@article{GerlachMonningerSchleieretal.2021, author = {Gerlach, Marius and Monninger, Sophie and Schleier, Domenik and Hemberger, Patrick and Goettel, James T. and Braunschweig, Holger and Fischer, Ingo}, title = {Photoelectron Photoion Coincidence Spectroscopy of NCl\(_{3}\) and NCl\(_{2}\)}, series = {ChemPhysChem}, volume = {22}, journal = {ChemPhysChem}, number = {21}, doi = {10.1002/cphc.202100537}, url = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-257322}, pages = {2164-2167}, year = {2021}, abstract = {We investigate NCl\(_{3}\) and the NCl\(_{2}\) radical by photoelectron-photoion coincidence spectroscopy using synchrotron radiation. The mass selected threshold photoelectron spectrum (ms-TPES) of NCl\(_{3}\) is broad and unstructured due to the large geometry change. An ionization energy of 9.7±0.1 eV is estimated from the spectrum and supported by computations. NCl2 is generated by photolysis at 213 nm from NCl\(_{3}\) and its ms-TPES shows an extended vibrational progression with a 90 meV spacing that is assigned to the symmetric N-Cl stretching mode in the cation. An adiabatic ionization energy of 9.94 ± 0.02 eV is determined.}, language = {en} } @article{SchleierReuschLummeletal.2019, author = {Schleier, Domenik and Reusch, Engelbert and Lummel, Lisa and Hemberger, Patrick and Fischer, Ingo}, title = {Threshold photoelectron spectroscopy of IO and IOH}, series = {ChemPhysChem}, volume = {20}, journal = {ChemPhysChem}, number = {19}, doi = {10.1002/cphc.201900813}, url = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-204751}, pages = {2413-2416}, year = {2019}, abstract = {Iodine oxides appear as reactive intermediates in atmospheric chemistry. Here, we investigate IO and HOI by mass-selective threshold photoelectron spectroscopy (ms-TPES), using synchrotron radiation. IO and HOI are generated by photolyzing iodine in the presence of ozone. For both molecules, accurate ionization energies are determined, 9.71±0.02 eV for IO and 9.79±0.02 eV for HOI. The strong spin-spin interaction in the 3Σ- ground state of IO+ leads to an energy splitting into the Ω=0 and Ω=±1 sublevels. Upon ionization, the I-O bond shortens significantly in both molecules; thus, a vibrational progression, assigned to the I-O stretch, is apparent in both spectra.}, language = {en} }