Journal
CHEMICAL PHYSICS
Volume 576, Issue -, Pages -Publisher
ELSEVIER
DOI: 10.1016/j.chemphys.2023.112118
Keywords
Vibronic excitation; Vibrational relaxation; Nonequilibrium dynamics; Reaction intermediates; Femtosecond spectroscopy
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Understanding the ultrafast electron transfer (ET) processes involving various vibronic excitation in biological systems is challenging. This study investigated the excitation dependence of the photo-induced ET dynamics by selecting mutants in flavodoxin with different ET lifetimes. The results showed that increasing excitation energies resulted in higher vibrational excitation in products for the ultrafast ET processes, but no dependence was found for slower ET due to complete vibrational relaxation.
Understanding the ultrafast electron transfer (ET) processes involving various vibronic excitation in biological systems remains challenging and requires well-defined model proteins for in-depth studies. In this work, we selected three types of mutants with different ET lifetimes in flavodoxin to explore the excitation dependence of the photo-induced ET dynamics. For the ultrafast ET processes within the time window of intramolecular vibrational relaxation, with increasing excitation energies, we observed no change of ET lifetimes but with higher vibrational excitation in products, both of which can be attributed to the unique nature of ultrafast ET. For the slower ET, we did not find any dependence of product vibration excitation relative to the initial different excitation due to the complete vibrational relaxation. These results strongly indicate the vibrational energy can be propagated to the subsequent reactions during ultrafast ET processes.
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