A dinuclear complex [DyFe(CN)6(DMF)4(H2O)3]·1.25H2O (DMF=N, N dimethylformamide) 1 based on the cyanide as linkage was prepared and structurally characterized by X ray single crystal structure analysis. The Dy?io...A dinuclear complex [DyFe(CN)6(DMF)4(H2O)3]·1.25H2O (DMF=N, N dimethylformamide) 1 based on the cyanide as linkage was prepared and structurally characterized by X ray single crystal structure analysis. The Dy?ion is eight coordinations in a square antiprism arrangement and the Fe?ion is six coordinations oriented octahedrally. The neutral units [DyFe(CN)6(DMF)4(H2O)3] are held together by hydrogen bonds formed by lattice water molecules, coordinated water molecules and nitrogen atoms of cyanide coming from other distinct complex units to afford a three dimensional framework. CCDC: 192314.展开更多
以N-乙基-3-吲哚三氟甲基β-二酮(EIFD)为主配体,分别以乙二醇单甲醚(EM)、乙二醇二甲醚(EDM)、二缩三乙二醇(TEG)为辅助配体,与DyCl3·6H2O反应合成了一系列Dy(Ⅲ)配合物[Dy(EIFD)3(EM)]·CH2Cl2(1)、[Dy(EIFD)3(EDM)]·CH...以N-乙基-3-吲哚三氟甲基β-二酮(EIFD)为主配体,分别以乙二醇单甲醚(EM)、乙二醇二甲醚(EDM)、二缩三乙二醇(TEG)为辅助配体,与DyCl3·6H2O反应合成了一系列Dy(Ⅲ)配合物[Dy(EIFD)3(EM)]·CH2Cl2(1)、[Dy(EIFD)3(EDM)]·CH2Cl2(2)和[Dy(EIFD)3(TEG)](3)。X射线单晶衍射分析表明,3个配合物都是八配位的单核结构,配位构型分别为双帽三棱柱、正十二面体和双帽三棱柱,分别具有C2v、D2d和C2v对称性。磁学性质显示了配合物1~3具有慢弛豫现象,能垒分别为95.1 K (1)、40.5 K (2)、53.8和13.4 K (3),且配合物1和3有明显的蝴蝶状磁滞回线。进一步讨论了配合物中Dy-O键长和含氧辅助配体的电子效应对配合物有效翻转能垒的影响。展开更多
In this paper, the molecular and crystal structures of the NH4[Y(trans CYDTA)(H2O)2]· 4.5 H2O(trans CYDTA=trans 1,2 cyclohexanediaminetetraacetic acid) are reported. The crystal data are as follows: Triclinic sys...In this paper, the molecular and crystal structures of the NH4[Y(trans CYDTA)(H2O)2]· 4.5 H2O(trans CYDTA=trans 1,2 cyclohexanediaminetetraacetic acid) are reported. The crystal data are as follows: Triclinic system, space group,a=0.8599(6)nm,b=1.0021(7)nm,c=1.4370(9)nm,α =88.095(13)° ,β =75.559(1)° ,γ =88.344(12)° ,V=1.1981(14)nm3,Z=2, M=708.68,Dc=1.570g· cm- 3, μ =2.506mm- 1 and F(000)=590. The final R1 and wR2 are 0.0571 and 0.1350 for 4205 [I >2.0σ (I)] unique reflections and 0.1007 and 0.1615 for all 4981 reflections, respectively. In the title complex, the anion [Y(trans CYDTA)(H2O)2]- has an eight coordination structure with distorted square antiprism. The trans CYDTA which acts as a hexadentate ligand with four O atoms and two N atoms and two H2O molecules directly coordinate to central metal Y? ion. It can be known that the Y? ion can form an eight coordinate compound with aminopolycarboxylic acid ligands in addition nine coordination structure.展开更多
The synthesis and structure of the title complex K_2[Y Ⅲ(dtpa)(H_2O)]·7H_2O (dtpa=diethylenetriaminepentaacetate) were studied. The crystal and molecular structures of the complex were determined by single-crys...The synthesis and structure of the title complex K_2[Y Ⅲ(dtpa)(H_2O)]·7H_2O (dtpa=diethylenetriaminepentaacetate) were studied. The crystal and molecular structures of the complex were determined by single-crystal X-ray structure analysis. The crystal of the complex K_2[Y Ⅲ(dtpa)(H_2O)]·7H_2O belongs to triclinic crystal system and P(-1) space group.The crystal data are as follows:a=0.9671(2)nm,b=1.1327(2)nm,c=1.3389(3)nm,β=86.76(3)°,γ=68.72(3)°,V=1.3324(5)nm3,Z=2,M=699.53,D_C=1.744 g·cm -3,μ=2.586 mm -1 and F(000)=720. The final R and R_W are 0.0467 and 0.1195 for 4524(I>2σ(I)) unique reflections, respectively. The complex anion [Y Ⅲ(dtpa)(H_2O)] 2- has a pseudo-monocapped square antiprismatic nine-coordinate structure in which eight coordinate atoms, three N and five O are from a dtpa ligand and one water molecule coordinates to Y Ⅲ ion directly as the ninth ligand.展开更多
