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The journal of chemical physics 158, 174305 (2023). doi:10.1063/5.0147456, Naphthalene and azulene are isomeric polycyclic aromatic hydrocarbons (PAHs) and are topical in the context of astrochemistry due to the recent discovery of substituted naphthalenes in the Taurus Molecular Cloud-1 (TMC-1). Here, the thermal- and photo-induced isomerization, dissociation, and radiative cooling dynamics of energized (vibrationally hot) naphthalene (Np$^+$) and azulene (Az$^+$) radical cations, occurring over the microsecond to seconds timescale, are investigated using a cryogenic electrostatic ion storage ring, affording “molecular cloud in a box” conditions. Measurement of the cooling dynamics and kinetic energy release distributions for neutrals formed through dissociation, until several seconds after hot ion formation, are consistent with the establishment of a rapid (sub-microsecond) Np$^+ ⇌$ Az$^+$ quasi-equilibrium. Consequently, dissociation by C$_2$H$_2$-elimination proceeds predominantly through common Az$^+$ decomposition pathways. Simulation of the isomerization, dissociation, recurrent fluorescence, and infrared cooling dynamics using a coupled master equation combined with high-level potential energy surface calculations [CCSD(T)/cc-pVTZ], reproduce the trends in the measurements. The data show that radiative cooling via recurrent fluorescence, predominately through the Np$^+$ D$_0$ ← D$_2$ transition, efficiently quenches dissociation for vibrational energies up to ≈1 eV above dissociation thresholds. Our measurements support the suggestion that small cations, such as naphthalene, may be more abundant in space than previously thought. The strategy presented in this work could be extended to fingerprint the cooling dynamics of other PAH ions for which isomerization is predicted to precede dissociation., Published by American Institute of Physics, Melville, NY

Physical chemistry, chemical physics 24, 23096 - 23105 (2022). doi:10.1039/D2CP02252D special issue: "Ions, electrons, coincidences and dynamics: Festschrift for John H.D. Eland", We investigated the dissociation of dications and trications of three polycyclic aromatic hydrocarbons (PAHs), fluorene, phenanthrene, and pyrene. PAHs are a family of molecules ubiquitous in space and involved in much of the chemistry of the interstellar medium. Ions are formed by ionization with 30.3 nm extreme ultraviolet (XUV) photons, and their velocity map images are recorded using a PImMS multi-mass imaging sensor. Application of recoil-frame covariance analysis allows the total kinetic energy release (TKER) associated with multiple fragmentation channels to be determined to high precision. Experimental measurements are supported by Born-Oppenheimer molecular dynamics (BOMD) molecular dynamics simulations., Published by RSC Publ., Cambridge

Physical chemistry, chemical physics 24(37), 22699 - 22709 (2022). doi:10.1039/D2CP03029B, We present results from an experimental ion imaging study into the fragmentation dynamics of 1-iodopropane and 2-iodopropane following interaction with extreme ultraviolet intense femtosecond laser pulses with a photon energy of 95 eV. Using covariance imaging analysis, a range of observed fragmentation pathways of the resulting polycations can be isolated and interrogated in detail at relatively high ion count rates (∼12 ions shot$^{−1}$). By incorporating the recently developed native frames analysis approach into the three-dimensional covariance imaging procedure, contributions from three-body concerted and sequential fragmentation mechanisms can be isolated. The angular distribution of the fragment ions is much more complex than in previously reported studies for triatomic polycations, and differs substantially between the two isomeric species. With support of simple simulations of the dissociation channels of interest, detailed physical insights into the fragmentation dynamics are obtained, including how the initial dissociation step in a sequential mechanism influences rovibrational dynamics in the metastable intermediate ion and how signatures of this nuclear motion manifest in the measured signals., Published by RSC Publ., Cambridge

Correction for ‘Multi-mass velocity map imaging study of the 805 nm strong field ionization of CF3I’ by Stuart W. Crane et al., Phys. Chem. Chem. Phys., 2022, DOI: https://doi.org/10.1039/d2cp02449g.