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首页> 外文期刊>Turkish journal of chemistry >Synthesis of metallo-supramolecular materials based on terpyridine functionalized double-decker silsesquioxane with improved complexation efficienc
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Synthesis of metallo-supramolecular materials based on terpyridine functionalized double-decker silsesquioxane with improved complexation efficienc

机译:基于三联吡啶官能化的双层倍半硅氧烷的金属超分子材料的合成及其络合效率的提高

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Silsesquioxane-based transition-metal complexes have come to the forefront due to the ability of silsesquioxane to control nanostructures and properties. However, some difficulties in complete complexation and purification limit the widespread use of transition-metal-based supramolecular coordination complexes comprising silsesquioxane. Herein, 2 different approaches have been proposed for the synthesis of metallo-supramolecular materials on the basis of ruthenium(II)-terpyridine functional double-layer silsesquioxane (DDSQ) (Tpy/Ru-DDSQ) (Routes 1 and 2). In Route 1, complexation was followed by functionalization of DDSQ with the ligand, whereas in Route 2, complexation was performed before the ligand was inserted into the DDSQ. Tpy/Ru-DDSQ obtained from both approaches was characterized by $^{1}$H NMR, X-ray photoelectron spectrometer, and FTIR and found in the same structure. Both methods were fully discussed and their merits were explored. The complexation yield of the routes was similar. However, the results based on NMR and UV-Vis spectroscopy demonstrated that the incorporation rate of DDSQ into the complex was quite high in Route 2. As far as is known, this is the first study based on the effects of complexing Tpy ligands before/after binding to the target compound, particularly to silsesquioxane-based materials.
机译:由于倍半硅氧烷具有控制纳米结构和性能的能力,因此倍半硅氧烷基过渡金属配合物已走在前列。然而,在完全络合和纯化中的一些困难限制了包含倍半硅氧烷的基于过渡金属的超分子配位化合物的广泛使用。在此,已经提出了两种基于钌(II)-叔吡啶功能的双层倍半硅氧烷(Tpy / Ru-DDSQ)合成金属超分子材料的方法(路线1和2)。在途径1中,络合之后是DDSQ与配体官能化,而在途径2中,络合物是在将配体插入DDSQ中之前进行的。从两种方法获得的Tpy / Ru-DDSQ的特征都在于$ ^ {1} $ H NMR,X射线光电子能谱仪和FTIR,并且结构相同。讨论了这两种方法,并探讨了它们的优点。路线的络合产率相似。但是,基于NMR和UV-Vis光谱的结果表明,路线2中DDSQ掺入配合物中的比率非常高。据了解,这是第一个基于配合Tpy配体之前/之后的作用的研究。与目标化合物,尤其是倍半硅氧烷化合物结合后。

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