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亚铜催化法^(131)I标记间碘苄胍的研究
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作者 李勇 李红全 《西南师范大学学报(自然科学版)》 CAS CSCD 北大核心 2005年第1期101-103,共3页
采用亚铜做催化剂, 研究了131I标记间碘苄胍的方法, 即是沸水浴温度, 标记时间 15 min, 用铜量 2. 5μg和抗坏血酸量5. 0 mg; 纸层析法分析标记物, 标记率大于97%. 此标记方法不需要进一步的分离, 具有简单、快速的特点.
关键词 胍乙啶 ^131I-间碘苄胍 亚铜催化 纸层析法 标记
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碘化亚铜催化下的两组分双环化反应构建氮杂环
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作者 范威 《好日子》 2020年第36期24-24,共1页
碘化亚铜是常用的催化剂,可以催化合成多种氮杂环化合物。本文综述了近几年来以碘化亚铜为催化剂的两组分双环化反应在构建氮杂环中的应用。
关键词 碘化亚铜催化 两组分双环化反应 构建 氮杂环
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亚铜催化的碳杂偶联反应机理 被引量:5
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作者 于海珠 傅尧 +1 位作者 白小宇 郭庆祥 《化学进展》 SCIE CAS CSCD 北大核心 2010年第4期557-572,共16页
近年来,亚铜催化的碳杂偶联反应以其高效、低成本和易制备等优点被广泛研究并应用于工业生产、有机合成及生物活性分子的制备中。目前对于这些碳杂偶联反应机理的探究仍然处于探索性阶段。本文主要评述了近年来亚铜催化的碳杂偶联反应... 近年来,亚铜催化的碳杂偶联反应以其高效、低成本和易制备等优点被广泛研究并应用于工业生产、有机合成及生物活性分子的制备中。目前对于这些碳杂偶联反应机理的探究仍然处于探索性阶段。本文主要评述了近年来亚铜催化的碳杂偶联反应机理的研究进展,重点综述近年来研究相对较多,对机理认识较为完善的碳-氮偶联(特别是酰胺类化合物的芳基化过程),碳氧偶联以及碳硼偶联(不饱和有机化合物的硼化、二硼化反应)机理等方面的进展。最后,基于目前这些机理研究工作的现状,展望了未来机理探究的主要方向。 展开更多
关键词 亚铜催化 碳-杂偶联 机理
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亚铜盐催化碱性水解法合成氟代苯酚及其工艺优化
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作者 窦杰 杨俊伟 +3 位作者 李程碑 杭磊 李浩 陈国珍 《应用化工》 CAS CSCD 北大核心 2017年第2期152-156,共5页
1-卤代氟苯在亚铜盐催化下发生碱性水解反应,生成氟代苯酚,以单因素结合正交实验,对合成工艺进行优化。结果表明,合成五氟苯酚的最佳工艺条件为:全氟苯93.0 g(0.5 mol),Raney Ni 5.0 g,Cu2O 7.5 g,90%工业KOH 65.0 g,水200 g,环丁砜60.0... 1-卤代氟苯在亚铜盐催化下发生碱性水解反应,生成氟代苯酚,以单因素结合正交实验,对合成工艺进行优化。结果表明,合成五氟苯酚的最佳工艺条件为:全氟苯93.0 g(0.5 mol),Raney Ni 5.0 g,Cu2O 7.5 g,90%工业KOH 65.0 g,水200 g,环丁砜60.0 g,转速500 r/min,120℃反应8 h,收率达到80.0%。经过非均相反应、脱色、除氟、分子精馏等工艺,五氟苯酚达到质量标准:含量≥99.8%,单杂含量≤0.1%,掉氟物≤0.01%,水分≤100 mg/kg,溶剂残留≤100 mg/kg,符合液晶中间体和医药中间体的质量要求。 展开更多
关键词 氟代苯酚 催化碱性水解 工艺优化 检测方法 质量标准
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碘化亚铜/乙二胺催化氮杂环化合物的N-芳基化反应 被引量:1
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作者 胡帅帅 郭海昌 +1 位作者 蒋华江 郑人华 《应用化学》 CAS CSCD 北大核心 2011年第10期1179-1183,共5页
以碘化亚铜/乙二胺为催化体系,研究了卤代芳烃和氮杂环化合物的Ullmann反应。结果表明,氮杂环化合物的pKa越小,芳基化反应越容易进行,p-π共轭形成的富电子卤代芳烃有利于反应,非p-π共轭的富电子卤代芳烃使反应变难。
关键词 ULLMANN反应 N-芳基化反应 氮杂环化合物 碘化/乙二胺催化
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RX/CuX/bpy催化体系中PEO大单体与PMMA接枝共聚物的合成与表征(英文) 被引量:2
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作者 冯松 李庆海 +1 位作者 杜宝辉 沈良骏 《安徽师范大学学报(自然科学版)》 CAS 2001年第3期231-235,238,共6页
本工作以正丁基溴为引发剂 ,卤化亚铜 /联吡啶 (bpy)为催化剂 ,研究了甲基丙烯酸甲酯 (MMA)与末端为丙烯酰胺基的聚氧化乙烯 (PEO)大单体的原子转移自由基聚合 (ATRP)反应 .得到了实测分子量与理论分子量相近 ,分子量分布较窄 ,有预期... 本工作以正丁基溴为引发剂 ,卤化亚铜 /联吡啶 (bpy)为催化剂 ,研究了甲基丙烯酸甲酯 (MMA)与末端为丙烯酰胺基的聚氧化乙烯 (PEO)大单体的原子转移自由基聚合 (ATRP)反应 .得到了实测分子量与理论分子量相近 ,分子量分布较窄 ,有预期结构的接枝共聚物 ,用IR ,1HNMR ,VPO ,GPC ,DSC等进行了表征 ,并对共聚物的组成和分子量受单体总浓度、投料比、引发剂及反应时间的影响进行了讨论 . 展开更多
关键词 PEO大单体 甲基丙烯酸甲酯 原子转移自由基共聚 接枝共聚物 合成 聚氧化乙烯 卤化/联吡啶催化
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一种合成薏苡素的新方法
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作者 梁大伟 袁野 +1 位作者 章斌 王悦秋 《化学试剂》 北大核心 2017年第7期790-792,共3页
以邻氨基苯酚与二(三氯甲基)碳酸酯为原料,经成环反应、溴代、碘化亚铜催化甲氧基取代反应合成薏苡素,反应的总收率为57.0%,其结构经1HNMR、13CNMR、IR、MS等进行表征。
关键词 薏苡素 碘化亚铜催化 甲氧基化 合成
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铜催化异氰酸酯加成反应机理研究 被引量:1
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作者 黄利 王毓浩 +3 位作者 刘吉英 李世俊 张文静 蓝宇 《有机化学》 SCIE CAS CSCD 北大核心 2021年第11期4347-4352,共6页
