Bimolecular photodissociation of interstellar 1-Cyanonaphthalene via Intermolecular Coulombic decay

被引:1
|
作者
Dutta, Saurav [1 ]
Behera, Nihar Ranjan [1 ]
Barik, Saroj [1 ]
Kushawaha, Rajesh Kumar [2 ]
Sajeev, Y. [3 ]
Aravind, G. [1 ]
机构
[1] Indian Inst Technol Madras, Chennai 600036, India
[2] Phys Res Lab, Ahmadabad 380009, India
[3] Bhabha Atom Res Ctr, Theoret Chem Sect, Mumbai 400085, India
来源
JOURNAL OF CHEMICAL PHYSICS | 2024年 / 161卷 / 12期
关键词
POLYCYCLIC AROMATIC-HYDROCARBONS; NITROGEN-HETEROCYCLIC COMPOUNDS; PHOTOELECTRON-SPECTRA; NAPHTHALENE; FRAGMENTATION; IONIZATION; DEPENDENCE; BENZENE; STATES;
D O I
10.1063/5.0226386
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous in space and govern the interstellar chemistry. The two isomers of cyanonaphthalene (1-CNN and 2-CNN) were the first PAHs to be recently identified in the Taurus Molecular Cloud (TMC-1). Their large abundance is attributed to high photostability with nearly no photofragmentation at photon energies above the ionization potential. Here, we show that at ambient light and at densities akin to dense molecular clouds and the upper atmosphere of planets and moons, 1-CNN could undergo extensive fragmentation through a new mechanism leading to daughter cations. On UV photoexcitation, at a photon energy way below the ionization threshold, 1-CNN monomers form photoexcited dimer units. Intermolecular Coulombic decay between the two photoexcited units of the dimer leads to ionization, and the subsequent molecular rearrangements form new daughter cations. These daughter cations could react further, contributing to rich bottom-up astrochemistry, and could play a pivotal role in developmental astrobiology. Photofragmentation in atmospheric and astrophysical environments is hitherto known to be unimolecular, while the present results point a pathway involving bimolecular photofragmentation.
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页数:8
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