A porous and redox active ferrocenedicarboxylic acid based aluminium MOF with a MIL-53 architecture

被引:17
作者
Benecke, Jannik [1 ]
Mangelsen, Sebastian [1 ]
Engesser, Tobias A. [1 ]
Weyrich, Thomas [1 ]
Junge, Jannik [1 ]
Stock, Norbert [1 ]
Reinsch, Helge [1 ]
机构
[1] Christian Albrechts Univ Kiel, Inst Anorgan Chem, Max Eyth Str 2, D-24118 Kiel, Germany
关键词
METAL-ORGANIC FRAMEWORKS; COORDINATION POLYMER; ELECTRONIC-STRUCTURE; SPECTRA;
D O I
10.1039/c9dt03489g
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A metallocene based linker 1,1 '-ferrocenedicarboxylic acid (H(2)FcDC) was used to synthesise the first permanently porous ferrocenedicarboxylate, exhibiting a MIL-53 architecture. This compound Al-MIL-53-FcDC [Al(OH)(FcDC)] is obtained in glass vials under mild synthesis conditions at <= 100 degrees C and after a short reaction time of 90 min. The crystal structure was determined from powder X-ray diffraction data and the compound shows porosity towards N-2 and H2O, exhibiting a BET surface area of 340 m(2) g(-1). Furthermore, the MOF was characterised via EPR and Mossbauer spectroscopy. The Mossbauer spectrum of Al-MIL-53-FcDC shows a characteristic doublet with an isomeric shift of 0.34 mm s(-1) and a quadrupole splitting of 2.39 mm s(-1), proving the persistence of the ferrocene moiety. A negligibly small amount of impurities of ferrocenium ions could be detected by EPR spectroscopy as a complementary technique. Cyclic voltammetric experiments demonstrated the accessible redox activity of the linker molecule FcDC(2-) in Al-MIL-53-FcDC. A reversible oxidation and reduction signal (0.75 V and 0.64 V, respectively, vs. Ag) of FcDC(2-) was observed and maintained during forty CV cycles, while the crystallinity of the MOF remained unchanged after the experiment.
引用
收藏
页码:16737 / 16743
页数:7
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