In this Article, we show that the aromaticity of a molecule can be turned off by controlling the electron dynamics. We present a controlled switching from the aromatic ground state of benzene to two different nonaromatic states, using a laser pulse. The propagation of the molecular wave function is carried out with the time-dependent configuration interaction method. The laser pulse for switching between the ground and excited states is optimized using optimal control theory. Bond orders and Mulliken charges serve as an aromaticity criterion. The nonaromatic target states exhibit localized bonds and partial charges on the carbon atoms; these localized electrons circulate on an attosecond time scale in the ring system.
The coupling of a molecular ensemble to the confined electromagnetic modes of a microcavity can strongly modify the photophysics and photochemistry of the molecules upon photoexcitation. We investigate here how collective coupling effects lead to modifications of the mechanisms and rates of photochemical processes, in particular, photodissociation and nonradiative decay in NaI and pyrazine, respectively. We show that, after direct excitation into the lower polaritonic states, the lower-energy light-matter hybrid states, the dynamics of the molecular ensemble coupled to light is very similar to the dynamics of the corresponding isolated molecules. Conversely, excitation into the upper polaritonic states results in more complex dynamics that involve as a first step the population transfer toward the manifold of intermediate dark states. These dynamics differ substantially from those of the isolated molecules and may result in measurable time delays for nonradiative decay or excited-state reaction mechanisms. Similarly, we describe how addition of a buffer of nonreactive molecules coupled to the cavity mode can be used to delay the onset of the photochemical processes of the reactive part of the ensemble, where the buffer medium is more effective in inhibiting the reactive process than only reactive molecules in the cavity.
Herein we present the results of a blind challenge to quantum chemical methods in the calculation of dimerization preferences in the low temperature gas phase. The target of study was the first step of the microsolvation of furan, 2-methylfuran and 2,5-dimethylfuran with methanol. The dimers were investigated through IR spectroscopy of a supersonic jet expansion. From the measured bands, it was possible to identify a persistent hydrogen bonding OH–O motif in the predominant species. From the presence of another band, which can be attributed to an OH-π interaction, we were able to assert that the energy gap between the two types of dimers should be less than or close to 1 kJ/mol across the series. These values served as a first evaluation ruler for the 12 entries featured in the challenge. A tentative stricter evaluation of the challenge results is also carried out, combining theoretical and experimental results in order to define a smaller error bar. The process was carried out in a double-blind fashion, with both theory and experimental groups unaware of the results on the other side, with the exception of the 2,5-dimethylfuran system which was featured in an earlier publication.
This paper was selected as Featured ARTICLES YOU MAY BE INTERESTED INProbabilistic performance estimators for computational chemistry methods: Systematic improvement probability and ranking probability matrix. I. Theory
The radiative and nonradiative relaxation dynamics of an ensemble of molecules in a microcavity are investigated with emphasis on the impact of the cavity lifetime on reactive and spectroscopic properties. We show that the dynamics of the ensemble and of single molecules are influenced by the presence of a cavity resonance as long as the polariton splitting can be resolved spectroscopically, which critically depends on the lifetime of the system. Our simulations illustrate how the branching between nonradiative intersystem crossing and radiative decay through the cavity can be tuned by selecting specific cavity photon energies resonant at specific molecular geometries. In the case of cavity-photon energies that are not resonant at the Franck-Condon geometry of the molecules, it is demonstrated numerically and analytically that collective effects are limited to a handful of molecules in the ensemble. File list (3) download file view on ChemRxiv main.pdf (3.69 MiB) download file view on ChemRxiv Ulusoy_Vendrell_SI.pdf (0.90 MiB) download file view on ChemRxiv WF_propagation_LP_med_fast.mp4 (545.97 KiB) Dynamics in a lossy microcavity Dynamics and spectroscopy of molecular ensembles in a lossy microcavity
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