The title complex [Nd(Gly)(H 2O) 7]Cl 3 was synthesized and its crystal structure was determined by X ray diffraction to obtain a final R value of 0 026 0 and a wR value of 0 086 8. The crystal is of m...The title complex [Nd(Gly)(H 2O) 7]Cl 3 was synthesized and its crystal structure was determined by X ray diffraction to obtain a final R value of 0 026 0 and a wR value of 0 086 8. The crystal is of monoclinic system with a space groug Pm . Every two neodymium ions in the crystal are connected with a carboxyl group to form a polymeric chain molecule. And each neodymium ion is further coordinated with seven oxygen atoms from water molecules. The counter ion(Cl -) is non coordinated to fill up the space between the polymeric chains. So the Nd 3+ cation is nine coordinated and the coordination polyhedron is a trigonotetradecahedron. In addition, there exists the mirror symmetry in the complex.展开更多
The title compound, [Nd(dmso) 7Cl][Bph 4] 2(dmso=dimethylsulfoxide, Bph 4=tetraphenylboron anion) was synthesized in organic solvent acetone/EtOH and the structure was determined by single crystal X ray diffract...The title compound, [Nd(dmso) 7Cl][Bph 4] 2(dmso=dimethylsulfoxide, Bph 4=tetraphenylboron anion) was synthesized in organic solvent acetone/EtOH and the structure was determined by single crystal X ray diffraction. The crystal is triclinic with space group P 1, and the crystal data are as follows: a =1 2554(1) nm, b = 1 2799(1) nm, c =2 4598(3) nm; α =93 53(1)°, β =104 50(1)°, γ =112 77(1)°, V =3 4722(6) nm 3, Z =2, M r=1365 01, D c=1 306 g·cm -3 . The crystal is composed of a big cation [Nd(dmso) 7Cl] 2+ and two big anions [BPh 4] -. The Nd 3+ is coordinated by a chlorine atom and seven oxygen atoms from seven dimethylsulfoxides forming a distorted square antiprism coordination polyhedron,while the BPh - 4 anion is charge equilibrium ion.展开更多
The crystal structure of Nd(ph-CH_2COO)_3H_2O has been determined by X-ray diffraction technique.The crystal behmgs to orthorhombic system with space group P_(na)2_1,cell parameters a=0.7983(1)nm, h=1.3957(1)nm,c=2.02...The crystal structure of Nd(ph-CH_2COO)_3H_2O has been determined by X-ray diffraction technique.The crystal behmgs to orthorhombic system with space group P_(na)2_1,cell parameters a=0.7983(1)nm, h=1.3957(1)nm,c=2.0282(2)nm;V=2.2598(15)nm^3,Z=4.The Mechanism and enthalpy changes of thermal decomposition reaction of the title complex have been studied by TG-DTG-DTA and DSC.展开更多
Single crystals of the title complex Na4 (NH4)10[Nd4Mo29O100(H2O)16]·34H2O obtained from the reaction of (NH4)6Mo7O24 and Nd (NO3)3, crystallize in themonoclinic, space group C2/c, with a= 19. 556(8), b= 43. 22 (...Single crystals of the title complex Na4 (NH4)10[Nd4Mo29O100(H2O)16]·34H2O obtained from the reaction of (NH4)6Mo7O24 and Nd (NO3)3, crystallize in themonoclinic, space group C2/c, with a= 19. 556(8), b= 43. 22 (2), c= 20. 389 (7) A,β= 117. 43(3)°, V= 15297(10) A3, Z=4, Dc= 1. 331g· cm-3, F(000) =5824, μ=1. 875 mm-1, final R(wR) = 0. 0816 (0. 2039) for 6128 unique intensity data [I≥2σ(I)]. In the molecule, each Nd heteroatom is coordinated by nine oxygen atoms with amono-capped square-antiprism configuration[1], while the Mo (VI) ions have severaldifferent coordination numbers (4, 5 and 6) with different configurations such as tetra-hedron, distorted square pyramid and octahedron respectively.展开更多
The title complex (Nd (C18H20N2O4) (NO3)3] was prepared and char-acterized by X-ray diffraction. The complex crystallizes in monociinic system, spacegroup P21/n, a= 14. 220(5) A, b= 11. 777(3) A, c= 14. 812(4) A, β= ...The title complex (Nd (C18H20N2O4) (NO3)3] was prepared and char-acterized by X-ray diffraction. The complex crystallizes in monociinic system, spacegroup P21/n, a= 14. 220(5) A, b= 11. 777(3) A, c= 14. 812(4) A, β= 105. 28(3)°, V= 2393(2) A3, Mr= 658. 63, Z=4, Dx= 1. 828 g/cm3, F(000) = 1308, thefinal R= 0. 053, Rw= 0. 065. In the complex the coordination number of Nd(Ⅲ) is 10with the geometry of a bicapped square antiprism. All of the coordination atoms areoxygen atoms.展开更多
