@article{HirschPachnerFischeretal.2020, author = {Hirsch, Florian and Pachner, Kai and Fischer, Ingo and Issler, Kevin and Petersen, Jens and Mitric, Roland and Bakels, Sjors and Rijs, Anouk M.}, title = {Do Xylylenes Isomerize in Pyrolysis?}, series = {ChemPhysChem}, volume = {21}, journal = {ChemPhysChem}, number = {14}, doi = {10.1002/cphc.202000317}, url = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-218316}, pages = {1515 -- 1518}, year = {2020}, abstract = {We report infrared spectra of xylylene isomers in the gas phase, using free electron laser (FEL) radiation. All xylylenes were generated by flash pyrolysis. The IR spectra were obtained by monitoring the ion dip signal, using a IR/UV double resonance scheme. A gas phase IR spectrum of para-xylylene  was recorded, whereas ortho- and meta-xylylene were found to partially rearrange to benzocyclobutene and styrene. Computations of the UV oscillator strength  for all molecules were carried out and provde an explanation for the observation of the isomerization products.}, language = {en} } @article{PreitschopfSturmStroganovaetal.2023, author = {Preitschopf, Tobias and Sturm, Floriane and Stroganova, Iuliia and Lemmens, Alexander K. and Rijs, Anouk M. and Fischer, Ingo}, title = {IR/UV Double Resonance Study of the 2-Phenylallyl Radical and its Pyrolysis Products}, series = {Chemistry - A European Journal}, volume = {29}, journal = {Chemistry - A European Journal}, number = {13}, doi = {10.1002/chem.202202943}, url = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-312338}, year = {2023}, abstract = {Isolated 2-phenylallyl radicals (2-PA), generated by pyrolysis from a nitrite precursor, have been investigated by IR/UV ion dip spectroscopy using free electron laser radiation. 2-PA is a resonance-stabilized radical that is considered to be involved in the formation of polycyclic aromatic hydrocarbons (PAH) in combustion, but also in interstellar space. The radical is identified based on its gas-phase IR spectrum. Furthermore, a number of bimolecular reaction products are identified, showing that the self-reaction as well as reactions with unimolecular decomposition products of 2-PA form several PAH efficiently. Possible mechanisms are discussed and the chemistry of 2-PA is compared with the one of the related 2-methylallyl and phenylpropargyl radicals.}, language = {en} }