College of Chemistry and Chemical Engineering, Taiyuan University of Technology, Taiyuan, 030024, Shanxi, China.
MOE Key Laboratory of Bioinorganic and Synthetic Chemistry, School of Chemistry, Sun Yat-Sen University, Guangzhou, 510275, Guangdong, China.
Nat Commun. 2022 Aug 5;13(1):4569. doi: 10.1038/s41467-022-32332-x.
The flexibility and guest-responsive behavior of some metal-organic frameworks (MOFs) indicate their potential in the fields of sensors and molecular recognition. As a subfamily of MOFs, the flexible zeolitic imidazolate frameworks (ZIFs) typically feature a small displacive transition due to the rigid zeolite topology. Herein, an atypical reversible displacive transition (6.4 Å) is observed for the sodalite (SOD) cage in flexible ZIF-65(Zn), which represents an unusually large breathing effect compared to other ZIFs. ZIF-65(Zn) exhibits a stepwise II → III → I expansion between an unusual ellipsoidal SOD cage (8.6 Å × 15.9 Å for II) and a spherical SOD cage (15.0 Å for I). The breathing behavior of ZIF-65(Zn) varies depending on the nature of the guest molecules (polarity and shape). Computational simulations are employed to rationalize the differences in the breathing behavior depending on the structure of the ZIF-65(Zn) cage and the nature of the guest-associated host-guest and guest-guest interactions.
一些金属-有机骨架(MOFs)的灵活性和客体响应行为表明它们在传感器和分子识别领域具有潜力。作为 MOFs 的一个亚家族,柔性沸石咪唑酯骨架(ZIFs)通常由于沸石拓扑结构的刚性而具有较小的位移转变。在此,柔性 ZIF-65(Zn)中观察到 sodalite(SOD)笼的非典型可逆位移转变(6.4 Å),与其他 ZIFs 相比,这代表了一种异常大的呼吸效应。ZIF-65(Zn)在不寻常的椭圆形 SOD 笼(II 为 8.6 Å × 15.9 Å)和球形 SOD 笼(I 为 15.0 Å)之间表现出逐步的 II → III → I 扩展。ZIF-65(Zn)的呼吸行为取决于客体分子的性质(极性和形状)而变化。计算模拟用于根据 ZIF-65(Zn)笼的结构和客体相关的主客体和客体-客体相互作用的性质来合理化呼吸行为的差异。