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Luminescent hybrid materials based on covalent attachment of Eu(III)-tris(bipyridinedicarboxylate) in the mesoporous silica host MCM-41

机译:发光杂化材料基于Eu(III)-tris(联吡啶二羧酸酯)在介孔二氧化硅主体mCm-41中的共价连接

摘要

A luminescent inorganic-organic hybrid material was synthesized by covalent immobilization of a europium bipyridine carboxylate complex on the inner pore walls of the mesoporous silica host MCM-41 using the grafting method. Guest-host binding was achieved through double functionalization of the host surface with organosilane reagents (trimethylsilyl, TMS, and aminopropyltriethoxysilane, APTES) followed by reaction of the active amino sites of the APTES residue with the ligand 2,2'-bipyridyl-6,6'-dicarboxylic acid. Addition of EuCl3 solution dissolved in ethanol results in the formation of an immobilized complex having the probable formula Eu(L)x(3 ≥ x ≥ 1)(H2O)y, whose detailed photophysical properties were investigated. In the final step, an additional 2,2'-bipyridine-6 monocarboxylic acid ligand was added in an attempt to complete the coordination sphere of the rare earth ion. Each of the synthesis steps was monitored by 1H, 13C, and 29Si solid state NMR spectroscopies, allowing for a quantitative assessment of the progress of the reaction and the influence of the paramagnetic species on the spectra. Based on these data and additional characterizations by chemical analysis, thermogravimetric analysis (TGA), N2 sorption, X-ray diffraction and FT-IR spectroscopy, a comprehensive quantitative picture of the covalent binding and complexation process was developed.
机译:使用接枝方法,通过将联吡啶羧酸盐络合物共价固定在介孔二氧化硅基质MCM-41的内孔壁上,合成了发光的无机-有机杂化材料。客体与主体的结合是通过利用有机硅烷试剂(三甲基甲硅烷基,TMS和氨基丙基三乙氧基硅烷,APTES)对主体表面进行双重功能化,然后使APTES残基的活性氨基与配体2,2'-联吡啶-6, 6'-二羧酸。加入溶解在乙醇中的EuCl3溶液导致形成了可能的式Eu(L)x(3≥x≥1)(H2O)y的固定化配合物,并对其详细的光物理性质进行了研究。在最后一步中,添加了额外的2,2'-联吡啶-6一元羧酸配体,以试图完成稀土离子的配位球。每个合成步骤均通过1H,13C和29Si固态NMR光谱仪进行监控,从而可以定量评估反应的进程以及顺磁性物质对光谱的影响。基于这些数据以及化学分析,热重分析(TGA),N2吸附,X射线衍射和FT-IR光谱的其他特征,开发了共价结合和络合过程的全面定量图片。

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