Dai Ruihan, Peng Fei, Ji Pengfei, Lu Kuangda, Wang Cheng, Sun Junliang, Lin Wenbin
College of Chemistry and Chemical Engineering, iCHEM, PCOSS, Xiamen University , Xiamen 361005, People's Republic of China.
Department of Materials and Environmental Chemistry, Stockholm University , 10691 Stockholm, Sweden.
Inorg Chem. 2017 Jul 17;56(14):8128-8134. doi: 10.1021/acs.inorgchem.7b00845. Epub 2017 Jun 22.
Nanoscale metal-organic frameworks (nMOFs) have shown tremendous potential in cancer therapy and biomedical imaging. However, their small dimensions present a significant challenge in structure determination by single-crystal X-ray crystallography. We report here the structural determination of nMOFs by rotation electron diffraction (RED). Two isostructural Zr- and Hf-based nMOFs with linear biphenyldicarboxylate (BPDC) or bipyridinedicarboxylate (BPYDC) linkers are stable under intense electron beams to allow the collection of high-quality RED data, which reveal a MOF structure with M(μ-O)(μ-OH)(μ-OH) (M = Zr, Hf) secondary building units (SBUs). The nMOF structures differ significantly from their UiO bulk counterparts with M(μ-O)(μ-OH) SBUs and provide the foundation for clarifying the structures of a series of previously reported nMOFs with significant potential in cancer therapy and biological imaging. Our work clearly demonstrates the power of RED in determining nMOF structures and elucidating the formation mechanism of distinct nMOF morphologies.
纳米级金属有机骨架(nMOFs)在癌症治疗和生物医学成像方面已展现出巨大潜力。然而,其微小尺寸给通过单晶X射线晶体学确定结构带来了重大挑战。我们在此报告通过旋转电子衍射(RED)对nMOFs进行结构测定的情况。两种具有线性联苯二甲酸酯(BPDC)或联吡啶二甲酸酯(BPYDC)连接体的同构Zr基和Hf基nMOFs在强电子束下稳定,从而能够收集高质量的RED数据,这些数据揭示了一种具有M(μ-O)(μ-OH)(μ-OH)(M = Zr、Hf)二级结构单元(SBUs)的金属有机骨架结构。这些nMOF结构与其具有M(μ-O)(μ-OH) SBUs的UiO本体对应物有显著差异,并为阐明一系列先前报道的在癌症治疗和生物成像方面具有巨大潜力的nMOFs的结构奠定了基础。我们的工作清楚地展示了RED在确定nMOF结构以及阐明不同nMOF形态形成机制方面的能力。