Direct tracking of H2 roaming reaction in real time
Debadarshini Mishra (),
Aaron C. LaForge (),
Lauren M. Gorman,
Sergio Díaz-Tendero,
Fernando Martín and
Nora Berrah
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Debadarshini Mishra: University of Connecticut
Aaron C. LaForge: University of Connecticut
Lauren M. Gorman: University of Connecticut
Sergio Díaz-Tendero: Universidad Autónoma de Madrid
Fernando Martín: Universidad Autónoma de Madrid
Nora Berrah: University of Connecticut
Nature Communications, 2024, vol. 15, issue 1, 1-8
Abstract:
Abstract Roaming is an unconventional type of molecular reaction where fragments, instead of immediately dissociating, remain weakly bound due to long-range Coulombic interactions. Due to its prevalence and ability to form new molecular compounds, roaming is fundamental to photochemical reactions in small molecules. However, the neutral character of the roaming fragment and its indeterminate trajectory make it difficult to identify experimentally. Here, we introduce an approach to image roaming, utilizing intense, femtosecond IR radiation combined with Coulomb explosion imaging to directly reconstruct the momentum vector of the neutral roaming H2, a precursor to $${{{{{{{{\rm{H}}}}}}}}_{3}}^{+}$$ H 3 + formation, in acetonitrile, CH3CN. This technique provides a kinematically complete picture of the underlying molecular dynamics and yields an unambiguous experimental signature of roaming. We corroborate these findings with quantum chemistry calculations, resolving this unique dissociative process.
Date: 2024
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-49671-6
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DOI: 10.1038/s41467-024-49671-6
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