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Synthesis, crystal structures, and photoluminescence of a series of coordination polymers with two homologous functional flexible ligands

机译:具有两个同源功能性柔性配体的一系列配位聚合物的合成,晶体结构和光致发光

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Two functional, flexible ligands, namely 3,6-dipyrazolyl-9-ethylcarbazole (L-1) and 3,6-diimidazolyl-9-ethylcarbazole (L-2) have been synthesized and characterized and their coordination to various Ag-I, Cd-II, and Co-II salts investigated. Six new complexes, 1-6, have been obtained and fully characterized by IR spectroscopy, elemental analysis, and single-crystal X-ray diffraction. The 2D double helix framework of the complex [(CdLI2)-I-1](n) (1) is formed by C-H center dot center dot center dot I hydrogen bonds, whereas the same 2D double helix framework of compound [{(AgLSO3PhCH3)-S-1}(2)(CH3OH)(H2O)](n) (2) is formed by S-O center dot center dot center dot H and C-H center dot center dot center dot O hydrogen bonds and weak pi-pi interactions. The coordination modes of Cd-II and Con in [CdL22(NCS)(2)](n) (3), [CoL22(NCS)(2)(CHCl3)(2)](n) (4), [CdL22(NO3)(2)(CH3OH)(2)](n) (5), and [CoL22(NO3)(2)(CH3OH)(2)](n) (6) are the same, but in the packing diagram interlayers form a 3D network through C-H center dot center dot center dot S interactions and pi-pi interactions in 3, interlayers form a 3D network through S center dot center dot center dot S interactions and pi-pi interactions in 4, novel 3D structures are formed by interchain O center dot center dot center dot H-C hydrogen bonding and interlayer O center dot center dot center dot H-C hydrogen-bonding and pi-pi interactions in 5 and 6. The structural differences between these complexes show the influence of the orientation of the coordinating group of the ligand. These results also show that the metal ion, anion, and nonbonding and pi-pi interactions are significant factors in controlling the structural topology of these metal-organic supramolecular architectures. In addition, the luminescence properties of L-1, 1, L-2 and 3 are investigated in the solid state at room temperature. ((C) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007).
机译:合成并表征了两个功能灵活的配体3,6-dipyrazolyl-9-ethylcarbazole(L-1)和3,6-diimidazolyl-9-ethylcarbazole(L-2),并对其与各种Ag-I的配位进行了表征研究了Cd-II和Co-II盐。获得了六个新的配合物1-6,并通过红外光谱,元素分析和单晶X射线衍射对其进行了全面表征。化合物[(CdLI2)-I-1](n)(1)的二维双螺旋骨架是由CH中心点中心点中心点I氢键形成的,而化合物[{(AgLSO3PhCH3 )-S-1}(2)(CH3OH)(H2O)](n)(2)由SO中心点中心点中心点H和CH中心点中心点中心点O的氢键和弱pi-pi相互作用形成。 [CdL22(NCS)(2)](n)(3),[CoL22(NCS)(2)(CHCl3)(2)](n)(4),[CdL22]中Cd-II和Con的配位模式(NO3)(2)(CH3OH)(2)](n)(5)和[CoL22(NO3)(2)(CH3OH)(2)](n)(6)相同,但在包装中图中间层通过3中的CH中心点中心点中心点S相互作用和pi-pi相互作用形成3D网络,中间层通过4中的S中心点中心点中心点S相互作用和pi-pi相互作用形成3D网络。由5和6中的链间O中心点中心点中心点HC氢键和层间O中心点中心点中心点HC氢键和pi-pi相互作用形成。这些配合物之间的结构差异显示了C的取向的影响。配体的配位基团。这些结果还表明,金属离子,阴离子以及非键和pi-pi相互作用是控制这些金属-有机超分子体系结构拓扑的重要因素。另外,在室温下以固态研究了L-1、1,L-2和3的发光性质。 ((C)Wiley-VCH Verlag GmbH&Co.KGaA,69451 Weinheim,Germany,2007)。

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