共查询到19条相似文献,搜索用时 46 毫秒
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建立了一种以有机碱1,8-二氮杂二环(5.4.0)十一稀-7(DBU)为催化剂的无溶剂反应条件的高效、快速和简便的Knoevenagel缩合芳香醛与活泼亚甲基化合物的反应体系。此反应体系能够在室温条件下顺利进行,而且在较短的反应时间内完成反应并得到大于85%的产物收率,且后处理非常简单。最后,讨论了可能的反应机理。 相似文献
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无溶剂条件下,无水CoCl2或干燥的强酸性阳离子交换树脂-SO3H催化醇和酸酐的反应,得到高产率的酯。实验证明无溶剂条件下反应简单,操作容易,反应时间短,产率高。 相似文献
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异丁醛1,4—丁烯二醇缩合反应的研究 总被引:1,自引:0,他引:1
将异丁醛与1,4-丁烯二醇缩合得到产物二氧七环,对产物进行了元素分析和IR分析,初步探讨了反应物浓度、温度、酸度和反应时间对产物产率的影响。 相似文献
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在超声波作用和无溶剂条件下,对氯苯甲醛与硝基甲烷发生缩合反应得到了β-硝基烯。最佳反应条件为反应时间2h,物料配比为n(对氯苯甲醛)∶n(硝基甲烷)∶n(氢氧化钠)=1∶40∶2.5。在此最佳反应条件下,β-硝基烯产率为80%。 相似文献
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Vladimir V. Pushkarev Zhongwei Zhu Kwangjin An Antoine Hervier Gabor A. Somorjai 《Topics in Catalysis》2012,55(19-20):1257-1275
We aim to develop novel catalysts that exhibit high activity, selectivity and stability under real catalytic conditions. In the recent decades, the fast development of nanoscience and nanotechnology has allowed synthesis of nanoparticles with well-defined size, shape and composition using colloidal methods. Utilization of mesoporous oxide supports effectively prevents the nanoparticles from aggregating at high temperatures and high pressures. Nanoparticles of less than 2?nm sizes were found to show unique activity and selectivity during reactions, which was due to the special surface electronic structure and atomic arrangements that are present at small particle surfaces. While oxide support materials are employed to stabilize metal nanoparticles under working conditions, the supports are also known to strongly interact with the metals through encapsulation, adsorbate spillover, and charge transfer. These factors change the catalytic performance of the metal catalysts as well as the conductivity of oxides. The employment of new in situ techniques, mainly high-pressure scanning tunneling microscopy (HPSTM) and ambient-pressure X-ray photoelectron spectroscopy (APXPS) allows the determination of the surface structure and chemical states under reaction conditions. HPSTM has identified the importance of both adsorbate mobility to catalytic turnovers and the metal substrate reconstruction driven by gaseous reactants such as CO and O2. APXPS is able to monitor both reacting species at catalyst surfaces and the oxidation state of the catalyst while it is being exposed to gases. The surface composition of bimetallic nanoparticles depends on whether the catalysts are under oxidizing or reducing conditions, which is further correlated with the catalysis by the bimetallic catalytic systems. The product selectivity in multipath reactions correlates with the size and shape of monodisperse metal nanoparticle catalysts in structure sensitive reactions. 相似文献
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Selim Alayoglu Simon K. Beaumont Fan Zheng Vladimir V. Pushkarev Haimei Zheng Viacheslav Iablokov Zhi Liu Jinghua Guo Norbert Kruse Gabor A. Somorjai 《Topics in Catalysis》2011,54(13-15):778-785
Cobalt and platinum?Ccobalt bimetallic alloy nanoparticles of uniform size distribution where prepared and supported on MCF-17 to produce a controlled and well-characterized model catalyst which was studied under reaction conditions during CO2 hydrogenation. Near edge X-ray absorption fine structure (NEXAFS) spectroscopy was used to elucidate the oxidation state of the catalyst under reaction conditions while the effect of reducing H2 gas on the composition and structure of the bimetallic PtCo nanoparticles was measured using ambient pressure X-ray photoelectron spectroscopy (AP-XPS) and environmental transmission electron microscopy (ETEM). NEXAFS indicates that Pt aids the reduction of Co to its metallic state under relevant reaction conditions, while AP-XPS and ETEM indicate that Pt is enriched at the surface by exchange with subsurface layers which become Pt deficient??in agreement with the ??Pt-like?? selectivity seen during catalytic testing of these materials. 相似文献
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Wieslaw Szeja 《Israel journal of chemistry》1985,26(3):235-238
Reaction derivatives of monosaccharides possessing a free anomeric hydroxyl group with methyl sulfate under phase-transfer catalysed conditions is described. Under phase-transfer conditions, which permit equilibrium control, the proportions of α- to β-glycosides are determined by the relative acidity of anomers. In the presence of alcohols the proportions of α to β-D-gluco- and galactopyranosides have been shifted in favor of the equatorial anomer. 相似文献
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异丁醛(IBA)的合成 总被引:1,自引:0,他引:1
甲醇与乙醇或正丙醇一步合成异丁醛,甲醇与正丙醇反应,催化剂为负载钒的TiO2,反应的转化率能够达到98.9%,异丁醛的产率可达64.2%。甲醇与乙醇反应,催化剂分别为V2O5/TiO2-SiO2,CuO-ZnO/Al2O3,CuO-MnO/Al2O3时,反应的转化率分别能达98%、93.1%、93.69%,异丁醛的选择性分别能达85%、53.1%、71%。 相似文献
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