异氰酸酯作为一种重要的单碳碳源,在合成化学中可以用于制备酰胺衍生物或杂环类化合物,其活化和转化机制是一个重要的问题.通过密度泛函理论(DFT)计算研究了亚铜催化异氰酸酯氢硼乙基化反应的机理.研究结果表明,该反应中叔丁醇亚铜是活... 异氰酸酯作为一种重要的单碳碳源,在合成化学中可以用于制备酰胺衍生物或杂环类化合物,其活化和转化机制是一个重要的问题.通过密度泛函理论(DFT)计算研究了亚铜催化异氰酸酯氢硼乙基化反应的机理.研究结果表明,该反应中叔丁醇亚铜是活性催化物种.反应经历了叔丁醇亚铜与硼烷转金属化、烯烃插入、异氰酸酯插入、与叔丁醇锂转金属化再生叔丁醇亚铜等步骤.其中,异氰酸酯插入为决速步,经历了一个特殊的三元环过渡态.如果使用手性的亚膦酰胺作为配体,则可实现立体选择性的异氰酸酯氢硼乙基化.对映体选择性控制步为烯烃插入,配体的空间调控决定了立体选择性.反应决速步同样是异氰酸酯插入,但相对使用卡宾配体,该过程活化能较低.因此,亚膦酰胺-亚铜催化体系可能具有较高催化活性. 展开更多
关键词 亚铜催化 密度泛函理论计算 异氰酸酯 插入反应
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Octahedral Cu_2O-modified TiO_2 nanotube arrays for efficient photocatalytic reduction of CO_2 被引量:5
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作者 李延芳 张文沛 +3 位作者 沈星 彭鹏飞 熊良斌 余颖 《Chinese Journal of Catalysis》 SCIE EI CAS CSCD 北大核心 2015年第12期2229-2236,共8页
A photocatalyst composed of TiO 2 nanotube arrays(TNTs) and octahedral Cu2 O nanoparticles was fabricated,and its performance in the photocatalytic reduction of CO2 under visible and simulated solar irradiation was ... A photocatalyst composed of TiO 2 nanotube arrays(TNTs) and octahedral Cu2 O nanoparticles was fabricated,and its performance in the photocatalytic reduction of CO2 under visible and simulated solar irradiation was studied. The average nanotube diameter and length was 100 nm and 5 μm,respectively. The different amount of octahedral Cu2 O modified TNTs were obtained by varying electrochemical deposition time. TNTs modified with an optimized amount of Cu2 O nanoparticles exhibited high efficiency in the photocatalysis,and the predominant hydrocarbon product was methane. The methane yield increased with increasing Cu2 O content of the catalyst up to a certain deposition time,and decreased with further increase in Cu2 O deposition time. Insufficient deposition time(5 min) resulted in a small amount of Cu2 O nanoparticles on the TNTs,leading to the disadvantage of harvesting light. However,excess deposition time(45 min) gave rise to entire TNT surface being most covered with Cu2 O nanoparticles with large sizes,inconvenient for the transport of photo-generated carriers. The highest methane yield under simulated solar and visible light irradiation was observed for the catalysts prepared at a Cu2 O deposition time of 15 and 30 min respectively. The morphology,crystallization,photoresponse and electrochemical properties of the catalyst were characterized to understand the mechanism of its high photocatalytic activity. The TNT structure provided abundant active sites for the adsorption of reactants,and promoted the transport of photogenerated carriers that improved charge separation. Modifying the TNTs with octahedral Cu2 O nanoparticles promoted light absorption,and prevented the hydrocarbon product from oxidation. These factors provided the Cu2O-modified TNT photocatalyst with high efficiency in the reduction of CO2,without requiring co-catalysts or sacrificial agents. 展开更多
关键词 Titania nanotube arrays Octahedral cuprous oxide nanoparticles Photocatalytic carbon dioxide reduction Hydrocarbon product PHOTOACTIVITY
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基于Buchwald-Hartwig反应合成N^6-芳氨基脱氧腺苷衍生物 被引量:1
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作者 时尚 刘刚 +1 位作者 王盼港 胡军林 《鲁东大学学报(自然科学版)》 2019年第2期136-142,共7页
N^6-芳氨基脱氧腺苷类化合物是一类重要的抗肿瘤药物分子,具有广泛的医疗价值.以2’-脱氧腺苷为原料,基于Buchwald-Hartwig反应,通过亚铜催化交叉偶联反应合成了一系列N^6-芳氨基脱氧腺苷衍生物(1a~1g),得到了一条高产率的N^6位修饰合... N^6-芳氨基脱氧腺苷类化合物是一类重要的抗肿瘤药物分子,具有广泛的医疗价值.以2’-脱氧腺苷为原料,基于Buchwald-Hartwig反应,通过亚铜催化交叉偶联反应合成了一系列N^6-芳氨基脱氧腺苷衍生物(1a~1g),得到了一条高产率的N^6位修饰合成路线,为新型抗肿瘤药物合成提供参考.所得关键中间体及产物结构经IR,~1H NMR和^(13)C NMR得到确证. 展开更多
关键词 Buchwald-Hartwig反应 N6-芳氨基脱氧腺苷 催化 合成
