News Release

Another advancement in imaging from INRS professor François Légaré's team

A molecule's transformation filmed at high resolution

Peer-Reviewed Publication

Institut national de la recherche scientifique - INRS

François Légaré's team at the INRS Énergie Matériaux Télécommunications Research Centre successfully imaged a chemical reaction with a spatial and temporal resolution greatly exceeding that obtained to date using microscopes. The team used a femtosecond laser source to shoot a molecular movie of how an acetylene molecule turns into vinylidene. An article presenting the advancement was recently published in the scientific journal Nature Communications.

"The approach we developed combines multiphoton ionization and Coulomb explosion imaging. With the significantly improved resolution of the image, we were able to reveal previously unknown details of this isomerization process and clarify the dynamics of proton migration. This form of imaging uses a compact laser source and is a simple option for studying the ultrafast molecular dynamics of other small organic molecules," said Banting postdoctoral fellow and primary author of the article Heide Ibrahim.

This isomerization process has already been observed using large equipment like free electron lasers with very energetic photons. However, the techniques most commonly employed to track nuclear rearrangement in a molecule were largely insensitive to the subtle and irregular changes that occur during a chemical reaction.

The experiments were designed by postdoctoral fellow Heide Ibrahim and professor François Légaré and conducted at INRS's Advanced Laser Light Source (ALLS) laboratory (Laboratoire de sources femtosecondes) in collaboration with the University of Waterloo, the National Research Council of Canada, and Université de Sherbrooke. The results showed for the first time that multiple oscillations can occur between the two isomers acetylene and vinylidene.


About This Publication

The article entitled "Tabletop imaging of structural evolutions in chemical reactions demonstrated for the acetylene cation" appeared in Nature Communications on July 18, 2014. The research was conducted by Heide Ibrahim, Samuel Beaulieu, Bruno E. Schmidt, Nicolas Thiré, Eric Bisson, Vincent Wanie, Mathieu Giguère, Jean-Claude Kieffer, and François Légaré of INRS, Benji Wales and Joseph Sanderson of the University of Waterloo, Emmanuel P. Fowe and André D. Brandrauk of Université de Sherbrooke, Michael Spanner and Michael S. Schuurman of the National Research Council of Canada (NRC), and Christoph T. Hebeisen of the University of Ottawa and NRC. Financial support was provided by the Natural Sciences and Engineering Research Council of Canada (NSERC), Fonds de recherche du Québec – Nature et technologies (FQRNT), and the Canadian Institute for Photonic Innovations.

About INRS

Institut national de recherche scientifique (INRS) is the top-ranking graduate research and training university in Canada in terms of research intensity. INRS brings together some 150 professors and close to 700 students and postdoctoral fellows in its centres in Montreal, Quebec City, Laval, and Varennes. Conducting fundamental research essential to the advancement of science in Quebec as well as internationally, INRS research teams also play a critical role in developing concrete solutions to problems facing our society.

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