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Photoinduced formation of peroxide ions on La2O3 and Nd2O3 under O2 was studied by in-situ microprobe Raman spectroscopy with attention focused on the effect of excitation wavelength and crystal structure on the O2(2-) formation. It was found that photoexcitations at 633, 532, 514, and 325 nm can induce O2(2-) formation over La2O3 at 450 °C. By contrast, photoexcitation at 785 nm does not cause formation of O2(2-) up to 500 °C. Photoexcitation at 325 nm can induce O2(2-) formation on cubic Nd2O3 at 25 °C, but cannot induce O2(2-) formation on hexagonal Nd2O3 up to 200 °C. The significant difference in the behavior of O2(2-) formation over the Nd2O3 samples of the two structures can be related to the difference in the capacity to adsorb O2. Since the number of oxygen vacancies in cubic Nd2O3 is larger than that in the hexagonal one, the former has a higher capacity than the latter to adsorb O2. As a result, cubic Nd2O3 is more favorable to the reaction of O2 with O(2-) to generate O2(2-). The structural similarity between cubic Nd2O3 and Nd2O2(O2) may be another factor in favor of peroxide formation.
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http://dx.doi.org/10.1002/asia.201500312 | DOI Listing |
Environ Res
August 2025
School of Resources and Environmental Engineering, Jiangsu University of Technology, Changzhou, Jiangsu, 213001, PR China.
MnOx-based materials have attracted significant attention for ozone decomposition due to their excellent catalytic activity. However, improving their stability and water resistance under humid conditions remains a major challenge. In this work, a K-doped ε-MnO catalyst was synthesized in situ using ozone as an oxidant.
View Article and Find Full Text PDFCell Mol Neurobiol
August 2025
Department of Biology, University of Ottawa, 30 Marie Curie Pvt., Ottawa, ON, K1N 6N5, Canada.
Deleterious perturbations in reactive oxygen species (ROS) and calcium (Ca) handling are key initiators of cell death in hypoxia-intolerant mammalian brain. Elevated cellular Ca can also inhibit ROS scavengers, exacerbating the deleterious impact of hypoxia on redox homeostasis. Conversely, such perturbations are typically absent in the brain of hypoxia-tolerant animals, including naked mole-rats (NMRs; Heterocephalus glaber), in which a remarkable ability to scavenge ROS has been observed in cardiac and skeletal muscle.
View Article and Find Full Text PDFInorg Chem
September 2025
Key Laboratory of Jiangxi Province for Environment and Energy Catalysis, School of Chemistry and Chemical Engineering, Nanchang University, Nanchang 330031, China.
At present, there are still controversy viewpoints on the reactive oxygen sites in the OCM reaction on ABO perovskites. Some researchers believe that electron-deficient chemisorbed oxygen species (O, O, and O) contribute to C product formation, and surface lattice oxygen (O) promotes the deep oxidation of methane, while others hold an opposite viewpoint. In addition, the influence of BO polyhedra on the reactive sites and reaction performance has rarely been elucidated.
View Article and Find Full Text PDFInorg Chem
September 2025
Beijing National Laboratory for Molecular Sciences (BNLMS), State Key Laboratory for Structural Chemistry of Unstable and Stable Species, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China.
Coumarin and its derivatives are common in biomolecules and function as pharmacophores in diverse medications. Here we studied the gas-phase reactions of coumarin with silver (Ag) and copper (Cu) using a compact tube reactor coupled to a custom reflection time-of-flight mass spectrometer (Re-TOFMS) featuring dual ionization sources of magnetron sputtering (MagS) and thermal evaporation (TVa). Interestingly, both Ag and Cu facilitated hydrogenated coumarin formation, yielding mono- and bis-coumarin complexes in varying ratios at different TVa temperatures.
View Article and Find Full Text PDFJACS Au
July 2025
LCC-CNRS, Université de Toulouse, CNRS, UPS, 205 route de Narbonne, BP44099, F-31077 cedex 4 Toulouse, France.
The bis-(borane) -{(CF)B}CF () reacts with dioxygen in the presence of decamethylferrocene (FeCp*, Cp* = pentamethylcyclopentadienyl) to deliver the salt [(μ-OH)-{B-(CF)}CF]-[FeCp*] () featuring a hydroxide sequestered by the two adjacent boron atoms. Mechanistic investigations of this formal 4-electron reduction of O suggest that it goes through the formation of a superoxide adduct [-O], which evolves through disproportionation into O and a peroxo-adduct [-O]. Upon coordination of another equivalent of , the thus-generated 4-fold boron-sequestered peroxide {[]-O} undergoes homolytic O-O bond cleavage to yield a pair of oxyl radicals [-O].
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