Bound and continuum-embedded states of cyanopolyyne anions

TL;DR

This study uses advanced ab initio methods to explore the electronic states of cyanopolyyne anions, revealing metastable resonances and stable bound states that are crucial for understanding their formation in space.

Contribution

It provides detailed predictions of bound and continuum electronic states of cyanopolyyne anions, including metastable resonances and their evolution with chain length, using complex ab initio calculations.

Findings

Multiple low-lying metastable states identified in CN$^-$.

Resonances become stabilized and turn into bound states with increasing chain length.

Some anions support dipole bound states due to large dipole moments.

Abstract

Cyanopolyyne anions were among the first anions discovered in the interstellar medium. The discovery have raised questions about routes of formation of these anions in space. Some of the proposed mechanisms assumed that anionic excited electronic states, either metastable or weakly bound, play a key role in the formation process. Verification of this hypothesis requires detailed knowledge of the electronic states of the anions. Here we investigate bound and continuum states of four cyanopolyyne anions, CN$^-$, C$_3$N$^-$, C$_5$N$^-$, and C$_7$N$^-$, by means of ab initio calculations. We employ the equation-of-motion coupled-cluster method augmented with complex absorbing potential. We predict that already in CN$^-$, the smallest anion in the family, there are several low-lying metastable states of both singlet and triplet spin symmetry. These states, identified as shape resonances, are located between 6.3-8.5 eV above the ground state of the anion (or 2.3-4.5 eV above the ground state of the parent radical) and have widths of a few tenths of eV up to 1 eV. We analyze the identified resonances in terms of leading molecular orbital contributions and Dyson orbitals. As the carbon chain length increases in the C$_{2n+1}$N$^-$ series, these resonances gradually become stabilized and eventually turn into stable valence bound states. The trends in energies of the transitions leading to both resonance and bound excited states can be rationalized by means of the H\"{u}ckel model. Apart from valence excited states, some of the cyanopolyynes can also support dipole bound states and dipole stabilized resonances, owing to a large dipole moment of the parent radicals in the lowest $^2\Sigma^+$ state. We discuss the consequences of open-shell character of the neutral radicals on the dipole-stabilized states of the respective anions.