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research article

Polychromatic femtosecond fluorescence studies of metal-polypyridine complexes in solution

Braem, Olivier  
•
Messina, Fabrizio  
•
El-Zohry, Ahmed M.  
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2012
Chemical Physics

Femtosecond-resolved broadband fluorescence studies are reported for M(bpy)(3) (M = Fe, Ru), RuN3 and RuN719 complexes in solution. We investigated the pump wavelength dependence of the fluorescence of aqueous Fe(bpy)(3) and the solvent and ligand dependence of the fluorescence of Ru-complexes excited at 400 nm. For all complexes, the (MLCT)-M-1 fluorescence appears at zero time delay with a mirror-like image with respect to the absorption. It decays in <= 30-45 fs due to intersystem crossing to the (MLCT)-M-3 states, but a longer lived component of similar to 190 fs additionally shows up in RuN719 and RuN3. No solvent effects are detected. The very early dynamics are characterized by internal conversion (IC) and intramolecular vibrational redistribution (IVR) processes on a time scale which we estimate to <= 10 fs using the (MLCT)-M-1 lifetime as an internal clock. (C) 2011 Elsevier B. V. All rights reserved.

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Type
research article
DOI
10.1016/j.chemphys.2011.11.022
Web of Science ID

WOS:000299013700008

Author(s)
Braem, Olivier  
Messina, Fabrizio  
El-Zohry, Ahmed M.  
Cannizzo, Andrea  
Chergui, Majed  
Date Issued

2012

Published in
Chemical Physics
Volume

393

Start page

51

End page

57

Subjects

Metal-polypyridine complexes

•

Ivr

•

Internal conversion

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Intersystem crossing

•

Ultrafast

•

Fluorescence up-conversion

•

Photoinduced Electron-Transfer

•

Titanium-Dioxide Films

•

Excited-State Dynamics

•

Anatase Tio2 Film

•

Ru-Dye Molecules

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Single-Crystal (Pf6)2

•

Nanocrystalline Tio2

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Relaxation Dynamics

•

Up-Conversion

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Solvent Dependence

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LSU  
Available on Infoscience
February 23, 2012
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/78078
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