Crystal structure of tetra(1,10-Phenanthroline)neodymium (Ⅲ) tetra(4-aminobenzoate)-hydrate, [Nd(p-ABA)4·2Phen]H+3O·2Phen (p-ABA:p-aminobenzoate,Phen:1,10-phenanthroline) has been determined by X-ray diffra...Crystal structure of tetra(1,10-Phenanthroline)neodymium (Ⅲ) tetra(4-aminobenzoate)-hydrate, [Nd(p-ABA)4·2Phen]H+3O·2Phen (p-ABA:p-aminobenzoate,Phen:1,10-phenanthroline) has been determined by X-ray diffraction.The complex crystallizes in monoclinic, space group C2/c.The cell dimensions are a=1.9067 (5) nm,b=1.9192 (3) nm,c=2.0190 (4) nm,β=117.25 (2) °.V=6.568 (3) nm3, Mr= 1428.63,Z=4 and Dx= 1.45 g·cm-3.The coordination number of Nd atom is 10, and the coordinated polyhedron around the Nd atom is distorted trigonal prism.展开更多
The effect of single coloring agent Nd(NO3)3 on the crystallization, microstructure and colorization of Li2O-Al2O3-SiO2 (LAS) glass ceramics were investigated by differential thermal analysis (DTA), X-ray diffractomet...The effect of single coloring agent Nd(NO3)3 on the crystallization, microstructure and colorization of Li2O-Al2O3-SiO2 (LAS) glass ceramics were investigated by differential thermal analysis (DTA), X-ray diffractometry (XRD) and scanning electron microscopy (SEM). The introduction of little neodymium has no effect on the crystallization manner and the formation of main crystallization phase, but more neodymium will weaken the crystallization of LAS glass. Little neodymium can increase the glossiness of LAS glass ceramic, while more neodymium can color LAS glass with light purple or red purple. The colorability of neodymium for LAS glass ceramic decreases with the increase of crystallization temperature.展开更多
The crystal structure of di-hydroxyisobutyrate)diaquo neodymium nitrate Nd(C_4H_7O_3)_2NO_32H_2O was determined by X-ray diffraction analysis. It belongs to monoclinic,space group C2/C,with cell dimensionsa=8.996(1), ...The crystal structure of di-hydroxyisobutyrate)diaquo neodymium nitrate Nd(C_4H_7O_3)_2NO_32H_2O was determined by X-ray diffraction analysis. It belongs to monoclinic,space group C2/C,with cell dimensionsa=8.996(1), b=8.601(1),c=21.111(3),β=92.38°,V=1632.O,Z=4,D_c=1.83g/cm^3.Crystal structure has been refined by full-matrix least-square techniques giving a final R value of 0.036.The neodymium atom is coordinated to eight oxygen atoms.The nitrate group in complex is not bonded to neodymium,each two neodymium atoms are linked by bridging carboxyl group forming a chain polymeric molecule.展开更多
The complex [Nd(L)(CH_3CN)(CF_3SO_3)_3] has been synthesized, where L=1-methyl-1,4,7,10-tetraazacyclododecane. The crystal structure of the complex has been determined by a fourcircle X-ray diffractometer to a final R...The complex [Nd(L)(CH_3CN)(CF_3SO_3)_3] has been synthesized, where L=1-methyl-1,4,7,10-tetraazacyclododecane. The crystal structure of the complex has been determined by a fourcircle X-ray diffractometer to a final R value of 0.0370 and Rw value of 0.0385 respectively. The crystal is triclinic system, space group P1 with a=8.738(2), b=12.870(3), c=12.900(3), α=85.63(2), β=87.25(2), γ=78.30(2)°, V=1415.71(60)~3, Z=2, Dc=1.92g/cm^3. The neodymiumion is eight-coordinated, forming a distorted square antiprism.展开更多
