The utility of coherent vacuum ultraviolet (VUV) single-photon ionization (SPI) combined with time-of-flight mass spectrometry (TOF-MS) for organic molecule detection by parent mass is explored in this short review. Nonresonant tripling in phase-matched XeAr gas mixtures was used to generate photons at a fixed energy of 10.5 eV. Representative organic molecules with different functional groups were examined, including aliphatic and aromatic alkanes, alkenes, alkynes, alkanols, ethers, amines, aldehydes, ketones, carboxylic acids, and esters. In almost every case, the intensity of the resultant parent molecular ion peak detected by TOF-MS was found to be superior to that obtained using 70 eV electron impact (EI), and comparable to that obtained with 12 eV EI. In those instances when fragmentation reactions did occur, the resultant ions were similar to those found using EI but with significantly reduced mass spectral intensities. It was still possible to establish one dominant fragmentation pathway that could be used for molecular identification even if the parent molecular ion was not the strongest feature in the spectrum, for example, in the case of alcohols, alcohol clusters, and alcoholether adducts. Several of the fragment ions were metastably broadened. Not surprisingly, their known appearance energies or estimated reaction enthalpies were very similar to the fixed photon energy used. The success of using VUV for organic molecule soft ionization is attributed to the low photon energy that removes predominantly a π- or non-bonding electron from the functionalized species. As most organic compounds have ionization potentials in the 10.5 eV region, this approach is expected to be near universal.Key words: vacuum ultraviolet laser, single photon ionization, organic molecule detection, soft-ionization, mass spectrometry.
Photophysics of indole upon X-ray absorption
