scholarly journals Photocatalytic primary alcohol oxidation on WO3 nanoplatelets

RSC Advances ◽  
2019 ◽  
Vol 9 (49) ◽  
pp. 28688-28694 ◽  
Author(s):  
Kori D. McDonald ◽  
Bart M. Bartlett

With the aid of direct heating through microwave irradiation in non-aqueous media, nanocrystalline tungsten(vi) oxide is achievable in 30 minutes at 200 °C, faster and at a lower temperature than conventional synthesis methods.

2013 ◽  
Vol 2013 ◽  
pp. 1-3
Author(s):  
Alekhya Venkata Madiraju ◽  
Kshitij Taneja ◽  
Manoj Kumar ◽  
Anup Kumar Keshri ◽  
Sarang Balkrushna Mahajan ◽  
...  

Copper-Zinc-Tin-Sulfide (CZTS), a promising material for absorber layer application in thin film solar cells, has been synthesized in aqueous media by microwave irradiation technique. Compared to conventional synthesis methods, microwave irradiation is highly efficient, reliable, and less time consuming. The synthesized nanopowders were characterized for particle size by dynamic light scattering (DLS), phase by X-ray diffraction (XRD), and band-gap by UV-Vis-NIR spectroscopy. Various atmospheric processing methods are being evaluated for the deposition of absorber layers from CZTS nanopowder based ink.


RSC Advances ◽  
2015 ◽  
Vol 5 (19) ◽  
pp. 14637-14645 ◽  
Author(s):  
Takuya Sumi ◽  
Ralf Dillert ◽  
Satoshi Horikoshi

On preparation of bimetal nanoparticles by using a single-mode microwave resonator, Ag–Ni and Pd–Ag nanocomposites were synthesized under microwave irradiation at 80 centigrade, which was a lower temperature than that for reduction of Ag ion.


Synthesis ◽  
2004 ◽  
Vol 2004 (11) ◽  
pp. 1859-1863 ◽  
Author(s):  
Santosh Tilve ◽  
Jyoti Shet ◽  
Vidya Desai

2018 ◽  
Vol 20 (14) ◽  
pp. 3214-3221 ◽  
Author(s):  
Christopher S. Lancefield ◽  
Lucas W. Teunissen ◽  
Bert M. Weckhuysen ◽  
Pieter C. A. Bruijnincx

A new Ir catalysed approach for the selective cleavage of the Cα–Cβ bond in lignin β-O-4 units, allowing access to novel and tuneable monomeric product mixtures.


Synthesis ◽  
2020 ◽  
Author(s):  
Travis J. Williams ◽  
Valeriy Cherepakhin

AbstractOxidation of primary alcohols to carboxylic acids is a fundamental transformation in organic chemistry, yet despite its simplicity, extensive use, and relationship to pH, it remains a subject of active research for synthetic organic chemists. Since 2013, a great number of new methods have emerged that utilize transition-metal compounds as catalysts for acceptorless dehydrogenation of alcohols to carboxylates. The interest in this reaction is explained by its atom economy, which is in accord with the principles of sustainability and green chemistry. Therefore, the methods for the direct synthesis of carboxylic acids from alcohols is ripe for a modern survey, which we provide in this review.1 Introduction2 Thermodynamics of Primary Alcohol Oxidation3 Oxometalate Oxidation4 Transfer Dehydrogenation5 Acceptorless Dehydrogenation6 Electrochemical Methods7 Outlook


2011 ◽  
Vol 391-392 ◽  
pp. 1354-1357 ◽  
Author(s):  
Bai Lin Li ◽  
Hua Ding Liang ◽  
Ai Guo Zhong ◽  
Dan Qian Xu

Novel SO3H-functionalized ionic liquids were successfully applied as catalysts for synthesis of xanthenediones under microwave irradiation in Aqueous. Various types of Xanthenes were provided in 90-97% yields using the catalytic system of [(HSO3-p)2im][CF3SO3]/H2O. The products could be conveniently separated from the reaction mixture by filtration and the dissolved catalyst could be reused without any treatment, which of the separation process was performed in water without using any organic solvents. The method not only has the adventages of shrot time and simple operation, but also is environmentally friendly.


2005 ◽  
Vol 2005 (11) ◽  
pp. 744-746 ◽  
Author(s):  
Xi-Cun Wang ◽  
Man-Gang Wang ◽  
Zhi Yang ◽  
Zheng-Jun Quan ◽  
Fang Wang ◽  
...  

A practical and rapid procedure is reported for the synthesis of a variety of 2-aryloxymethylene-6-arylimidazo[2,1-b][1,3,4]thiadiazole 3a–m by condensation reaction of 2-amino-5-aryloxymethylene-1,3,4-thiadiazole 1a–g with ω-bromoacetophenone derivatives 2a–b in aqueous media under microwave irradiation and yielded a series of novel compounds. The procedure is simple and the yields are good to excellent.


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