The synthesis is and crystal structure are reported for the sheet-like compourd [CU2(oxpn)Fe(CN )5(NO)]. there oxpn is the dianion of M, M'-bis(3-aminopropyl)oxamide. This compound crustallizes in the orthogonal s...The synthesis is and crystal structure are reported for the sheet-like compourd [CU2(oxpn)Fe(CN )5(NO)]. there oxpn is the dianion of M, M'-bis(3-aminopropyl)oxamide. This compound crustallizes in the orthogonal space group Puma. with a=11 .413(4), b=22.242(5), c=7.736(2) A, and Z=4.The structure was refined to conventionat discrepancy factors R=0.047 and Pw=0.054. The Cu(II ) and Fe(III)centers are bridged by oxpn and cyanide, the formal behaves as a his-terdentate tigand bound to cooper(II)ion to form (II) dimers. whereas the latter bridges Cu(II) and Fe(III) centers in both symmetric and asymetric end- to-end bis-monodentate fashions, spreading out along be plane to form a 20 network. The Structure is made up of CuFe unit with Cu(II) and Fe(III) ions locating in a distorted square-based pyramid and a compressed octahedron, respectively.展开更多
Reaction of 2-pyridone, copper acetate and terbium(or yttrium) perchlorate in acetone with the mole ratio 6: 2: 1 results in the formation of heteronuclear complex Ln_2Cu_4L_8 (HL)_4 (OH)_2 (ClO_4)_4 (H_20)_(10) 2CH_3...Reaction of 2-pyridone, copper acetate and terbium(or yttrium) perchlorate in acetone with the mole ratio 6: 2: 1 results in the formation of heteronuclear complex Ln_2Cu_4L_8 (HL)_4 (OH)_2 (ClO_4)_4 (H_20)_(10) 2CH_3COCH_3(Ln = Tb (1), Y (2)). By recrystallizing (1) in CHCl_3 single crystals were obtained and the structure was determined by four-circle diffractometer. Data showed that the crystal is in space group C2/m with a=27. 454(9)A, b=13, 608A, c=30. 556(11)A, β=99. 89(3)°, v=11245. 7(7. 5)A^3. The structure was solved by a combination of Patterson method and Fourier technique. The final R value is 0. 103. In the structure, four copper and two terbium ions are bridged by 2-pyridone anions to form an essentially octahedral Cu_4Tb_2 core. The terbium atoms are each eight-coordinate and the copper atoms are five-coordinate.展开更多
The ordering of the α-Fe(Si) crystallization phase in annealed Fe73.5Cu1Mo3Si13.5B9 alloy has been studied using XRD method. The α-Fe(Si) phase in Fe73.5Cu1Mo3Si13.5B9 alloy annealed at 460℃ for 1 h consists of th...The ordering of the α-Fe(Si) crystallization phase in annealed Fe73.5Cu1Mo3Si13.5B9 alloy has been studied using XRD method. The α-Fe(Si) phase in Fe73.5Cu1Mo3Si13.5B9 alloy annealed at 460℃ for 1 h consists of the DO3-type ordered region with spherical shape and disordered region. The size of DO3 ordered region increases with the annealing temperature. When the annealing temperature is 560℃, the size of the ordered region in the α-Fe(Si) grain is 14.0nm,which is nearly as large as that of the α-Fe(Si) grain (14.2 nm) and the degree of order of the α-Fe(Si) phase is about 0.78. When Fe73.5Cu1 Mo3Si13.5B9 amorphous alloy is annealed at 520℃， with the increment of the annealing time, the shape of the DO3 ordered region in the α-Fe(Si) phase is spheroidal at the beginning of the annealing and becomes spherical and has asize of 12.8 nm when the annealing time is 60 min. In addition, the DO3 superlattice lines of the α-Fe(Si) phase will vanish if Fe73.5Cu1Mo3Si13.5 B9 amorphous alloy is annealed for 1 h at 750℃.展开更多
Fe（0.2 mol%）：Cu（0.04 mol%）：LiNbO3 crystals with different doping concentration of In^3＋ （0, 1.0, 2.0, 3.0mol%） were grown by Czochralski method, and then oxidized and reduced. The infrared transmittance spect...Fe（0.2 mol%）：Cu（0.04 mol%）：LiNbO3 crystals with different doping concentration of In^3＋ （0, 1.0, 2.0, 3.0mol%） were grown by Czochralski method, and then oxidized and reduced. The infrared transmittance spectra of crystals were measured to investigate the location of doping ion and its threshold concentration. The photorefractive properties of the crystals were tested by two beam coupling experiment. The