Broadband Vibrational Spectroscopy of Protonated and Radical Cationic Forms of Interstellar Formamide, [HCONH ₂ ]H ⁺ and [HCONH ₂ ] ⁺

Formamide (HCONH₂), the simplest organic molecule with a peptide bond, has been detected in various interstellar environments and is regarded as a potential precursor to essential biomolecules, such as amino acids and nucleic acids. Many of the proposed synthetic routes involve its ionized and protonated forms in the interstellar medium, where ion-molecule gas-phase reactions are predominant. However, spectroscopic data on cationic and protonated formamide is limited. In this work, we report the first bare-ion and Ne-tagged broadband vibrational spectra of isomeric forms of the formamide cation [HCONH₂]⁺ (<i>m</i>/<i>z</i> 45) and protonated formamide [HCONH₂]H⁺ (<i>m</i>/<i>z</i> 46). The vibrational spectra were obtained using two techniques, leak-out spectroscopy and Ne-tagging infrared predissociation spectroscopy, in a cryogenic 22-pole ion trap at the infrared free-electron laser facility HFML-FELIX. The measured spectra within the fingerprint region 650-1800 cm^-1 are compared to anharmonic vibrational frequency calculations at the B2PLYP-D3/aug-cc-pVTZ level of theory for structural identification and band assignments. For the formamide cation, spectral signatures of both the low-energy aminohydroxycarbene isomer (NH₂-C^•+-OH) and the higher-energy canonical cation (HCONH₂^•+) were detected, while protonated formamide was observed exclusively as the more stable O-protonated isomer with no indication of N-protonation. Additionally, a comparative analysis of the two spectroscopic techniques, supported by potential energy surface and vibrational frequency calculations, highlights how the weakly bound Ne tag subtly affects the vibrational signatures of the ions.