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An analytical method for Fe(Ⅱ) and Fe(Ⅲ) determination in pharmaceutical grade iron sucrose complex and sodium ferric gluconate complex 被引量:5
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作者 Daniele Merli Antonella Profumo Carlo Dossi 《Journal of Pharmaceutical Analysis》 SCIE CAS 2012年第6期450-453,共4页
A robust voltammetric method has been developed and validated for the determination of Fe(Ⅱ) and Fe(Ⅲ) in pharmaceutical iron polysaccharidic complexes. Undesirable low molecular weight iron complexes, at concen... A robust voltammetric method has been developed and validated for the determination of Fe(Ⅱ) and Fe(Ⅲ) in pharmaceutical iron polysaccharidic complexes. Undesirable low molecular weight iron complexes, at concentration about 3% in the pharmaceutical formulation, can be easily determined with good accuracy and precision. This methodology can be proposed as a viable, environmentally sustainable substitute for the conventional Normal Pulse Polarographic method in US Pharmacopeia, with better analytical figures of merit, and reduced Hg consumption. A deeper insight in Fe(Ⅱ) and Fe(Ⅲ) composition can be gained by the combined use of a new potentiometric technique after chemical decomposition of the complex. 展开更多
关键词 Sodium ferric gluconatecomplex iron sucrose complex iron polysaccharides VOLTAMMETRY
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Electric Conductivity Study of o-Substituted Phenoxo Iron (Ⅲ) Complexes 被引量:2
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作者 Ramadan Ali Bawa 《Journal of Chemistry and Chemical Engineering》 2010年第5期54-58,共5页
关键词 铁() 导电性 配合物 取代酚 电动 紫外可见光谱 金属离子 水杨酸甲酯
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Fe(Ⅲ)-XG配合物选择性絮凝微细粒赤铁矿与石英及其机理研究
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作者 韩英棋 杨志超 +4 位作者 滕青 张郭阳 方淑华 张素红 刘生玉 《有色金属(选矿部分)》 CAS 2024年第1期116-125,共10页
基于金属离子配位理论,将FeCl_(3)·6H_(2)O与黄原胶(XG)按一定比例混合制备Fe(Ⅲ)-XG配合物,用于改善微细粒赤铁矿难沉降、回收效果差的问题。采用沉降实验研究了不同条件下Fe(Ⅲ)-XG对微细粒赤铁矿和石英的选择性絮凝行为,结合动... 基于金属离子配位理论,将FeCl_(3)·6H_(2)O与黄原胶(XG)按一定比例混合制备Fe(Ⅲ)-XG配合物,用于改善微细粒赤铁矿难沉降、回收效果差的问题。采用沉降实验研究了不同条件下Fe(Ⅲ)-XG对微细粒赤铁矿和石英的选择性絮凝行为,结合动电位、红外光谱和显微镜分析,揭示Fe(Ⅲ)-XG对赤铁矿的絮凝作用机理。矿物絮凝沉降试验结果表明:以黄原胶和Fe(Ⅲ)为絮凝剂,无法实现赤铁矿与石英的选择性絮凝,而黄原胶与FeCl_(3)·6H_(2)O质量比为1︰9时生成的Fe(Ⅲ)-XG配位絮凝剂,对赤铁矿和石英表现出较强的选择性絮凝作用,pH值为6时两者沉降率差异最大,分别为91.50%和39.96%。显微镜观察结果证实,Fe(Ⅲ)-XG作用下,赤铁矿颗粒形成块状絮体,且絮体密实程度更大,而石英颗粒间未发生团聚作用,处于相对分散的状态。Zeta电位、溶液化学计算、吸附量实验与红外光谱分析结果表明:黄原胶主要通过羧酸基团的羰基C=O与Fe^(3+)发生配位作用形成Fe(Ⅲ)-XG配合物,Fe(Ⅲ)-XG在石英和赤铁矿表面吸附方式不同,因而在两种矿物表面吸附量不同。Fe(Ⅲ)-XG中的羟基氧和赤铁矿表面的铁元素发生化学键合特异性吸附在赤铁矿表面,而在石英表面只有微弱的氢键吸附。通过FeCl_(3)·6H_(2)O与黄原胶配位组装可显著提升微细粒赤铁矿选择性絮凝分离效果,为赤铁矿选择性絮凝分选提供新的策略和理论指导。 展开更多
关键词 Fe()-XG配合物 赤铁矿 石英 絮凝剂 选择性絮凝 微细粒
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Synthesis and DNA cleavage activity of diiron(Ⅲ) complex bearing pyrene group 被引量:1
