Researchers at European XFEL in Germany have tracked in real time the movement of individual atoms during a chemical reaction in the gas phase. Using extremely short X-ray flashes, they were able to observe the formation of an iodine molecule (I₂) after irradiating diiodomethane (CH₂I₂) molecules by infrared light, which involves breaking two bonds and forming a new one. At the same time, they were able to distinguish this reaction from two other reaction pathways, namely the separation of a single iodine atom from the diiodomethane, or the excitation of bending vibrations in the bound molecule. The results provide new insights into fundamental reaction mechanisms that have so far been very difficult to distinguish experimentally.
So-called elimination reactions in which small molecules are formed from a larger molecule are central to many chemical processes—from atmospheric chemistry to catalyst research. However, the detailed mechanism of many reactions, in which several atoms break and re-form their bonds, often remains obscure. The reason: The processes take place in incredibly short times—in femtoseconds, or a few millionths of a billionth of a second.
An innovative experimental approach was now used at the SQS instrument at European XFEL to visualize such reaction dynamics. The researchers irradiated diiodomethane molecules with ultrashort infrared laser pulses, which triggered the molecular reactions. Femtoseconds later, intense X-ray flashes shattered the molecules, causing their atomic components to fly apart in a “Coulomb explosion.” The trajectories and velocities of the ions were then recorded by a detection device called the COLTRIMS reaction microscope (COLd Target Recoil Ion Momentum Spectroscopy)—one of the detection instruments at the SQS experimental station that is made available to users.
“Using this method, we were able to precisely track how the iodine atoms assemble while the methylene group is cleaved off,” explains Artem Rudenko from Kansas State University, USA, the principal investigator of the experiment. The analysis revealed that both synchronous and asynchronous mechanisms contribute to the formation of the iodine molecule—a result that was supported by theoretical calculations.
Remarkably, “Although this reaction pathway only accounts for about ten percent of the resulting products, we were able to clearly distinguish it from the other competing reactions,” explains Rebecca Boll from the European XFEL’s SQS (Small Quantum Systems) instrument in Schenefeld near Hamburg. This was made possible by the precise selection of specific ion fragmentation channels and their time-resolved analysis.
Read more on European XFEL website
