Fe（NO3）3-9H2O/Fe（HSO4）3 was used as an efficient reagent system for the oxidation of alcohols to their corresponding carbonyl compounds. All reactions were performed in the absence of solvent in good to high yield...Fe（NO3）3-9H2O/Fe（HSO4）3 was used as an efficient reagent system for the oxidation of alcohols to their corresponding carbonyl compounds. All reactions were performed in the absence of solvent in good to high yields. Under the same reaction conditions, thiols and sulfides were also converted to their corresponding disulfides and sulfoxides, respectively. 2007 Farhad Shirini. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved.展开更多
A LiFePO4/（C＋Fe2P） composite cathode material was prepared by a sol-gel method using Fe（NO3）3.9H20, LiAc·H2O）, NHaH2PO4 and citric acid as raw materials, and the physical properties and electrochemical perf...A LiFePO4/（C＋Fe2P） composite cathode material was prepared by a sol-gel method using Fe（NO3）3.9H20, LiAc·H2O）, NHaH2PO4 and citric acid as raw materials, and the physical properties and electrochemical performance of the composite cathode material were investigated by X-ray diffractometry （XRD）, scanning electron microscopy （SEM）, transmission electron microscopy （TEM） and electrochemical tests. The Fe2P content, morphology and electrochemical performance of LiFePOa/（C＋Fe2P） composite depend on the calcination temperature. The optimized LiFePO4/（C＋FeeP） composite is prepared at 650 ~C and the optimized composite exhibits sphere-like morphology with porous structure and Fe2P content of about 3.2% （mass fraction）. The discharge capacity of the optimized LiFePO4/（C＋FeRP） at 0.1C is 156 and 161 mA.h/g at 25 and 55 ℃, respectively, and the corresponding capacity retentions are 96% after 30 cycles; while the capacity at 1C is 142 and 149 mA.h/g at 25 and 55 ℃, respectively, and the capacity still remains 135 and 142 mA-h/g after 30 cycles at 25 and 55℃, respectively.展开更多
A mild and efficient method for the oxidative deprotection of 1,3-oxathiolanes with Fe（NO3）3·9H2O and Cu（NO3）2·3H2O in the absence of solvent is reported.
Y-shaped structure was synthesized by ethanol catalytic combustion(ECC) technique on the copper plate substrate, without directly seeding catalyst into the flame. The as-grown Y-junction carbon nanofibres were investi...Y-shaped structure was synthesized by ethanol catalytic combustion(ECC) technique on the copper plate substrate, without directly seeding catalyst into the flame. The as-grown Y-junction carbon nanofibres were investigated by transmission electron microscopy (TEM). The very common laboratory ethanol burner was used for synthesizing carbon nanofibres. Two kinds of the catalyst precursor, which are iron nitrate (Fe(NO3)3) and nickel nitrate (Ni(NO3)2), were respectively employed to assist the formation of Y-junction carbon nanofibres. TEM analysis confirm the formation of Y-junction in the coiled and noncoiled carbon nanofibres. The type of the catalyst is found to be crucial to grow different Y-junction carbon nanofibres. Different Y-shaped structure may possess different mechanical and electronic properties. These three-terminal nanofibres provide the nanoelectronics community with a novel material for the development of molecular-scale electronic devices.展开更多
文摘Fe（NO3）3-9H2O/Fe（HSO4）3 was used as an efficient reagent system for the oxidation of alcohols to their corresponding carbonyl compounds. All reactions were performed in the absence of solvent in good to high yields. Under the same reaction conditions, thiols and sulfides were also converted to their corresponding disulfides and sulfoxides, respectively. 2007 Farhad Shirini. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved.
基金Project(50571091) supported by the National Natural Science Foundation of ChinaProject(09C947) supported by the Scientific Research Fund of Hunan Provincial Education Department,China
文摘A LiFePO4/（C＋Fe2P） composite cathode material was prepared by a sol-gel method using Fe（NO3）3.9H20, LiAc·H2O）, NHaH2PO4 and citric acid as raw materials, and the physical properties and electrochemical performance of the composite cathode material were investigated by X-ray diffractometry （XRD）, scanning electron microscopy （SEM）, transmission electron microscopy （TEM） and electrochemical tests. The Fe2P content, morphology and electrochemical performance of LiFePOa/（C＋Fe2P） composite depend on the calcination temperature. The optimized LiFePO4/（C＋FeeP） composite is prepared at 650 ~C and the optimized composite exhibits sphere-like morphology with porous structure and Fe2P content of about 3.2% （mass fraction）. The discharge capacity of the optimized LiFePO4/（C＋FeRP） at 0.1C is 156 and 161 mA.h/g at 25 and 55 ℃, respectively, and the corresponding capacity retentions are 96% after 30 cycles; while the capacity at 1C is 142 and 149 mA.h/g at 25 and 55 ℃, respectively, and the capacity still remains 135 and 142 mA-h/g after 30 cycles at 25 and 55℃, respectively.
基金Supported by National Nature Science Foundation of China ( No .60477003) Projects fromthe Shanghai ScienceTechnology Committee (No .0552nm006 , No .0652nm033) +3 种基金Shanghai Pujiang Program ( No .05PJ14320) KeyProject of Photonic Technology (No .06DZ11404) Development Program of High Technology and Innovation ofShanghai Economic Committee Key Project of EXPO Plan ( No .05dz05803) Project of Key Laboratory ofAdvanced Display and System Applications (Shanghai University ) Ministry of Education ,China(No .P200503)
文摘A mild and efficient method for the oxidative deprotection of 1,3-oxathiolanes with Fe（NO3）3·9H2O and Cu（NO3）2·3H2O in the absence of solvent is reported.
基金Project(KM200510772013) supported by Beijing City Education Committee Science and Technology Development Program Project(2005-2007) supported by Beijing City Education Committee Academic Innovative Team Program
文摘Y-shaped structure was synthesized by ethanol catalytic combustion(ECC) technique on the copper plate substrate, without directly seeding catalyst into the flame. The as-grown Y-junction carbon nanofibres were investigated by transmission electron microscopy (TEM). The very common laboratory ethanol burner was used for synthesizing carbon nanofibres. Two kinds of the catalyst precursor, which are iron nitrate (Fe(NO3)3) and nickel nitrate (Ni(NO3)2), were respectively employed to assist the formation of Y-junction carbon nanofibres. TEM analysis confirm the formation of Y-junction in the coiled and noncoiled carbon nanofibres. The type of the catalyst is found to be crucial to grow different Y-junction carbon nanofibres. Different Y-shaped structure may possess different mechanical and electronic properties. These three-terminal nanofibres provide the nanoelectronics community with a novel material for the development of molecular-scale electronic devices.