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Fabrication and photocatalytic properties of Cu_2S/T-ZnO_w heterostructures via simple polyol process 被引量:1
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作者 吴德智 范希梅 +2 位作者 田轲 代佳 刘花蓉 《Transactions of Nonferrous Metals Society of China》 SCIE EI CAS CSCD 2012年第7期1620-1628,共9页
The Cu2S/tetrapod-like ZnO whisker(T-ZnOw) heterostructures were successfully synthesized via a simple polyol process employing the poly(vinyl pyrrolidone)(PVP) as a surfactant.The as-prepared heterostructures w... The Cu2S/tetrapod-like ZnO whisker(T-ZnOw) heterostructures were successfully synthesized via a simple polyol process employing the poly(vinyl pyrrolidone)(PVP) as a surfactant.The as-prepared heterostructures were characterized by X-ray diffraction(XRD),field emission scanning electron microscopy(FESEM),X-ray photoelectron spectroscopy(XPS) and Fourier transform infrared(FTIR).The photocatalytic properties of Cu2S/T-ZnOw nanocomposites synthesized with different PVP concentrations were evaluated by photodegradation of methyl orange(MO) under UV irradiation.The results show that the Cu2S/T-ZnOw nanocomposites exhibit remarkable improved photocatalytic property compared with the pure T-ZnOw.The sample prepared with 3.0 g/L PVP shows an excellent photocatalytic property and the highest photodegradation rate of MO is 97% after UV irradiation for 120 min.Besides,the photocatalytic activity of the photocatalyst has no evident decrease even after four cycles,which demonstrates that the Cu2S/T-ZnOw photocatalyst exhibits an excellent photostability.Moreover,the photocatalytic mechanism of the Cu2S/T-ZnOw nanocomposites was also discussed. 展开更多
关键词 Cu2S/T-ZnOw heterostructure photocatalytic property Cu2S nanoparticle
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Synergistic effects of CuO and Au nanodomains on Cu_2O cubes for improving photocatalytic activity and stability 被引量:5
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作者 Denghui Jiang Yuegang Zhang Xinheng Li 《Chinese Journal of Catalysis》 SCIE EI CAS CSCD 北大核心 2019年第1期105-113,共9页
Cu2O is a promising photocatalyst,but it suffers from poor photocatalytic activity and stability,especially for Cu2O cubes.Herein,we report the deposition of CuO and Au nanodomains on Cu2O cubes to form dual surface h... Cu2O is a promising photocatalyst,but it suffers from poor photocatalytic activity and stability,especially for Cu2O cubes.Herein,we report the deposition of CuO and Au nanodomains on Cu2O cubes to form dual surface heterostructures(HCs)to improve photocatalytic activity and stability.The apparent quantum efficiency of Au/CuO/Cu2O HCs was ca.123 times that of pristine Cu2O.In addition,the Au/CuO/Cu2O HCs maintained nearly 80%of its original activity after eight cycles in contrast to five cycles for the Au/Cu2O material.Therefore,CuO and Au domains greatly improved the photocatalytic activity and stability of the Cu2O cubes due to the synergistic effect of the HCs. 展开更多
关键词 Cuprous oxide Photocatalytic activity STABILITY Sequential surface engineering Charge transfer
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Electrocatalytic Oxidation of Calcium Folinate on Carboxyl Graphene Modified CuxO/Cu Electrode 被引量:2
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作者 Li-wen Wang Shou-guo Wu +2 位作者 Tian-yang Shi Wei Wei Pan Pan 《Chinese Journal of Chemical Physics》 SCIE CAS CSCD 2016年第6期729-734,I0002,共7页
