A new binuclear copper(Ⅱ) complex, [Cu2(phen)2(H2O)2( μ2-C2O4)](NO3)2, has been synthesized and characterized by elemental analysis, IR and UV-Vis spectrum. Its crystal structure was determined by single crystal X-r...A new binuclear copper(Ⅱ) complex, [Cu2(phen)2(H2O)2( μ2-C2O4)](NO3)2, has been synthesized and characterized by elemental analysis, IR and UV-Vis spectrum. Its crystal structure was determined by single crystal X-ray diffraction techniques. Crystal data: monoclinic, space group P21/c, a=0.712 21(8) nm, b=1.170 93(14) nm, c=1.783 7(2) nm, β=111.828(2)°, and V=1.380 8(3) nm3, Dc=1.769 Mg·m-3, Z=2, F(000)=744, R1=0.025 4, wR2=0.069 5, Gof=1.077, Δρ=328^-455 e·nm-3. The complex is packed by one centrosymmetry binuclear copper(Ⅱ) unit, oxalate dianion and NO3- anion. In the molecule structure of the title complex, two Cu(Ⅱ) ions are bridged by oxalate dianion and each Cu(Ⅱ) ions coordinates with two nitrogen atoms from 1,10-phenanthroline ligand and one oxygen atom from water to form a five-coordinate distorted square-pyramidal configuration. The hydrogen bonds are observed between coordinated water molecules and NO3- anions. The analysis of the crystal structure indicates that the complex has a two-dimensional stacking network structure, which is formed by intramolecular hydrogen bonds, intermolecular hydrogen bonds and stacking effect of aromatic ring. CCDC: 255345.展开更多
A ( μ oxo)( μ CO 3)diiron(Ⅲ) complex of tri(2 pyridylmethyl)amine(TPA), [Fe 2L 2( μ O) ( μ CO 3)] (ClO 4) 2·MeOH·EtOH·H 2O], was synthesized and characterized, where L represents TPA. This complex ...A ( μ oxo)( μ CO 3)diiron(Ⅲ) complex of tri(2 pyridylmethyl)amine(TPA), [Fe 2L 2( μ O) ( μ CO 3)] (ClO 4) 2·MeOH·EtOH·H 2O], was synthesized and characterized, where L represents TPA. This complex crystallizes in the monoclinic space group P2 1/c with a =1.181 0(3) nm, b =3.728 1(8) nm, c = 1.377 0(3) nm , β =115.393(3)°, V =5.477(2) nm 3, Z =4. R 1=0.084 9 and wR 2=0.196 2. The UV Vis spectra of this compound show multiply absorption bands in 200-800 nm range, which are similar to that of N - 3 coordinated met hemerythrin. , was synthesized and characterized, where L represents TPA. This complex crystallizes in the monoclinic space group P2 1/c with a =1.181 0(3) nm, b =3.728 1(8) nm, c = 1.377 0(3) nm , β =115.393(3)°, V =5.477(2) nm 3, Z =4. R 1=0.084 9 and wR 2=0.196 2. The UV Vis spectra of this compound show multiply absorption bands in 200-800 nm range, which are similar to that of N - 3 coordinated met hemerythrin.展开更多
Three binuclear Nickel(Ⅱ) complexes were synthesized, bridged with dithiooxalate, Ni2(Bpy)3(Dto)2(H2O)3 (1), Ni2(Phen)3(Dto)2(H2O)3 (2) and Ni2(Me2Bpy)3(Dto)2(H2O)2 (3) (Bpy=2,2′-Bipyridine, Phen=1,10-phenanthroline...Three binuclear Nickel(Ⅱ) complexes were synthesized, bridged with dithiooxalate, Ni2(Bpy)3(Dto)2(H2O)3 (1), Ni2(Phen)3(Dto)2(H2O)3 (2) and Ni2(Me2Bpy)3(Dto)2(H2O)2 (3) (Bpy=2,2′-Bipyridine, Phen=1,10-phenanthroline, Me2Bpy=4,4′-dimethyl-2,2′-bipyridine, Dto2-=Dithiooxalate), and characterized by elemental analyses, IR, UV-Visible spectra, conductance. The variable temperature magnetic susceptibilities for the complexes were measured in the range of temperature between 1.5 K and 298 K. Experimental data of magnetic susceptibility were successfully fit to theoretical value based on the spin Hamiltonian operator: H=-2JS1S2, S1=S2=1, giving the magnetic exchange parameters of 2J=-52.8 cm-1. This result indicates the presence of a strong antiferromagnetic spin exchange interaction between the Ni(Ⅱ) ions. The magnetic exchange parameters of the binuclear Nickel(Ⅱ) complexes bridged with dithiooxalate is larger than that of the binuclear Nickel(Ⅱ) complexes bridged with oxalate. Dithiooxalate is more effective to transfer antiferromagnetic spin exchange interaction between the Ni(Ⅱ) ions than oxalate.展开更多
