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基于具有提高的络合效率的三联吡啶功能化双层倍半硅氧烷的金属超分子材料的合成。

Synthesis of metallo-supramolecular materials based on terpyridine functionalized double-decker silsesquioxane with improved complexation efficiency.

作者信息

Çelİk KÜÇÜk Asuman, Matsui Jun, Miyashita Tokuji

机构信息

Department of Metallurgical and Materials Engineering, Marmara University, İstanbul Turkey.

Department of Material and Biological Chemistry, Yamagata University, Yamagata Japan.

出版信息

Turk J Chem. 2020 Apr 1;44(2):296-308. doi: 10.3906/kim-1909-60. eCollection 2020.

Abstract

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 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.

摘要

基于倍半硅氧烷的过渡金属配合物因倍半硅氧烷控制纳米结构和性质的能力而备受关注。然而,完全络合和纯化方面的一些困难限制了包含倍半硅氧烷的过渡金属基超分子配位配合物的广泛应用。在此,基于钌(II)-三联吡啶功能化双层倍半硅氧烷(DDSQ)(Tpy/Ru-DDSQ)提出了两种不同的方法来合成金属超分子材料(路线1和路线2)。在路线1中,先进行络合,然后用配体对DDSQ进行功能化;而在路线2中,在将配体插入DDSQ之前进行络合。通过1H NMR、X射线光电子能谱仪和FTIR对两种方法得到的Tpy/Ru-DDSQ进行了表征,发现其结构相同。对两种方法都进行了充分讨论并探讨了它们的优点。两条路线的络合产率相似。然而,基于NMR和UV-Vis光谱的结果表明,在路线2中DDSQ掺入配合物的速率相当高。据所知,这是第一项基于在与目标化合物(特别是基于倍半硅氧烷的材料)结合之前/之后络合Tpy配体的影响的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e548/7671228/734a394c3f5a/turkjchem-44-296-fig001.jpg

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