A Low-Temperature Approach for the Phase-Pure Synthesis of MIL-140 Structured Metal-Organic Frameworks

被引:22
|
作者
Schulz, Marcel [1 ,2 ]
Marquardt, Nele [1 ,2 ]
Schaefer, Malte [1 ,2 ]
Warwas, Dawid Peter [1 ,2 ]
Zailskas, Saskia [1 ,2 ]
Schaate, Andreas [1 ,2 ]
机构
[1] Leibniz Univ Hannover, Inst Inorgan Chem, Callinstr 9, D-30167 Hannover, Germany
[2] Leibniz Univ Hannover, ZFM Ctr Solid State Chem & New Mat, Callinstr 9, D-30167 Hannover, Germany
关键词
hybrid materials; metal-organic frameworks; MIL-140; phase purity; synthesis field diagrams; ASSISTED SOLVOTHERMAL SYNTHESIS; DETERMINING SURFACE-AREAS; POSTSYNTHETIC LIGAND; MODULATED SYNTHESIS; BET METHOD; UIO-66; APPLICABILITY; ADSORPTION; EXCHANGE; INSIGHTS;
D O I
10.1002/chem.201902981
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In a systematic investigation, the synthesis of metal-organic frameworks (MOFs) with MIL-140 structure was studied. The precursors of this family of MOFs are the same as for the formation of the well-known UiO-type MOFs although the synthesis temperature for MIL-140 is significantly higher. This study is focused on the formation of Zr-based MIL-140 MOFs with terephthalic acid (H(2)bdc), biphenyl-4,4 '-dicarboxylic acid (H(2)bpdc), and 4,4 '-stilbenedicarboxylic acid (H(2)sdc) and the introduction of synthesis field diagrams to discover parameters for phase-pure products. In this context, a MIL-140 network with H(2)sdc as linker molecule is first reported. Additionally, an important aspect is the reduction of the synthesis temperature to make MIL-140 MOFs more accessible even though linkers with a more delicate nature are used. The solvothermal syntheses were conducted in highly concentrated reaction mixtures whereby a targeted synthesis to yield the MIL-140 phase is possible. Furthermore, the effect of the often-used modulator approach is examined for these systems. Finally, the characteristics of the synthesized MOFs are compared with physisorption measurements, thermogravimetric analyses, and scanning electron microscopy.
引用
收藏
页码:13598 / 13608
页数:11
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