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Mission Statement
Chemical reactions involve the rearrangements of atoms, the
breaking of bonds and the formation of new ones. At the atomic level, such motions
occur on time scales as short as a few tens of femtoseconds ( 1 fs = 10-15 s
). We are using spectroscopic techniques that are able to temporally resolve such
incredibly fast events and at the same time, are sensitive to the molecular structural changes
accompanying the elementary chemical process.
In particular, femtosecond nonlinear spectroscopy in the
ultraviolet, the visible, and the infrared spectral regions are used to exploit
the time-dependent molecular-optical properties that are associated with
chemical transformations. We are interested in reactive processes such as
light-triggered dissociations, proton and electron transfer reactions, and
conformational isomerizations. In addition, we explore non-reactive dynamics such as intermolecular vibrational energy transfer, intramolecular vibrational
redistribution, electronic dephasing and time-dependent solvation.
To this end, we implement in our laboratories novel
techniques of femtosecond electronic and vibrational spectroscopies such as
rapid-scan time and frequency-resolved transient absorption, fluorescence
upconversion, IR and VIS
photon echoes, Raman-induced
optical Kerr effect and femtosecond nonlinear infrared spectroscopy. Such
tools are being supplemented by single-molecule methods like confocal
fluorescence lifetime imaging and fluorescence correlation spectroscopy.
We are particularly interested in observing chemical dynamics in
hydrogen-bonded systems and in disclosing the influence of hydrogen-bonding on
chemical reactivity. The hydrogen-bonded systems we focus on range from simple
molecular liquids such as water and aqueous solutions to highly complex
supramolecular architectures. Hydrogen-bonded liquids are studied under a wide
variety of thermodynamic conditions ranging from nanoscopic liquid droplets with
interfaces to soft matter, to bulk liquid and supercritical phases at elevated pressures and temperatures. Supramolecular
hydrogen-bonded architectures are being fabricated artificially by our synthetically oriented project partners using advanced
methods of organic and inorganic synthesis.
Click on the hyperlinks below to download a poster on:
Femtosecond spectroscopy of the primary relaxation dynamics of solvated electrons in liquid ammonia
Femtosecond vibrational relaxation dynamics of the OH-stretching vibration of HOD in liquid-to-supercritical D2O
Primary processes in green fluorescent protein (wt) studied by femtosecond UV/VIS pump-probe spectroscopy
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