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@ARTICLE{Walmsley:642750,
      author       = {Walmsley, Tiffany and Allum, Felix and Harries, James and
                      Kumagai, Yoshiaki and McManus, Joseph and Nagaya, Kiyonobu
                      and Britton, Mathew and Brouard, Mark and Bucksbaum, Philip
                      and Fushitani, Mizuho and Gabalski, Ian and Gejo, Tatsuo and
                      Hockett, Paul and Howard, Andrew and Iwayama, Hiroshi and
                      Kukk, Edwin and Lam, Chow-shing and Minns, Russell and
                      Niozu, Akinobu and Nishimuro, Sekito and Niskanen, Johannes
                      and Owada, Shigeki and Razmus, Weronika and Rolles, Daniel
                      and Somper, James and Ueda, Kiyoshi and Unwin, James and
                      Wada, Shin-ichi and Woodhouse, Joanne and Forbes, Ruaridh
                      and Burt, Michael and Warne, Emily},
      title        = {{T}he inner-shell ionization and fragmentation of
                      selenophene at 120 e{V}},
      reportid     = {PUBDB-2025-05599},
      year         = {2025},
      abstract     = {Three-dimensional velocity-map imaging and covariance
                      analysis were used to identify over 50 fragmentation
                      channels produced following the inner-shell ionization of
                      selenophene at 120 eV. The majority resulted in two or three
                      'heavy' products containing selenium or carbon, many of
                      which had identical mass-to-charge ratios but different
                      chemical compositions due to the degree of hydrogenation and
                      the selenium isotope involved. Covariance analysis was used
                      to isolate these reaction channels and to provide estimates
                      of their relative yields. In combination with prior similar
                      studies on thiophene and furan, the current results indicate
                      that the nature of the heteroatom significantly influences
                      the charge redistribution and bond cleavage dynamics induced
                      by the Auger-Meitner process, and demonstrate the
                      sensitivity of inner-shell ionization dynamics to the
                      molecular and electronic structures of heterocyclic
                      systems.},
      cin          = {FS-FLASH},
      cid          = {I:(DE-H253)FS-FLASH-20140814},
      pnm          = {631 - Matter – Dynamics, Mechanisms and Control
                      (POF4-631)},
      pid          = {G:(DE-HGF)POF4-631},
      experiment   = {EXP:(DE-MLZ)External-20140101},
      typ          = {PUB:(DE-HGF)25},
      doi          = {10.21203/rs.3.rs-7925497/v1},
      url          = {https://bib-pubdb1.desy.de/record/642750},
}