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Synthesis, Structure, and Properties of Aromatic Ring-Layered Polymers Containing Ferrocene as a Terminal Unit

机译:含二茂铁为末端单元的芳环层状聚合物的合成,结构与性能

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摘要

[2.2]Paracyclophane-layered polymers 4a and 4b end-capped by ferrocene and [2.2]paracyclophane, respectively, were synthesized by using a xanthene skeleton as a scaffold. Two model compounds, 4, 5-bis(ferrocenylethynyl)-9, 9-dimethylxanthene 7 and pseudo-p-bis(4-ferrocenylethynyl-9, 9-dimethylxanthen-5-yl)[2.2]paracyclophane 8, comprising ferrocenes arranged in a face-to-face manner were also prepared. According to the X-ray molecular structure of compound 8, [2.2]paracyclophane between the ferrocenes had sufficient space for twisting and there was no interaction between two ferrocenes via [2.2]paracyclophane in the ground state. These polymers exhibited blue-light emission originating from the layered cyclophanes; however, the photoluminescence intensity of polymer 4a was lower than that of polymer 4b. The fluorescence emission of polymer 4a was effectively quenched by the end-capping ferrocene group.
机译:使用x吨骨架作为骨架,分别合成了由二茂铁和[2.2]对环环烷封端的[2.2]环环烷酮层聚合物4a和4b。两种模型化合物,4,5-双(二茂铁基乙炔基)-9,9-二甲基x吨7和伪对-双-(4-二茂铁基乙炔基-9,9-二甲基黄嘌呤-5-基)[2.2]对环烷8,包括二茂铁,排列在还准备了面对面的方式。根据化合物8的X射线分子结构,二茂铁之间的[2.2]对环环烷具有足够的扭曲空间,并且两个二茂铁之间通过基态的[2.2]对环环烷之间没有相互作用。这些聚合物表现出源自层状环烷的蓝光发射;因此,该化合物具有较高的发射光。然而,聚合物4a的光致发光强度低于聚合物4b的光致发光强度。聚合物4a的荧光发射被封端的二茂铁基团有效地猝灭。

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