Incorporation of silicon into heterocycles for polymethine dyes can impart red-shifts of up to 100 nm, while also enhancing photostability up to 10-fold, resulting in photostable fluorophores with emission above 900 nm.
Molecular photoswitches use light to interconvert from a thermodynamically stable isomer into a meta-stable isomer. Chemists and materials scientists have applied photoswitches in photopharmacology, catalysis, and molecular solar thermal (MOST) materials. Visible-light-absorbing photoswitches are attractive because the relatively low-energy light minimizes undesired photochemical reactions and enables biological applications.Designing ideal photoswitches requires long-lived metastable states; predicting their half-lives with theory is difficult because it requires locating transition structures. We now report the EZ-TS code, which automates the prediction of rate constants for the thermal Z → E isomerization. We leverage EZ-TS to automate the location of the favored transition structure and to comprehensively benchmark the performance of 140 model chemistries against the experimental rate constants of 11 azoarenes. We used 28 density functionals [local spin density approximation, generalized gradient approximation, meta-GGA, hybrid GGA, hybrid meta-GGA], and five basis sets [6-31G(d), 6-31+G(d,p), 6-311+G(d,p), cc-pvdz, and aug-cc-pvdz]. The hybrid GGA functionals performed the best of all tested functional classes. We demonstrate that the mean absolute errors of 14 model chemistries approach chemical accuracy, and mPWPW91/6-31+G (d,p) achieves chemical accuracy and should be used with EZ-TS. File list (2) download file view on ChemRxiv Azoarene thermal benchmarking -Final.pdf (1.39 MiB) download file view on ChemRxiv Azoarene benchmarking supporting information.pdf (466.14 KiB) Benchmarking of density functionals for Z-azoarene half-lives via automated transition state search
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