ChemInform Abstract: An Efficient and Scalable Room Temperature Aerobic Alcohol Oxidation Catalyzed by Iron Chloride Hexahydrate/Mesoporous Silica Supported TEMPO.

ChemInform ◽  
2013 ◽  
Vol 44 (48) ◽  
pp. no-no
Author(s):  
Lianyue Wang ◽  
Jun Li ◽  
Xiaoping Zhao ◽  
Ying Lv ◽  
Hengyun Zhang ◽  
...  
Tetrahedron ◽  
2013 ◽  
Vol 69 (30) ◽  
pp. 6041-6045 ◽  
Author(s):  
Lianyue Wang ◽  
Jun Li ◽  
Xiaoping Zhao ◽  
Ying Lv ◽  
Hengyun Zhang ◽  
...  

2016 ◽  
Vol 20 (3) ◽  
pp. 967-972 ◽  
Author(s):  
Peng Liu ◽  
Chun-Hui He ◽  
Fujuan Liu ◽  
Lan Xu ◽  
Yuqin Wan ◽  
...  

In this work, ?-Fe2O3 nanobulk with high aspect ratio were successfully prepared via a facile bubble electrospinning technique using polyvinylidene fluoride and iron chloride hexahydrate (FeCl3?6H2O) as ?-Fe2O3 precursor followed by annealing in air at 600?C. The products were characterized with field emission scanning electron microscope, Fourier transform infrared, X-ray photoelectron spectroscopy, and thermogravimetric analysis. The results showed that ?-Fe2O3 nanobulk has a hierarchical heterostructure which has an extremely broad application prospect in many areas.


2021 ◽  
Vol 43 (2) ◽  
pp. 193-193
Author(s):  
Taiping Gao Taiping Gao ◽  
Xiaolin Ma Xiaolin Ma ◽  
Xin Li Xin Li ◽  
Qiang Xu and Yubao Wang Qiang Xu and Yubao Wang

The first mesoporous silica nanoparticles (MSNs) supported atomically precise palladium nanoclusters catalyzed alcohol oxidation reactions in water have been achieved. The catalysts was synthesized with simple impregnation method and well characterized by TEM, FT-IR, XPS anddiffuse reflectance optical spectrum and the results proved that the Pd nanoclustersimmobilized into the pores of MSNs.The as-prepared catalyst show excellent activity for the alcohol oxidation reactions with high yield under extremely mild aqueous conditions utilizes 1 atmosphere of molecular oxygen as sole oxidant. The features of clean system, gram-scale oxidation and easy recovery catalyst make this method cost effectively and environmentally benign.


2020 ◽  
Vol 22 (9) ◽  
Author(s):  
Shewaye Yismaw ◽  
Stefan G. Ebbinghaus ◽  
Marianne Wenzel ◽  
David Poppitz ◽  
Roger Gläser ◽  
...  

2016 ◽  
Vol 88 (4) ◽  
pp. 349-361 ◽  
Author(s):  
Ana R. Jesus ◽  
Ana P. Marques ◽  
Amélia P. Rauter

AbstractDihydrochalcones are polyphenols that exhibit a diversity of bioactivities, namely anti-inflammatory, antimicrobial and antiviral. We have explored the synthetic access to such molecular entities, and describe now an easy and scalable approach based on reduction of the olefinic double bond of chalcone precursors via in situ hydrogenation with the system Et3SiH-Pd/C in very high yield. The intermediate chalcones were synthesized also by a simple and efficient microwave-assisted Claisen–Schmidt condensation of aromatic aldehydes with acetophenones, conveniently protected with ethoxymethyl ether, if required. Chalcones were obtained as single reaction product in high yield in 2–3 h, while under conventional conditions at room temperature the reaction was carried out with completion only after 24 h. In addition, microwave irradiation has proven very efficient for deprotection of ethoxymethyl ether with iron chloride in only 10 min and very high yield.


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