The title complex was obtained by reaction of hydrated neodymium(Ⅲ) nitrate with N,N-disalicyclideneethylenediamine in DMSO. The complex [Nd(C_6H_4OHCHNC_2H_4NCHC_6H_4OH)(NO_3)_3(CH_3SOCH_3)] crystallizes in monoclin...The title complex was obtained by reaction of hydrated neodymium(Ⅲ) nitrate with N,N-disalicyclideneethylenediamine in DMSO. The complex [Nd(C_6H_4OHCHNC_2H_4NCHC_6H_4OH)(NO_3)_3(CH_3SOCH_3)] crystallizes in monoclinic system, space group- P2_1/n, a=9.663(2), b=16.610(6),c=16.322(5),β=102.77(2)°,V=2555(3),M_r=676.71,Z=4,Dx=1.759 gcm-3. The coordination number of Nd(Ⅲ) is 9 with the geometry of a monocapped square antiprism.All of coordination atoms are oxygen atoms from three bidentate nitrate groups, two dischiff base molecules and one DMSO molecule.展开更多
Nd∶NBW laser crystal with the size of Φ8 mm×20 mm was grown by the process of lifting and pulling. The growth technological parameters which have influence on the completeness of crystal were analyzed and the r...Nd∶NBW laser crystal with the size of Φ8 mm×20 mm was grown by the process of lifting and pulling. The growth technological parameters which have influence on the completeness of crystal were analyzed and the reasonable technological parameters were ascertained.展开更多
The reaction of the THF solution of （C5H5）2NdCl· 2LiCl with n-butyllithium was studied and the neodymium hydride complex, [ Li （ DME ）3 ] [ （C5H5）3Nd （μ-H） Nd （ C5H5 ）3 ] 1 was isolated from the reacti...The reaction of the THF solution of （C5H5）2NdCl· 2LiCl with n-butyllithium was studied and the neodymium hydride complex, [ Li （ DME ）3 ] [ （C5H5）3Nd （μ-H） Nd （ C5H5 ）3 ] 1 was isolated from the reaction solution. Complex 1 was crystallized from a mixture solvent of THF-DME and structurally characterized by single crystal X-ray diffraction method at - 80 ℃. The crystal is monoclinic, space group P21/c with unit cell dimensions a = 0.9670（2） nm, b =2.1001（5） nm, c=2.1279（7） nm, β=9.089（2）°, Z = 4. The structure was solved by heavy atom method and refined by the least-squares method to a final R = 0.094. The complex consists of disconnected ion pairs of [ Li （ DME ）3 ]^＋ and [ （ C5H5 ）3Nd （μ-H） Nd （C5H5）3]^-. The neodymium atom is coordinated by three η5-cyclopentadienyls, and two （C5H5）3Nd species are connected by one hydrogen bridge to form the anion with Nd-H 0.218（1） nm.展开更多
The title complex crystallized in triclinic system with space group P1;Mr=5862. 35 a= 17.04(1), b= 18. 989(5), c= 24. 240(6) A ;a= 100. 18(2), β=92. 24(3), γ= 113. 04(3)°; V=7054(6) A3, Z=2, Dc= 2. 664 g. cm-3,...The title complex crystallized in triclinic system with space group P1;Mr=5862. 35 a= 17.04(1), b= 18. 989(5), c= 24. 240(6) A ;a= 100. 18(2), β=92. 24(3), γ= 113. 04(3)°; V=7054(6) A3, Z=2, Dc= 2. 664 g. cm-3, F(000) =5306, μ= 4. 036 mm-1 and final R= 0. 0763 and Rw= 0. 2176 for 15951 reflections [Ⅰ>2δ(I)]. The Nd(Ⅲ) coordinated with 9 oxygen atoms forms a mono-capped square-antiprism configuration, while the Mo (Ⅵ) ions have several different coordinationnumbers such as 4, 5 and 6 with different configurations such as tetrahedron, distortedsquare pyramid and octahedron respectively.展开更多
A new sulfate inorganic framework, {（C2H8N）9[Nds（SO4）12]·2H2O}n （1） templated by organic amine, has been solvothermally synthesized and characterized by TGA, PXRD and single-crystal X-ray diffraction. Compo...A new sulfate inorganic framework, {（C2H8N）9[Nds（SO4）12]·2H2O}n （1） templated by organic amine, has been solvothermally synthesized and characterized by TGA, PXRD and single-crystal X-ray diffraction. Compound 1 crystalizes in monoclinic, space group C2/c with a = 20.570（5）, b = 35.815（8）, c = 10.106（2） A, C108H72NgNd5050S12, Mr = 2315.73, V= 6765（3） A3, Z = 4, Dc = 2.274 g·cm-3, μ = 4.253 mm-1, F（000 = 4520, 2.52〈θ〈25°, λ（MoKa） = 0.71073 A, T= 273（2） K, the final R =0.0401, wR = 0.1022 and S = 1.042. X-ray diffraction analysis reveals that complex 1 possesses a 3D inorganic sulfate framework with large 20-membered ring （20 MR） and 10-membered ring （10 MR） channels constructed by two kinds of SBUs. Moreover, the UV-vis and luminescent properties of comolex I were also investigated展开更多
