Control over Catenation in Pillared Paddlewheel Metal-Organic Framework Materials via Solvent-Assisted Linker Exchange

被引：141

作者：

Bury, Wojciech ^{[1
,2
,3
]}

Fairen-Jimenez, David ^{[4
,5
]}

Lalonde, Marianne B. ^{[1
,2
]}

Snurr, Randall Q. ^{[4
]}

Farha, Omar K. ^{[1
,2
]}

Hupp, Joseph T. ^{[1
,2
]}

机构：

[1] Northwestern Univ, Dept Chem, Evanston, IL 60208 USA

[2] Northwestern Univ, Int Inst Nanotechnol, Evanston, IL 60208 USA

[3] Warsaw Univ Technol, Dept Chem, PL-00664 Warsaw, Poland

[4] Northwestern Univ, Dept Chem & Biol Engn, Evanston, IL 60208 USA

[5] Univ Cambridge, Dept Chem Engn & Biotechnol, Cambridge CB2 3RA, England

来源：

CHEMISTRY OF MATERIALS | 2013年 / 25卷 / 05期

关键词：

catenation; metal-organic frameworks; SALE; linker exchange; POSTSYNTHETIC LIGAND; RATIONAL DESIGN; SURFACE-AREA; STRATEGY; INTERPENETRATION; PURIFICATION; POROSITY; STORAGE; SOLIDS; ROUTE;

D O I：

10.1021/cm303749m

中图分类号：

O64 [物理化学（理论化学）、化学物理学];

学科分类号：

070305 [高分子化学与物理];

摘要：

Control over catenation in a pillared paddlewheel metal-organic framework was achieved via solvent-assisted linker exchange. The linker exchange was demonstrated on the noncatenated structure of DO-MOF, by using 4,4'-bipyridine (L4) and 4,4'-azobis(pyridine) (L5) as linkers, leading to noncatenated materials SALEM-3 and SALEM-4. The de novo synthesized analogues of SALEM-3 and SALEM-4 can only be obtained as 2-fold interpenetrated frameworks. The reaction progress of the linker exchange was monitored by NMR spectroscopy, and structure and framework catenation were characterized by powder X-ray diffraction and thermogravimetric methods.

引用

页码：739 / 744

页数：6

共 55 条

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