Zedler L, Müller C, Wintergerst P, Mengele AK, Rau S, Dietzek-Ivanšić B (2022)
Publication Type: Journal article
Publication year: 2022
Book Volume: 28
Article Number: e202200490
Journal Issue: 35
To optimize light-driven catalytic processes, light-mediated multi-electron transfer dynamics in molecular dyads need to be studied and correlated with structural changes focusing on the catalytically active metastable intermediates. Here, spectro-electrochemistry has been employed to investigate the structure-dependent photoelectron transfer kinetics in catalytically active intermediates of two Ru−Rh catalysts for light-driven NAD+ reduction. The excited-state reactivity of short-lived intermediates was studied along different photoreaction pathways by resonance Raman and time-resolved transient absorption spectro-electrochemistry with sub-picosecond time resolution under operando conditions. The results demonstrate, for the first time, how the bridging ligand serves as a (multi-)electron storage structure, mediates the strength of the electronic coupling of catalytic and photocenter and impacts the targeted electron transfer as well as parasitic electron-transfer kinetics.
APA:
Zedler, L., Müller, C., Wintergerst, P., Mengele, A.K., Rau, S., & Dietzek-Ivanšić, B. (2022). Influence of the Linker Chemistry on the Photoinduced Charge-Transfer Dynamics of Hetero-dinuclear Photocatalysts. Chemistry - A European Journal, 28(35). https://doi.org/10.1002/chem.202200490
MLA:
Zedler, Linda, et al. "Influence of the Linker Chemistry on the Photoinduced Charge-Transfer Dynamics of Hetero-dinuclear Photocatalysts." Chemistry - A European Journal 28.35 (2022).
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