization:
- Univ. of Hawaii, Honolulu, HI (United States)
- Sponsoring Organization:
- USDOE Office of Science (SC), Basic Energy Sciences (BES); Ministry of Education and Science of the Russian Federation
- Grant/Contract Number:
- FG02-03ER15411; FG02-04ER15570; 14.Y26.31.0020
- OSTI ID:
- 1602966
- Journal Information:
- Journal of Physical Chemistry. A, Molecules, Spectroscopy, Kinetics, Environment, and General Theory, Vol. 122, Issue 12; ISSN 1089-5639
- Publisher:
- American Chemical SocietyCopyright Statement
- Country of Publication:
- United States
- Language:
- English
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