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作者 Xiao Qiang Chen Jing Yun Wang +2 位作者 Tong Yan Zhang Li Zhu Zhang Xiao Jun Peng 《Chinese Chemical Letters》 SCIE CAS CSCD 2008年第3期342-344,共3页
As DNA cleavage agent, a new diiron(Ⅲ) complex (Fe2Lb), in which a DNA-intercalator (pyrene) is covalently linked to a diferric moiety, has been synthesized and characterized. The DNA-binding property and DNA c... As DNA cleavage agent, a new diiron(Ⅲ) complex (Fe2Lb), in which a DNA-intercalator (pyrene) is covalently linked to a diferric moiety, has been synthesized and characterized. The DNA-binding property and DNA cleavage activity of the complex have also been investigated. 展开更多
关键词 Diiron complex INTERCALATOR PYRENE DNA cleavage
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OXIDATION OF ALKYLBENZENES CATALYZED BY IRON( Ⅱ,Ⅲ)-1,10-PHENANTHROLINE AND 2, 2'-BIPYRIDINE COMPLEXES 被引量:1
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作者 Zi Qiang LEI Yun Pu WANG 《Chinese Chemical Letters》 SCIE CAS CSCD 1993年第1期21-22,共2页
Oxidation of alkybenzenes PhCH_2R(R=H, CH_3, C_2H_5 and n-C_3H_7) under 1 atm. of O_2 or air catalyzed by iron(Ⅱ, Ⅲ)-2,2'-bipyridine and 1,10-phenanthroline complexes, affords the aryl-substituted ketones and al... Oxidation of alkybenzenes PhCH_2R(R=H, CH_3, C_2H_5 and n-C_3H_7) under 1 atm. of O_2 or air catalyzed by iron(Ⅱ, Ⅲ)-2,2'-bipyridine and 1,10-phenanthroline complexes, affords the aryl-substituted ketones and alcohols with the conversion of 15.00%~34.58% containing of 97.60%~99.80% ketones and alcohols. The turnover numbers of these catalysts are over 3500 mol-cat. ^(-1)for 3.5 h. 展开更多
关键词 PHENANTHROLINE AND 2 BIPYRIDINE complexES OXIDATION OF ALKYLBENZENES CATALYZED BY iron
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Aerobic Enantioselective Epoxidation of Styrene Analogues Induced by (β-Diketone)-iron( Ⅲ ) Complex
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作者 Qing Fang CHENG Xing You XU +2 位作者 Wei Xing MA Shu Jie YANG Tian Pa YOU 《Chinese Chemical Letters》 SCIE CAS CSCD 2005年第11期1467-1470,共4页
Tris(d,d-dicampholylmethanato) iron (Ⅲ) complex, Fe(dcm)3, was found to be an excellent catalyst for asymmetric oxygenation of styrene analogues into the corresponding epoxides. Good chemical yields and higher ... Tris(d,d-dicampholylmethanato) iron (Ⅲ) complex, Fe(dcm)3, was found to be an excellent catalyst for asymmetric oxygenation of styrene analogues into the corresponding epoxides. Good chemical yields and higher enantioselectivity were obtained with combined use of molecular oxygen and an aldehyde at 30℃, Some factors influencing enantioselectivity were discussed. 展开更多
关键词 EPOXIDATION oliefin asymmetric catalysis (β-diketone)-iron complex.
