The title compound, [Ni(acac)2(Im)2] (acac = acetylacetone), has been obtained by the reaction of Ni(acac)2 with imidazole ligand in the ethanol solvent. The blue crystal is of triclinic, space group Pi with a = 7.472...The title compound, [Ni(acac)2(Im)2] (acac = acetylacetone), has been obtained by the reaction of Ni(acac)2 with imidazole ligand in the ethanol solvent. The blue crystal is of triclinic, space group Pi with a = 7.472(2), b = 9.456(2), c = 13.823(3) ? a = 85.55(3), = 89.03(3), ? = 80.63(3)o, C16H22N4NiO4, Mr = 393.09, V = 960.7(3) 3, Z = 2, Dc = 1.359 g/cm3, F(000) = 412, = 1.036 mm-1, R = 0.0549 and wR = 0.1615. The crystal structure consists of two disconnected structural units. Each Ni atom coordinated by two N atoms from two imidazole ligands and four O atoms from two acetylactone ligands adopts a slightly distorted octahedron. The structure characterization was performed by means of IR, UV, TG, elemental analysis and single-crystal X-ray analysis. The thermal gravity (TG) data indicate that thermal decomposition of the title compound takes place in two steps, and the residue is NiO.展开更多
A fluorescent Ni（II） complex 1, [Ni（OH-H2Bdc）（Bibimp）]n·nH2O, constructed with 5-hydroxyisophthalic acid（OH-H2Bdc） and 2,6-bis（2-benzimidazolyl）pyridine）（Bibimp） has been synthesized by hydrothermal ...A fluorescent Ni（II） complex 1, [Ni（OH-H2Bdc）（Bibimp）]n·nH2O, constructed with 5-hydroxyisophthalic acid（OH-H2Bdc） and 2,6-bis（2-benzimidazolyl）pyridine）（Bibimp） has been synthesized by hydrothermal methods and structurally characterized by elemental analysis, IR spectroscopy, TG/DTG, fluorescence spectrum and single-crystal X-ray diffraction. The title complex crystallizes in triclinic system, space group P1 with a = 10.187（2）, b = 10.273（2）, c = 13.401（3）A, α = 69.65（3）, β = 69.66（3）, γ = 70.61（3）°, V = 1196.8（4） A3, and Z = 2. The adjacent chains of complex 1 are stacked offset with respect to each other in an ABAB fashion by van der Waals interactions, and only a weak interlayer nonclassical C–H…O hydrogen bond has been observed. Complex 1 displays strong blue fluorescent emissions at 483 nm in the solid state upon photo-excitation at 365 nm at room temperature.展开更多
A new binuclear nickel(II) complex Ni_(2)(HPT)_4(H_(2)O)_(3) (1) has been hydrothermally synthesized with nickel hydroxide,3,4-pyridine dicarboxylic acid and 3-(pyridin-2-yl)-1,2,4-triazole (HPT) in the mixed solution...A new binuclear nickel(II) complex Ni_(2)(HPT)_4(H_(2)O)_(3) (1) has been hydrothermally synthesized with nickel hydroxide,3,4-pyridine dicarboxylic acid and 3-(pyridin-2-yl)-1,2,4-triazole (HPT) in the mixed solution (the volume ratio of methanol and water is 1:4).It crystallizes in tetragonal space group P4_(2)/n,with a=20.844(1),b=20.844(1),c=7.2463(7)A,V=3148.2(5)A^(3),D_(c)=1.587 g/cm^(3),Z=4,μ(Mo Ka)=1.257,F(000)=1544,the final GOOF=1.043,R=0.0437 and w R=0.1297.The crystal structure shows that the whole molecule consists of two nickel ions which are bridged by fourμ_(2)-η^(1):η^(0-3)-(pyridin-2-yl)-1,2,4-triazole anions.The coordination environment of Ni(II) ion is Ni N_(6),giving a distorted octahedral geometry.The thermal stability and fluorescent and magnetic properties of the complex were investigated.展开更多
基金This work was supported bythe Natural Science Foundation of Shandong Province (No. Y2002B06) and Science Research Foundation of Qingdao University of Science and Technology (No. 03Z08)
文摘The title compound, [Ni(acac)2(Im)2] (acac = acetylacetone), has been obtained by the reaction of Ni(acac)2 with imidazole ligand in the ethanol solvent. The blue crystal is of triclinic, space group Pi with a = 7.472(2), b = 9.456(2), c = 13.823(3) ? a = 85.55(3), = 89.03(3), ? = 80.63(3)o, C16H22N4NiO4, Mr = 393.09, V = 960.7(3) 3, Z = 2, Dc = 1.359 g/cm3, F(000) = 412, = 1.036 mm-1, R = 0.0549 and wR = 0.1615. The crystal structure consists of two disconnected structural units. Each Ni atom coordinated by two N atoms from two imidazole ligands and four O atoms from two acetylactone ligands adopts a slightly distorted octahedron. The structure characterization was performed by means of IR, UV, TG, elemental analysis and single-crystal X-ray analysis. The thermal gravity (TG) data indicate that thermal decomposition of the title compound takes place in two steps, and the residue is NiO.
