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Gas‐Phase Synthesis of 3‐Vinylcyclopropene via the Crossed Beam Reaction of the Methylidyne Radical (CH; X 2 Π) with 1,3‐Butadiene (CH 2 CHCHCH 2 ; X 1 A g )
Author(s) -
He Chao,
Zhao Long,
Doddipatla Srinivas,
Thomas Aaron M.,
Nikolayev Anatoliy A.,
Galimova Galiya R.,
Azyazov Valeriy N.,
Mebel Alexander M.,
Kaiser Ralf I.
Publication year - 2020
Publication title -
chemphyschem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.016
H-Index - 140
eISSN - 1439-7641
pISSN - 1439-4235
DOI - 10.1002/cphc.202000183
Subject(s) - chemistry , crossed molecular beam , cyclopropene , deuterium , hydrogen atom , hydrocarbon , transition state , decomposition , acetylene , hydrogen , ab initio , carbon fibers , computational chemistry , photochemistry , atomic physics , molecule , medicinal chemistry , physics , organic chemistry , materials science , catalysis , alkyl , composite number , composite material
The crossed molecular beam reactions of the methylidyne radical (CH; X 2 Π) with 1,3‐butadiene (CH 2 CHCHCH 2 ; X 1 A g ) along with their (partially) deuterated counterparts were performed at collision energies of 20.8 kJ mol −1 under single collision conditions. Combining our laboratory data with ab initio calculations, we reveal that the methylidyne radical may add barrierlessly to the terminal carbon atom and/or carbon−carbon double bond of 1,3‐butadiene, leading to doublet C 5 H 7 intermediates with life times longer than the rotation periods. These collision complexes undergo non‐statistical unimolecular decomposition through hydrogen atom emission yielding the cyclic cis‐ and trans‐3‐vinyl‐cyclopropene products with reaction exoergicities of 119±42 kJ mol −1 . Since this reaction is barrierless, exoergic, and all transition states are located below the energy of the separated reactants, these cyclic C 5 H 6 products are predicted to be accessed even in low‐temperature environments, such as in hydrocarbon‐rich atmospheres of planets and cold molecular clouds such as TMC‐1.