Carboxyl graphene modified CuxO/Cu electrode was fabricated. The bare copper electrode was firstly anodic polarized in 1.0 mol/L NaOH solution in order to get CuxO nanoparticles, then the carboxyl graphene (CG) was ... Carboxyl graphene modified CuxO/Cu electrode was fabricated. The bare copper electrode was firstly anodic polarized in 1.0 mol/L NaOH solution in order to get CuxO nanoparticles, then the carboxyl graphene (CG) was electrodeposited on the CuxO/Cu electrode by cyclic potential sweeping. The electrocatalytic oxidation behaviors of calcium folinate (CF) at the graphene modified CuxO/Cu electrode were investigated by cyclic voltammetry. A positive scan polarization reverse catalytic voltammetry was used to obtain the pure catalytic oxidation current. The graphene modified CuxO/Cu electrode was served as the electrochemical sensor of CF, a highly sensitivity of 22.0μA.(μmol/μL)^-1cm^-2 was achieved, and the current response was linear with increasing CF concentration in the range of 2.0×10^-7 mol/L to 2.0×10^-5 mol/L, which crossed three orders of magnitude, and the detection limit was found 7.6×10^-5 mol/L (S/N=3). In addition, the proposed sensor was successfully applied in determination of CF in drug sample. 展开更多
关键词 Calcium folinate Carboxyl graphene CuxO/Cu electrode Chemically modi-fied electrode Positive scan polarization reverse catalytic voltammetry
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Semi-heterogeneous photo-Cu-dual-catalytic cross-coupling reactions using polymeric carbon nitrides 被引量:3
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作者 Zhaofei Zhang Yangsen Xu +4 位作者 Qitao Zhang Shaofan Fang Hongli Sun Wei Ou Chenliang Su 《Science Bulletin》 SCIE EI CSCD 2022年第1期71-78,M0004,共9页
A merger of copper catalysis and semiconductor photocatalysis using polymeric carbon nitride(PCN)for multi-type cross-coupling reactions was developed.This dual-catalytic system enables mild C-H arylation,chalcogenati... A merger of copper catalysis and semiconductor photocatalysis using polymeric carbon nitride(PCN)for multi-type cross-coupling reactions was developed.This dual-catalytic system enables mild C-H arylation,chalcogenation,and C-N cross-coupling reactions under visible light irradiation with a broad substrate scope.Good-to-excellent yields were obtained with appreciable site selectivity and functional group tolerance.Metal-free and low-cost PCN photocatalyst can easily be recovered and reused several times. 展开更多
关键词 Dual catalysis Polymeric carbon nitride Heterogeneous photocatalysis C-H functionalization C-N coupling
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Synthesis and Enhanced Photocatalytic Activity of Regularly Shaped Cu2O Nanowire Polyhedra 被引量:12
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作者 Jing Shi Jin LI Xiaojian Huang Yiwei Tan 《Nano Research》 SCIE EI CAS CSCD 2011年第5期448-459,共12页
A series of unique nanowire superstructures, Cu2O nanowire polyhedra, have been synthesized through a cost-effective hydrothermal route. Three types of nanowire polyhedra, namely octahedra, concave octahedra, and hexa... A series of unique nanowire superstructures, Cu2O nanowire polyhedra, have been synthesized through a cost-effective hydrothermal route. Three types of nanowire polyhedra, namely octahedra, concave octahedra, and hexapods, were formed in high morphological yields (90%) by reducing cupric acetate with o-anisidine or o-phenetidine in the presence