results showed that the threshold concentration of In ions is 2.0～ 3.0 mol% and In ions take the place of NbLi^4＋ to form （ InLi^2＋） before reaching its threshold concentration, and then the location of normal Nb ions. In the （2.0 mol%）：Fe：Cu：LiNbO3 crystal with the oxidation treatment having the highest diffraction efficiency （η = 45.8%）, the photo-damage resistance threshold value R of In（3.0 mol%）：Fe：Cu：LiNbO3 was 3.67×10^4 W/cm^2 which was two orders of magnitude higher than that of Fe：Cu：LiNbO3 crystal （4.30×10^2 W/cm^2）. And the photo-damage resistance ability was enhanced by oxidized treatment. The In（2.0～3.0 mol%）：Fe：Cu：LiNbO3 crystals with oxidized treatment have the best photorefractive properties.展开更多
ZnO(4mol%),In 2O 3(1mol%)and Fe 2O 3(0.05mol%)were doped in LiNbO 3 and Czochralski method was used to grow Zn∶In∶Fe∶LiNbO 3 crystal.The diameter of the crystal we grew is 30mm.The technology parameter we took is t...ZnO(4mol%),In 2O 3(1mol%)and Fe 2O 3(0.05mol%)were doped in LiNbO 3 and Czochralski method was used to grow Zn∶In∶Fe∶LiNbO 3 crystal.The diameter of the crystal we grew is 30mm.The technology parameter we took is that the axial temperature gradient is 40℃/cm,the growth rate is 1mm/h, the rotation rate is 15-25r/min,the temperature of polarization is 1220℃ and the current density of polarization is 5mA/cm 2.The wafer dimension is 10mm×10mm×3mm and was covered in Li 2CO 3 powder to reduce.The reduction temperature is 500℃ and reduction time is 30 hours. OH - stretch vibration transmission spectra were measured by Fourier infrared spectrophotometer. There are two absorption peaks in OH - spectra of Zn∶In∶Fe∶LiNbO 3,in which one is at 3534cm -1 (2.83μm) and the other is at 3505cm -1 (2.85μm).The peak at 2.85μm is far lower than that at 2.83μm. Because of the threshold effect of Zn 2+ and In 3+ ,the peak at 2.83μm is generated and the peak at 2.85μm is related with Fe 3+ .In LiNbO 3 only doped with Fe,Li + site is taken place by Fe 3+ .When doping Zn 2+ and In 3+ in high concentration,these two ions take place Nb that is at Li site and Fe 3+ substitutes for Nb 5+ at the same time.The interaction between Fe 3+ and OH - make the OH - peak shift to 2.85μm.展开更多
文摘The synthesis is and crystal structure are reported for the sheet-like compourd [CU2(oxpn)Fe(CN )5(NO)]. there oxpn is the dianion of M, M'-bis(3-aminopropyl)oxamide. This compound crustallizes in the orthogonal space group Puma. with a=11 .413(4), b=22.242(5), c=7.736(2) A, and Z=4.The structure was refined to conventionat discrepancy factors R=0.047 and Pw=0.054. The Cu(II ) and Fe(III)centers are bridged by oxpn and cyanide, the formal behaves as a his-terdentate tigand bound to cooper(II)ion to form (II) dimers. whereas the latter bridges Cu(II) and Fe(III) centers in both symmetric and asymetric end- to-end bis-monodentate fashions, spreading out along be plane to form a 20 network. The Structure is made up of CuFe unit with Cu(II) and Fe(III) ions locating in a distorted square-based pyramid and a compressed octahedron, respectively.
基金Project supported by China National Climbing plan and National Nature Science Foundation
文摘Reaction of 2-pyridone, copper acetate and terbium(or yttrium) perchlorate in acetone with the mole ratio 6: 2: 1 results in the formation of heteronuclear complex Ln_2Cu_4L_8 (HL)_4 (OH)_2 (ClO_4)_4 (H_20)_(10) 2CH_3COCH_3(Ln = Tb (1), Y (2)). By recrystallizing (1) in CHCl_3 single crystals were obtained and the structure was determined by four-circle diffractometer. Data showed that the crystal is in space group C2/m with a=27. 454(9)A, b=13, 608A, c=30. 556(11)A, β=99. 89(3)°, v=11245. 7(7. 5)A^3. The structure was solved by a combination of Patterson method and Fourier technique. The final R value is 0. 103. In the structure, four copper and two terbium ions are bridged by 2-pyridone anions to form an essentially octahedral Cu_4Tb_2 core. The terbium atoms are each eight-coordinate and the copper atoms are five-coordinate.