The electroreduction of Y(Ⅲ)on tungsten electrode in NaCl-KCl-YCl_3 melt has been investi- gated by cyclic voltammetry.Deposition of Y(Ⅲ)to Y(0)is reversible in one step.The cyclic voltammetry, convolution voltammet...The electroreduction of Y(Ⅲ)on tungsten electrode in NaCl-KCl-YCl_3 melt has been investi- gated by cyclic voltammetry.Deposition of Y(Ⅲ)to Y(0)is reversible in one step.The cyclic voltammetry, convolution voltammetry,potential-time curve after potentiostatic electrolysis and X-ray diffraction analy- sis were used to study the electrode process of Y(Ⅲ)reduced on iron electrode.Several Y-Fe intermetallic compounds are formed before the deposition of metallic yttrium.The diffusion coefficient and diffusion activation energy of Y in Y_6Fe_(23) were determined by current-time curve at potential step. The results indicate the diffusion of Y in its alloy phase is so slow that this step will control the electrode pro- cess.展开更多
A novel compound, {[Y（HPIDC）（OX）1/2（H2O）]·2H2O}n （1, H3PIDC = 2-（pyridin-4- yl）-1H-imidazole-4,5-dicarboxylic acid, H2OX = oxalic acid）, has been synthesized under hydrothermal conditions and characteri...A novel compound, {[Y（HPIDC）（OX）1/2（H2O）]·2H2O}n （1, H3PIDC = 2-（pyridin-4- yl）-1H-imidazole-4,5-dicarboxylic acid, H2OX = oxalic acid）, has been synthesized under hydrothermal conditions and characterized by thermal analysis （TGA）, powder X-ray diffraction （PXRD）, and single-crystal X-ray diffraction. Complex 1 crystallizes in monoclinic space group P21/c with a = 8.342（8）, b = 14.61（1）, c = 11.487（1）, β = 90.78（9）°, V = 1400.4（2）3, Z = 4, C11H11N3O9Y, Mr = 418.14, Dc = 1.983 g/cm3, F（000） = 836, Rint = 0.0509, T = 293（2） K, μ = 4.240 mm-1, the final R = 0.0477 and wR = 0.1125 for 2770 observed reflections with I 2σ（I）. Compound 1 exhibits a 3D framework and generates the 1D open channels filled with free water molecules. The structure of 1 can be rationalized as a diamondoid network when the atom yttrium is regarded as a 4-connected node linking four surrounding yttrium atoms. The luminescent property of compound 1 is also investigated.展开更多
文摘A dinuclear complex [DyFe(CN)6(DMF)4(H2O)3]·1.25H2O (DMF=N, N dimethylformamide) 1 based on the cyanide as linkage was prepared and structurally characterized by X ray single crystal structure analysis. The Dy?ion is eight coordinations in a square antiprism arrangement and the Fe?ion is six coordinations oriented octahedrally. The neutral units [DyFe(CN)6(DMF)4(H2O)3] are held together by hydrogen bonds formed by lattice water molecules, coordinated water molecules and nitrogen atoms of cyanide coming from other distinct complex units to afford a three dimensional framework. CCDC: 192314.
