A5101997388- Sulfur-Based Synthesis Techniques
- Carbon Dioxide Capture Technologies
- Membrane Separation and Gas Transport
- Chemical Synthesis and Reactions
- Supercapacitor Materials and Fabrication
- Synthesis of heterocyclic compounds
- Advanced Combustion Engine Technologies
- Cyberloafing and Workplace Behavior
- Catalysis and Oxidation Reactions
- Copper-based nanomaterials and applications
- Catalytic Processes in Materials Science
- Combustion and flame dynamics
- Nanocluster Synthesis and Applications
- Synthesis and Reactivity of Sulfur-Containing Compounds
- Combustion and Detonation Processes
- Radical Photochemical Reactions
- Carbon dioxide utilization in catalysis
Changzhou University
2022-2024
Hebei University of Engineering
2023
A sustainable and green catalytic strategy for C‐S coupling reactions is developed by combining micelle transition metal. The synergistic AGA8@Cu(I) catalyst forms spontaneous anchoring of the in situ generated Cu(I) nanoclusters onto AGA8 micelles has been fully characterized FT‐IR, XPS, SEM, TEM, EDS, ICP‐OES. recyclable highly effective mediating conversion halides to disulfides water at room temperature with a broad substrate scope.
A sugar-based surfactant AGA8 was designed and demonstrated to promote the synthesis of disulfides thioamides in water.
Aryl sulfides play an important role in pharmaceuticals, biologically active molecules and polymeric materials. Herein, a general efficient protocol for Pd@COF-TB (a kind of Pd nanocatalyst supported by covalent organic framework)/DIPEA-catalyzed one-pot synthesis symmetrical diaryl through C-S coupling reaction from aryl iodides Na2S2O3 is developed. More importantly, the addition N,N-diisopropylethylamine (DIPEA) can not only enhance catalytic activity nanocatalyst, but also effectively...
A sustainable and green catalytic strategy for C-S coupling reactions is developed by combining micelle transition metal catalysis. The synergistic AGA8@Cu(I) catalyst forms spontaneous anchoring of the in-situ generated Cu(I) nanoclusters onto AGA8 micelles, has been fully characterized XPS, FT-IR, TEM. highly effective recyclable in mediating conversion halides to disulfides water at room temperature with a broad substrate scope.
ABSTRACT A methodology of using chloroacetylated polystyrene resin (PS‐COCH 2 ‐Cl) to initiate the ring‐opening polymerization oxazolines was established prepare highly amininated (PS) beads for CO adsorption. The structure resulting material fully characterized by FTIR, BET, TGA, and XPS, results suggested that chloroacetyl group more reactive in initiating than known chloromethyl groups, which eliminated use iodide salts are costly. could adsorb at an equilibrium adsorption capacity 3.15...