Buday P, Kasahara C, Hofmeister E, Kowalczyk D, Farh MK, Riediger S, Schulz M, Wachtler M, Furukawa S, Saito M, Ziegenbalg D, Gräfe S, Bauerle P, Kupfer S, Dietzek-Ivansic B, Weigand W (2022)
Publication Type: Journal article
Publication year: 2022
Book Volume: 61
Article Number: e202202079
Journal Issue: 20
Inspired by the active center of the natural [FeFe] hydrogenases, we designed a compact and precious metal-free photosensitizer-catalyst dyad (PS-CAT) for photocatalytic hydrogen evolution under visible light irradiation. PS-CAT represents a prototype dyad comprising π-conjugated oligothiophenes as light absorbers. PS-CAT and its interaction with the sacrificial donor 1,3-dimethyl-2-phenylbenzimidazoline were studied by steady-state and time-resolved spectroscopy coupled with electrochemical techniques and visible light-driven photocatalytic investigations. Operando EPR spectroscopy revealed the formation of an active [FeIFe0] species—in accordance with theoretical calculations—presumably driving photocatalysis effectively (TON≈210).
APA:
Buday, P., Kasahara, C., Hofmeister, E., Kowalczyk, D., Farh, M.K., Riediger, S.,... Weigand, W. (2022). Activating a [FeFe] Hydrogenase Mimic for Hydrogen Evolution under Visible Light**. Angewandte Chemie International Edition, 61(20). https://doi.org/10.1002/anie.202202079
MLA:
Buday, Philipp, et al. "Activating a [FeFe] Hydrogenase Mimic for Hydrogen Evolution under Visible Light**." Angewandte Chemie International Edition 61.20 (2022).
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