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Structure and Magnetic Property of an Oxygenand Carboxamide-bridged One-dimensional Iron(Ⅲ) Complex [Fe_2(μ-O)(bpb)_2]_n
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作者 聂景 李国玲 +2 位作者 苗宝喜 倪中海 张丽芳 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2012年第8期1129-1134,共6页
The structure of the title complex [Fe2(μ-O)(bpb)2]n (bpb 2=1,2-bis(pyridine-2carboxamido) benzenate) has been characterized by single-crystal X-ray diffraction analysis.The complex (C36 H24 Fe2N8O5,Mr=760.3... The structure of the title complex [Fe2(μ-O)(bpb)2]n (bpb 2=1,2-bis(pyridine-2carboxamido) benzenate) has been characterized by single-crystal X-ray diffraction analysis.The complex (C36 H24 Fe2N8O5,Mr=760.33) crystallizes in the monoclinic space group P2 1/c with a=8.4615(17),b=33.704(7),c=11.173(2),β=91.12(3)o,V=3185.7(11)3,Z=4,D c=1.585 g/cm 3,μ(MoK)=0.970 mm-1,F(000)=1552,R int=0.0381,the final R=0.0454 and wR=0.1114.The magnetic susceptibilities of the complex have been examined in the temperature range of 2-300 K.The magnetic data were fitted to give the parameters of J d=-77.7(9) and J c=-11.5(6) cm-1. 展开更多
关键词 crystal structure magnetic property iron complex
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Synthesis,Crystal Structure and Electrochemistry Properties of an Iron(Ⅲ) Complex Based on the 3,5-Pyridinedicarboxylate and Water Ligands
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作者 冯勋 赵建社 +1 位作者 王利亚 师新阁 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2010年第2期290-296,共7页
Reaction of 3,5-pyridine-dicarboxylic acid(3,5-PydcH2) with iron salt in hydrothermal condition results in the formation of a three-dimensional self-assembly network formulated as [C14H14Fe2N2O12]n,and it has been s... Reaction of 3,5-pyridine-dicarboxylic acid(3,5-PydcH2) with iron salt in hydrothermal condition results in the formation of a three-dimensional self-assembly network formulated as [C14H14Fe2N2O12]n,and it has been structurally characterized by elemental analysis,IR spectra and X-ray diffraction.It crystallizes in the monoclinic system,space group C2/c with a=9.9633(15),b=12.0942(18),c=7.4297(11)A and β=105.822o.The units of Fe2(pydc)2·2H2O are linked into a one-dimensional structure via the chelate carboxylate groups from the 3,5-pyridine-dicarboxylate.The interlayer hydrogen bonding interactions result in a three-dimensional supramolecular architecture.In the complex,the Fe(Ⅲ) ion displays a slightly distorted pentagonal bipyramidal geometry with seven coordination numbers.Cyclic-voltammetry measurement reveals the oxidation and reduction processes for the complex are quasi-reversible in nature. 展开更多
关键词 X-ray structure iron complex topology cyclic-voltammetry
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羟胺强化Fe(Ⅲ)-NTA络合物活化过二硫酸盐降解磺胺甲恶唑
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作者 王真然 彭藴斓 +1 位作者 刘义青 付永胜 《安全与环境学报》 CAS CSCD 北大核心 2024年第3期1163-1172,共10页
