Two chiral Mn complexes synthesized and characterized by single-crystal X-ray diffraction were grafted onto mesoporous silica MCM-41. The MCM-41-immobilized solid chiral catalysts were characterized by various spectrochemical and physicochemical methods (XRD, FTIR, Si NMR, TGA, UV/Vis/DRS, EPR, cyclic voltammetry, SEM, BET). Both the homogeneous and heterogeneous Mn chiral complexes are found to be effective catalysts for epoxidation of styrene. MCM-41-supported chiral catalysts are found to retain their catalytic activity up to five cycles. When an ionic liquid was implemented to enhance the catalytic recyclability of the homogeneous catalysts, they can be recycled up to three times. However, after the third cycle the catalytic activities of the complexes were found to decrease due to rupturing of the chiral catalyst.
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http://dx.doi.org/10.1002/cplu.201402446 | DOI Listing |
Int J Biol Macromol
December 2024
Graduate Program in Chemistry, Federal University of Alfenas, Alfenas, MG 37130-001, Brazil; Institute of Chemistry, Federal University of Alfenas, Alfenas, MG 37130-001, Brazil. Electronic address:
The objective of this study was to produce new and renewable bio-based plasticizers from used soybean cooking oil (USCO). First, USCO was completely converted into free fatty acids (FFAs) using lipase from Candida rugosa. Next, these FFAs were enzymatically esterified with benzyl alcohol in solvent-free systems.
View Article and Find Full Text PDFNanomaterials (Basel)
December 2024
Institute of Physical Chemistry-Ilie Murgulescu of the Romanian Academy, 202 Splaiul Independentei, 060021 Bucharest, Romania.
Bimetallic (Ta/Ti, V, Co, Nb) mesoporous MCM-41 nanoparticles were obtained by direct synthesis and hydrothermal treatment. The obtained mesoporous materials were characterized by XRD, XRF, N adsorption/desorption, SEM, TEM, XPS, Raman, UV-Vis, and PL spectroscopy. A more significant effect was observed on the mesoporous structure, typically for MCM-41, and on optic properties if the second metal (Ti, Co) did not belong to the same Vb group with Ta as V and Nb.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2024
Fuzhou University, Chemistry, 523 Gongye Rd, Gulou, 350000, Fuzhou, CHINA.
Heterogeneous photoelectrocatalysis systems have recently seen significant growth in organic transformations, but are limited by the inherent physicochemical properties of electrode materials. To enhance selectivity in these processes, we propose an innovative advancement in the rational design of photoanodes. Specifically, we incorporated cobalt porphyrin co-catalysts with confined Co sites onto bismuth vanadate films as a photoanode.
View Article and Find Full Text PDFChemistry
December 2024
Lanzhou University, College of Chemistry and Chemical Engineering, Lanzhou Tianshui south street 222, 730000, Lanzhou, CHINA.
Dual single-atom catalysts have attracted considerable research interest due to their higher metal atom loading and more flexible active sites compared to single-atom catalysts (SACs). We pioneered the one-step synthesis of sheets copper-cobalt graphitic carbon nitride dual single-atom (S-Cu/Co-g-C3N4) using folding fan-shaped aluminum foil as a template, and used them as catalysts in the epoxidation of styrene respectively. Through XAFS(X-ray Absorption Fine Structure) and other characterizations, it is found that Cu and Co single atoms are stabilized separately on g-C3N4 via coordination with nitrogen (N), hindered the ordered growth of sheets, and formed more pore structures, which not only increased more catalytically active sites, but also effectively prevented the flakes re-aggregate during the catalytic process.
View Article and Find Full Text PDFAcc Chem Res
December 2024
State Key Laboratory of Elemento-Organic Chemistry, Frontiers Science Center for New Organic Matter, Haihe Laboratory of Sustainable Chemical Transformations, College of Chemistry, Nankai University, Tianjin 300071, China.
ConspectusElectrochemistry has been used as a tool to drive chemical reactions for more than two centuries. With the help of an electrode and a power source, chemists are provided with a system whose potential can be precisely dialed in. The theoretically infinite redox range renders electrochemistry capable of oxidizing or reducing some of the most tenacious compounds.
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