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Abstract Identifying the short-lived intermediates and reaction mechanisms of multi-channel radical cation fragmentation processes remains a current and important challenge to understanding and predicting mass spectra. We find that coherent oscillations in the femtosecond time-dependent yields of several product ions following ultrafast strong-field ionization represent spectroscopic signatures that elucidate their mechanism of formation and identify the intermediate(s) they originate from. Experiments on endo-dicyclopentadiene show that vibrational frequencies from various intermediates are mapped onto their resulting products. Aided by ab initio methods, we identify the vibrational modes of both the cleaved and intact molecular ion intermediates. These results confirm stepwise and concerted fragmentation pathways of the dicyclopentadiene ion. This study highlights the power of tracking the femtosecond dynamics of all product ions simultaneously and sheds further light onto one of the fundamental reaction mechanisms in mass spectrometry, the retro-Diels Alder reaction.
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This content will become publicly available on September 4, 2026
On the Chlorobenzene-Ammonia Cluster Reaction: Entrance Channel Dynamics, 2CR2PI Spectroscopy, and Ion Imaging of the Reaction Dynamics
Prior studies of halobenzene−ammonia complexes have shown that the nature of the cationic intermediate (i.e., Wheland-type vs ion-radical) may play a key role in determining the reaction products. To probe this link, we report here the reaction dynamics of the chlorobenzene-ammonia 1:1 complex (PhCl···NH3) using product ion imaging following two-color resonant two-photon ionization. A threshold value of 8.863 ± 0.008 eV was determined for the appearance of protonated aniline, which accompanies Cl atom loss and is the dominant product channel at energies near threshold. Scanning down to energies close to threshold, we find no evidence for a roaming halogen radical mechanism leading to HCl products, which was evidenced in the related bromobenzene−ammonia complex, and proceeded through an ion-radical intermediate structure. Here, supporting calculations indicate that both types of intermediates are present, but the Wheland-type structure is significantly more stable. Addressing a key question of earlier work, analysis of the PhCl···NH3 potential energy surface (PES) in the reactant region establishes a complicated entrance channel pathway linking the in-plane σ-type complex to the Wheland intermediate (iWH) on the [PhCl···NH3]+• cationic surface. This pathway involves stepwise transition of the weakly bound ammonia from the initial in-plane σ-type complex to an ortho Wheland intermediate, followed by rearrangement to the ipso position. Finally, given that fluorine has been shown to stabilize aromatic ions, we hypothesized that fluorine substitution might alter the structure of the intermediate, favoring the ion-radical intermediate. To test this hypothesis, as an illustrative example the PES of the meta-PhClF-NH3 system on the cationic surface was computed. Confirming our hypothesis, these calculations show an inversion in stability for the Wheland-type and ion−radical complex intermediates, with the latter preferred energetically at the examined level of theory.
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- PAR ID:
- 10653503
- Publisher / Repository:
- American Chemical Socieity
- Date Published:
- Journal Name:
- The Journal of Physical Chemistry A
- Volume:
- 129
- Issue:
- 35
- ISSN:
- 1089-5639
- Page Range / eLocation ID:
- 8056 to 8063
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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