High Surface Area Conjugated Microporous Polymers: The Importance of Reaction Solvent Choice

被引:197
作者
Dawson, Robert
Laybourn, Andrea
Khimyak, Yaroslav Z.
Adams, Dave J.
Cooper, Andrew I. [1 ]
机构
[1] Univ Liverpool, Dept Chem, Liverpool L69 7ZD, Merseyside, England
基金
英国工程与自然科学研究理事会;
关键词
COVALENT ORGANIC FRAMEWORKS; REVERSIBLE HYDROGEN STORAGE; INTRINSIC MICROPOROSITY; HETEROGENEOUS CATALYSIS; NANOPOROUS POLYMERS; NETWORKS; PIMS; CRYSTALLINE; PALLADIUM; METHANE;
D O I
10.1021/ma101541h
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The choice of reaction solvent has a major influence on the surface area and pore volume in conjugated microporous polymer (CMP) networks synthesized by Sonogashira-Hagihara palladium-catalyzed cross-coupling chemistry of aromatic dibromo monomers with 1,3,5-triethynylbenzene. Four solvents were evaluated for these reactions: N,N-dimethylformamide (DMF), 1,4-dioxane, tetrahydrofuran (THF), and toluene. Networks synthesized in DMF tend to exhibit the highest surface areas (up to 1260 m(2)/g), whereas those synthesized in toluene have on average significantly lower surface areas and pore volumes. By judicious choice of reaction solvent, microporous materials can he prepared which combine high surface area with a variety of functional groups of interest in applications such as gas storage, molecular separations, and catalysis.
引用
收藏
页码:8524 / 8530
页数:7
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