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Time-resolved molecular dynamics of single and double hydrogen migration in ethanol

Author

Listed:
  • Nora G. Kling

    (University of Connecticut)

  • S. Díaz-Tendero

    (Universidad Autónoma de Madrid
    Universidad Autónoma de Madrid
    Universidad Autónoma de Madrid)

  • R. Obaid

    (University of Connecticut)

  • M. R. Disla

    (University of Connecticut)

  • H. Xiong

    (University of Connecticut)

  • M. Sundberg

    (University of Connecticut)

  • S. D. Khosravi

    (University of Connecticut)

  • M. Davino

    (University of Connecticut)

  • P. Drach

    (University of Connecticut)

  • A. M. Carroll

    (University of Connecticut)

  • T. Osipov

    (LCLS, SLAC National Accelerator Laboratory)

  • F. Martín

    (Universidad Autónoma de Madrid
    Universidad Autónoma de Madrid
    Instituto Madrileño de Estudios Avanzados en Nanociencia (IMDEA-Nano), Campus de Cantoblanco
    Donostia International Physics Center (DIPC), Paseo Manuel de Lardizabal 4)

  • N. Berrah

    (University of Connecticut)

Abstract

Being the lightest, most mobile atom that exists, hydrogen plays an important role in the chemistry of hydrocarbons, proteins and peptides and most biomolecules. Hydrogen can undergo transfer, exchange and migration processes, having considerable impact on the chemical behavior of these molecules. Although much has been learned about reaction dynamics involving one hydrogen atom, less is known about those processes where two or more hydrogen atoms participate. Here we show that single and double hydrogen migrations occurring in ethanol cations and dications take place within a few hundred fs to ps, using a 3D imaging and laser pump-probe technique. For double hydrogen migration, the hydrogens are not correlated, with the second hydrogen migration promoting the breakup of the C–O bond. The probability of double hydrogen migration is quite significant, suggesting that double hydrogen migration plays a more important role than generally assumed. The conclusions are supported by state-of-the-art molecular dynamics calculations.

Suggested Citation

  • Nora G. Kling & S. Díaz-Tendero & R. Obaid & M. R. Disla & H. Xiong & M. Sundberg & S. D. Khosravi & M. Davino & P. Drach & A. M. Carroll & T. Osipov & F. Martín & N. Berrah, 2019. "Time-resolved molecular dynamics of single and double hydrogen migration in ethanol," Nature Communications, Nature, vol. 10(1), pages 1-8, December.
  • Handle: RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-10571-9
    DOI: 10.1038/s41467-019-10571-9
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    Cited by:

    1. Debadarshini Mishra & Aaron C. LaForge & Lauren M. Gorman & Sergio Díaz-Tendero & Fernando Martín & Nora Berrah, 2024. "Direct tracking of H2 roaming reaction in real time," Nature Communications, Nature, vol. 15(1), pages 1-8, December.
    2. Travis Severt & Eleanor Weckwerth & Balram Kaderiya & Peyman Feizollah & Bethany Jochim & Kurtis Borne & Farzaneh Ziaee & Kanaka Raju P & Kevin D. Carnes & Marcos Dantus & Daniel Rolles & Artem Rudenk, 2024. "Initial-site characterization of hydrogen migration following strong-field double-ionization of ethanol," Nature Communications, Nature, vol. 15(1), pages 1-11, December.

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