针对Fe(Ⅱ)/过二硫酸盐(Peroxydisulfate,PDS)高级氧化技术存在的pH值应用范围窄、铁泥产量大等缺陷,研究构建Fe(Ⅲ)-氨三乙酸(Nitrilotriacetic Acid,NTA)/羟胺(Hydroxylamine,HAm)/PDS体系,以在中性条件下高效降解水中新污染物磺胺甲... 针对Fe(Ⅱ)/过二硫酸盐(Peroxydisulfate,PDS)高级氧化技术存在的pH值应用范围窄、铁泥产量大等缺陷,研究构建Fe(Ⅲ)-氨三乙酸(Nitrilotriacetic Acid,NTA)/羟胺(Hydroxylamine,HAm)/PDS体系,以在中性条件下高效降解水中新污染物磺胺甲恶唑(Sulfamethoxazole,SMX)。研究结果显示,Fe(Ⅲ)-NTA/HAm/PDS体系在pH=7条件下对SMX的降解率可达91%,该体系降解SMX的主要活性物种为·SO_(4)^(-)和·OH。SMX在Fe(Ⅲ)-NTA/HAm/PDS体系中的降解效率随溶液pH值的升高而降低,且增加Fe(Ⅲ)、PDS的用量会加速SMX降解。NTA的引入可将Fe(Ⅱ)/PDS体系的pH值应用范围由酸性拓展至弱碱性,与此同时,向体系内加入HAm可有效减少铁泥的产量。根据检测到的降解产物,提出SMX在Fe(Ⅲ)-NTA/HAm/PDS体系中可能的降解途径包括断键反应、羟基化反应、氨基氧化反应。双酚AF、双氯芬酸、土霉素等其他新污染物也能在Fe(Ⅲ)-NTA/HAm/PDS体系中被高效去除,表明该体系在新污染物的降解领域有较大的应用潜力。 展开更多
关键词 环境工程学 磺胺甲恶唑 羟胺 Fe()-NTA络合物 过二硫酸盐
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Fe(Ⅲ)/2,6-吡啶二羧酸活化高碘酸盐强化染料脱色的效能与机制
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作者 陈文政 苏晗 +2 位作者 钟欣洋 牛丽君 冯明宝 《化学试剂》 CAS 2024年第4期59-64,共6页
有色染料是环境中非常重要的污染源之一,严重威胁着水生生态环境和人类健康。由于其难以被天然降解,且传统的污水处理工艺亦无法实现其高效去除,因此急需开发绿色、高效的水处理工艺进行有色染料污染控制。发现Fe(Ⅲ)/2,6-吡啶二羧酸(2,... 有色染料是环境中非常重要的污染源之一,严重威胁着水生生态环境和人类健康。由于其难以被天然降解,且传统的污水处理工艺亦无法实现其高效去除,因此急需开发绿色、高效的水处理工艺进行有色染料污染控制。发现Fe(Ⅲ)/2,6-吡啶二羧酸(2,6-PDA)可高效活化高碘酸盐(PI)实现亚甲基蓝(MB)这一典型染料的高效降解。实验结果表明,该体系在Fe(Ⅲ)浓度为10μmol/L、2,6-PDA浓度为10μmol/L和PI浓度为200μmol/L时,可在pH 3.0条件下使5 mg/L MB降解率在120 s内大于97%。该方法依托高级氧化原理和配位强化策略,利用PI对有色染料进行降解,为目前染料废水治理提供了新思路从而有效地修复了污染水体。 展开更多
关键词 亚甲基蓝 高碘酸盐 配位活化 Fe() 高级氧化
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基于三氰基铁(Ⅲ)酸盐的Fe^(Ⅲ)_(4)Ni^(Ⅱ)_(2)六核配合物的合成、结构及磁性 被引量:2
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作者 李国玲 王蒙蒙 +2 位作者 唐新学 张然 倪中海 《无机化学学报》 SCIE CAS CSCD 北大核心 2023年第8期1564-1570,共7页
利用三氰基铁酸盐(Bu_(4)N)[FeⅢ(Tp)(CN)_(3)](Tp=氢化三(1-吡唑基)硼酸)与配体2,9-二吡唑基-1,10-菲咯啉(dpzpen)以及高氯酸镍反应合成了一例氰根桥联的Fe^(Ⅲ)_(4)Ni^(Ⅱ)_(2)六核配合物[Fe_(4)Ni_(2)(Tp)_(4)(CN)_(12)(dpzpen)_(2)]... 利用三氰基铁酸盐(Bu_(4)N)[FeⅢ(Tp)(CN)_(3)](Tp=氢化三(1-吡唑基)硼酸)与配体2,9-二吡唑基-1,10-菲咯啉(dpzpen)以及高氯酸镍反应合成了一例氰根桥联的Fe^(Ⅲ)_(4)Ni^(Ⅱ)_(2)六核配合物[Fe_(4)Ni_(2)(Tp)_(4)(CN)_(12)(dpzpen)_(2)]·12H_(2)O·3CH_(3)OH (1)。结构研究表明配合物1具有近似菱形的Fe^(Ⅲ)_(2)Ni^(Ⅱ)_(2)骨架结构,另外2个Fe则通过氰根延伸在菱形的外侧。磁性研究表明在配合物1中氰根桥联的Fe和Ni表现出铁磁相互作用。更为重要的是,基于配合物1的结构模型,对它的变温磁化率数据进行拟合得到了不同Fe-Ni之间的磁耦合常数,得到的最佳磁耦合常数J3d(15.73 cm^(-1))>J2d(3.53 cm^(-1))≈J1d(3.50 cm^(-1))与Ni-N键的键长以及Ni-N≡C键角的变化趋势有关(J3d:0.206 5 nm,169.8°;J2d:0.206 2 nm,163.1°;J1d:0.198 7 nm,161.6°)。以上结果表明Ni-N键长越短,Ni-N≡C键角越大,Fe与Ni之间的铁磁耦合越强。 展开更多
关键词 三氰基铁酸盐 FeNi配合物 晶体结构 磁性 磁性-结构相互关系
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铜离子选择性电极研究铁(Ⅲ)与Tiron,HOx配位化合物
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作者 魏昌明 陈连山 +1 位作者 马桂芝 何钟林 《辽宁师范大学学报(自然科学版)》 CAS 1994年第3期217-221,共5页
用固态膜铜离子选择性电极研究Fe(Ⅲ)与1,2-二羟基苯-3,5-二磺酸钠溶液配合物的组成和表观稳定常数.离于强度I=0.1mol·L-1,pH=2.1时生成1:1型配合物,pH=3.08时Fe(Ⅲ)与8-羟基喹... 用固态膜铜离子选择性电极研究Fe(Ⅲ)与1,2-二羟基苯-3,5-二磺酸钠溶液配合物的组成和表观稳定常数.离于强度I=0.1mol·L-1,pH=2.1时生成1:1型配合物,pH=3.08时Fe(Ⅲ)与8-羟基喹啉生成1:1和1:2型两种溶液配位化合物. 展开更多
关键词 铁络合物 离子选择电极
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三核铜(Ⅱ)-稀土(Ⅲ)席夫碱配合物的合成、分子结构和性质
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作者 刘一夫 马方伟 《黑龙江大学工程学报(中英俄文)》 2023年第4期18-25,共8页
通过四齿铜(Ⅱ)席夫碱配合物(CuSaltn)与硝酸镧(Ⅲ)反应,合成了一系列的3d-4f异金属席夫碱配合物(CuSaltn)_(2)Ln(H_(2)O)(NO_(3))_(3)(Ln=镧(1),铈(2),镨(3),钕(4),钐(5)),其中Saltn为1,3-丙二胺缩双水杨醛席夫碱配体。对配体和配合物... 通过四齿铜(Ⅱ)席夫碱配合物(CuSaltn)与硝酸镧(Ⅲ)反应,合成了一系列的3d-4f异金属席夫碱配合物(CuSaltn)_(2)Ln(H_(2)O)(NO_(3))_(3)(Ln=镧(1),铈(2),镨(3),钕(4),钐(5)),其中Saltn为1,3-丙二胺缩双水杨醛席夫碱配体。对配体和配合物进行了元素分析、热失重、红外光谱、紫外光谱等分析表征。在室温下测定了配合物5的晶体结构,钐(Ⅲ)离子与两个双齿铜配合物、两个双齿硝酸盐离子和一个水分子形成九配位构型。形成三核铜(Ⅱ)-稀土(Ⅲ)配合物后,配合物的荧光显著降低。该类化合物的结构研究为其他类似的席夫碱配合物的研究提供有价值的信息,并且会被应用于荧光性能的研究。 展开更多
