4.7 Article

Rational Design and Synthesis of Hybrid Porous Polymers Derived from Polyhedral Oligomeric Silsesquioxanes via Heck Coupling Reactions

期刊

MACROMOLECULAR RAPID COMMUNICATIONS
卷 34, 期 10, 页码 861-866

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/marc.201200835

关键词

functionalization of polymers; Heck coupling reaction; non-crystalline polymers; polyhedral oligomeric silsesquioxanes; porous polymers

资金

  1. National Natural Science Foundation of China [21274080, 21274081]
  2. Postdoctoral Science Foundation of China [2012M511018]
  3. Key Natural Science Foundation of Shandong Province [ZR2011BZ001]
  4. Special Funds for Postdoctoral Innovative Projects of Shandong Province [201103037]
  5. Independent Innovation Foundation of Shandong University (IIFSDU)

向作者/读者索取更多资源

Heck coupling reactions are introduced as an efficient method to prepare porous polymers. Novel inorganic-organic hybrid porous polymers (HPPs) were constructed via Heck coupling reactions from cubic functional polyhedral oligomeric silsesquioxanes (POSS), iodinated octaphenylsilsesquioxanes (OPS) and octavinylsilsesquioxanes (OVS) using Pd(OAc)2/PPh3 as the catalyst. Here, two iodinated OPS were used, IOPS and p-I8OPS. IOPS was a mixture with 90% octasubstituted OPS (I8) and some nonasubstituted OPS (I9), while p-I8OPS was a nearly pure compound with 99% I8 and 93% para-substitution. IOPS and p-I8OPS reacted with OVS to produce the porous materials HPP-1 and HPP-2, which exhibited comparable specific surface areas with SBET of 418 +/- 20 m2 g1 and 382 +/- 20 m2 g1, respectively, with total pore volumes of 0.28 +/- 0.01 cm3 g1 and 0.23 +/- 0.01 cm3 g1, respectively. HPP-1 showed a broader pore size distribution and possessed a more significant contribution from the mesopores, when compared with HPP-2, thereby indicating that IOPS may induce more disorder because of the geometrical asymmetry. HPP-1 and HPP-2 possessed moderate carbon dioxide uptakes of 134 and 124 cm3 g1 at 1 bar at 195 K, making them promising candidates for CO2 capture and storage. The synthesized porous polymers may be easily post-functionalized using the retained ethenylene groups.

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