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Photoinduced radical sulfur dioxide insertion with asymmetric cyclization of alkenes:accessingβ-chiral sulfones bearing S-stereocentric cyclic sulfinamides

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Science china chemistry 2025年第1期68卷 257-263页

作者： Jiapian Huang chenxin wang Xu wang Xiaoyu Zhou Wei Xiao Jie Wu School of Pharmaceutical and chemical Engineering&Institute for Advanced Studies Taizhou UniversityTaizhou 318000China State Key Laboratory of Organometallic chemistry Shanghai Institute of Organic ChemistryChinese Academy of SciencesShanghai 200032China School of chemistry and chemical Engineering Henan Normal UniversityXinxiang 453007China

The generation of variousβ-chiral sulfones bearing chiral cyclic sulfinamides through photoredox-catalyzed sulfur dioxide insertion with asymmetric radical cyclization is *** method features a broad substrate scope and excellent *** studies reveal that the dispersion interaction between sulfinyl group and ch_(2)SO_(2)Ph group plays a crucial role in the stereoselectivity control.

关键词： β-chiral sulfones chiral cyclic sulfinamides sulfur dioxide insertion asymmetric radical cyclization stereoselectivity

Co-loading Pd and CeO_(2)on Silicalite-1 as High-performance Catalyst for Methane Dry Reforming Reaction

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chemical Research in chinese Universities 2025年第1期41卷 15-20页

作者： XU Jing ZHANG Rui wang Ke wang Xiao SONG Shuyan ZHANG Hongjie State Key Laboratory of Rare Earth Resource Utilization Changchun Institute of Applied ChemistryChinese Academy of SciencesChangchun130022P.R.China School of Applied chemistry and Engineering University of Science and Technology of ChinaHefei230026P.R.China Department of chemistry Tsinghua UniversityBeijing100084P.R.China

The methane dry reforming(DRM)reaction can convert CO_(2)and ch_(4),both of which contribute to climate change,into syngas,which holds great significance in mitigating specific environmental issues stemming from the greenhouse ***,the challenges that persist include the substantial energy consumption and the catalyst’s susceptibility to deactivation,both of which necessitate ***,we developed a catalyst,PdCe/S1,featuring small-sized Pd species and CeO_(2)stabilized on pure silicon zeolite(silicalite-1),which is employed in the DRM *** can achieve 97%ch_(4)conversion and 98%CO_(2)conversion at 750℃,surpassing binary Pd/CeO_(2)and Pd/S1 *** small size of CeO_(2)stabilized by silicalite-1 promotes oxygen defects formation and enhances the CO_(2)adsorption *** introduction of silicalite-1 further enhances the interaction between Pd and CeO_(2),boosting DRM performance.

关键词： Dry reforming of methane CeO_(2) Zeolite

Human neural stem cell-derived extracellular vesicles protect against ischemic stroke by activating the PI3K/AKT/mTOR pathway

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Neural Regeneration Research 2025年第11期20卷 3245-3258页

作者： Jiayi wang Mengke Zhao Dong Fu Meina wang chao Han Zhongyue Lv Liang wang Jing Liu Stem Cell Clinical Research Center The First Affiliated Hospital of Dalian Medical UniversityDalianLiaoning ProvinceChina Dalian Innovation Institute of Stem Cell and Precision Medicine DalianLiaoning ProvinceChina Institute(College)of Integrative Medicine Dalian Medical UniversityDalianLiaoning ProvinceChina

Human neural stem cell-derived extracellular vesicles exhibit analogous functions to their parental cells,and can thus be used as substitutes for stem cells in stem cell therapy,thereby mitigating the risks of stem cell therapy and advancing the frontiers of stem cell-derived *** lays a foundation for the development of potentially potent new treatment modalities for ischemic ***,the precise mechanisms underlying the efficacy and safety of human neural stem cell-derived extracellular vesicles remain unclear,presenting challenges for clinical *** promote the translation of therapy based on human neural stem cell-derived extracellular vesicles from the bench to the bedside,we conducted a comprehensive preclinical study to evaluate the efficacy and safety of human neural stem cell-derived extracellular vesicles in the treatment of ischemic *** found that administration of human neural stem cell-derived extracellular vesicles to an ischemic stroke rat model reduced the volume of cerebral infarction and promoted functional recovery by alleviating neuronal *** human neural stem cell-derived extracellular vesicles reduced neuronal apoptosis by enhancing phosphorylation of phosphoinositide 3-kinase,mammalian target of rapamycin,and protein kinase B,and these effects were reversed by treatment with a phosphoinositide 3-kinase *** findings suggest that human neural stem cell-derived extracellular vesicles play a neuroprotective role in ischemic stroke through activation of phosphoinositide 3-kinase/protein kinase B/mammalian target of rapamycin signaling ***,we showed that human neural stem cell-derived extracellular vesicles have a good in vivo safety ***,human neural stem cell-derived extracellular vesicles are a promising potential agent for the treatment of ischemic stroke.

