Cross-linking Zr-based metal-organic polyhedra via postsynthetic polymerization

被引:132
|
作者
Nam, Dongsik [1 ]
Huh, Jihyun [1 ]
Lee, Jiyoung [1 ]
Kwak, Ja Hun [2 ]
Jeong, Hu Young [3 ]
Choi, Kyungmin [4 ]
Choe, Wonyoung [1 ]
机构
[1] Ulsan Natl Inst Sci & Technol, Dept Chem, 50 UNIST Gil, Ulsan 44919, South Korea
[2] Ulsan Natl Inst Sci & Technol, Dept Chem Engn, 50 UNIST Gil, Ulsan 44919, South Korea
[3] Ulsan Natl Inst Sci & Technol, UNIST Cent Res Facil, 50 UNIST Gil, Ulsan 44919, South Korea
[4] Sookmyung Womens Univ, Dept Chem & Biol Engn, 100 Cheongpa Ro 47 Gil, Seoul 04310, South Korea
基金
新加坡国家研究基金会;
关键词
RETICULAR CHEMISTRY; FRAMEWORKS; DESIGN; FUNCTIONALIZATION; CONSTRUCTION; ADSORPTION; COMPLEXES; CAVITIES; LINKERS; UIO-66;
D O I
10.1039/c7sc03847j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Metal organic polyhedra (MOPs) have potential as supramolecular building blocks, but utilizing MOPs for postsynthetic polymerization has not been explored. Although MOPs with flexible organic moieties have been recently reported to target enhanced processability, permanent porosity has not been demonstrated. Here, a novel synthetic strategy involving the cross-linking of MOPs via a covalent bond is demonstrated by exploiting a condensation reaction between the MOP and flexible organic linkers. An amine-functionalized Zr-based MOP is cross-linked with acyl chloride linkers in the crystalline state to form cross-linked MOPs. The condensation reaction results in a cross-linked system without significant changes to the structure of the Zr-based MOP. Such cross-linked MOPs provide a microporous tetrahedral cage based on gas sorption analysis. This cross-linking strategy highlights the potential of MOPs as building blocks and provides access to a new class of porous material.
引用
收藏
页码:7765 / 7771
页数:7
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