Answers are grounded in this paper and cite their sources.
Computational simulations demonstrate quenching dynamics in solution, suggesting new modeling approaches for reactions.
A computational method to simulate bimolecular quenching reactions using coarse-grained reaction-diffusion dynamics is presented and applied to the quenching of molecular photosensitizers in solution. The simulations describe photoinduced reactions involving explicit excited states of light-harvesting species together with intrinsic deactivation, as well as collision quenching from separate quencher species. The simulation methodology is applied to time-resolved quenching of light-harvesting Fe(III) complexes in electron-donating solvents as a prototype system for reaction-diffusion dynamics of experimental interest over a wide range of quencher concentrations. The results show clear signatures for the transition from classical diffusion-limited Stern-Volmer dynamics to close-contact quencher-photosensitizer interactions at high quencher concentrations, and the simulations are used to elucidate physically realistic photosensitizer-quenching collision interaction parameters for photoinduced dynamics beyond the classical Stern-Volmer model. The simulation method provides the means to directly model and analyze system kinetics and dynamics beyond standard theoretical equations, opening up significant opportunities to simulate a broad range of reactions in solutions.
No takes yet. Share an insight, caveat, or question.
Liedtke et al. (2026) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: