X-ray-Induced Molecular Catapult: Ultrafast Dynamics Driven by Lightweight Linkages.
Oksana Travnikova1, Victor Kimberg2, Barbara Cunha de Miranda1
1Sorbonne Université, CNRS, UMR 7614, Laboratoire de Chimie Physique-Matière et Rayonnement, F-75005 Paris, France.
The Journal of Physical Chemistry Letters
|November 21, 2024
Summary
X-ray photons trigger a "molecular catapult" effect, breaking chemical bonds in femtoseconds. Light atomic groups control this ultrafast dissociation, similar to projectiles from a catapult.
Area of Science:
- Chemical Physics
- Molecular Dynamics
- Ultrafast Spectroscopy
Background:
- Chemical bond dissociation is fundamental to chemical reactions.
- Understanding ultrafast dynamics is key to controlling chemical processes.
- X-ray-driven processes offer unique insights into molecular behavior.
Purpose of the Study:
- To investigate the
- molecular catapult
- effect initiated by X-ray photons.
- To elucidate the role of light atomic groups in ultrafast molecular dissociation.
- To analyze three-body dissociation dynamics in bromochloromethane.
Main Methods:
- Utilizing X-ray photons to induce molecular dissociation.
- Reconstructing fragment momenta using the ion pair average (IPA) reference frame.
- Performing ab initio calculations to support experimental findings.
Main Results:
- Demonstrated X-ray-induced molecular dissociation via a
- molecular catapult
- mechanism.
- Observed dissociation into heavy fragments within femtoseconds.
- Identified light atomic groups (alkylene, alkanylene) governing nuclear dynamics.
Conclusions:
- Low-reduced-mass vibrational modes play a critical role in driving ultrafast chemical processes.
- The
- molecular catapult
- effect provides a new perspective on bond dissociation dynamics.
- This study enhances understanding of X-ray-matter interactions at the molecular level.


