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Anaerobic oxidation of methane (AOM) coupled electron acceptor reduction has been shown to regulate methane (CH) emissions from the habitats. Landfill is one of the most important anthropogenic CH emission sources. However, the effect of electron acceptors on the AOM process and its microbial mechanism in landfills is poorly characterized. Herein, electron acceptors including nitrate, nitrite, sulfate and ferric iron were used to regulate the AOM process in landfill microcosms by using stable isotope probing analysis. The addition of electron acceptors could promote AOM in the landfilled waste. Among them, nitrate and nitrite had the strongest promoting effect on AOM in the waste with the maximum activities of 5.60-5.76 μg g d, which increased by 1070.9%-1103.6% compared with the control without electron acceptor amendation. Candidatus Methylomirabilis was only detected in assimilating CH in the ferric iron-amended treatment. The proteobacterial methanotrophs and Methylacidiphilum were mainly observed in the ferric iron C-DNA, likely due to O released from the conversion of nitric oxide. Methanomassiliicoccus were the most abundant archaea in the treatments with nitrate, nitrite and sulfate, while Methanosarcina dominated in the ferric iron-amended treatment. Nitrate, nitrite, sulfate and ferric iron all could prompt the growth of sulfur, iron, nitrate and nitrite metabolizing microorganisms. Partial least squares path modeling indicated that AOM in the landfilled waste could be driven by electron acceptors via the changes of environmental variables, while the direct effect of electron acceptors on the AOM activity was weak with an intensity of 0.06. Taken together, this study demonstrated that the AOM process in landfills can be regulated by electron acceptors, especially nitrate and nitrite, to mitigate CH emissions from landfills.
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http://dx.doi.org/10.1016/j.envres.2025.121139 | DOI Listing |
mSystems
September 2025
Graduate School of Oceanography, University of Rhode Island, Narragansett, Rhode Island, USA.
Dinitrogen (N) fixation provides bioavailable nitrogen to the biosphere. However, in some habitats (e.g.
View Article and Find Full Text PDFChem Sci
August 2025
College of Chemistry and Materials Science, Key Laboratory of Chemical Biology of Hebei Province, Hebei Research Center of the Basic Discipline of Synthetic Chemistry, Institute of Life Science and Green Development Hebei University Baoding Hebei 071002 P. R. China
The photocatalytic oxidative dipolar [3 + 2] cycloaddition reaction is a promising green approach for producing pyrrolo[2,1-]isoquinolines. However, developing sustainable cycloaddition methods with heterogeneous photocatalysts is still in its infancy, largely owing to their low reactivity and photostability. Herein, we propose a charge-oxygen synergy strategy through a dual-engineered covalent organic framework (COF) by integrating π-spacers with donor-acceptor motifs to promote intermolecular cycloaddition.
View Article and Find Full Text PDFNatl Sci Rev
August 2025
Center for AIE Research, Shenzhen Key Laboratory of Polymer Science and Technology, Guangdong Provincial Key Laboratory of New Energy Materials Service Safety, College of Material Science and Engineering, Shenzhen University, Shenzhen 518060, China.
Multimodal phototheranostics has been recognized as one of the most momentous advances in cancer treatment. Of particular interest is a single molecular species simultaneously featuring in multiple imaging and synergistic phototherapies; the development of such a molecular species is nevertheless a formidably challenging task. Herein, we innovatively designed and synthesized three aggregation-induced emission (AIE)-active molecules with emission in the second near-infrared (NIR-II) window, by employing 10-indeno[1,2-][1,2,5]thiadiazolo[3,4-]quinoxalin-10-one as the electron acceptor, 4-(-butyl)--(4-(-butyl)phenyl)--phenylaniline as the electron donor, and different π-bridge moieties.
View Article and Find Full Text PDFOrg Lett
September 2025
College of Chemistry and Chemical Engineering and Luoyang Key Laboratory of Green Synthesis and Photofunctional Materials, Luoyang Normal University, Luoyang, Henan 471934, China.
Inspired by the excellent stereoinduction of palladium catalytic glycosylation with glycals via an inner-sphere pathway, a nickel-catalyzed, stereoselective -aryl glycosylation has been developed for glucals bearing a pentafluorobenzoate (PFB) group at the C3 position. The extremely electron-deficient nature of PFB not only endows stronger activity compared to the traditional leaving groups but also functions as an orientation group, presumably through the strong π-π interactions with the bipyridine ligand coordinated to the nickel center, thereby enabling the β-selective formation of a -aryl glycosidic bond with aryl iodides as glycosyl acceptors under mild conditions. This method features a broad substrate scope, high efficiency, and scalability, providing a general solution to the synthesis of challenging β--glycosides.
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September 2025
N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry SB RAS, Novosibirsk 630090, Russia.
While fluorene-containing materials are widely used in organic optoelectronics as bright emitters and hole semiconductors, their diazafluorene analogues have been poorly explored, though their nitrogen atoms could result in electron transport and bring sensory abilities. Here, we report the synthesis, characterization, and detailed study of a series of 4,5-diazafluorene-derivatives with different donor/acceptor substituents and organic semiconductors based on these molecules. The crystal structures of all the materials were solved by X-ray diffraction, indicating the presence of extensive π-stacking and anisotropic charge-transfer pathways.
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