关键词 铜(Ⅱ)-稀土()配合物 席夫碱 晶体结构
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Influence of shape anisotropy on microwave complex permeability in carbonyl iron flakes/epoxy resin composites 被引量:7
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作者 温福昇 乔亮 +3 位作者 周栋 左文亮 伊海波 李发伸 《Chinese Physics B》 SCIE EI CAS CSCD 2008年第6期2263-2267,共5页
To explore the mechanism of carbonyl iron flake composites for microwave complex permeability, this paper investigates the feature of the flakes. The shape anisotropy was certified by the results of the magnetization ... To explore the mechanism of carbonyl iron flake composites for microwave complex permeability, this paper investigates the feature of the flakes. The shape anisotropy was certified by the results of the magnetization hysteresis loops and the Mossbauer spectra. Furthermore, the shape anisotropy was used to explain the origin of composite microwave performance, and the calculated results agree with the experiment. It is believed that the shape anisotropy dominates microwave complex permeability, and the natural resonance plays main role in flake. 展开更多
关键词 carbonyl iron flake complex permeability shape anisotropy Mossbauer spectroscopy
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Thermal Decomposition Kinetics and Mechanism of Tb(Ⅲ) m-Methylbenzoate Complex with 1,10-Phenanthroline in Static Air Atmosphere 被引量:5
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作者 ZHANG Jian-jun WANG Rui-fen +1 位作者 ZHANG Jian-ling WANG Shu-ping 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2002年第1期25-29,共5页
The thermal behavior of [Tb_2( m -MBA)_6(phen)_2](H_2O)_2( m -MBA=C_8H_7O_2, methoxybenzoate; phen=C_ 12 H_8N_2, 1,10-phenanthroline) in static air atmosphere was investigated by means of TG-DTG and DTA methods. The... The thermal behavior of [Tb_2( m -MBA)_6(phen)_2](H_2O)_2( m -MBA=C_8H_7O_2, methoxybenzoate; phen=C_ 12 H_8N_2, 1,10-phenanthroline) in static air atmosphere was investigated by means of TG-DTG and DTA methods. The thermal decomposition of the title compound takes place mainly in two steps. The intermediate and the residue for each decomposition were identified by the TG curve. By the kinetic method of processing thermal analysis data put forward by Malek et al ., it is defined that the kinetics model for the first-step thermal decomposition is SB( m,n ). 展开更多
关键词 Thermal decomposition Non-isothermal kinetics Tb() complex m-Methylbenzoate 1 10-PHENANTHROLINE
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Synthesis of Eu(Ⅲ) and Tb(Ⅲ) Complexes with New Aryl Amide Type Tetrapodal Ligand and Their Luminescence Properties 被引量:3
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作者 蔡正洪 谭民裕 《Journal of Rare Earths》 SCIE EI CAS CSCD 2002年第5期382-384,共3页