关键词： behavior exosome extracellular vesicles ischemic stroke mammalian target of rapamycin(mTOR) middle cerebral artery occlusion neural stem cells neuronal apoptosis phosphoinositide 3-kinase(PI3K) protein kinase B(AKT)

An integrated photocatalytic redox architecture for simultaneous overall conversion of CO_(2)and H_(2)O toward ch_(4)and H_(2)O_(2)

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Science Bulletin 2025年第3期70卷 373-382页

作者： Muhammad Salman Nasir Bowen Sheng Ying Zhao Haotian Ye Jun Song Jinglin Li Ping wang Tao wang Xinqiang wang Zhen Huang Baowen Zhou Key Laboratory for Power Machinery and Engineering of Ministry of Education Research Center for Renewable Synthetic FuelSchool of Mechanical EngineeringShanghai Jiao Tong UniversityShanghai 200240China State Key Laboratory of Artificial Microstructure and Mesoscopic Physics School of PhysicsNano-Optoelectronics Frontier Center of Ministry of Education(NFC-MOE)Peking UniversityBeijing 100871China Department of Mining and Materials Engineering McGill UniversityMontrealH3A 0G4Canada Electron Microscopy Laboratory School of PhysicsPeking UniversityBeijing 100871China Peking University Yangtze Delta Institute of Optoelectronics Nantong 226010China Collaborative Innovation Center of Quantum Matter School of PhysicsPeking UniversityBeijing 100871China

Solar-driven overall conversion of CO_(2)and H_(2)O into fuels and chemicals shows an ultimate strategy for carbon neutrality yet remains a huge ***,an integrated photocatalytic redox architecture of Zn NPs/GaN Nanowires(NWs)/Si is explored for light-driven overall conversion of CO_(2)and H_(2)O into ch_(4)and H_(2)O_(2)simultaneously without any external sacrificial agents and *** as-designed architecture affords a benchmark ch_(4)activity of 189 mmol gcat^(-1)h^(-1)with a high selectivity of 93.6%,in the synchronized formation of H_(2)O_(2)at a considerable rate of 25 m g^(-1)h^(-1).Moreover,a considerable turnover number of 27,280 mol ch_(4)per mol Zn was achieved over a long-term operation of 80 *** operando spectroscopic characterizations,isotope experiments,and density functional theory calculations,it is unraveled that Zn sites are synergetic with GaN to drive CO_(2)-to-ch_(4)conversion with a lowered energy barrier of 0.27 eV while inhibiting hydrogen evolution reaction with a relatively high energy barrier of 0.93 ***,owing to the unique surface properties of GaN,water is split into*OH and*H,followed by the formation of H_(2)O_(2)because of the alleviated adsorption strength of*OH by Zn ***,the hierarchical architecture enables the achievement of high activity and high selectivity of ch_(4)from CO_(2)reduction in distilled water along with the generation of H_(2)O_(2).This work provides an integrated photocatalytic redox architecture for the synchronized production of ch_(4)and H_(2)O_(2)with the only inputs of CO_(2),distilled water,and light.

关键词： Zn nanoparticles GaN nanowires/Si Integrated redox architecture Artificial photosynthesis ch_(4)and H_(2)0_(2)

Merging polymers of intrinsic microporosity and porous carbon-based zinc oxide composites in novel mixed matrix membranes for efficient gas separation

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Green Energy & Environment 2025年第1期10卷 203-213页

作者： Muning chen Jiemei Zhou Jing Ma Weigang Zheng Guanying Dong Xin Li Zhihong Tian Yatao Zhang Jing wang Yong wang School of chemical Engineering Zhengzhou UniversityZhengzhou450001HenanChina State Key Laboratory of Materials-Oriented chemical Engineering and College of chemical Engineering Nanjing Tech UniversityNanjing211816JiangsuChina Singapore Membrane Technology Centre Nanyang Environment and Water Research InstituteNanyang Technological UniversitySingapore637141Singapore Engineering Research Center for Nanomaterials Henan UniversityKaifeng475004HenanChina State Key Laboratory of Coking Coal Resources Green Exploitation Zhengzhou UniversityZhengzhou 450001China School of Energy and Environment Southeast UniversityNanjing210096JiangsuChina

