Journal of Physical Chemistry B 2007-05-31

Tracking ultrafast excited-state bond-twisting motion in solution close to the Franck-Condon point.

Benjamin Dietzek, Torbjörn Pascher, Arkady Yartsev

Index: J. Phys. Chem. B 111(21) , 6034-41, (2007)

Full Text: HTML

Abstract

Applying optimal control to photoinduced trans-cis isomerization in condensed phase, the dynamics of bond-twisting motion of 1,1'-diethyl-4,4'-cyanine in methanol and propanol is revealed. The shape of the optimized pulse resulting from minimization of the photoisomer formation can be directly related to the initial excited-state dynamics in close proximity to the Franck-Condon point. The solvent viscosity-dependent ultrafast wavepacket motion is reflected in the prominent down-chirp of the optimized pulses and reveals a detailed picture of the control mechanism: The reduction of the isomer production is achieved by most efficient dumping of excited population back to the trans ground state. In the higher-viscosity solvent, propanol, wavelength-dependent oscillatory features are superimposed to the overall chirp structure pointing to the importance of excited-state vibrational coherences for the dumping process.

Related Compounds

Structure Name/CAS No. Articles
Quinolinium,1-ethyl-4-[3-(1-ethyl-4(1H)-quinolinylidene)-1-propen-1-yl]-, iodide (1:1) Structure Quinolinium,1-ethyl-4-[3-(1-ethyl-4(1H)-quinolinylidene)-1-propen-1-yl]-, iodide (1:1)
CAS:4727-50-8