A new aryl amide type tetrapodal ligand L (1, 1, 1, 1 tetrakis-{[(2 benzylaminoformyl) phenoxyl]methyl}methane) and its europium and terbium nitrate complexes were synthesized. The luminescence properties of these c... A new aryl amide type tetrapodal ligand L (1, 1, 1, 1 tetrakis-{[(2 benzylaminoformyl) phenoxyl]methyl}methane) and its europium and terbium nitrate complexes were synthesized. The luminescence properties of these complexes were also studied. 展开更多
关键词 rare earths aryl amide tetrapodal ligand Eu() and Tb() complexes luminescence property
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Photochemical degradation of environmentally persistent perfluorooctanoic acid (PFOA) in the presence of Fe(Ⅲ) 被引量:3
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作者 Yuan Wang Peng Yi Zhang +1 位作者 Gang pan Hao chen 《Chinese Chemical Letters》 SCIE CAS CSCD 2008年第3期371-374,共4页
Environmentally persistent and bioaccumulative perfluorooctanic acid (PFOA) was difficult to be decomposed under the irradiation of 254 nm UV light. However, in the presence of 80μmol/L Fe(Ⅲ), 80% of PFOA with i... Environmentally persistent and bioaccumulative perfluorooctanic acid (PFOA) was difficult to be decomposed under the irradiation of 254 nm UV light. However, in the presence of 80μmol/L Fe(Ⅲ), 80% of PFOA with initial concentration of 48μmol/L (20 mg/L) was effectively degraded and 47.8% of fluorine atoms in PFOA molecule were transformed into inorganic fluoride ion after 4 h reaction. Shorter chain perfluorocarboxylic acids bearing C3-C7 and fluoride ion were detected and identified by LC/MS and IC as the degradation products in the aqueous solution. It was proposed that complexes of PFOA with Fe(Ⅲ) initiated degradation of PFOA irradiated with 254 nm UV light. 展开更多
关键词 Perfluorooctanoic acid iron Photochemical degradation 254 nm UV light
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Synthesis,Fluorescence and Magnetic Properties of a New Europium(Ⅲ)Complex Eu(C14H9O3)2(C12H8N2)2(NO3) 被引量:5
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作者 杨颖群 李玉林 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2018年第11期1781-1785,共5页
A new europium(III)complex Eu(CHO)(CHN)(NO)has been synthesized with 2-benzoylbenzoic acid and 1,10-phenanthroline as ligands.Crystal data for the complex are as follows:monoclinic,space group P2/c,a=9.6733(6),b=22.95... A new europium(III)complex Eu(CHO)(CHN)(NO)has been synthesized with 2-benzoylbenzoic acid and 1,10-phenanthroline as ligands.Crystal data for the complex are as follows:monoclinic,space group P2/c,a=9.6733(6),b=22.9521(14),c=19.7701(12)?,β=94.9800(10)o,V=4372.8(5)?~3,D=1.557 g/cm~3,Z=4,μ(Mo Kα)=1.501 mm,F(000)=2064,the final R=0.0214 and w R=0.0510.The Eu(III)ion is coordinated by ten atoms to give a bicapped square antiprism coordination geometry.The complex shows two intense fluorescence emission bands arising from the transitions of Eu:~5D→~7F(594 nm)and ~5D→~7F(618 nm).In addition,its XT decreases from 1.29767 cm~3?mol?K at 300 K to 0.01531 cm~3?mol?K at 2 K. 展开更多
关键词 europium() complex crystal structure fluorescent and magnetic properties
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Intercalation Assembly, Characterization and Luminescent Properties of Novel Supramolecular Composite Materials, Tb(Ⅲ) Complex with Tetrapodal Ligand-Montmorillonite 被引量:3
