@article{59901,
  author       = {{Keksel, Ewald and Kluge, Sebastian and Schleier, Domenik and Höner, Martin and Karakaya, Yasin and Bierkandt, Thomas and Köhler, Markus and Kasper, Tina}},
  issn         = {{0010-2180}},
  journal      = {{Combustion and Flame}},
  publisher    = {{Elsevier BV}},
  title        = {{{Sensitizing effect of acetylene and 1,3-butadiene on toluene oxidation in laminar flames}}},
  doi          = {{10.1016/j.combustflame.2025.113978}},
  volume       = {{274}},
  year         = {{2025}},
}

@article{60552,
  abstract     = {{<jats:title>Abstract</jats:title><jats:p>The incorporation of heteroatoms into the framework of polycyclic aromatic hydrocarbons (PAHs), in particular of nitrogen to yield polycyclic aromatic nitrogen heterocycles (PANHs), has been proposed for both astronomical and combustion environments, but no suitable precursors and pathways have been found. Analogous pathways to PAH formation are kinetically or energetically inhibited in the presence of a nitrogen heteroatom. We report on the reaction of phenylnitrene (<jats:sup>3</jats:sup>PhN, <jats:italic>c</jats:italic>‐C<jats:sub>6</jats:sub>H<jats:sub>5</jats:sub>N) with resonance‐stabilized propargyl radicals (C<jats:sub>3</jats:sub>H<jats:sub>3</jats:sub>) and find that the association reaction bifurcates depending on the orientation of the attacking propargyl radical and yields multiple isomeric products. Among them, we identify the condensed‐ring quinoline and conclude that nitrenes are viable candidates to drive the formation of PANHs.</jats:p>}},
  author       = {{Arns, Rahel and McClish, Rory and Hemberger, Patrick and Bodi, Andras and Bouwman, Jordy and Kasper, Tina and Schleier, Domenik}},
  issn         = {{1433-7851}},
  journal      = {{Angewandte Chemie International Edition}},
  publisher    = {{Wiley}},
  title        = {{{Is Phenylnitrene a Missing Link in the Formation of Polycyclic Aromatic Nitrogen Heterocycles?}}},
  doi          = {{10.1002/anie.202503940}},
  year         = {{2025}},
}

@article{48639,
  abstract     = {{The seven parallel dissociative ionization channels of benzonitrile yield highly stable fragment ions with commensurate abundance, underlining the potential role of the benzonitrile cation as hub species in the interstellar medium.}},
  author       = {{Kamer, Jerry and Schleier, Domenik and Donker, Merel and Hemberger, Patrick and Bodi, Andras and Bouwman, Jordy}},
  issn         = {{1463-9076}},
  journal      = {{Physical Chemistry Chemical Physics}},
  keywords     = {{Physical and Theoretical Chemistry, General Physics and Astronomy}},
  number       = {{42}},
  pages        = {{29070--29079}},
  publisher    = {{Royal Society of Chemistry (RSC)}},
  title        = {{{Threshold photoelectron spectroscopy and dissociative photoionization of benzonitrile}}},
  doi          = {{10.1039/d3cp03977c}},
  volume       = {{25}},
  year         = {{2023}},
}

@article{44231,
  abstract     = {{<jats:p>A new decomposition mechanism for trimethylborane at high temperatures has been discovered.</jats:p>}},
  author       = {{Schleier, Domenik and Gerlach, Marius and Schaffner, Dorothee and Mukhopadhyay, Deb Pratim and Hemberger, Patrick and Fischer, Ingo}},
  issn         = {{1463-9076}},
  journal      = {{Physical Chemistry Chemical Physics}},
  keywords     = {{Physical and Theoretical Chemistry, General Physics and Astronomy}},
  number       = {{6}},
  pages        = {{4511--4518}},
  publisher    = {{Royal Society of Chemistry (RSC)}},
  title        = {{{Threshold photoelectron spectroscopy of trimethylborane and its pyrolysis products}}},
  doi          = {{10.1039/d2cp04513c}},
  volume       = {{25}},
  year         = {{2022}},
}