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Fulleropyrrolidines derived from dioxa- and trioxaalkyl-tethered diglycines

机译:富含二氧化硅和三元烷基拴系的二甘油苷的富罗啉

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摘要

Two different alpha,omega-diglicynes linked by linear polyoxaalkyl chains in the presence of formaldehyde underwent Prato reaction to the fullerene C-60. The shorter linker templated formation of only cis-bisadducts, while the longer one afforded a mixture of four bisadducts (all cis and the equatorial) and difullerene dumbbell compound. Their structures were confirmed by the extensive analysis of the spectral data and molecular symmetry, as well. All compounds expressed an ability to arrange into hierarchically ordered supramolecular aggregates, the form of which depended both on the addition pattern and the spacer structure. The attenuated electron-accepting affinity, examined by cyclic voltammetry was in agreement with diminished delocalization of the pi-electronic system. In addition, all compounds exerted a notable radical scavenging activity.
机译:两种不同的α,ω-diglicynes在甲醛的存在下通过线性聚氧烷基链连接到富勒烯C-60的Prato反应的存在下。 只有CIS-BISADDUCTS的较短接头模板形成,而较长的接头形成了四种双层(所有顺式和赤道)和差异哑铃化合物的混合物。 通过对光谱数据和分子对称的广泛分析来证实了它们的结构。 所有化合物都表达了布置成分层有序的超分子聚集体的能力,其形式依赖于添加图案和间隔结构。 通过循环伏安法检测的衰减的电子接受亲和力与PI-Electronic系统的临床化减少了一致。 此外,所有化合物都施加着显着的激进清除活性。

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