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基于噻吩异构体的芘核共价有机聚合物、其气体吸附性能及光物理性质

Pyrene-cored covalent organic polymers by thiophene-based isomers, their gas adsorption, and photophysical properties.

作者信息

Li Changfeng, Li Peixian, Chen Linjiang, Briggs Michael E, Liu Ming, Chen Kai, Shi Xiaoxiao, Han Deman, Ren Shibin

机构信息

School of Chemistry and materials Science Shanxi Normal University Lin Fen 041004 China.

School of Pharmaceutical and Chemical Engineering Taizhou University Taizhou 317000 China.

出版信息

J Polym Sci A Polym Chem. 2017 Jul 15;55(14):2383-2389. doi: 10.1002/pola.28627. Epub 2017 May 7.

Abstract

Two new pyrene-cored covalent organic polymers (COPs), and , were synthesized via the one-step polymerization of two thiophene-based isomers, 1,3,6,8-tetra(thiophene-2-yl) pyrene ( ) and 1,3,6,8-tetra(thiophene-3-yl) pyrene ( ). The resulting pyrene-cored COPs exhibit rather different surface areas of 54 m g and 615 mg for and , respectively. The CO uptake capacities of and also show different values of 2.85 and 9.73 wt % at 273 K, respectively. Furthermore, offers not only a larger CO adsorption capacity but also a better CO/CH selectivity at 273 K compared with . and also exhibit considerable differences in their photophysical property. The different structure and properties of could be attributed to the isomer effect of their corresponding thiophene-based monomers. © 2017 Authors. Journal of Polymer Science Part A: Polymer Chemistry Published by Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. , , 2383-2389.

摘要

通过两种噻吩基异构体1,3,6,8 - 四(噻吩 - 2 - 基)芘( )和1,3,6,8 - 四(噻吩 - 3 - 基)芘( )的一步聚合反应,合成了两种新型的以芘为核的共价有机聚合物(COPs),即 和 。所得的以芘为核的COPs表现出截然不同的比表面积, 和 的比表面积分别为54 m²/g和615 m²/g。 和 在273 K时的CO吸附容量也显示出不同的值,分别为2.85 wt%和9.73 wt%。此外,与 相比, 在273 K时不仅具有更大的CO吸附容量,而且具有更好的CO/CH选择性。 和 在光物理性质方面也表现出显著差异。 的不同结构和性质可归因于其相应噻吩基单体的异构体效应。© 2017作者。《聚合物科学杂志》A辑:聚合物化学由威利期刊公司出版。J. Polym. Sci., Part A: Polym. Chem., , 2383 - 2389。

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