Ultrafast isomerization initiated by X-ray core ionization
File(s)
Author(s)
Type
Journal Article
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.
Date Issued
2015-09-10
Date Acceptance
2015-07-28
Citation
Nature Communications, 2015, 6 (10)
ISSN
2041-1723
Publisher
Nature Publishing Group
Journal / Book Title
Nature Communications
Volume
6
Issue
10
Copyright Statement
© 2015, Rights Managed by Nature Publishing Group
Sponsor
Engineering & Physical Science Research Council (EPSRC)
Commission of the European Communities
Grant Number
EP/I032517/1
290467
Subjects
Science & Technology
Multidisciplinary Sciences
Science & Technology - Other Topics
MEMBRANE-PROTEIN STRUCTURE
ACETYLENE
DISSOCIATION
SPECTROSCOPY
VINYLIDENE
DYNAMICS
PULSES
LASERS
C2H2
Publication Status
Published
Article Number
ARTN 8199