Coordination Chemistry Reviews, Journal Year: 2021, Volume and Issue: 442, P. 213996 - 213996
Published: May 13, 2021
Language: Английский
Coordination Chemistry Reviews, Journal Year: 2021, Volume and Issue: 442, P. 213996 - 213996
Published: May 13, 2021
Language: Английский
Nature Catalysis, Journal Year: 2023, Volume and Issue: 6(6), P. 464 - 475
Published: May 18, 2023
Language: Английский
Citations
56Journal of the American Chemical Society, Journal Year: 2024, Volume and Issue: 146(23), P. 16229 - 16236
Published: May 30, 2024
Employing covalent organic frameworks (COFs) for the photocatalytic CO2 reduction reaction (CDRR) to generate high-value chemical fuels and mitigate greenhouse gas emissions represents a sustainable catalytic conversion approach. However, achieving superior CDRR performance is hindered by challenges of low charge separation efficiency, poor stability, high preparation costs associated with COFs. Herein, in this work, we utilized perfluorinated metallophthalocyanine (MPcF16) biomolecule compound ellagic acid (EA) as building blocks actualize functional named EPM-COF (M = Co, Ni, Cu). The designed EPCo-COF, featuring cobalt metal active sites, demonstrated an impressive CO production rate selectivity (CDRR). Moreover, following alkaline treatment (EPCo-COF-AT), COF exposed carboxylic anion (COO–) hydroxyl group (OH), thereby enhancing electron-donating capability EA. This modification achieved heightened 17.7 mmol g–1 h–1 outstanding 97.8% efficient CDRR. Theoretical calculations further illustrated that EPCo-COF-AT functionalized COO– OH can effectively alleviate energy barriers involved process, which facilitates proton-coupled electron transfer processes enhances on sites within EPCo-COF-AT.
Language: Английский
Citations
38Journal of the American Chemical Society, Journal Year: 2024, Volume and Issue: 146(15), P. 10550 - 10558
Published: April 8, 2024
Implementing the synergistic effects between metal and ligand has successfully streamlined energetics for CO2 activation gained high catalytic activities, establishing important breakthroughs in photocatalytic reduction. Herein, we describe a Ni(II) N-confused porphyrin complex (NiNCP) featuring an acidic N–H group. It is readily deprotonated exists anion form during catalysis. Owing to this functional site, NiNCP gave rise outstanding turnover number (TON) as 217,000 with 98% selectivity reduction CO, while parent (NiTPP) was found be nearly inactive. Our mechanistic analysis revealed nonclassical reaction pattern where effectively activated via attack of Lewis-basic ligand. The resulting ligand-bound adduct could further reduced produce CO. This new metal–ligand effect anticipated inspire design highly active catalysts small molecule activations.
Language: Английский
Citations
22Nature Catalysis, Journal Year: 2025, Volume and Issue: unknown
Published: Feb. 7, 2025
Language: Английский
Citations
4Coordination Chemistry Reviews, Journal Year: 2021, Volume and Issue: 442, P. 213996 - 213996
Published: May 13, 2021
Language: Английский
Citations
90