Ultrafast electron diffraction imaging of bond breaking in di-ionized acetylene

• Autores: B. Wolter, M. Baudisch, K. Doblhoff Dier
• Localización: Science, ISSN 0036-8075, Vol. 354, Nº 6310, 2016, págs. 308-312
• Idioma: inglés
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• Resumen

  • Visualizing chemical reactions as they occur requires atomic spatial and femtosecond temporal resolution. Here, we report imaging of the molecular structure of acetylene (C2H2) 9 femtoseconds after ionization. Using mid-infrared laser–induced electron diffraction (LIED), we obtained snapshots as a proton departs the [C2H2]2+ ion. By introducing an additional laser field, we also demonstrate control over the ultrafast dissociation process and resolve different bond dynamics for molecules oriented parallel versus perpendicular to the LIED field. These measurements are in excellent agreement with a quantum chemical description of field-dressed molecular dynamics.