Mixed matrix membranes(MMMs)have demonstrated significant promise in energy-intensive gas separations by amalgamating the unique properties of fillers with the facile processability of ***,achieving a simultaneous enhancement of permeability and selectivity remains a formidable challenge,due to the difficulty of achieving an optimal match between polymers and *** this study,we incorporate a porous carbon-based zinc oxide composite(C@ZnO)into high-permeability polymers of intrinsic microporosity(PIMs)to fabricate *** dipole–dipole interaction between C@ZnO and PIMs ensures their exceptional compatibility,mitigating the formation of non-selective voids in the resulting ***,C@ZnO with abundant interconnected pores can provide additional low-resistance pathways for gas transport in *** a result,the CO_(2) permeability of the optimized C@ZnO/PIM-1 MMMs is elevated to 13,215 barrer,while the CO_(2)/N_(2) and CO_(2)/ch_(4) selectivity reached 21.5 and 14.4,respectively,substantially surpassing the 2008 Robeson upper ***,molecular simulation results further corroborate that the augmented membrane gas selectivity is attributed to the superior CO_(2) affinity of C@*** summary,we believe that this work not only expands the application of MMMs for gas separation but also heralds a paradigm shift in the application of porous carbon materials.

关键词： Mixed matrix membranes Polymers of intrinsic microporosity CO_(2)separation Porous carbon materials

Thermal effects on wear behavior of additively manufactured NiTi shape memory alloys

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chinese Journal of Aeronautics 2025年第1期38卷 147-164页

作者： Xianghui HUANG Nan KANG Pei wang Mohamed EL MANSORI Arts et Metiers Institute of Technology MSMPHESAM UniversitéChâlons-en-Champagne 51006France Henan Key Laboratory of High-Performance Carbon Fiber Reinforced Composites Institute of Carbon Matrix CompositesHenan Academy of SciencesZhengzhou 450046China Texas A&M Engineering Experiment Station Institute for Manufacturing SystemsCollege StationTX 77843USA

NiTi alloys fabricated by laser powder bed fusion(LPBF)additive manufacturing technology not only address the compositional instability resulting from complex processes but also solve the challenges of difficult machining of intricate aerospace ***,there are very few reports on the wear behavior of LPBF-NiTi *** the present work,the effects of microstructure and thermal treatment,including heat treatment and frictional heat,on the wear behavior of LPBF-NiTi alloy and 100Cr6 ball were analyzed through a series of tribological experiments with different sliding *** the average sliding speed increases(0.079–0.216 m/s),the wear rate of the as-built and heat-treated samples tends to decrease in the range of 2.69×10^(-3)–0.97×10^(-3)mm^(3)/*** the heat-treated LPBF-NiTi alloy is 46%harder than the as-built alloy is,the latter has a higher toughness(505 MJ/m^(3))and greater transformation strain of SIM(0.097).This leads to a coupling effect of heat treatment and sliding speed on the wear *** addition,the wear track morphologies under different sliding speeds are asymmetric due to the 24% greater acceleration at the far end from the motor and the 2.15 mm deviation between the maximum speed position and the geometric center of the *** wear modes of the as-built and heat-treated samples included adhesive,abrasive and delamination ***,the wear morphologies and dominant wear modes change with the frictionally caused heat release induced by the sliding speed.

关键词： Additive manufacturing Laser powder bed fusion NiTi alloys Wear resistance Sliding speed

Discovery of a new family member of arsenic–vanadium polyoxometalates with high catalytic performance for one-pot coupling of CO2, epoxides and amines

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Tungsten 2025年第1期7卷 80-87页

作者： Fang-Qian wang Yin Zhang Wei-Wei wang Mei-Qian Fu Hong-Bing Mo Wei-Dong Yu chao Liu Jun Yan College of chemistry and chemical Engineering Central South University Junior Education Department Changsha Normal University School of Science Hunan University of Technology and Business

Arsenic-vanadium polyoxometalates（POMs） represent a family of tremendous potential catalysts owing to their peculiar physical and chemical *** in CO2conversion,using POMs to catalyze the conversion of CO2and epoxide into chemical intermediates is the research ***,A new family number of arsenic-vanadium POMs,[N（ch3）4]4[As8V12O38（H2O）]·2H2O({As8V12O38}),was reported and characterized by single-crystal X-ray diffraction,fourier transform infrared spectroscopy,X-ray photoelectron spectroscopy,*** from other allotropicity,{As8V12O38}shows a different structure pattern with an I-43d *** obtained {As8V12O38} was employed as a catalyst for the *** initial catalytic reaction confirmed that {As8V12O38} can catalyze the formation of epoxy carbonate by using 1.01 kPa CO2and epoxide at 70℃.Furtherly,when added amine in the catalytic system,oxazolidinone could be obtained by high yields,which provides an efficient way to convert CO2into profitable ***,a possible catalytic reaction mechanism was proposed by using different characterization analyses.{As8V12O38} first catalyzes the epoxide and CO2to form an epoxy carbonate and then catalyzes epoxy carbonate and benzylamine into oxazolidinone.

