由4,4’-(乙烷-1,2-二氧基)-二苯甲酸构筑的钴(II)配合物的水热合成与晶体结构 Hydrothermal Synthesis and Crystal Structure of a Cobalt(II) Coordination Polymer Assembled by 4,4?-(Ethane-1,2-diyldioxy)dibenzoic Acid
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引用次数: 0
Abstract
采用水热法合成了一个分子式为[Co(eoba)(phen)(H2O)2]•H2O的配合物(H2boba = 4,4’-(乙烷-1,2-二氧基)-二苯甲酸,phen = 1,10-邻菲咯啉),并对其进行了元素分析、红外光谱、热重和X-射线单晶衍射的结构解析。该配合物(C28H26CoN2O9)属于单斜晶系,P2(1)/c空间群,晶体学数据:a = 13.708(5) A,b = 20.237(5) A,c =10.158(5) A,β = 105.071(5)˚,V = 2721.0(18) A3,Mr = 593.44,Dc = 1.449 g/cm3,μ(MoKα) = 0.688 mm-1,F(000) = 1228,Z = 4。直接法解析原子位置的结果显示:R = 0.0409,wR = 0.0933。该配合物为二维网状结构,并通过氢键和π–π堆积形成超分子结构。 A coordination polymer formulated as [Co(eoba)(phen)(H2O)2]•H2O (H2boba = 4,4΄-(ethane- 1,2-diyldioxy) dibenzoic acid, phen = 1,10-phenanthroline) has been hydrothermally synthesized and structurally characterized by elemental analysis, IR, TG and single-crystal X-ray diffraction. The title compound (C28H26CoN2O9) crystallizes in the monoclinic system, space group P2(1)/c with a = 13.708(5) A, b = 20.237(5) A, c = 10.158(5) A, β = 105.071(5)˚, V = 2721.0(18) A3, Mr = 593.44, Dc= 1.449 g/cm3, μ(MoKα) = 0.688 mm-1, F(000) = 1228, Z = 4, the final R = 0.0409 and wR = 0.0933. It exhibits a two-dimensional network structure and extended into a supramolecular framework through hydrogen bonds and π-π interactions.
由4,4’-(乙烷-1,2-二氧基)-二苯甲酸构筑的钴(II)配合物的水热合成与晶体结构 Hydrothermal Synthesis and Crystal Structure of a Cobalt(II) Coordination Polymer Assembled by 4,4?-(Ethane-1,2-diyldioxy)dibenzoic Acid
采用水热法合成了一个分子式为[Co(eoba)(phen)(H2O)2]•H2O的配合物(H2boba = 4,4’-(乙烷-1,2-二氧基)-二苯甲酸,phen = 1,10-邻菲咯啉),并对其进行了元素分析、红外光谱、热重和X-射线单晶衍射的结构解析。该配合物(C28H26CoN2O9)属于单斜晶系,P2(1)/c空间群,晶体学数据:a = 13.708(5) A,b = 20.237(5) A,c =10.158(5) A,β = 105.071(5)˚,V = 2721.0(18) A3,Mr = 593.44,Dc = 1.449 g/cm3,μ(MoKα) = 0.688 mm-1,F(000) = 1228,Z = 4。直接法解析原子位置的结果显示:R = 0.0409,wR = 0.0933。该配合物为二维网状结构,并通过氢键和π–π堆积形成超分子结构。 A coordination polymer formulated as [Co(eoba)(phen)(H2O)2]•H2O (H2boba = 4,4΄-(ethane- 1,2-diyldioxy) dibenzoic acid, phen = 1,10-phenanthroline) has been hydrothermally synthesized and structurally characterized by elemental analysis, IR, TG and single-crystal X-ray diffraction. The title compound (C28H26CoN2O9) crystallizes in the monoclinic system, space group P2(1)/c with a = 13.708(5) A, b = 20.237(5) A, c = 10.158(5) A, β = 105.071(5)˚, V = 2721.0(18) A3, Mr = 593.44, Dc= 1.449 g/cm3, μ(MoKα) = 0.688 mm-1, F(000) = 1228, Z = 4, the final R = 0.0409 and wR = 0.0933. It exhibits a two-dimensional network structure and extended into a supramolecular framework through hydrogen bonds and π-π interactions.