Cousinié Sandra, Gressier Marie, Reber Christian, Dexpert-Ghys Jeannette, Menu Marie-Joëlle
Centre Interuniversitaire de Recherche et d'Ingénierie des Matériaux, UMR-CNRS 5085, Université Paul Sabatier, 118 route de Narbonne, 31062 Toulouse Cedex 9, France.
Langmuir. 2008 Jun 17;24(12):6208-14. doi: 10.1021/la7035983. Epub 2008 May 20.
This work focuses on the grafting of transition metal complexes on silica surface nanoparticles. Nanoscale silica particles in aqueous sols are used as starting silicated materials. We have undertaken the synthesis of europium(III) complexes containing organosilyldipyridine ligands, (EtO)3Si(CH2)3NHCH2-bipy (1) and (EtO)(CH3)2Si(CH2) 3NHCH 2-bipy (2), in view of a direct grafting reaction on silica nanoparticles. Reaction of one molar equivalent of 1 and 2 with Eu(tmhd)3 (tmhd= 2,2,6,6-tetramethyl-3,5-heptanedionato), as precursor, leads to octacoordinated silylated europium(III) complexes [Eu(tmhd)3(1)] (3) and [Eu(tmhd)3(2)] (4) as white solids in 34-54% yields. Europium complexes were characterized by elemental analysis, mass spectrometry, FT-IR, UV, and luminescence spectroscopies. These new complexes are reacting in a 1:10 (v/v) water and ethanol mixture with silica nanoparticles colloidal sol. Elemental analysis and thermogravimetric data indicated grafting ratios of 0.41 and 0.26 mmol of europium(III) complexes per gram of silica. Functionalized silica nanoparticles were characterized by DRIFT spectroscopy and TEM microscopy. The first analysis shows that the chemical integrity of the complexes is retained on the silica surface together with the size and the monodispersity of the nanoscale particles. As expected for europium(III) complexes, luminescence is observed under UV irradiation. Emission and excitation spectra indicate that the metal coordination environment is not modified on the silica surface. Moreover, the sharpness of the luminescence bands and the strong antenna effect are maintained when complexes are covalently bonded to silica. New luminescent europium(III) complexes grafted on silica nanoparticles are therefore obtained from our approach.
这项工作聚焦于过渡金属配合物在二氧化硅表面纳米颗粒上的接枝。水溶胶中的纳米级二氧化硅颗粒被用作起始硅基材料。鉴于要在二氧化硅纳米颗粒上进行直接接枝反应,我们已开展了含有有机硅二吡啶配体(EtO)3Si(CH2)3NHCH2 - bipy(1)和(EtO)(CH3)2Si(CH2)3NHCH2 - bipy(2)的铕(III)配合物的合成。一摩尔当量的1和2与作为前体的Eu(tmhd)3(tmhd = 2,2,6,6 - 四甲基 - 3,5 - 庚二酮)反应,生成八配位的硅烷化铕(III)配合物[Eu(tmhd)3(1)](3)和[Eu(tmhd)3(2)](4),为白色固体,产率为34 - 54%。通过元素分析、质谱、傅里叶变换红外光谱、紫外光谱和发光光谱对铕配合物进行了表征。这些新配合物在水和乙醇体积比为1:10的混合物中与二氧化硅纳米颗粒胶体溶液发生反应。元素分析和热重数据表明,每克二氧化硅上铕(III)配合物的接枝率为0.41和0.26 mmol。通过漫反射红外傅里叶变换光谱和透射电子显微镜对功能化二氧化硅纳米颗粒进行了表征。首次分析表明,配合物的化学完整性在二氧化硅表面得以保留,同时纳米颗粒的尺寸和单分散性也得以保持。正如铕(III)配合物所预期的那样,在紫外照射下观察到了发光现象。发射光谱和激发光谱表明,金属配位环境在二氧化硅表面未发生改变。此外,当配合物与二氧化硅共价键合时,发光带的锐度和强烈的天线效应得以保持。因此,通过我们的方法获得了接枝在二氧化硅纳米颗粒上的新型发光铕(III)配合物。