电子顺磁共振
结晶度
氧化还原
部分
穆斯堡尔谱学
化学
多孔性
连接器
结晶学
二茂铁
四极分裂
材料科学
物理化学
无机化学
电化学
立体化学
核磁共振
有机化学
操作系统
物理
计算机科学
电极
作者
Jannik Benecke,Sebastian Mangelsen,Tobias A. Engesser,Thomas Weyrich,Jannik Junge,Norbert Stock,Helge Reinsch
出处
期刊:Dalton Transactions
[Royal Society of Chemistry]
日期:2019-01-01
卷期号:48 (44): 16737-16743
被引量:16
摘要
A metallocene based linker 1,1'-ferrocenedicarboxylic acid (H2FcDC) 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 °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 N2 and H2O, exhibiting a BET surface area of 340 m2 g-1. Furthermore, the MOF was characterised via EPR and Mössbauer spectroscopy. The Mössbauer 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 FcDC2- in Al-MIL-53-FcDC. A reversible oxidation and reduction signal (0.75 V and 0.64 V, respectively, vs. Ag) of FcDC2- was observed and maintained during forty CV cycles, while the crystallinity of the MOF remained unchanged after the experiment.
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