Synthesis of π-conjugated porous polymers via direct arylation of fluoroarenes with three-arm triazine

被引：21

作者：

Hayashi, Shotaro ^{[1
]}

Togawa, Yuki ^{[1
]}

Ashida, Jun ^{[2
,3
]}

Nishi, Koji ^{[1
]}

Asano, Atsushi ^{[1
]}

Koizumi, Toshio ^{[1
]}

机构：

[1] Natl Def Acad, Dept Appl Chem, 1-10-20 Hashirimizu, Yokosuka, Kanagawa 2398686, Japan

[2] Agilent Technol Japan Ltd, Minato Ku, Sumitomo Shibaura Bldg 8F 4-16-36 Shibaura, Tokyo 1080023, Japan

[3] JEOL RESONANCE Inc, Chiyoda Ku, Ohtemachi Nomura Bldg 13F 2-1-1 Ohtemachi, Tokyo 1000004, Japan

来源：

POLYMER | 2016年 / 90卷

关键词：

Conjugated microporous polymers; Direct arylation; Fluorine; C-H ARYLATION; MICROPOROUS POLYMERS; ORGANIC POLYMERS; ALTERNATING COPOLYMERS; SURFACE-AREA; GAS UPTAKE; POLYCONDENSATION; FRAMEWORKS; CATALYST; POROSITY;

D O I：

10.1016/j.polymer.2015.11.056

中图分类号：

O63 [高分子化学（高聚物）];

学科分类号：

070305 ; 080501 ; 081704 ;

摘要：

We have successfully synthesized pi-conjugated microporous polymers (CMPs) via direct arylation of fluoroarenes with 2,4,6-tris(4-bromophenyl)-1,3,5-triazine. Both 1,2,4,5-tetrafluorobenzene and 1,3,5-trifluorobenzene were good monomers to give the networks, CMP1 and CMP2, respectively. Characterization of the insoluble materials was successfully achieved by high performance solid-state C-13 and F-19 CP/MAS NMR spectroscopy. The signals appeared in the aromatic region. No end group signals were observed in the C-13 NMR spectrum of CMP1, but CMP2 showed the unreacted C-H signal of the trifluorobenzene unit. CMP2 showed higher Brunauer-Emmett-Teller (BET) surface area than CMP1. The number of branch controlled (or tailored) the porosity of the polymer networks. The polymers have microporocity with CO2 capture capacity. The CO2 capture capacity of CMP2 (16.75 cm(3) g(-1)) was higher than that of CMP1 (11.49 cm(3) g(-1)) at 1.0 bar. (C) 2016 Elsevier Ltd. All rights reserved.

引用

页码：187 / 192

页数：6

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