Department of Physics, Stanford University, 382 Via Pueblo Mall, Stanford, California 94305, USA.
PULSE Institute for Ultrafast Energy Science, 2575 Sand Hill Road, Menlo Park, California 94025, USA.
Nat Commun. 2015 Sep 10;6:8199. doi: 10.1038/ncomms9199.
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.
快速质子迁移是碳氢化合物光化学中的关键过程。当较重的原子吸收 X 射线时,电荷迁移和随后的质子运动可以减轻辐射损伤。如果速度足够快,这可以提高在 X 射线自由电子激光器中对生物分子结构进行衍射前破坏测量的保真度。在这里,我们研究了乙炔的 X 射线引发的异构化,这是碳氢化合物中质子动力学的模型。我们的时间分辨测量捕捉到了碳 K 壳层电子 X 射线电离后质子的瞬态运动。我们用第二束精确延迟的 X 射线脉冲使分子库仑爆炸,然后记录所有碎片的动量。这些不同延迟的快照被组合成一个演化分子的“分子电影”,显示出在最初的 12fs 内质子有明显的重新分布。我们得出的结论是,在与填充 K 壳空位的俄歇弛豫相当的时间尺度上,会发生显著的质子运动。