A low-lying resonance in FeCN− anion was identified through abrupt changes in the spectral dependence of the photoelectron angular distribution. Non-Franck–Condon transitions from the resonance to the neutral FeCN (4Δ), and the corresponding photoelectron angular distributions revealed that the resonance is a dipole scattering state. Significant thermionic electron emission was observed in the resonant photoelectron spectra, indicating a strong coupling of the resonance with the ground state of this triatomic anion and its competition over autodetachment. This low-lying resonance is identified to be an efficient pathway for the formation of FeCN− anion in the outer envelope of IRC+10216. The results in general reveal formation pathways in space for anions with low-lying resonances and large permanent dipole moment.
Nitrogen-bearing polycyclic aromatic hydrocarbons (PANHs) are ubiquitous in space. They are considered precursors to advanced biomolecules identified in meteorites. However, their chemical evolution into biomolecules in photodestructive astrophysical mediums remains a paradox. Here, we show that light can efficiently initiate the molecular mass growth of PANHs. Ultraviolet-photoexcited quinoline monomers, the smallest PANH, were observed to associate and intermolecular Coulombic decay between the associating monomers formed the cations of quinoline-dimer. Molecular rearrangements in the dimer cation lead to a dominant formation of cations heavier than quinoline. The enrichment of these heavier cations over all the other cations reveals the efficiency of this route for the mass growth of PANHs in space. This mechanism also leads to a highly reactive unsaturated PANH-ring via CH loss, a hitherto unknown channel in any photon-driven process. The occurrence of this efficient pathway toward complex molecules points to a rich chemistry in dense interstellar clouds.
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