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金属配位诱导的以发光金属环为核的液晶

Luminescent Metallacycle-Cored Liquid Crystals Induced by Metal Coordination.

作者信息

Chen Long, Chen Changlong, Sun Yue, Lu Shuai, Huo Haohui, Tan Tianyi, Li Anquan, Li Xiaopeng, Ungar Goran, Liu Feng, Zhang Mingming

机构信息

State Key Laboratory for Mechanical Behavior of Materials, Shaanxi International Research Center for Soft Matter, School of Materials Science and Engineering, Xi'an Jiaotong University, Xi'an, 710049, P. R. China.

Hubei Key Laboratory of Catalysis and Materials Science, College of Chemistry and Material Sciences, South-Central University for Nationalities, Wuhan, 430074, P. R. China.

出版信息

Angew Chem Int Ed Engl. 2020 Jun 15;59(25):10143-10150. doi: 10.1002/anie.201915055. Epub 2020 Mar 13.

Abstract

Two rhomboidal metallacycles based on metal-coordination-driven self-assembly are presented. Because metal-coordination interactions restrict the rotation of phenyl groups on tetraphenylethene units, these metallacycles were emissive both in solution and in solid state, and their aggregation-induced emission properties were well-retained. Moreover, the rhomboidal metallacyclic structures offer a platform for intermolecular packing beneficial for the formation of liquid crystalline phases. Therefore, although neither of building blocks shows mesogenic properties, both thermotropic and lyotropic (in DMF) mesophases were observed in one of metallacycles, indicating that mesophases could be induced by metal-coordination interactions. This study not only reveals the mechanism for the formation of cavity-cored liquid crystals, but also provides a convenient approach to preparing supramolecular luminescent liquid crystals, which will serve as good candidates for chemo sensors and liquid crystal displays.

摘要

本文展示了两种基于金属配位驱动自组装的菱形金属环。由于金属配位相互作用限制了四苯乙烯单元上苯基的旋转,这些金属环在溶液和固态中均具有发光性,且其聚集诱导发光特性得到了很好的保留。此外,菱形金属环结构为分子间堆积提供了一个平台,有利于液晶相的形成。因此,尽管两种构建块均不显示介晶性质,但在其中一种金属环中观察到了热致和溶致(在N,N-二甲基甲酰胺中)介相,这表明介相可以由金属配位相互作用诱导产生。这项研究不仅揭示了空穴核液晶的形成机制,还提供了一种制备超分子发光液晶的简便方法,这些超分子发光液晶将成为化学传感器和液晶显示器的良好候选材料。

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