A new Nd（Ⅲ） nitronyl nitroxide complex [Nd（NIT2Py）2（NO3）3] （NIT2Py = 2-（2＇-pyridyl）-4,4,5,5-tetramethylimidazoline-l-oxyl-3-oxide） has been synthesized and structurally characterized by X-ray diffraction. ...A new Nd（Ⅲ） nitronyl nitroxide complex [Nd（NIT2Py）2（NO3）3] （NIT2Py = 2-（2＇-pyridyl）-4,4,5,5-tetramethylimidazoline-l-oxyl-3-oxide） has been synthesized and structurally characterized by X-ray diffraction. It crystallizes in monoclinic, space group P21/n with a = 12.396（4）, b =11.134（4）, c = 23.360（7） A°, β = 98.178（6）°, V= 3191.2（18） A°^3, C24H32N9NdO13, Mr = 798.83, Dc =1.663 g/cm^3, μ（MoKa） = 1.704 mm^-1, F（000） = 1612, Z = 4, the final R = 0.0425 and wR = 0.0957 for 6532 independentreflections with Rint = 0.0642 and 4552 observed reflections （I 〉 2σ（I））. The complex exists as discrete mononuclear molecules and the neodymium（Ⅲ） ion is ten-coordinated with three bidentate nitrate anions and two radical ligands （NIT2Py） via bidentate chelating mode.The optical properties of the complex are discussed.展开更多
文摘The title complex [Nd(Gly)(H 2O) 7]Cl 3 was synthesized and its crystal structure was determined by X ray diffraction to obtain a final R value of 0 026 0 and a wR value of 0 086 8. The crystal is of monoclinic system with a space groug Pm . Every two neodymium ions in the crystal are connected with a carboxyl group to form a polymeric chain molecule. And each neodymium ion is further coordinated with seven oxygen atoms from water molecules. The counter ion(Cl -) is non coordinated to fill up the space between the polymeric chains. So the Nd 3+ cation is nine coordinated and the coordination polyhedron is a trigonotetradecahedron. In addition, there exists the mirror symmetry in the complex.
文摘The title compound, [Nd(dmso) 7Cl][Bph 4] 2(dmso=dimethylsulfoxide, Bph 4=tetraphenylboron anion) was synthesized in organic solvent acetone/EtOH and the structure was determined by single crystal X ray diffraction. The crystal is triclinic with space group P 1, and the crystal data are as follows: a =1 2554(1) nm, b = 1 2799(1) nm, c =2 4598(3) nm; α =93 53(1)°, β =104 50(1)°, γ =112 77(1)°, V =3 4722(6) nm 3, Z =2, M r=1365 01, D c=1 306 g·cm -3 . The crystal is composed of a big cation [Nd(dmso) 7Cl] 2+ and two big anions [BPh 4] -. The Nd 3+ is coordinated by a chlorine atom and seven oxygen atoms from seven dimethylsulfoxides forming a distorted square antiprism coordination polyhedron,while the BPh - 4 anion is charge equilibrium ion.
文摘The crystal structure of Nd(ph-CH_2COO)_3H_2O has been determined by X-ray diffraction technique.The crystal behmgs to orthorhombic system with space group P_(na)2_1,cell parameters a=0.7983(1)nm, h=1.3957(1)nm,c=2.0282(2)nm;V=2.2598(15)nm^3,Z=4.The Mechanism and enthalpy changes of thermal decomposition reaction of the title complex have been studied by TG-DTG-DTA and DSC.
文摘Single crystals of the title complex Na4 (NH4)10[Nd4Mo29O100(H2O)16]·34H2O obtained from the reaction of (NH4)6Mo7O24 and Nd (NO3)3, crystallize in themonoclinic, space group C2/c, with a= 19. 556(8), b= 43. 22 (2), c= 20. 389 (7) A,β= 117. 43(3)°, V= 15297(10) A3, Z=4, Dc= 1. 331g· cm-3, F(000) =5824, μ=1. 875 mm-1, final R(wR) = 0. 0816 (0. 2039) for 6128 unique intensity data [I≥2σ(I)]. In the molecule, each Nd heteroatom is coordinated by nine oxygen atoms with amono-capped square-antiprism configuration[1], while the Mo (VI) ions have severaldifferent coordination numbers (4, 5 and 6) with different configurations such as tetra-hedron, distorted square pyramid and octahedron respectively.