文摘A fluorescent Ni（II） complex 1, [Ni（OH-H2Bdc）（Bibimp）]n·nH2O, constructed with 5-hydroxyisophthalic acid（OH-H2Bdc） and 2,6-bis（2-benzimidazolyl）pyridine）（Bibimp） has been synthesized by hydrothermal methods and structurally characterized by elemental analysis, IR spectroscopy, TG/DTG, fluorescence spectrum and single-crystal X-ray diffraction. The title complex crystallizes in triclinic system, space group P1 with a = 10.187（2）, b = 10.273（2）, c = 13.401（3）A, α = 69.65（3）, β = 69.66（3）, γ = 70.61（3）°, V = 1196.8（4） A3, and Z = 2. The adjacent chains of complex 1 are stacked offset with respect to each other in an ABAB fashion by van der Waals interactions, and only a weak interlayer nonclassical C–H…O hydrogen bond has been observed. Complex 1 displays strong blue fluorescent emissions at 483 nm in the solid state upon photo-excitation at 365 nm at room temperature.
基金Supported by the Natural Science Foundation of Hunan Province(2019JJ60021)Industry and Research Key Project of Hengyang City(2019jhzx1093,2018k KJ016)。
文摘A new binuclear nickel(II) complex Ni_(2)(HPT)_4(H_(2)O)_(3) (1) has been hydrothermally synthesized with nickel hydroxide,3,4-pyridine dicarboxylic acid and 3-(pyridin-2-yl)-1,2,4-triazole (HPT) in the mixed solution (the volume ratio of methanol and water is 1:4).It crystallizes in tetragonal space group P4_(2)/n,with a=20.844(1),b=20.844(1),c=7.2463(7)A,V=3148.2(5)A^(3),D_(c)=1.587 g/cm^(3),Z=4,μ(Mo Ka)=1.257,F(000)=1544,the final GOOF=1.043,R=0.0437 and w R=0.1297.The crystal structure shows that the whole molecule consists of two nickel ions which are bridged by fourμ_(2)-η^(1):η^(0-3)-(pyridin-2-yl)-1,2,4-triazole anions.The coordination environment of Ni(II) ion is Ni N_(6),giving a distorted octahedral geometry.The thermal stability and fluorescent and magnetic properties of the complex were investigated.
文摘以高氯酸镍、二苯甲酰甲烷、二乙酰丙酮为原料合成了新型固态三元配合物[Ni_2(C_(10)H_(12)O_4)(C_(15)H_(11)O_2)_2]·3H_2O,并用元素分析、电导率、红外光谱、电子光谱和电喷雾质谱对其进行了表征,确定了配合物的组成,研究了配合物在氮气气氛中的热分解行为.其变温磁化率(2～300K)的测定结果表明桥联双核Ni^(2+)配合物为弱的反铁磁性自旋交换作用,交换参数为J=-1.04cm^(-1),Weiss常数θ=-2.5 K.
