Co-reporter:Xueyin Bai, Ziwei Liu, Kaiqi Ye, Yu Wang, Xianlong Zhang, Huijuan Yue, Ge Tian, Shouhua Feng
Tetrahedron Letters 2014 Volume 55(Issue 2) pp:319-321
Publication Date(Web):8 January 2014
DOI:10.1016/j.tetlet.2013.11.005
Here we report experimental evidence for the simple synthesis of N,N-diethylhydroxylamine and an amide bond formation reaction from oxidation of the alpha-carbon of tertiary amines by the reaction of triethylamine and hydrogen peroxide in hydrothermal conditions. It is proved that 120 °C is a turning point: when the temperature is lower than that, the main product is N,N-diethylhydroxylamine as a result of a cope rearrangement reaction mechanism; on the contrary, the product is more complex and the main products are amides via a radical chain mechanism involving three steps: initiation, propagation, and oxidation, followed by decarbonylation and electrocyclization because the radical is easier to form under high temperature.
Co-reporter:Gull Maheen;Yu Wang;Yingwu Wang;Zhan Shi;Shouhua Feng
Heteroatom Chemistry 2011 Volume 22( Issue 2) pp:186-191
Publication Date(Web):
DOI:10.1002/hc.20675
Abstract
Prebiotic acidic hydrothermal conditions were mimicked, and biological phosphate esters such as glucose-1-phosphate, glucose-6-phosphate, and glucose-di-phosphate were synthesized under hydrothermal conditions, in the presence of a mixture of montmorillonite and kaolinite. Phosphorus was incorporated into the biological world under hydrothermal conditions, leading to the formation of phosphate esters. The synthesis was successfully carried out within a temperature range of 100–160°C. Both isomers of glucose phosphate were obtained, with some detectable amount of glucose-di-phosphate. Selected mixture of montmorillonite and kaolinite was found to be essential for the reaction. No products were detected without this catalyst mixture. © 2011 Wiley Periodicals, Inc. Heteroatom Chem 22:186–191, 2011; View this article online at wileyonlinelibrary.com. DOI 10.1002/hc.20675
Co-reporter:Hui Liu, Weijian Zou, Xingliang Xu, Xianlong Zhang, Yongquan Yang, Huijuan Yue, Yang Yu, Ge Tian, Shouhua Feng
Journal of CO2 Utilization (January 2017) Volume 17() pp:43-49
Publication Date(Web):1 January 2017
DOI:10.1016/j.jcou.2016.11.006
In order to correlate the physico-chemical properties of CexZr1-xO2 catalysts with their catalytic activities for direct carboxylation of methanol to dimethyl carbonate (DMC), ceria-zirconia mixed oxides with the same nominal composition (Ce0.5Zr0.5O2), which were prepared by different methods, were applied. The catalysts were characterized by means of XRD, N2 adsorption, ICP-MS, NH3-TPD, CO2-TPD, Raman spectroscopy and XPS. Significant variations in their physico-chemical properties were observed by varying the preparation conditions. The results showed that the catalytic activity of the ceria-zirconia mixed oxides increased with improving the proportion of Ce4+, acidity and basicity of the catalyst surface. And the number of surface Ce4+ content is the most important factor.We reported that different preparation methods of Ce0.5Zr0.5O2 catalysts have great influences on their surface and bulk properties and catalytic activities of synthesis of DMC from methanol and CO2.Download high-res image (163KB)Download full-size image
Co-reporter:Xingliang Xu, Xianlong Zhang, Weijian Zou, Huijuan Yue, Ge Tian, Shouhua Feng
Catalysis Communications (5 March 2015) Volume 62() pp:67-70
Publication Date(Web):5 March 2015
DOI:10.1016/j.catcom.2015.01.011
•The sulfated MMT catalysts were synthesized through a simple impregnation method.•The sulfate groups promote the amount of strong acid sites and the acidic amount.•The 20-SO42 −/MTT exhibits the best performance for the conversion of glucose to ML.•The layers of MMT were damaged when the concentration of sulfuric acid is 30 wt.%.We reported a highly efficient conversion of carbohydrates such as glucose to methyl levulinate (ML) in methanol with a series of sulfated montmorillonite (MMT) as simple and inexpensive catalysts. Among these catalysts, the MMT treated by H2SO4 after calcination (especially the MMT treated by 20% H2SO4) showed a high catalytic activity. Under the optimal conditions, the conversion of glucose and fructose was up to 100%, and the ML yields obtained from glucose and fructose were 48% and 65%, respectively. The reaction conditions were optimized. Further, the structure and properties of sulfated MMT were characterized.We reported a highly efficient conversion of carbohydrates such as glucose to methyl levulinate (ML) in methanol with a series of sulfated montmorillonite (MMT) as an affordable and easily prepared solid acid catalyst.Download high-res image (164KB)Download full-size image