关键词： Arsenic CO2 conversion Oxazolidinone Polyoxometalates Vanadium

Encapsulating perovskite quantum dots into 3D COF for visible light-driven CO2 reduction

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Science china chemistry 2025年

作者： Xinxin wang Yucheng Jin Xiya Yang Qingyu Luan Tianyu wang Dongdong Qi Kang wang Jianzhuang Jiang College of chemistry and Materials Science Anhui Normal University Beijing Advanced Innovation Center for Materials Genome Engineering Beijing Key Laboratory for Science and Application of Functional Molecular and Crystalline Materials Department of Chemistry and Chemical Engineering School of Chemistry and Biological EngineeringUniversity of Science and Technology Beijing

Lead halide perovskite quantum dots（LHP QDs） have been revealed to possess great potential in photocatalytic applications including CO2reduction, which however suffer from poor stability. Herein, a high crystalline hydrazine-linked three-dimensional（3D） covalent organic framework, USTB-17, was fabricated from the reaction between 12-connected building block and 4-connected 3,5,7-tetrakis（4-aldophenyl）-adamantane. Post-modification with Ni2+affords the metallic framework USTB-17（Ni）followed by sequential deposition of the ch3NH2PbI3（MAPbI3） perovskite QDs into its pores, generating the USTB-17（Ni）@MAPbI3composite. Powder X-ray diffraction analysis together with theoretical simulations and transmission electron microscopy discloses the crystalline nature of USTB-17, USTB-17（Ni）, and USTB-17（Ni）@MAPbI3with an unprecedented noninterpenetrated hpt topology. The close contact of QDs inside the COF pores with the Ni catalytic site locating at the pore surface of COF allows a rapid transfer of the photogenerated electrons in QDs to the Ni catalytic sites, enhancing the photocatalytic activity for CO2reduction. This endows USTB-17（Ni）@MAPbI3with efficient photocatalysis performance for photocatalytic CO2reduction with CO generation rate of 365 μmol g-1h-1and CO selectivity up to 96% under visible-light irradiation, 7 times higher than that of USTB-17（Ni）. After four cycles of reactions, the photocatalytic CO generation rate remains almost unchanged, demonstrating its excellent cycle stability.

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Electrochemical conversion of methane to bridge the gap in the artificial carbon cycle

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Journal of Energy chemistry 2025年第1期100卷 286-308页

作者： Yuhao Peng Yuefeng Song Ihar Razanau Juanxiu Xiao Wei Xiao Di Hu Guoxiong wang College of chemistry and Molecular Sciences Hubei Key Laboratory of Electrochemical Power SourcesWuhan UniversityWuhan 430072HubeiChina State Key Laboratory of Catalysis Dalian National Laboratory for Clean EnergyiChEM(Collaborative Innovation Center of Chemistry for Energy Materials)Dalian Institute of Chemical PhysicsChinese Academy of SciencesDalian 116023LiaoningChina Laboratory of Physical-chemical Technologies SSPA Scientific and Practical Materials Research Centre of NAS of BelarusMinsk 220072Belarus State Key Laboratory of Marine Resources Utilization in South china Sea Collaborative Innovation Center of Marine Science and TechnologySchool of Marine Science and EngineeringHainan UniversityHaikou 570228HainanChina Department of chemical and Environmental Engineering University of Nottingham Ningbo ChinaNingbo 315100ZhejiangChina

Methane, an abundant one-carbon(C_(1)) resource, is extensively used in the industrial production of vital fuels and value-added chemicals. However, current industrial methane conversion technologies are energy-and carbon-intensive, mainly due to the high activation energy required to break the inert C–H bond, low selectivity, and problematic side reactions, including CO_(2)emissions and coke deposition. Electrochemical conversion of methane(ECM) using intermittent renewable energy offers an attractive solution, due to its modular reactor design and operational flexibility across a broad spectrum of temperatures and pressures. This review emphasizes conversion pathways of methane in various reaction systems, highlighting the significance and advantages of ECM in facilitating a sustainable artificial carbon cycle. This work provides a comprehensive overview of conventional methane activation mechanisms and delineates the complete pathways of methane conversion in electrolysis contexts. Based on surface/interface chemistry, this work systematically analyzes proposed reaction pathways and corresponding strategies to enhance ECM efficiency towards various target products, including syngas, hydrocarbons, oxygenates, and advanced carbon materials. The discussion also encompasses opportunities and challenges for the ECM process, including insights into ECM pathways, rational electrocatalyst design, establishment of benchmarking protocols, electrolyte engineering, enhancement of ch4conversion rates, and minimization of CO_(2)emission.

关键词： Methane Electrochemical conversion Reaction mechanism Catalyst design Electrode Electrocatalysis