文摘The title complex (Nd (C18H20N2O4) (NO3)3] was prepared and char-acterized by X-ray diffraction. The complex crystallizes in monociinic system, spacegroup P21/n, a= 14. 220(5) A, b= 11. 777(3) A, c= 14. 812(4) A, β= 105. 28(3)°, V= 2393(2) A3, Mr= 658. 63, Z=4, Dx= 1. 828 g/cm3, F(000) = 1308, thefinal R= 0. 053, Rw= 0. 065. In the complex the coordination number of Nd(Ⅲ) is 10with the geometry of a bicapped square antiprism. All of the coordination atoms areoxygen atoms.
文摘Crystal structure of tetra(1,10-Phenanthroline)neodymium (Ⅲ) tetra(4-aminobenzoate)-hydrate, [Nd(p-ABA)4·2Phen]H+3O·2Phen (p-ABA:p-aminobenzoate,Phen:1,10-phenanthroline) has been determined by X-ray diffraction.The complex crystallizes in monoclinic, space group C2/c.The cell dimensions are a=1.9067 (5) nm,b=1.9192 (3) nm,c=2.0190 (4) nm,β=117.25 (2) °.V=6.568 (3) nm3, Mr= 1428.63,Z=4 and Dx= 1.45 g·cm-3.The coordination number of Nd atom is 10, and the coordinated polyhedron around the Nd atom is distorted trigonal prism.
文摘The effect of single coloring agent Nd(NO3)3 on the crystallization, microstructure and colorization of Li2O-Al2O3-SiO2 (LAS) glass ceramics were investigated by differential thermal analysis (DTA), X-ray diffractometry (XRD) and scanning electron microscopy (SEM). The introduction of little neodymium has no effect on the crystallization manner and the formation of main crystallization phase, but more neodymium will weaken the crystallization of LAS glass. Little neodymium can increase the glossiness of LAS glass ceramic, while more neodymium can color LAS glass with light purple or red purple. The colorability of neodymium for LAS glass ceramic decreases with the increase of crystallization temperature.
文摘The crystal structure of di-hydroxyisobutyrate)diaquo neodymium nitrate Nd(C_4H_7O_3)_2NO_32H_2O was determined by X-ray diffraction analysis. It belongs to monoclinic,space group C2/C,with cell dimensionsa=8.996(1), b=8.601(1),c=21.111(3),β=92.38°,V=1632.O,Z=4,D_c=1.83g/cm^3.Crystal structure has been refined by full-matrix least-square techniques giving a final R value of 0.036.The neodymium atom is coordinated to eight oxygen atoms.The nitrate group in complex is not bonded to neodymium,each two neodymium atoms are linked by bridging carboxyl group forming a chain polymeric molecule.
文摘The complex [Nd(L)(CH_3CN)(CF_3SO_3)_3] has been synthesized, where L=1-methyl-1,4,7,10-tetraazacyclododecane. The crystal structure of the complex has been determined by a fourcircle X-ray diffractometer to a final R value of 0.0370 and Rw value of 0.0385 respectively. The crystal is triclinic system, space group P1 with a=8.738(2), b=12.870(3), c=12.900(3), α=85.63(2), β=87.25(2), γ=78.30(2)°, V=1415.71(60)~3, Z=2, Dc=1.92g/cm^3. The neodymiumion is eight-coordinated, forming a distorted square antiprism.
文摘The title complex was obtained by reaction of hydrated neodymium(Ⅲ) nitrate with N,N-disalicyclideneethylenediamine in DMSO. The complex [Nd(C_6H_4OHCHNC_2H_4NCHC_6H_4OH)(NO_3)_3(CH_3SOCH_3)] crystallizes in monoclinic system, space group- P2_1/n, a=9.663(2), b=16.610(6),c=16.322(5),β=102.77(2)°,V=2555(3),M_r=676.71,Z=4,Dx=1.759 gcm-3. The coordination number of Nd(Ⅲ) is 9 with the geometry of a monocapped square antiprism.All of coordination atoms are oxygen atoms from three bidentate nitrate groups, two dischiff base molecules and one DMSO molecule.
