A5100326442- Supercapacitor Materials and Fabrication
- Advancements in Battery Materials
- Advanced battery technologies research
- Covalent Organic Framework Applications
- Metal-Organic Frameworks: Synthesis and Applications
- Asymmetric Hydrogenation and Catalysis
- Conducting polymers and applications
- Catalytic C–H Functionalization Methods
- Electrocatalysts for Energy Conversion
- Graphene research and applications
- Catalytic Cross-Coupling Reactions
- Layered Double Hydroxides Synthesis and Applications
- Advanced Sensor and Energy Harvesting Materials
- Catalytic Processes in Materials Science
- Nanomaterials for catalytic reactions
- Magnetism in coordination complexes
- Carbon Nanotubes in Composites
- Radical Photochemical Reactions
- Asymmetric Synthesis and Catalysis
- Polymer composites and self-healing
- Carbon dioxide utilization in catalysis
- Surface Chemistry and Catalysis
- Cyclopropane Reaction Mechanisms
- Electrospun Nanofibers in Biomedical Applications
- MXene and MAX Phase Materials
Wuhan Third Hospital
2025
Tongren Hospital
2025
Huanggang Normal University
2018-2024
Institute of New Materials
2017-2024
State Key Laboratory of High Performance Civil Engineering Materials
2017-2024
Nanjing University
2017-2024
Collaborative Innovation Center of Advanced Microstructures
2024
Xi'an Polytechnic University
2024
Central China Normal University
2020-2023
Hubei University
2023
We report a new nonwrapping approach to noncovalent engineering of carbon nanotube surfaces by short, rigid functional conjugated polymers, poly(aryleneethynylene)s. Our technique not only enables the dissolution various types nanotubes in organic solvents, which represents first example solubilization via π-stacking without polymer wrapping, but could also introduce numerous neutral and ionic groups onto surfaces.
Single-atom catalysts have emerged as a new frontier in catalysis science. However, their applications are still limited to small molecule activations the gas phase, classic organic transformations catalyzed by single-atom rare. Here, we report use of Pd catalyst for Suzuki-Miyaura carbon-carbon coupling reaction under phosphine-free and open-air conditions at room temperature. The is prepared through anchoring on bimetal oxides (Pd-ZnO-ZrO2). significant synergetic effect ZnO ZrO2 observed....
Direct condensation of β-arylketones with acetamide afforded both Z and E enamides. The Z-configured substrates underwent hydrogenation excellent enantioselectivity by using the Rh/tangphos catalytic system (see scheme; tangphos=1,1′-di-tert-butyl-[2,2′]-diphospholanyl). product β-arylisopropylamines are important precursors to several drugs.
A novel tetraoxolene-bridged Fe two-dimensional honeycomb layered compound, (NPr4 )2 [Fe2 (Cl2 An)3 ] ⋅2 (acetone)⋅H2 O (1), where Cl2 Ann- =2,5-dichloro-3,6-dihydroxy-1,4-benzoquinonate and NPr4+ =tetrapropylammonium cation, has been synthesized. 1 revealed a thermally induced valence tautomeric transition at T1/2 =236 K (cooling)/237 (heating) between Fem+ (m=2 or 3) (n=2 that modulations [FeIIHS FeIIIHS An2- An.3- )]2- T>T1/2 [FeIIIHS )(Cl2 ]2- T<T1/2 . Even in network structure, the...
Purpose: Locked nucleic acid (LNA)-modified anti-microRNAs have been demonstrated to target mesenchymal stem cells (MSCs) treat bone diseases. However, the "off-target" effect limits its clinical application. Methods: We selected specific aptamer M4 of MSCs and employed three-way junction (3WJ) as core scaffold construct nanoparticles (3WJ-M4-LNA) for delivery anti-miRNA 138. Results: Our results suggested that 3WJ-M4-LNA nanoparticles, not 3WJ-M4 or 3WJ-LNA, can specifically deliver MSCs,...
It is demonstrated that toxic pollutants such as phenols in industrial wastewaters can be eliminated efficiently by photochemical methods using a combination of UV and heterogeneous photocatalyst, combinations UV, H2O2, ferric compounds. The photocatalyst even decreases the COD some wastewater around 60–70% 1–4 hour treatment time depending on source wastewater. different (200 W high pressure mercury lamp, wavelength 313 ≤ λ 456 nm), magnetite or aluminium oxide (as photocatalyst), H2O2 iron...
[reaction: see text] Ruthenium porphyrins catalyze three-component coupling reaction of alpha-diazo esters with a series N-benzylidene imines and alkenes to form functionalized pyrrolidines in excellent diastereoselectivities. The proceeds via reactive ruthenium-carbene intermediate its subsequent imine generate azomethine ylide, which reacts 1,3-diploar cycloaddition.