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作者 Jiang Wei Tang Yu +2 位作者 Xu Li Liu Weisheng Tan Minyu 《Journal of Rare Earths》 SCIE EI CAS CSCD 2006年第5期537-537,共1页
Two kinds of Tb( Ⅲ ) complexes with tetrapodal ligand, [TbL(NO3)]^3+ and [TbL]^3+ (L: 1,1, 1', 1'-tera ( 2-pyridinecarboxylester )-di ( trimethylpropane)) were intercalated into the interlayer space of... Two kinds of Tb( Ⅲ ) complexes with tetrapodal ligand, [TbL(NO3)]^3+ and [TbL]^3+ (L: 1,1, 1', 1'-tera ( 2-pyridinecarboxylester )-di ( trimethylpropane)) were intercalated into the interlayer space of montmorillonite (MT) by ion exchange and coordination reaction of L with the Tb^3+ ion existing in the interlayer space of Tb-MT respectively. The obtained luminescent supramolecular composite materials, [ TbL (NO3) ]^2+-MT and [TbL]^3+-MT were characterized by elemental analysis, XRD, FT-IR, UV-vis and thermal analysis. At the same time, the luminescent properties of the materials were also studied. The results show that the intercalated materials with regular layered structure, good thermal stability and the interlayer spacing (d001) approximates to the size of the complex ions which are located in the interlayer space of MT in the form of a monolayer. 展开更多
关键词 Tb( complexes with tetrapodal ligand MONTMORILLONITE supramolecular composite materials intercalation assembly luminescent properties rare earths
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Catalytic performance of cerium iron complex oxides for partial oxidation of methane to synthesis gas 被引量:2
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作者 李孔斋 王华 +1 位作者 魏永刚 刘明春 《Journal of Rare Earths》 SCIE EI CAS CSCD 2008年第5期705-710,共6页
The cerium iron complex oxides oxygen carrier was prepared by the co-precipitation method. The reactions between methane and lattice oxygen from the complex oxides were investigated in a fixed micro-reactor system. Th... The cerium iron complex oxides oxygen carrier was prepared by the co-precipitation method. The reactions between methane and lattice oxygen from the complex oxides were investigated in a fixed micro-reactor system. The reduced oxygen carder could be re-oxidized by air and its initial state could be restored. The characterizations of the oxygen carders were studied using XRD, O2-TPD, and H2-TPR. The results showed that the bulk lattice oxygen of CeO2-Fe2O3 was found to be suitable for the partial oxidation of methane to synthesis gas. There were two kinds of oxygen species on the oxygen carrier: the stronger oxygen species that was responsible for the complete oxidation of methane, and the weaker oxygen species (bulk lattice oxygen) that was responsible for the selective oxidation of methane to CO and H2 at a higher temperature. Then, the lost bulk lattice oxygen could be selectively supplemented by air re-oxidation at an appropriate reaction condition. CeFeO3 appeared on the oxygen carrier after 10 successive redox cycles, however, it was not bad for the selectivity of CO and H2. 展开更多
关键词 METHANE cerium iron complex oxides lattice oxygen selective oxidation SYNGAS cycles rare earths
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