Ultrafast intramolecular electronic charge separation during photo-chemical reactions cause up to ten thousand surrounding molecules to perform aligning pirouettes. Researchers observed for the first time such light induced reorientations in an organic molecular crystal.
Scientists from the Max-Born-Institute for Nonlinear Optics and Ultrafast Spectroscopy and of the Ludwig-Maximilians-University in Munich performed the study. In their study they initiated a separation of positive and negative electronic charge in a small number of particular molecules with extremely short light pulses. In turn the surrounding molecules responded by aligning their respective dipole axes along the photoinduced electric fields. The researchers observed this fundamental process for the first time by means of femtosecond x-ray diffraction with high spatial precision and in real time.
In nature chemical and biochemical reactions are strongly influenced by the surroundings, for instance water, a macromolecular or crystalline environment. During the course of reaction the structure of the surroundings changes considerably, which in turn determines backwards the reaction speed and the stability of the reaction products. Quite often such processes occur in the time regime of picoseconds, i.e. shorter than a millionth of a millionth of a second.
Ultrafast x-ray pulses provide a sequence of “x-ray snapshots” which directly image the structure of the molecular surroundings during the photoinduced reaction. From those x-ray pictures the separation and orientation of the molecules is deduced. For the generation of x-ray pulses, the scientists from Berlin and Munich used a tabletop femtosecond laser system, a method that is complementary to the planned large-scale free electron x-ray lasers.
In order to resolve changes of molecular distances and orientations simultaneously the researchers chose a crystal made of periodically ordered
4-(Diisopropylamino)benzonitrile (DIABN) molecules as a model system. They were successful in detecting structural changes in the molecular surroundings with a precision of fractions of an atomic diameter.
They found that the charge separation in the photo-excited molecules generates electric fields forcing molecules in the vicinity to rotate up to angles of 10 degrees. Due to the distant action of electric fields up to tenthousand surrounding molecules participate in this process. The molecular rotations take place without detectable delay with respect to the intramolecular charge separation occuring within 10 picoseconds. The separation of lattice planes is left unchanged.
The novel experiments with an unprecedented spatial and temporal resolution show that in nature local chemical reactions cause structural changes in a spatially extended vicinity on ultrafast time scales via electric fields. Such studies pave the way to investigations of more complex systems right up to crystalline biological macromolecules. Besides laser-driven x-ray sources ultrashort x-ray pulses from free electron lasers will be used in future for such investigations, e.g. the XFEL in Hamburg which is currently under construction.
Reference: M. Braun et al.: Ultrafast changes of molecular crystal structure induced by dipole solvation. In: Physical Review Letters (Vol. 98, 248301)
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