Hydroxyl-Decorated Diiron Complex as a [FeFe]-Hydrogenase Active Site Model Complex: Light-Driven Photocatalytic Activity and Heterogenization on Ethylene-Bridged Periodic Mesoporous Organosilica
نویسندگان
چکیده
A biomimetic model complex of the [FeFe]-hydrogenase active site (FeFeOH) with an ethylene bridge and a pendant hydroxyl group has been synthesized, characterized evaluated as catalyst for light-driven hydrogen production. The interaction present in 3-isocyanopropyltriethoxysilane provided carbamate triethoxysilane bearing diiron dithiolate (NCOFeFe), thus becoming potentially promising candidate anchoring on heterogeneous supports. As proof concept, NCOFeFe precursor was anchored by grafting procedure into periodic mesoporous organosilica ethane bridges (EthanePMO@NCOFeFe). Both molecular heterogenized complexes were tested catalysts generation aqueous solutions. photocatalytic conditions optimized homogenous varying reaction time, pH, amount or photosensitizer, photon flux, type light source (light-emitting diode (LED) Xe lamp). It shown that FeFeOH achieved decent turnover number (TON) 70 after 6 h, while EthanePMO@NCOFeFe had slightly lower activities showing TONs 37 5 at respectively.
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ژورنال
عنوان ژورنال: Catalysts
سال: 2022
ISSN: ['2073-4344']
DOI: https://doi.org/10.3390/catal12030254