In search of the cause behind the similarities often seen in the fragmentation of PANHs, vacuum ultraviolet (VUV) photodissociation of two pairs of isomers quinoline-isoquinoline and 2-naphthylamine-3-methyl-quinoline are studied using the velocity map imaging technique. The internal energy dependence of all primary fragmentation channels is obtained for all four target molecules. The decay dynamics of the four molecules is studied by comparing their various experimental signatures.
View Article and Find Full Text PDFA detailed exploration of the potential energy surface of quinoline cation (CHN) is carried out to extend the present understanding of its fragmentation mechanisms. Density functional theory calculations have been performed to explore new fragmentation schemes, giving special attention to previously unexplored pathways, such as isomerization and elimination of HNC. The isomerization mechanisms producing five- to seven-membered ring intermediates are described and are found to be a dominant channel both energetically and kinetically.
View Article and Find Full Text PDFPolycyclic aromatic hydrocarbons are major species in astrophysical environments, and this motivates their study in samples of astrochemical interest such as meteorites and laboratory analogues of stardust. Molecular analyses of carbonaceous matter in these samples show a dominant peak at / = 202.078 corresponding to CH.
View Article and Find Full Text PDFDissociative photoionization of quinoline induced by vacuum ultraviolet radiation is investigated using photoelectron-photoion coincidence spectroscopy. Branching ratios of all the detectable fragment ions are measured as a function of internal energy ranging from 2 to 30 eV. A specific generation hierarchy is observed in the breakdown curves of a set of dissociation channels.
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