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Polymers of Intrinsic Microporosity Derived from Novel Disulfone-Based Monomers

机译:新型二砜基单体衍生的本征微孔性聚合物

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摘要

The synthesis of three novel disulfone-based monomers from readily available hexafluorobenzene and thiols for the preparation of homopolymers and copolymers of intrinsic microporosity (PIMs) is described. The disulfonyl-based PIMs derived from 5,5',6,6'-tetrahydroxy-3,3,3',3'-tetramethylspirobisindane (TTSBI) with tetrafluoroterephthalonitrile (TFTPN) and disulfone-based monomers were prepared at high temperature (160 degrees C) within 1 h. Three new copolymers (monomer molar ratio of TTSBI and disulfone-based monomers = 3: 1) show a good combination of properties, such as excellent film-forming characteristics and gas transport properties. Compared with a previously reported microporous nitrile-based homopolymer, referred to as PIM-1, the present sulfone-based copolymers have higher gas selectivities for O-2/N-2 and CO2/N-2, while showing some reduction in pure-gas permeabilities. The relationship between the structure and gas permeation behavior of the copolymers is discussed.
机译:描述了从容易获得的六氟苯和硫醇合成三种新颖的基于二砜的单体,用于制备固有微孔性(PIM)的均聚物和共聚物。在高温下(160)制备了由5,5',6,6'-四羟基-3,3,3',3'-四甲基螺双茚满(TTSBI)与四氟对苯二甲腈(TFTPN)和二砜基单体衍生的基于二磺酰基的PIM。摄氏度)。三种新的共聚物(TTSBI与二砜基单体的单体摩尔比= 3:1)表现出良好的性能组合,例如出色的成膜特性和气体传输特性。与先前报道的微孔腈基均聚物PIM-1相比,本砜基共聚物对O-2 / N-2和CO2 / N-2的气体选择性更高,而纯正丁二烯的含量却有所降低。气体渗透率。讨论了共聚物的结构与气体渗透行为之间的关系。

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