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Polymers of intrinsic microporosity (PIMs) formed by means of dioxane-forming reactions exhibit apparent Brunauer¨CEmmet¨CTeller (BET) specific surface areas of 500¨C 1000 m2 g1 depending on the structure of the monomers.Hyper-cross-linked polymers are another example of porous organic polymers that can display permanent porosity because of extensive chemical cross-links that prevent the polymer chains collapsing into dense solids. The simplest networks constructed from styrenic monomers have a wide range of BET surface areas (100¨C2000 m2g1) that depend mainly on the degree of cross-linking and the monomers.Amorphous conjugated microporous polymers can be synthesized with BET surface areas in the range 500¨C1200 m2 g1 by means of Pd0/CuI-catalyzed Sonogashira cross-coupling.[19] Micropore distributions of these conjugated poly(arylene ethynylene) materials could be controlled by means of the rigid node¨Cstrut topology, in particular by the average strut length,[19a,b] and this implies that order and crystallinity are not prerequisites for precise control over porosity of materials. These previous reports strongly suggest that selection of the right monomer is a critical factor to achieve synthetic porous organic polymers with high surface area and narrow pore size distribution. |
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°®ÓëÓêÏÂ: ½ð±Ò+1 2015-03-20 22:27:00
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°®ÓëÓêÏÂ: ½ð±Ò+1 2015-03-20 22:27:00
´óËÄдÂÛÎÄ: ½ð±Ò+40, ¡ï¡ï¡ïºÜÓаïÖú 2015-03-21 12:16:34
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Polymers of intrinsic microporosity (PIMs) formed by means of dioxane-forming reactions exhibit apparent Brunauer¨CEmmet¨CTeller (BET) specific surface areas of 500¨C1000 m2 g1 depending on the structure of the monomers. ÒÀ¿¿µ¥Ìå½á¹¹£¬Í¨¹ý¶þÑõ¼º»·Ðγɷ´Ó¦Éú³ÉµÄ×Ô¾ß΢¿×¾ÛºÏÎï(PIMs) £¬Õ¹ÏÖ³öµÄÃ÷ÏÔ²¼BET(³ŵ(Brunauer)¡¢°£ÂóÌØ(Emmet)ºÍÌ©ÀÕ(Teller))±È±íÃæ»ý´ï 500¨C1000 m2 g1. Hyper-cross-linked polymers are another example of porous organic polymers that can display permanent porosity because of extensive chemical cross-links that prevent the polymer chains collapsing into dense solids. ¶à¿×Óлú¾ÛºÏÎïµÄÁíÒ»¸öÀý×Ó-³¬¸ß½»Áª¾ÛºÏÎÒòÆä¹ã·ºµÄ»¯Ñ§½»Áª·´Ó¦£¬ÓÐЧµÄ×èÖ¹Á˸߷Ö×ÓÁ´µ¹Ëúµ½³íÃܵĹÌÌå×éÖ¯ÖУ¬Òò¶øËüÃÇÄܹ»Õ¹ÏÖ³öÓÀ¾ÃµÄ¶à¿×ÐÔ¡£ The simplest networks constructed from styrenic monomers have a wide range of BET surface areas (100¨C2000 m2g1) that depend mainly on the degree of cross-linking and the monomers. Óɱ½ÒÒÏ©¹¹½¨³ÉµÄ×î¼òµ¥µÄÍøÂ磬Óй㷺µÄBET±È±íÃæ»ý·¶Î§£¨100¨C2000 m2g1£©£¬ÆäÖ÷Ҫȡ¾öÓÚÓÚ½»Áª³Ì¶ÈºÍµ¥Ìå·Ö×Ó¡£ Amorphous conjugated microporous polymers can be synthesized with BET surface areas in the range 500¨C1200 m2 g1 by means of Pd0/CuI-catalyzed Sonogashira cross-coupling. Pd0/CuI×÷´ß»¯¼ÁµÄËQͷżºÏ·´Ó¦£¬¿ÉÒԺϳɱȱíÃæ»ý·¶Î§Îª500¨C1200 m2 g1µÄ·Ç¾§Ì¬¹²éî΢¿×¾ÛºÏÎï¡£ [19] Micropore distributions of these conjugated poly(arylene ethynylene) materials could be controlled by means of the rigid node¨Cstrut topology, in particular by the average strut length,[19a,b] and this implies that order and crystallinity are not prerequisites for precise control over porosity of materials. ÔËÓøÕÐÔ½Úµã-Ö§ÖùÍØÆË£¨ÓÈÆäÊÇ£¬Æ½¾ùÖ§Öù³¤¶È[19a,b]£©£¬¿ÉÒÔ¿ØÖÆÕâЩ¹²éî¾ÛºÏ²ÄÁÏ£¨ÑÇ·¼»ù£¬ÑÇÒÒȲ»ù£©µÄ΢¿×·Ö²¼¡£Õâ±íÃ÷½á¾§¶ÈºÍ˳Ðò£¬²»ÊÇ׼ȷ¿ØÖƲÄÁ϶à¿×ÐÔµÄÏȾöÌõ¼þ¡£ These previous reports strongly suggest that selection of the right monomer is a critical factor to achieve synthetic porous organic polymers with high surface area and narrow pore size distribution. ´ËǰÕâЩ±¨µÀ£¬Ç¿ÁÒ½¨Ò飬ѡÔñÕýÈ·µÄµ¥ÌåÊǾö¶¨ÐÔÒòÊý£¬¾ö¶¨×ÅÄÜ·ñ³É¹¦ºÏ³É£¬¸ß±íÃæ»ý£¬ÕÆø¿×µÄ¶à¿×Óлú¾ÛºÏÎï¡£ |
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