Bifunctional chiral urea-containing quaternary ammonium salts can be straightforwardly synthesised in good yield and with high structural diversity a scalable and operationally simple highly telescoped sequence starting from -1,2-cyclohexanediamine. These novel hybrid catalysts were systematically investigated for their potential to control glycine Schiff bases in asymmetric addition reactions. It was found that Michael addition reactions and the herein presented aldol-initiated cascade reaction can be carried out to provide enantiomeric ratios up to 95 : 5 and good yields under mild conditions at room temperature.
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http://dx.doi.org/10.1039/C5RA14466C | DOI Listing |
Acc Chem Res
January 2025
State Key Laboratory of Physical Chemistry of Solid Surfaces, Key Laboratory of Chemical Biology of Fujian Province, College of Chemistry and Chemical Engineering, and Discipline of Intelligent Instrument and Equipment, Xiamen University, Xiamen 361005, P. R. China.
ConspectusMolecular photoelectrocatalysis, which combines the merits of photocatalysis and organic electrosynthesis, including their green attributes and capacity to offer novel reactivity and selectivity, represents an emerging field in organic chemistry that addresses the growing demands for environmental sustainability and synthetic efficiency. This synergistic approach permits access to a wider range of redox potentials, facilitates redox transformations under gentler electrode potentials, and decreases the use of external harsh redox reagents. Despite these potential advantages, this area did not receive significant attention until 2019, when we and others reported the first examples of modern molecular photoelectrocatalysis.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
Department of Civil and Environmental Engineering, Hanyang University, 222 Wangsimni-ro, Seongdong-Gu, Seoul 04763, Republic of Korea.
In this research, S-scheme heterojunction photocatalysts are prepared through the hybridization of nitrogen-rich g-CN with TiO (coded as TCN-(): as the weight ratio of TiO:g-CN). The photocatalytic potential of TCN-() is evaluated against benzene (1-5 ppm) across varying humidity levels using a dynamic flow packed-bed photocatalytic reactor. Among the prepared composites, TCN-(10) exhibits the highest synergy between g-CN and TiO at "" ratio of 10%, showing superior best benzene degradation performance (e.
View Article and Find Full Text PDFJ Colloid Interface Sci
January 2025
School of Materials Science and Engineering, Chongqing Jiaotong University, Chongqing 400074, China. Electronic address:
Defect engineering is considered one of the most powerful strategies for regulating the catalytic activity of electrocatalysts. A deep understanding of the defect-involved mechanism in electrocatalytic process is of great importance but remains a challenging task. In this study, an anionic Se-vacancy (V) was introduced into iron diselenide (FeSe) nanoarrays, enabling the catalyst to exhibit improved electrocatalytic performance for sulfion oxidation reaction (SOR).
View Article and Find Full Text PDFOrg Lett
January 2025
Anhui Province Key Laboratory of Chemistry for Inorganic/Organic Hybrid Functionalized Materials, College of Chemistry & Chemical Engineering, Anhui University, Hefei, Anhui 230601, China.
Boron compounds are widely employed in organic chemistry, pharmaceuticals, and materials science. Among them, borylated heterocycles serve as versatile synthons for the construction of new C-C or C-heteroatom bonds via coupling or radical processes. Such methods for direct C-H borylation reactions are of high synthetic value to reduce the number of synthetic steps and the amount of waste and to improve efficiency.
View Article and Find Full Text PDFJ Colloid Interface Sci
January 2025
College of Physics and Electronic Information, Yunnan Normal University, 650500 Kunming, China. Electronic address:
Rational design of effective cathode host materials is an effective way to solve the problems of serious shuttle and slow conversion of polysulfides in lithium-sulfur batteries (LSBs). However, the redox reaction of sulfur differs from conventional "Rocking chair" type batteries and involves a cumbersome phase transition process, so a single-component catalyst cannot consistently and steadily enhance the reaction rate throughout the redox process. In this work, a hybrid composed of magnetopyrite FeS catalyst-modified with N/S-doped porous carbon spheres (FeS@NSC) is proposed as a novel sulfur host to synergistically promote the adsorption and redox catalysis conversion of polysulfides.
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