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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+

Authors :
Gilles Doumy
Martin Nielsen
György Vankó
T. B. van Driel
Stephen H. Southworth
Anne Marie March
Kristoffer Haldrup
Henrik T. Lemke
Wojciech Gawelda
Asmus Ougaard Dohn
Jens Uhlig
Andreas Galler
Elliot P. Kanter
Villy Sundström
Linda Young
Christian Bressler
Amélie Bordage
Kasper S. Kjær
Sophie E. Canton
Institute of Electrical Engineering, SAS Bratislava
Consejo Superior de Investigaciones Científicas [Madrid] (CSIC)
European XFEL GmbH
Department of Physics
Ohio State University [Columbus] (OSU)
Laboratoire Géomatériaux et Environnement (LGE)
Université Paris-Est Marne-la-Vallée (UPEM)
GKSS Research Center Geesthacht
Lund University [Lund]
Source :
Journal of Physical Chemistry A, Journal of Physical Chemistry A, American Chemical Society, 2012, 116 (40), pp.9878-9887. ⟨10.1021/jp306917x⟩, The Journal of Physical Chemistry A
Publication Year :
2012
Publisher :
American Chemical Society (ACS), 2012.

Abstract

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.

Details

ISSN :
15205215 and 10895639
Volume :
116
Database :
OpenAIRE
Journal :
The Journal of Physical Chemistry A
Accession number :
edsair.doi.dedup.....2335bc1bf649a0aaaee4d25177e34fce
Full Text :
https://doi.org/10.1021/jp306917x