A5043667682- Catalysis and Oxidation Reactions
- Catalysis and Hydrodesulfurization Studies
- Nanomaterials for catalytic reactions
- Quantum Dots Synthesis And Properties
- Catalysis for Biomass Conversion
- Catalytic Processes in Materials Science
- Chemical Synthesis and Reactions
- Sulfur-Based Synthesis Techniques
- Radical Photochemical Reactions
- Oxidative Organic Chemistry Reactions
- Metal-Organic Frameworks: Synthesis and Applications
- Advanced Nanomaterials in Catalysis
- Catalytic C–H Functionalization Methods
University of Colorado Boulder
2024
Imperial College London
2024
Leibniz-Institute for New Materials
2024
National Science and Technology Development Agency
2023-2024
National Nanotechnology Center
2023-2024
Environmental Energy & Engineering
2024
National Renewable Energy Laboratory
2024
The University of Adelaide
2024
The University of Melbourne
2019
Catalytic partial oxidation of methane presents a promising route to convert the abundant but environmentally undesired gas liquid methanol with applications as an energy carrier and platform chemical. However, outstanding challenge for this process remains in developing catalyst that can oxidize selectively good activity under continuous flow conditions phase using O2 oxidant. Here, we report Fe supported by metal-organic framework (MOF), Fe/UiO-66, selective on-stream methanol. Kinetic...
Active surface oxygen and hydroxyl groups play a decisive role in catalyzing the oxidation of 5-hydroxymethylfurfural (HMF) to 2,5-furandicarboxylic acid (FDCA) over β-MnO 2 .
Abstract The catalytic oxidation of 5‐hydroxymethylfurfural (HMF) is an important process for producing a renewable furan‐2,5‐dicarboxylic acid (FDCA). Although several Pt‐based catalysts have been reported to efficiently catalyze the HMF, functional roles catalyst supports, as corroborated by spectroscopic techniques, not fully described. Here, we report on Pt nanoparticles supported metal‐organic frameworks (MOFs) that HMF FDCA in absence base. Several are prepared immobilizing...
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A methodology for a radical Pictet–Spengler reaction promoted by visible light photoredox catalysis is described. This strategy furnishes tetrahydroisoquinoline derivatives bearing electron poor and rich substituents. The proceeds at room temperature with excellent regioselectivity the 6-endo intramolecular cyclisation. approach provides complementary method synthesis of scaffold substitution patterns inaccessible via established thermal transformations.