2018
DOI: 10.1007/s00214-018-2377-y
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Conical intersection properties unraveled by the position spread tensor

Abstract: We explore the application of the electron position spread tensor, i.e., a quantitative measure of the electron delocalization and mobility, to the conical intersection regions of three relevant compounds showing either photoisomerization or chemiluminescence properties. The electronic structure of the involved states has been solved using the complete active space self-consistent field method, and the position spread tensor has been computed at the same level of theory. In particular, we show that the total p… Show more

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Cited by 5 publications
(2 citation statements)
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“…All MEP calculations and CIX optimizations were obtained with the CASPT2//CASSCF methodology, in which the geometries were determined at the CASSCF level and then, the CASPT2 method was used on top of the CASSCF geometries to obtain high‐accuracy energies. The ANO‐L basis set contracted to C,N,O[4 s,3p,1d]/H,[2 s1p] i. e .…”
Section: Computational Detailsmentioning
confidence: 99%
“…All MEP calculations and CIX optimizations were obtained with the CASPT2//CASSCF methodology, in which the geometries were determined at the CASSCF level and then, the CASPT2 method was used on top of the CASSCF geometries to obtain high‐accuracy energies. The ANO‐L basis set contracted to C,N,O[4 s,3p,1d]/H,[2 s1p] i. e .…”
Section: Computational Detailsmentioning
confidence: 99%
“…A deep knowledge of the PES regions around CIs (since CIs themselves are rare to be encountered directly) is critical since nonadiabatic phenomena are ubiquitous in the photophysics and photochemistry of a broad set of photoactive molecules, encompassing biopolymer components and novel photovoltaic materials. Various spectroscopic techniques have emerged as powerful tools for monitoring electronic wave packet dynamics in proximity to nonadiabatic CI regions, including two-dimensional electronic–vibrational spectroscopy and femtosecond stimulated Raman spectroscopy. , These methods facilitate the correlation of electronic and nuclear degrees of freedom, especially during the initial stages of the photon absorption and subsequent nuclear rearrangement. Femtosecond stimulated Raman spectroscopy is a particularly favored method for studying vibrational coherence in molecular systems within nonadiabatic regions. Transient absorption spectroscopy represents another crucial tool for monitoring the vibrational wave packet dynamics in proximity to points or seams of PES degeneracy, as observed during singlet exciton fission and excited-state (ES) isomerization events. ,, In addition, the advent of attosecond spectroscopic techniques has paved the way for the mapping of wave packet bifurcation and the discernment of curve crossings. These advances have significantly expanded the exploration of a wide array of physical phenomena, spanning from the dynamics of large protein assemblies tumbling in the nanosecond domain to the ultrafast electron dynamics occurring on attosecond time scales.…”
Section: Introductionmentioning
confidence: 99%