苯并咪唑-5,6-二甲酸-锰配合物的合成,晶体结构和磁性质(英文)
Synthesis, Crystal Structure and Magnetic Properties of Mn(Ⅱ) Benzimidazole-5,6-dicarboxylate Complex
作者单位
林培喜 广东石油化工学院化学与生命科学学院茂名 525000 
康新平 广东石油化工学院化学与生命科学学院茂名 525000 
安 哲 广东石油化工学院化学与生命科学学院茂名 525000 
摘要: 采用水热法将MnCl2与苯并咪唑-5,6-二甲酸混合反应合成出一个新的具有二维层状结构的锰金属配位聚合物{[Mn(Hbim)(H2O)2]·(H2O)2}n (1),并分别用元素分析,红外谱图,差热分析和X-射线单晶衍射表征该结构。X-射线单晶衍射分析表明,晶体属于正交晶系,Pbca空间群,晶胞参数a=0.728 2(14) nm,b=1.804 5(4) nm,c=1.915 5(4) nm,V=2.429 3(8) nm3,Z=8,C9H12MnN2O8Mr=331.15,Dc=1.811 g·cm-3F(000)=1 352,μ(Mo Kα)=1.130 mm-1,最终R=0.037 1,wR=0.085 8。在配位聚合物中,锰-羧基Z字形链相互连接成具有尺寸为0.57 nm×0.75 nm一维通道的二维网络结构,并进一步被分子间的氢键作用构筑成三维超分子结构。磁性质测试表明该化合物为反铁磁。
关键词: 锰配合物  晶体结构  水热合成  磁性质
基金项目: 
Abstract: A new manganese coordination polymer {[Mn(Hbim)(H2O)2]·(H2O)2}n(1) (where Hbim=1H-benzimidazole-5,6-dicarboxylate) has been synthesized by hydrothermal method and characterized by elemental analysis, IR, TGA and single-crystal X-ray diffraction. It crystallizes in orthorhombic, space group Pbca with a=0.728 2(14) nm, b=1.804 5(4) nm, c=1.915 5(4) nm, V=2.429 3(8) nm3, Z=8, C9H12MnN2O8, Mr=331.15, Dc=1.811 g·cm-3, F(000)=1 352, μ(Mo Kα)=1.130 mm-1, the final R=0.037 1 and wR=0.085 8 for observed reflections with I>2σ(I). Compound 1 is a 2D coordination polymer including 1D channels of 0.57 nm×0.75 nm (excluding van der Waals radii) along the c axis made up of interconnected Mn-carboxylate zigzag chains, and displays a three-dimensional (3D) supramolecular network via multiple intermolecular hydrogen bonds. Furthermore, the temperature dependent magnetic susceptibility has been evaluated under 1 000 Oe, and reveals the antiferromagnetic coupling. CCDC: 805737.
Keywords: manganese coordination polymer  crystal structure  hydrothermal synthesis  magnetic properties
 
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林培喜,康新平,安 哲.苯并咪唑-5,6-二甲酸-锰配合物的合成,晶体结构和磁性质(英文)[J].无机化学学报,2011,27(7):1446-1450.
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