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探索含机械互锁分子梭的 Zr 基金属有机骨架的动态特性。

Exploring the dynamics of Zr-based metal-organic frameworks containing mechanically interlocked molecular shuttles.

机构信息

Department of Chemistry and Biochemistry, University of Windsor, Ontario, N9B 3P4, Canada.

出版信息

Faraday Discuss. 2021 Feb 1;225:358-370. doi: 10.1039/d0fd00004c. Epub 2020 Oct 22.

Abstract

Zr(iv) metal-organic frameworks (MOFs) UiO-68 and PCN-57, containing triphenylene dicarboxylate (TPDC) and tetramethyl-triphenylene dicarboxylate (TTDC) linkers, respectively, were doped with an H-shaped tetracarboxylate linker that contains a [2]rotaxane molecular shuttle. The new MOFs, UWDM-8 and UWDM-9, contain a [2]rotaxane crossbar spanning the tetrahedral cavities of the fcu topology while the octahedral cavities remain empty. C solid-state NMR (SSNMR) spectra and solution H NMR spectra verified that the [2]rotaxanes were included as designed. Variable-temperature (VT) cross polarization (CP) magic-angle spinning (MAS) C SSNMR was used to explore the translational motion of the macrocyclic ring in both MOFs. The SSNMR results clearly show that the structure of the linker (TPDCvs.TTDC) affects the shuttling rate of the macrocyclic ring, although questions remain as to how rotation of the central phenylene unit of the strut might also affect the motion of the macrocycle.

摘要

Zr(iv) 金属有机骨架(MOFs)UiO-68 和 PCN-57 分别含有联苯二甲酸(TPDC)和四甲基联苯二甲酸(TTDC)连接体,用含有[2]轮烷分子梭的 H 形四羧酸连接体掺杂。新的 MOFs UWDM-8 和 UWDM-9 包含一个横跨 fcu 拓扑的四面体腔的[2]轮烷横杆,而八面体腔仍然是空的。C 固体核磁共振(SSNMR)谱和溶液 H NMR 谱证实了[2]轮烷的包含是按设计进行的。变温(VT)交叉极化(CP)魔角旋转(MAS)C SSNMR 用于探索两种 MOF 中环的平移运动。SSNMR 结果清楚地表明,连接体的结构(TPDCvs.TTDC)影响大环的穿梭速率,尽管关于支柱中心苯单元的旋转如何也可能影响大环的运动仍存在疑问。

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