SIMBAD references

Atomic nitrogen reacts efficiently with polycyclic aromatic hydrocarbons species, and potentially generates a diverse array of complex organic molecules in the interstellar medium. In this work, the gas-phase chemical evolution of large, astronomically relevant PAH, tetra-benzo-pero-pyrene (TBPP, C₃₆H₁₆) cations under N-atom bombardment is investigated experimentally and theoretically. A series of nitridated TBPP cations, including [C₃₆H₁₆N_n]⁺ (n=1-5) and dehydrogenated species [C₃₆H_10–15N_n]⁺ (n=1-5), are effectively formed. Additionally, we identify denitridation pathways of nitridated TBPP cations that, through loss of a CN or HCN/HNC unit, lead to the formation of smaller PAH cations (with odd carbon numbers and five-membered carbon cycles, e.g., [C₃₅H₁₅]⁺). We investigated the structures and the vibrational infrared spectra of newly formed nitridated TBPP cations and the bonding energy for the reaction pathways using theoretical calculations, which were based on density functional theory with the hybrid density functional B3LYP/6-311++G(d, p). The reaction energy is relatively high, which indicates that the addition of N atoms to the carbon skeleton is a random and independent event, i.e., there is no carbon-edge structural effect. Furthermore, theoretical analyses confirm that denitridation pathways involving the loss of CN or HCN/HNC units are energetically favorable, which underscores their potential role in the top-down evolution of large PAHs. The obtained results highlight the importance of PAH cations evolution under N-atom bombardment, and demonstrate the formation of complex organic species containing nitrogen functionalities, such as C=N, C-N-H, and C-N-C groups. Furthermore, these findings provide insights into the molecular diversity and chemical evolution of PAHs, where ion-atom collisions drive both the functionalization and structural truncation of large molecules in astrophysical environments.