of carboxylic acids. The architectures of these Cu2O nanowire polyhedra were examined by electron microscopy, which revealed ordered, highly aligned CU2O nanowires within the polyhedral outlines. The growth of the Cu2O nanowire polyhedra is controlled by the orientation and growth rates of the nanowire branches which are adjusted by addition of carboxylic acids. Compared to the Cu2O samples reported in the recent literature, the Cu2O nanowire octahedra exhibit notably enhanced photocatalytic activities for dye degradation in the presence of H202 under visible light, probably due to the high-density charge carriers photoexcited from the branched nanowires with their special structures. Additionally, the discussion in the recent literature of the photocatalytic activity of Cu2O in the absence of H2O2 for direct photodegradation of dyes seems questionable. 展开更多
关键词 Nanowire superstructures POLYHEDRA cuprous oxide PHOTOCATALYSIS morphology control
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Cu2O-Au Nanocomposites with Novel Structures and Remarkable Chemisorption Capacity and Photocatalytic Activity 被引量:3
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作者 Qing Hua Fucheng Shi +5 位作者 Kai Chen Sujie Chang Yunsheng Ma Zhiquan Jiang Guoqiang Pan Weixin Huang 《Nano Research》 SCIE EI CAS CSCD 2011年第10期948-962,共15页
The decomposition of Cull nanoparticles in aqueous solution has been successfully developed as a novel method for the preparation of Cu2O nanoparticles. In particular, we found that the decomposition of Cull nanoparti... The decomposition of Cull nanoparticles in aqueous solution has been successfully developed as a novel method for the preparation of Cu2O nanoparticles. In particular, we found that the decomposition of Cull nanoparticles in aqueous solution could be catalyzed by Au colloids, forming CU2O-Au nanocomposites. The composition and structure of the resulting Cu2O-Au nanocomposites have been characterized in detail by inductively coupled plasma atomic emission spectroscopy, powder X-ray diffraction, N2 adsorption-desorption isotherms, infrared spectroscopy, X-ray photoelectron spectroscopy, scanning electron microscopy and transmission electron microscopy. Their visible-light-driven photocatalytic activity toward various dye molecules has also been investigated. Depending on the Au:Cu ratio, Cu20-Au nanocomposites exhibit different novel nanostructures including a beautiful flower-like nanostructure that consists of polycrystalline Cu2O, amorphous Cu2O and Au colloids. We propose that the rapidly-generated bubbles of H2 during the course of the catalytic decomposition reaction drive the simultaneously-formed Cu2O to form amorphous curved thin foils and might also act as a template to assemble curved thin foils of amorphous Cu2O, polycrystalline Cu2O and Au colloids into uniform nanostructures. A Cu2O-Au nanocomposite with a Cu:Au ratio of 40 exhibits remarkable chemisorption capacity and visible-light-driven photocatalytic activity towards methyl orange and acid orange 7 and is a promising chemisorption-photocatalysis integrated catalyst. The catalytic decomposition of the metal hydride might open up a new approach for the fabrication of other metal/metal oxide nanocomposites with novel nanostructures and properties. 展开更多
关键词 Cu2O-Au nanocomposites metal hydride decomposition chemisorption-photocatalysis integrated catalyst
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