文摘以N-乙基-3-吲哚三氟甲基β-二酮(EIFD)为主配体,分别以乙二醇单甲醚(EM)、乙二醇二甲醚(EDM)、二缩三乙二醇(TEG)为辅助配体,与DyCl3·6H2O反应合成了一系列Dy(Ⅲ)配合物[Dy(EIFD)3(EM)]·CH2Cl2(1)、[Dy(EIFD)3(EDM)]·CH2Cl2(2)和[Dy(EIFD)3(TEG)](3)。X射线单晶衍射分析表明,3个配合物都是八配位的单核结构,配位构型分别为双帽三棱柱、正十二面体和双帽三棱柱,分别具有C2v、D2d和C2v对称性。磁学性质显示了配合物1~3具有慢弛豫现象,能垒分别为95.1 K (1)、40.5 K (2)、53.8和13.4 K (3),且配合物1和3有明显的蝴蝶状磁滞回线。进一步讨论了配合物中Dy-O键长和含氧辅助配体的电子效应对配合物有效翻转能垒的影响。
文摘In this paper, the molecular and crystal structures of the NH4[Y(trans CYDTA)(H2O)2]· 4.5 H2O(trans CYDTA=trans 1,2 cyclohexanediaminetetraacetic acid) are reported. The crystal data are as follows: Triclinic system, space group,a=0.8599(6)nm,b=1.0021(7)nm,c=1.4370(9)nm,α =88.095(13)° ,β =75.559(1)° ,γ =88.344(12)° ,V=1.1981(14)nm3,Z=2, M=708.68,Dc=1.570g· cm- 3, μ =2.506mm- 1 and F(000)=590. The final R1 and wR2 are 0.0571 and 0.1350 for 4205 [I >2.0σ (I)] unique reflections and 0.1007 and 0.1615 for all 4981 reflections, respectively. In the title complex, the anion [Y(trans CYDTA)(H2O)2]- has an eight coordination structure with distorted square antiprism. The trans CYDTA which acts as a hexadentate ligand with four O atoms and two N atoms and two H2O molecules directly coordinate to central metal Y? ion. It can be known that the Y? ion can form an eight coordinate compound with aminopolycarboxylic acid ligands in addition nine coordination structure.
文摘The synthesis and structure of the title complex K_2[Y Ⅲ(dtpa)(H_2O)]·7H_2O (dtpa=diethylenetriaminepentaacetate) were studied. The crystal and molecular structures of the complex were determined by single-crystal X-ray structure analysis. The crystal of the complex K_2[Y Ⅲ(dtpa)(H_2O)]·7H_2O belongs to triclinic crystal system and P(-1) space group.The crystal data are as follows:a=0.9671(2)nm,b=1.1327(2)nm,c=1.3389(3)nm,β=86.76(3)°,γ=68.72(3)°,V=1.3324(5)nm3,Z=2,M=699.53,D_C=1.744 g·cm -3,μ=2.586 mm -1 and F(000)=720. The final R and R_W are 0.0467 and 0.1195 for 4524(I>2σ(I)) unique reflections, respectively. The complex anion [Y Ⅲ(dtpa)(H_2O)] 2- has a pseudo-monocapped square antiprismatic nine-coordinate structure in which eight coordinate atoms, three N and five O are from a dtpa ligand and one water molecule coordinates to Y Ⅲ ion directly as the ninth ligand.
基金The project supported by the National Natural Science Foundation of China
文摘The electroreduction of Y(Ⅲ)on tungsten electrode in NaCl-KCl-YCl_3 melt has been investi- gated by cyclic voltammetry.Deposition of Y(Ⅲ)to Y(0)is reversible in one step.The cyclic voltammetry, convolution voltammetry,potential-time curve after potentiostatic electrolysis and X-ray diffraction analy- sis were used to study the electrode process of Y(Ⅲ)reduced on iron electrode.Several Y-Fe intermetallic compounds are formed before the deposition of metallic yttrium.The diffusion coefficient and diffusion activation energy of Y in Y_6Fe_(23) were determined by current-time curve at potential step. The results indicate the diffusion of Y in its alloy phase is so slow that this step will control the electrode pro- cess.
基金supported by the 973 key program of the MOST(2010CB933501,2012CB821705)the Chinese Academy of Sciences(KJCX2-YW-319,KJCX2-EW-H01)+1 种基金the National Natural Science Foundation of China(20873150,20821061,20973173,50772113 and 91022008)the Natural Science Foundation of Fujian Province(2007HZ0001-1,2009HZ0004-1,2009HZ0005-1,2009HZ0006-1,2006L2005)
文摘A novel compound, {[Y（HPIDC）（OX）1/2（H2O）]·2H2O}n （1, H3PIDC = 2-（pyridin-4- yl）-1H-imidazole-4,5-dicarboxylic acid, H2OX = oxalic acid）, has been synthesized under hydrothermal conditions and characterized by thermal analysis （TGA）, powder X-ray diffraction （PXRD）, and single-crystal X-ray diffraction. Complex 1 crystallizes in monoclinic space group P21/c with a = 8.342（8）, b = 14.61（1）, c = 11.487（1）, β = 90.78（9）°, V = 1400.4（2）3, Z = 4, C11H11N3O9Y, Mr = 418.14, Dc = 1.983 g/cm3, F（000） = 836, Rint = 0.0509, T = 293（2） K, μ = 4.240 mm-1, the final R = 0.0477 and wR = 0.1125 for 2770 observed reflections with I 2σ（I）. Compound 1 exhibits a 3D framework and generates the 1D open channels filled with free water molecules. The structure of 1 can be rationalized as a diamondoid network when the atom yttrium is regarded as a 4-connected node linking four surrounding yttrium atoms. The luminescent property of compound 1 is also investigated.
