首页> 外文期刊>Zeitschrift fur Naturforschung, B. A Journal of Chemical Sciences >Halogen bonds in two silver(I) mixed-ligand supramolecular frameworks: Synthesis, structure and photoluminescence
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Halogen bonds in two silver(I) mixed-ligand supramolecular frameworks: Synthesis, structure and photoluminescence

机译:两个银(I)混合配体超分子框架中的卤素键:合成,结构和光致发光

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摘要

Two silver(I) tetrachlorophthalates incorporating aminopyrimidyl ligands, namely [Ag_4(apym)_4(tcpta)_2]_n (1) and [Ag_2(dmapym)(tcpta)]_n (2), (apym = 2-aminopyrimidine, dmapym = 2-amino-4,6-dimethylpyrimidine, H_2tcpta = tetrachlorophthalic acid), were synthesized and characterized by elemental analysis, IR spectroscopy and single-crystal X-ray diffraction. Both 1 and 2 form sheets which are assembled into 3D supramolecular frameworks via halogen bonds, hydrogen bonds and π ? π interactions. Even adding two more methyl groups to the pyrimidyl ring does not change the dimensions of 1 and 2, but it influences the arrangement of the N- and O-donors in the solid state which in turn results in different types of halogen bonds. The photoluminescence properties of 1 and 2 were investigated in the solid state at room temperature.
机译:两种结合了氨基嘧啶基配体的四氯邻苯二甲酸银(I),即[Ag_4(apym)_4(tcpta)_2] _n(1)和[Ag_2(dmapym)(tcpta)] _ n(2),(apym = 2-氨基嘧啶,dmapym =合成了2-氨基-4,6-二甲基嘧啶(H_2tcpta =四氯邻苯二甲酸),并通过元素分析,红外光谱和单晶X射线衍射进行了表征。 1和2模板均通过卤素键,氢键和π键组装成3D超分子框架。 π相互作用。即使在嘧啶环上再添加两个甲基也不会改变1和2的尺寸,但会影响固态的N和O供体的排列,进而导致形成不同类型的卤素键。在室温下固态下研究1和2的光致发光特性。

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