文摘The ordering of the α-Fe(Si) crystallization phase in annealed Fe73.5Cu1Mo3Si13.5B9 alloy has been studied using XRD method. The α-Fe(Si) phase in Fe73.5Cu1Mo3Si13.5B9 alloy annealed at 460℃ for 1 h consists of the DO3-type ordered region with spherical shape and disordered region. The size of DO3 ordered region increases with the annealing temperature. When the annealing temperature is 560℃, the size of the ordered region in the α-Fe(Si) grain is 14.0nm,which is nearly as large as that of the α-Fe(Si) grain (14.2 nm) and the degree of order of the α-Fe(Si) phase is about 0.78. When Fe73.5Cu1 Mo3Si13.5B9 amorphous alloy is annealed at 520℃， with the increment of the annealing time, the shape of the DO3 ordered region in the α-Fe(Si) phase is spheroidal at the beginning of the annealing and becomes spherical and has asize of 12.8 nm when the annealing time is 60 min. In addition, the DO3 superlattice lines of the α-Fe(Si) phase will vanish if Fe73.5Cu1Mo3Si13.5 B9 amorphous alloy is annealed for 1 h at 750℃.
基金This work was supported by Harbin Science and Technology Project (No. 2005AA5CG058)Natural Science Foundation of Heilongjiang Province (No. A0203)
文摘Fe（0.2 mol%）：Cu（0.04 mol%）：LiNbO3 crystals with different doping concentration of In^3＋ （0, 1.0, 2.0, 3.0mol%） were grown by Czochralski method, and then oxidized and reduced. The infrared transmittance spectra of crystals were measured to investigate the location of doping ion and its threshold concentration. The photorefractive properties of the crystals were tested by two beam coupling experiment. The results showed that the threshold concentration of In ions is 2.0～ 3.0 mol% and In ions take the place of NbLi^4＋ to form （ InLi^2＋） before reaching its threshold concentration, and then the location of normal Nb ions. In the （2.0 mol%）：Fe：Cu：LiNbO3 crystal with the oxidation treatment having the highest diffraction efficiency （η = 45.8%）, the photo-damage resistance threshold value R of In（3.0 mol%）：Fe：Cu：LiNbO3 was 3.67×10^4 W/cm^2 which was two orders of magnitude higher than that of Fe：Cu：LiNbO3 crystal （4.30×10^2 W/cm^2）. And the photo-damage resistance ability was enhanced by oxidized treatment. The In（2.0～3.0 mol%）：Fe：Cu：LiNbO3 crystals with oxidized treatment have the best photorefractive properties.
文摘ZnO(4mol%),In 2O 3(1mol%)and Fe 2O 3(0.05mol%)were doped in LiNbO 3 and Czochralski method was used to grow Zn∶In∶Fe∶LiNbO 3 crystal.The diameter of the crystal we grew is 30mm.The technology parameter we took is that the axial temperature gradient is 40℃/cm,the growth rate is 1mm/h, the rotation rate is 15-25r/min,the temperature of polarization is 1220℃ and the current density of polarization is 5mA/cm 2.The wafer dimension is 10mm×10mm×3mm and was covered in Li 2CO 3 powder to reduce.The reduction temperature is 500℃ and reduction time is 30 hours. OH - stretch vibration transmission spectra were measured by Fourier infrared spectrophotometer. There are two absorption peaks in OH - spectra of Zn∶In∶Fe∶LiNbO 3,in which one is at 3534cm -1 (2.83μm) and the other is at 3505cm -1 (2.85μm).The peak at 2.85μm is far lower than that at 2.83μm. Because of the threshold effect of Zn 2+ and In 3+ ,the peak at 2.83μm is generated and the peak at 2.85μm is related with Fe 3+ .In LiNbO 3 only doped with Fe,Li + site is taken place by Fe 3+ .When doping Zn 2+ and In 3+ in high concentration,these two ions take place Nb that is at Li site and Fe 3+ substitutes for Nb 5+ at the same time.The interaction between Fe 3+ and OH - make the OH - peak shift to 2.85μm.
