Abstract
In this study, we utilized the infrared (IR)–vacuum-ultraviolet (VUV) non-resonant ionization and fragmentation detected IR spectroscopy (NRIFD-IR) technique to explore the IR spectra (2700–7200 cm-1) and the structures of both neutral and cationic hydroxyacetone. By comparing the experimentally obtained IR spectra with the anharmonic frequencies calculated at the B2PLYP-D3/cc-pVTZ and B3LYP-D3(BJ)/def2-TZVPP level of theory, we assigned the structures of hydroxyacetone and its cation. Notably, we observed a discrepancy in the neutral spectrum within the CH stretch region, depending on whether the parent or fragment channel was monitored. This observation suggests that the near-threshold dissociative ionization process exhibits mode-selectivity, implying that certain vibrational modes play a crucial role in either facilitating or inhibiting the dissociation event.
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