文摘Nd∶NBW laser crystal with the size of Φ8 mm×20 mm was grown by the process of lifting and pulling. The growth technological parameters which have influence on the completeness of crystal were analyzed and the reasonable technological parameters were ascertained.
文摘The reaction of the THF solution of （C5H5）2NdCl· 2LiCl with n-butyllithium was studied and the neodymium hydride complex, [ Li （ DME ）3 ] [ （C5H5）3Nd （μ-H） Nd （ C5H5 ）3 ] 1 was isolated from the reaction solution. Complex 1 was crystallized from a mixture solvent of THF-DME and structurally characterized by single crystal X-ray diffraction method at - 80 ℃. The crystal is monoclinic, space group P21/c with unit cell dimensions a = 0.9670（2） nm, b =2.1001（5） nm, c=2.1279（7） nm, β=9.089（2）°, Z = 4. The structure was solved by heavy atom method and refined by the least-squares method to a final R = 0.094. The complex consists of disconnected ion pairs of [ Li （ DME ）3 ]^＋ and [ （ C5H5 ）3Nd （μ-H） Nd （C5H5）3]^-. The neodymium atom is coordinated by three η5-cyclopentadienyls, and two （C5H5）3Nd species are connected by one hydrogen bridge to form the anion with Nd-H 0.218（1） nm.
文摘The title complex crystallized in triclinic system with space group P1;Mr=5862. 35 a= 17.04(1), b= 18. 989(5), c= 24. 240(6) A ;a= 100. 18(2), β=92. 24(3), γ= 113. 04(3)°; V=7054(6) A3, Z=2, Dc= 2. 664 g. cm-3, F(000) =5306, μ= 4. 036 mm-1 and final R= 0. 0763 and Rw= 0. 2176 for 15951 reflections [Ⅰ>2δ(I)]. The Nd(Ⅲ) coordinated with 9 oxygen atoms forms a mono-capped square-antiprism configuration, while the Mo (Ⅵ) ions have several different coordinationnumbers such as 4, 5 and 6 with different configurations such as tetrahedron, distortedsquare pyramid and octahedron respectively.
基金Supported by the NSFC(No.21001115)the Fundamental Research Funds for the Central Universities(13CX02006A,13CX05015A)the scientific research foundation of Shandong province Outstanding Young Scientist Award(BS2011CL041)
文摘A new sulfate inorganic framework, {（C2H8N）9[Nds（SO4）12]·2H2O}n （1） templated by organic amine, has been solvothermally synthesized and characterized by TGA, PXRD and single-crystal X-ray diffraction. Compound 1 crystalizes in monoclinic, space group C2/c with a = 20.570（5）, b = 35.815（8）, c = 10.106（2） A, C108H72NgNd5050S12, Mr = 2315.73, V= 6765（3） A3, Z = 4, Dc = 2.274 g·cm-3, μ = 4.253 mm-1, F（000 = 4520, 2.52〈θ〈25°, λ（MoKa） = 0.71073 A, T= 273（2） K, the final R =0.0401, wR = 0.1022 and S = 1.042. X-ray diffraction analysis reveals that complex 1 possesses a 3D inorganic sulfate framework with large 20-membered ring （20 MR） and 10-membered ring （10 MR） channels constructed by two kinds of SBUs. Moreover, the UV-vis and luminescent properties of comolex I were also investigated
基金This work was supported by the National Natural Science Foundation of China (No. 20331010) and Natural Science Foundation of Tianjin (No. 033602011)
文摘A new Nd（Ⅲ） nitronyl nitroxide complex [Nd（NIT2Py）2（NO3）3] （NIT2Py = 2-（2＇-pyridyl）-4,4,5,5-tetramethylimidazoline-l-oxyl-3-oxide） has been synthesized and structurally characterized by X-ray diffraction. It crystallizes in monoclinic, space group P21/n with a = 12.396（4）, b =11.134（4）, c = 23.360（7） A°, β = 98.178（6）°, V= 3191.2（18） A°^3, C24H32N9NdO13, Mr = 798.83, Dc =1.663 g/cm^3, μ（MoKa） = 1.704 mm^-1, F（000） = 1612, Z = 4, the final R = 0.0425 and wR = 0.0957 for 6532 independentreflections with Rint = 0.0642 and 4552 observed reflections （I 〉 2σ（I））. The complex exists as discrete mononuclear molecules and the neodymium（Ⅲ） ion is ten-coordinated with three bidentate nitrate anions and two radical ligands （NIT2Py） via bidentate chelating mode.The optical properties of the complex are discussed.
