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1,3,5-Tris(functionalised-phenylethynyl)benzene–metal complexes: synthetic survey of mesoporous coordination polymers and investigation of their carbonisation

机译:1,3,5-Tris(官能化的苯基乙炔基)苯-金属配合物:介孔配位聚合物的合成调查及其碳化研究

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摘要

A series of multicoordinate 1,3,5-tris(functionalised-phenylethynyl)benzenes (1–9) was synthesised, and coordination polymers were constructed from these organic linkers and copper ions in high yields. The carbonisation of the linkers 1–9 afforded a microporous carbon that shows type I adsorption–desorption isotherm. Although most of the coordination polymers prepared in this study turned out to be low porous materials, the coordination polymer 7e prepared from the reaction of 1,3,5-tris(4-carboxyphenylethynyl)benzene tripotassium salt (K37) and copper(II) nitrate was a microporous material in addition to the mesoporous materials (7c and 7d) prepared from the reaction of K37 with copper(II) acetate and copper(II) chloride, respectively. The carbonisation of the coordination polymers unexceptionally brought about an increase of micropore volume. A stepwise analysis of 7c pyrolysed at 350, 600, and 900 °C revealed that the mesoporosity hardly changed upon heat treatment, which in other words, demonstrates that microporosity could be successfully added to the mesoporous coordination polymer through the carbonisation process.
机译:合成了一系列多配位的1,3,5-三(官能化的苯基乙炔基)苯(1–9),并由这些有机连接基和铜离子以高收率构建了配位聚合物。接头1–9的碳化提供了微孔碳,该碳显示I型吸附-解吸等温线。尽管本研究中制备的大多数配位聚合物均为低多孔材料,但由1,3,5-三(4-羧苯基乙炔基)苯三钾盐(K37)与铜(II)反应制备的配位聚合物7e除了由K37分别与乙酸铜(II)和氯化铜(II)反应制得的中孔材料(7c和7d)以外,硝酸盐是微孔材料。配位聚合物的碳化毫无例外地导致微孔体积的增加。对在350、600和900°C下热解的7c的分步分析显示,介孔率在热处理后几乎不变,换句话说,这表明微孔率可以通过碳化过程成功地添加到介孔配位聚合物中。

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