% IMPORTANT: The following is UTF-8 encoded.  This means that in the presence
% of non-ASCII characters, it will not work with BibTeX 0.99 or older.
% Instead, you should use an up-to-date BibTeX implementation like “bibtex8” or
% “biber”.

@ARTICLE{VelaPerz:585154,
      author       = {Vela-Peréz, I. and Ota, Fukiko and Mhamdi, A. and Tamura,
                      Y. and Rist, Jonas and Melzer, Niklas and Uerken, S. and
                      Nalin, Giammarco and Anders, Nils and You, Daehyun and
                      Kircher, Max and Janke, Christian and Waitz, Markus and
                      Trinter, Florian and Guillemin, Renaud and Piancastelli,
                      Maria Novella and Simon, Marc and Davis, V. T. and Williams,
                      Joshua and Doerner, Reinhard and Hatada, Keisuke and
                      Yamazaki, Kaoru and Fehre, Kilian and Demekhin, Philipp and
                      Ueda, Kiyoshi and Schoeffler, Markus and Jahnke, Till},
      title        = {{H}igh-energy molecular-frame photoelectron angular
                      distributions: a molecular bond-length ruler},
      journal      = {Physical chemistry, chemical physics},
      volume       = {25},
      number       = {19},
      issn         = {1463-9076},
      address      = {Cambridge},
      publisher    = {RSC Publ.},
      reportid     = {PUBDB-2023-03427},
      pages        = {13784 - 13791},
      year         = {2023},
      abstract     = {We present a study on molecular-frame photoelectron angular
                      distributions (MFPADs) of small molecules using circularly
                      polarized synchrotron light. We find that the main
                      forward-scattering peaks of the MFPADs are slightly tilted
                      with respect to the molecular axis. This tilt angle is
                      directly connected to the molecular bond length by a simple,
                      universal formula. We apply the derived formula to several
                      examples of MFPADs of C 1s and O 1s photoelectrons of CO,
                      which have been measured experimentally or obtained by means
                      of ab initio modeling. In addition, we discuss the influence
                      of the back-scattering contribution that is superimposed
                      over the analyzed forward-scattering peak in the case of
                      homo-nuclear diatomic molecules such as N2.},
      cin          = {FS-PETRA-S / DOOR ; HAS-User / $XFEL_E2_SQS$},
      ddc          = {540},
      cid          = {I:(DE-H253)FS-PETRA-S-20210408 /
                      I:(DE-H253)HAS-User-20120731 /
                      $I:(DE-H253)XFEL_E2_SQS-20210408$},
      pnm          = {631 - Matter – Dynamics, Mechanisms and Control
                      (POF4-631) / SFB 1319 C03 - Trennung und Aufreinigung von
                      Enantiomer-Gemischen mittels Quantenkontrolle (C03)
                      (389895275)},
      pid          = {G:(DE-HGF)POF4-631 / G:(GEPRIS)389895275},
      experiment   = {EXP:(DE-MLZ)External-20140101},
      typ          = {PUB:(DE-HGF)16},
      pubmed       = {37159272},
      UT           = {WOS:000992632600001},
      doi          = {10.1039/D2CP05942H},
      url          = {https://bib-pubdb1.desy.de/record/585154},
}