Postsynthetic ligand exchange as a route to functionalization of 'inert' metal-organic frameworks

被引:376
|
作者
Kim, Min [1 ]
Cahill, John F. [1 ]
Su, Yongxuan [1 ]
Prather, Kimberly A. [1 ,2 ]
Cohen, Seth M. [1 ]
机构
[1] Univ Calif San Diego, Dept Chem & Biochem, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Scripps Inst Oceanog, La Jolla, CA 92093 USA
关键词
LASER-DESORPTION/IONIZATION; MASS-SPECTROMETRY; PARTICLES; CRYSTAL; ATOFMS; POLYHEDRA; LINKERS;
D O I
10.1039/c1sc00394a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Herein, we report that the exchange of ligands from an intact metal-organic framework (MOF) can be exploited as a means to introduce functionalized ligands into MOFs under mild conditions. It is shown that ligand exchange can occur with 'inert' Zr(IV)-based UiO-66 MOFs in a solvent dependent manner. We call this process postsynthetic exchange (PSE) and show that it provides access to MOFs that are not readily prepared in high quality by solvothermal methods. It was found that ligand exchange can occur between UiO-66 MOFs as monitored by aerosol time-of-flight mass spectrometry (ATOFMS). ATOFMS was used to analyze the chemical composition of microcrystalline MOFs on the single particle level, providing information not available through bulk analysis. PSE is an important postsynthetic approach to the modification of MOFs, and the ligand exchange revealed by ATOFMS requires a re-evaluation of the assumed 'stability' of even the most robust MOFs.
引用
收藏
页码:126 / 130
页数:5
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