| Literature DB >> 26354002 |
Chelsea E Liekhus-Schmaltz1,2, Ian Tenney1,2, Timur Osipov3, Alvaro Sanchez-Gonzalez4, Nora Berrah3, Rebecca Boll5,6, Cedric Bomme5, Christoph Bostedt7, John D Bozek7, Sebastian Carron7, Ryan Coffee7, Julien Devin1,2, Benjamin Erk5, Ken R Ferguson7,8, Robert W Field9, Lutz Foucar10, Leszek J Frasinski4, James M Glownia7, Markus Gühr2, Andrei Kamalov1,2, Jacek Krzywinski7, Heng Li2,7, Jonathan P Marangos4, Todd J Martinez2,11, Brian K McFarland2, Shungo Miyabe2,11, Brendan Murphy3, Adi Natan2, Daniel Rolles5, Artem Rudenko12, Marco Siano4, Emma R Simpson4, Limor Spector1,2, Michele Swiggers7, Daniel Walke4, Song Wang1,2, Thorsten Weber13, Philip H Bucksbaum1,2,8, Vladimir S Petrovic1,2.
Abstract
Rapid proton migration is a key process in hydrocarbon photochemistry. Charge migration and subsequent proton motion can mitigate radiation damage when heavier atoms absorb X-rays. If rapid enough, this can improve the fidelity of diffract-before-destroy measurements of biomolecular structure at X-ray-free electron lasers. Here we study X-ray-initiated isomerization of acetylene, a model for proton dynamics in hydrocarbons. Our time-resolved measurements capture the transient motion of protons following X-ray ionization of carbon K-shell electrons. We Coulomb-explode the molecule with a second precisely delayed X-ray pulse and then record all the fragment momenta. These snapshots at different delays are combined into a 'molecular movie' of the evolving molecule, which shows substantial proton redistribution within the first 12 fs. We conclude that significant proton motion occurs on a timescale comparable to the Auger relaxation that refills the K-shell vacancy.Entities:
Year: 2015 PMID: 26354002 DOI: 10.1038/ncomms9199
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919