4.6 Article

Guest-Host Interactions Investigated by Time-Resolved X-ray Spectroscopies and Scattering at MHz Rates: Solvation Dynamics and Photoinduced Spin Transition in Aqueous Fe(bipy)32+

Journal

JOURNAL OF PHYSICAL CHEMISTRY A
Volume 116, Issue 40, Pages 9878-9887

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jp306917x

Keywords

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Funding

  1. European Research Council [ERC-StG-259709]
  2. Danish National Research Foundation's Centre for Molecular Movies
  3. European XFEL
  4. DANSCATT
  5. U.S. Department of Energy (DOE) Office of Science, Division of Chemical, Geological and Biological Sciences [DE-AC02-06CH11357]
  6. Carlsberg and Villum Foundations
  7. Bolyai Janos Fellowship of the Hungarian Academy of Sciences
  8. European Research Council
  9. Advanced Investigator Grant [VISCHEM-226136]
  10. Swedish Research Council
  11. German Research Association DFG [SFB925]
  12. U.S. DOE [DE-AC02-06CH11357]

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We have studied the photoinduced low spin (LS) to high spin (HS) conversion of [Fe(bipy)(3)](2+) in aqueous solution. In a laser pump/X-ray probe synchrotron setup permitting simultaneous, time-resolved X-ray diffuse scattering (XDS) and X-ray spectroscopic measurements at a 3.26 MHz repetition rate, we observed the interplay between intramolecular dynamics and the intermolecular caging solvent response with better than 100 ps time resolution. On this time scale, the initial ultrafast spin transition and the associated intramolecular geometric structure changes are long completed, as is the solvent heating due to the initial energy dissipation from the excited HS molecule. Combining information from X-ray emission spectroscopy and scattering, the excitation fraction as well as the temperature and density changes of the solvent can be closely followed on the subnanosecond time scale of the HS lifetime, allowing the detection of an ultrafast change in bulk solvent density. An analysis approach directly utilizing the spectroscopic data in the XDS analysis effectively reduces the number of free parameters, and both combined permit extraction of information about the ultrafast structural dynamics of the caging solvent, in particular, a decrease in the number of water molecules in the first solvation shell is inferred, as predicted by recent theoretical work.

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