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过渡金属—羧酸配位聚合物的合成、结构及其形貌传递研究
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摘要
本论文致力于利用不同类型的芳香羧酸配体,与过渡金属离子构筑新型的一维链结构配合物,研究配体结构与合成条件对一维链结构形成的影响,探讨其结构与性能的关系。研究以一维链结构配合物作为前驱体转化为无机纳米晶的形貌传递机理和规律,为一维氧化物纳米结构材料的控制合成开辟新的思路。
     论文主要研究了苯二甲酸、异烟酸配体与过渡金属离子构筑的具有一维链结构的配位聚合物的合成、结构及其性能;对利用具有一维链状结构的配位聚合物作为前驱体通过固相转化合成氧化物纳米线的方法做了重点的研究和讨论。
     以苯二甲酸为配体利用溶剂热方法合成了3个配位聚合物[C_8H_6CdO_5]_n(1)、[C_8H_(10)CdO_7]_n·4H_2O(2)和[C_8H_6CdO_5]_n(3),利用单晶X-射线衍射方法确定了其晶体结构。结构分析表明配合物(2)具有一维链结构,(1)和(3)为三维网状结构。固态荧光光谱分析表明三个配位聚合物均表现出较强的蓝色荧光。以异烟酸为配体利用溶剂热方法合成了4个异质同构的超分子化合物[C_(12)H_(16)MN_2O_8](M=Co(4),Zn(5),Cd(6),Mn(7))和两个配位聚合物[C_2H_6CoO_6]_n(8)、[C_(12)H_(10)CoN_2O_4]_n(9),利用单晶X-射线衍射确定了其晶体结构。结构分析表明配合物(4-7)为单核结构,单核结构之间通过氢键作用形成三维超分子结构。配合物(8)和(9)为三维网状结构。荧光光谱分析表明由Zn~(2+)、Cd~(2+)两种金属离子形成的配合物(5)和(6)发射出较强的蓝色荧光。
     以所合成的具有一维链结构的镉配位聚合物作为前驱体,通过控制一定的条件实现了从一维链结构的配位聚合物前驱体到CdO纳米晶的转化,得到了尺寸均匀的超长CdO纳米线,分别对其做了XRD、TEM、EDX、HRTEM以及光学性能表征,并讨论了纳米线的生长机理。该结果表明,前驱体在分子尺度上的一维链几何形态在固相转化过程中被传递下来,揭示了从分子尺度上的形貌向纳米尺度形貌进行传递的可能性,为从分子尺度上实现纳米材料形貌的控制提供了思路。
The aim of this thesis is to synthesize new coordination polymer with one-dimensional chain structure on the basis of aromatic carboxylic acid ligands and transition metal ions, to study the influence of ligands structure and synthetic conditions to the formation of one-dimensional chain, and to explore the relationships between structure and property. Another aim of this thesis is to study the morphology transfer mechanism and rules of coordination compound precursors with one-dimensional chain transformed to inorganic nano-crystals, to find a new way for the controlling synthesis of one-dimensional nano-structural materials.
     This thesis investigated the synthesis, structure and property of coordination polymers with one-dimensional chain structure constructed from benzene-dicarboxylic acid, iso-nicotinic acid and transition metal ion; the procedure via solid-state transformation of coordination polymer with one-dimensional chain to synthesize oxide nanowires has been especially investigated and discussed.
     Three coordination polymers: [C_8H_6CdO_5]_n(1), [C_8H_(10)CdO_7]_n·4H_2O (2) and [C_8H_6ZnO_5]_n (3) on the basis of benzene-dicarboxylic acid were synthesized by sovol-thermal method and characterized by single crystal X-ray diffraction. Structural analysis revealed that compound (2) displayed one-dimensional chain structure and compound (2) and (3) were three-dimensional network structure. Solid-state fluorescent spectrum revealed that three compounds all displayed strong blue fluorescent. Four iso-structural supra-molecular compounds [C_(12)H_(16)MN_2O_8]_n(M = Co (4), Zn (5), Cd (6), Mn (7)) and two coordination polymers [C_2H_6CoO_6]_n(7), [C_(12)H_(10)CoN_2O_4]_n (8) on the basis of iso-nicotinic acid were synthesized by sovol-thermal method and characterized by single crystal X-ray diffraction. Structural analysis revealed that compound (4-7) were three-dimensional network constructed from hydrogen-bonding interaction between mononuclear structure, compound (8) and (9) were three-dimensional network structure. Solid-state fluorescent spectrum revealed that two compounds (5 and 6) formed by Zn~(2+) and Cd~(2+) displayed strong blue fluorescence.
     To control reaction condition, the transformation from coordination polymer to supra-long CdO nano-wires with average diameter was achieved by using synthesized cadmium coordination polymer with one-dimensional structure as precursors. The prepared nano-wires were characterized using XRD, TEM, EDX, HRTEM and its optical properties were examined, and the growth mechanism of nano-wires was discussed. The results indicated that the one-dimensional chain geometry of molecular scale was inherited during the solid-state transformation course. The successful preparation of CdO nano-wires from coordination polymer with one-dimensional chain structure made it possible of morphology transfer from molecular scale to nano-scale and provided a new way for the controlling synthesis of nano-materials in molecular dimensionality.
引文
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