Directed Gas-Phase Formation of the 1-Cyanovinyl Radical (H _<b>2</b> CCCN, X ^<b>2</b> A′) in the Interstellar Medium

The formation pathways to nitrogen-containing molecules and radicals are crucial to the understanding of the carbon-nitrogen chemistry in interstellar and atmospheric environments. While over 65 nitrogen-containing neutral species have been observed in deep space to date, their formation mechanisms─in particular, those of radical species─remain largely speculative. The crossed molecular beam technique in conjunction with electronic structure and statistical calculations was utilized to offer a detailed overview of the fundamental pathways in the gas-phase bimolecular reaction of ground-state atomic carbon (C, ³P) with acetonitrile-<i>d</i>_<i>3</i> (CD₃CN, X¹A₁) under single-collision conditions leading to the formation of the 1-cyanovinyl radical (D₂CCCN, X²A') coupled with deuterium atom loss. The indirect reaction was initiated by barrierless carbon-atom addition, with the most probable route involving carbon addition across the carbon-nitrogen nitrile triple bond of acetonitrile, forming a three-membered ring intermediate followed by ring-opening and unimolecular decomposition via atomic deuterium loss from the C3 carbon atom. The reaction was overall exoergic, and intermediates and transition states lie lower in energy than the separated reactants, unlocking the reaction of carbon with acetonitrile in low-temperature environments such as cold molecular clouds, e.g., Taurus Molecular Cloud (TMC-1), and planetary atmospheres, e.g., Saturn's moon Titan. In these environments, the 1-cyanovinyl radical may act as a building block for cyano-substituted polycyclic aromatic hydrocarbons and N-heterocycles, thus furthering our understanding of the complex carbon-nitrogen chemistry in deep space.