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Photoelectron Imaging of Anions Illustrated by 310 Nm Detachment of F−
Published on: July 27, 2018
Contrasting Dynamics in Isoelectronic Anions Formed by Electron Attachment.
P Nag1, M Ranković1, M Polášek1
1J. Heyrovský Institute of Physical Chemistry, The Czech Academy of Sciences, Dolejškova 3, 18223 Prague, Czech Republic.
Isoelectronic molecules cyanogen (NCCN) and cyanoacetylene (HCCCN) exhibit distinct dissociation dynamics following electron attachment. Differences in CN- fragment energy partitioning and angular distributions reveal unique molecular responses to electron-induced bond cleavage.
Area of Science:
- Physical Chemistry
- Chemical Physics
- Molecular Dynamics
Background:
- Cyanogen (NCCN) and cyanoacetylene (HCCCN) are isoelectronic molecules with similar properties.
- Dissociative electron attachment (DEA) is a key process for studying molecular bond cleavage.
Purpose of the Study:
- To investigate and compare the dissociation dynamics of NCCN and HCCCN induced by DEA.
- To understand the factors contributing to the different fragmentation pathways observed in these isoelectronic molecules.
Main Methods:
- Velocity map imaging (VMI) was used to analyze the CN- fragment produced from DEA.
- Electron energy loss (EEL) spectra were employed to identify parent resonance states.
Main Results:
- Both NCCN and HCCCN produce CN- with similar energy dependence via resonant electron attachment.
- VMI revealed significant differences in excess energy partitioning and fragment angular distributions between the two molecules.
- The observed differences were attributed to nuclear frame distortion during resonance formation in HCCCN.
Conclusions:
- The study elucidates distinct dissociation dynamics in isoelectronic NCCN and HCCCN following DEA.
- A mechanism involving nuclear frame distortion in HCCCN explains the observed dynamic differences and the CN- cross-section magnitude discrepancy.
- This research provides insights into electron-molecule interactions and fragmentation pathways.
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