文摘A new binuclear copper(Ⅱ) complex, [Cu2(phen)2(H2O)2( μ2-C2O4)](NO3)2, has been synthesized and characterized by elemental analysis, IR and UV-Vis spectrum. Its crystal structure was determined by single crystal X-ray diffraction techniques. Crystal data: monoclinic, space group P21/c, a=0.712 21(8) nm, b=1.170 93(14) nm, c=1.783 7(2) nm, β=111.828(2)°, and V=1.380 8(3) nm3, Dc=1.769 Mg·m-3, Z=2, F(000)=744, R1=0.025 4, wR2=0.069 5, Gof=1.077, Δρ=328^-455 e·nm-3. The complex is packed by one centrosymmetry binuclear copper(Ⅱ) unit, oxalate dianion and NO3- anion. In the molecule structure of the title complex, two Cu(Ⅱ) ions are bridged by oxalate dianion and each Cu(Ⅱ) ions coordinates with two nitrogen atoms from 1,10-phenanthroline ligand and one oxygen atom from water to form a five-coordinate distorted square-pyramidal configuration. The hydrogen bonds are observed between coordinated water molecules and NO3- anions. The analysis of the crystal structure indicates that the complex has a two-dimensional stacking network structure, which is formed by intramolecular hydrogen bonds, intermolecular hydrogen bonds and stacking effect of aromatic ring. CCDC: 255345.
文摘A ( μ oxo)( μ CO 3)diiron(Ⅲ) complex of tri(2 pyridylmethyl)amine(TPA), [Fe 2L 2( μ O) ( μ CO 3)] (ClO 4) 2·MeOH·EtOH·H 2O], was synthesized and characterized, where L represents TPA. This complex crystallizes in the monoclinic space group P2 1/c with a =1.181 0(3) nm, b =3.728 1(8) nm, c = 1.377 0(3) nm , β =115.393(3)°, V =5.477(2) nm 3, Z =4. R 1=0.084 9 and wR 2=0.196 2. The UV Vis spectra of this compound show multiply absorption bands in 200-800 nm range, which are similar to that of N - 3 coordinated met hemerythrin. , was synthesized and characterized, where L represents TPA. This complex crystallizes in the monoclinic space group P2 1/c with a =1.181 0(3) nm, b =3.728 1(8) nm, c = 1.377 0(3) nm , β =115.393(3)°, V =5.477(2) nm 3, Z =4. R 1=0.084 9 and wR 2=0.196 2. The UV Vis spectra of this compound show multiply absorption bands in 200-800 nm range, which are similar to that of N - 3 coordinated met hemerythrin.
文摘Three binuclear Nickel(Ⅱ) complexes were synthesized, bridged with dithiooxalate, Ni2(Bpy)3(Dto)2(H2O)3 (1), Ni2(Phen)3(Dto)2(H2O)3 (2) and Ni2(Me2Bpy)3(Dto)2(H2O)2 (3) (Bpy=2,2′-Bipyridine, Phen=1,10-phenanthroline, Me2Bpy=4,4′-dimethyl-2,2′-bipyridine, Dto2-=Dithiooxalate), and characterized by elemental analyses, IR, UV-Visible spectra, conductance. The variable temperature magnetic susceptibilities for the complexes were measured in the range of temperature between 1.5 K and 298 K. Experimental data of magnetic susceptibility were successfully fit to theoretical value based on the spin Hamiltonian operator: H=-2JS1S2, S1=S2=1, giving the magnetic exchange parameters of 2J=-52.8 cm-1. This result indicates the presence of a strong antiferromagnetic spin exchange interaction between the Ni(Ⅱ) ions. The magnetic exchange parameters of the binuclear Nickel(Ⅱ) complexes bridged with dithiooxalate is larger than that of the binuclear Nickel(Ⅱ) complexes bridged with oxalate. Dithiooxalate is more effective to transfer antiferromagnetic spin exchange interaction between the Ni(Ⅱ) ions than oxalate.
